Plant Bioactive Metabolites and Drugs Produced by Endophytic Fungi of Spermatophyta

Nicoletti, Rosario; Fiorentino, Antonio

doi:10.3390/agriculture5040918

Open AccessReview

Plant Bioactive Metabolites and Drugs Produced by Endophytic Fungi of Spermatophyta

by

Rosario Nicoletti

^1,2,* and

Antonio Fiorentino

³

¹

Council for Agricultural Research and Economics. Rome 00185, Italy

²

Department of Agriculture, University Federico II of Naples, Via Università 100, Portici 80055, Italy

³

Department of Environmental Biological and Pharmaceutical Sciences and Technologies, Second University of Naples, Via Vivaldi 43, Caserta 81100, Italy

^*

Author to whom correspondence should be addressed.

Agriculture 2015, 5(4), 918-970; https://0-doi-org.brum.beds.ac.uk/10.3390/agriculture5040918

Submission received: 13 May 2015 / Revised: 17 September 2015 / Accepted: 21 September 2015 / Published: 29 September 2015

(This article belongs to the Special Issue Phytotoxic Fungal Metabolites)

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Abstract

:

It is known that plant-based ethnomedicine represented the foundation of modern pharmacology and that many pharmaceuticals are derived from compounds occurring in plant extracts. This track still stimulates a worldwide investigational activity aimed at identifying novel bioactive products of plant origin. However, the discovery that endophytic fungi are able to produce many plant-derived drugs has disclosed new horizons for their availability and production on a large scale by the pharmaceutical industry. In fact, following the path traced by the blockbuster drug taxol, an increasing number of valuable compounds originally characterized as secondary metabolites of plant species belonging to the Spermatophyta have been reported as fermentation products of endophytic fungal strains. Aspects concerning sources and bioactive properties of these compounds are reviewed in this paper.

Keywords:

plant-derived drugs; bioactive compounds; endophytic fungi

1. Introduction

Endophytic fungi are polyphyletic microorganisms that inhabit plant tissues without inciting disease symptoms, and eventually establish mutualistic associations with their host plants. Until recently these microbial entities have been generally overlooked as a component of ecosystems, the reason why lately they have been regarded as a trove of unexplored biodiversity. Investigations on the biosynthetic potential of endophytes have gained impetus owing to the ongoing discovery of strains capable to synthesize plant compounds, a property which may reflect an adaptative functional role in biocenosis. The intrinsic nature of the interactions among and between endophytes and host plants, and pests, which are mediated by such compounds, is an area open to future discoveries. The elucidation of such connections can not only enhance the understanding of evolution of complex defense mechanisms in plants and their associated organisms, but also help to exploit the latter for a sustained production of a few valuable compounds to be used in biotechnologies [1].

Secondary metabolites serve in multiple physiologic functions, many of which are common to both plants and microorganisms, and in a way it is intuitive that the same or similar compounds can be produced by ecologically associated entities. Thus, the aim to exploit botanical diversity for the discovery of novel drugs has led to the finding of microbial strains able to synthesize bioactive compounds previously considered as typical plant products. In the last 25 years, the general evidence that all plants are inhabited by endophytic microorganisms, together with an ongoing finding that the latter are also capable of producing plant metabolites, has depicted a research context which is more inclined to consider these compounds as a major factor influencing the establishment and evolution of mutualistic interrelations. Moreover, a refined tool enabling endophytes to regulate the metabolism of host plants in their delicately balanced association [2].

This paper offers an overview on the extremely varied assortment of organic molecules occurring as secondary metabolites both in plants and endophytic fungi. Our attention is particularly focused on products occurring in single or a restricted range of plant species, with a few exceptions. Therefore, compounds representing metabolic products of a wide array of organisms, such as carbohydrates, aliphatic compounds, aminoacids, peptides, nucleobases, phenolic and benzoic acids, tannins and pseudotannins, sterols, and carotenoids, are not treated in this review.

2. Phytohormones

Plant hormones are undoubtedly among the main secondary metabolites that can influence plant fitness and enhance development when exogenously administered. Many fungal species have been reported to be able to produce compounds such as indole-3-acetic acid (IAA) and gibberellins (GAs), particularly species inhabiting rhizosphere which are presumed to exert a consistent effect on plant development [3]. Likewise, the observation of such an aptitude by endophytic fungal strains, which in most instances establishes an even closer association with plant tissues, is indicative of a possible functional meaning of mutualistic relationships in certain associations, and provides ground for a more direct impact of an exogenous provision of phytohormones. Unlike what is generally thought for other products synthesized by both plants and endophytes, experimental findings have shown that biosynthetic pathways for these compounds may have evolved independently in plants and fungi [4,5].

The interaction of crop plants with endophytic fungi producing gibberellins could be exploited as a strategy to overcome the adverse effects of abiotic stresses, considering the increased plant growth and biomass production that have been documented even in extreme environmental conditions [6]. On the other hand, it must be considered that hormones are characterized by a dose-related effect, the reason why exceeding supplies may result into abnormal growth. In fact, gibberellins were discovered as products of the plant pathogenic fungus Fusarium (=Gibberella) fujikuroi inducing disease symptoms (elongation of internodes, leaf yellowing, etc.) in rice plants [7]. Until recently, a number of fungal plant pathogens have proved to be able to produce these phytohormones as a means for altering physiology of their hosts, but these cases are not a subject for this review. We also do not consider the complex case of the endophytic fungi inhabiting a series of fodder plants, which cause noxious effects to livestock because of their attitude to permeate host tissues with mycotoxins, and are also able to produce phytohormones [8,9,10]. A few excellent reviews on this bordering subject are available in the literature [11,12,13].

Production of IAA by fungi establishing a mutualistic relationship with plants was first evidenced by a few mycorrhizal species recovered from pine and orchid roots [14,15,16]. Afterwards it has been reported by strains of Colletotrichum sp. from Artemisia annua [17], Talaromyces verruculosus (=Penicillium verruculosum) from roots of Potentilla fulgens [18], and Penicillium glabrum from pomegranate (Punica granatum) fruits [19]. An isolate of the yeast Williopsis saturnus endophytic in maize roots was found to produce IAA and indole-3-pyruvic acid [20]. Finally, IAA is also produced by Piriformospora indica [21], the quite famous Basidiomycetes species first described as a mycorrhizal agent of shrubs growing in the Rajahstan desert [22], but later found to be widespread and able to colonize roots of many host plants, disclosing a potential for applications in crop production [23]. However, all these reports should be carefully verified considering the growth medium used for culturing the producing strains; in fact, it has been observed that the addition of tryptophan incited auxin synthesis by a couple of yeast strains of Rhodotorula graminis and R. mucilaginosa recovered from poplar stems [24].

Other endophytic fungi have been found to produce both IAA and GAs, such as two strains of Fusarium sp. from Euphorbia pekinensis [25]. Moreover, a strain of Galactomyces geotrichum isolated from the aquatic plant Trapa japonica produced IAA and biologically active GAs (GA₁, GA₄, and GA₇) [26], while two strains from cucumber roots (Phoma glomerata and Penicillium sp.) were found to produce gibberellic acid (GA₃) along with GA₁, GA₄, GA₇, and IAA in Czapek-Dox broth. This medium is based on sucrose as the only organic compound, which demonstrates an intrinsic ability by these strains to synthesize phytohormones. When experimentally inoculated in cucumber plants under drought stress, the plant biomass and related growth parameters significantly increased, together with a higher assimilation of essential nutrients (K, Ca and Mg), while effects of sodium toxicity were reduced. Moreover, a modulation of stress was also ensured through alteration in jasmonic acid level, down-regulation of abscissic acid, and increased salicylic acid content [27]. Similar effects resulted in the evaluation of another cucumber endophytic strain (Paecilomyces formosus) by the same research group [28].

Production of GAs only has been documented in a higher number of endophytic fungi. A strain of Fusarium proliferatum from roots of Physalis alkekengi var. francheti displayed a plant growth-promoting activity twice stronger than a wild-type of F. fujikuroi, due to the production of the physiologically active GA₁, GA₃, GA₄, and GA₇, along with GA₉, GA₂₀ and GA₂₄ [29]. Another strain of F. proliferatum from orchid roots was found to produce GA₄ and GA₇ as the major forms, and smaller amounts of GA₁, GA₃, GA₉, GA₁₃, GA₁₄, GA₁₆, GA₂₄, GA₂₅, and GA₃₆, together with additional side products in the GA-biosynthetic pathway [30]. A strain of Scolecobasidium tshawytschae from soybean produced GA₃ together with both active (GA₁, GA₄, and GA₇) and inactive (GA₁₅ and GA₂₄) analogs [31]. Root isolates of Penicillium citrinum from the dune plant Ixeris repens [32], and Arthrinium phaeospermum from a sedge species (Carex kobomugi) [33] both produced GA₁, GA₃, GA₄, and GA₇, along with inactive forms (GA₅, GA₉, GA₁₂, GA₁₅, GA₁₉, GA₂₀, and GA₂₄). Strains of Aspergillus fumigatus, Cladosporium sphaerospermum and Talaromyces funiculosus (=Penicillium funiculosum) from soybean were found to produce bioactive GAs (respectively G₄, G₉, and G₁₂ the former; GA₃, GA₄, and GA₇ the intermediate; GA₁, GA₄, GA₈, and GA₉ the latter), besides the inactive GA₅, GA₁₅, GA₁₉, and GA₂₄ [34,35,36,37]. Another strain of Penicillium sp. from crown daisy (Chrysanthemum coronarium) was found to promote shoot elongation due to the production of all bioactive GAs (GA₁, GA₃, GA₄, GA₇), along with a few inactive forms (GA₉, GA₁₂, GA₁₅, GA₁₉, GA₂₀) [38]. Finally, GA₃ has been reported as a fermentation product of an unidentified endophytic strain from Curcuma wenyujin [39].

Cytokinins are a group of N⁶-substituted adenine derivatives influencing cell division, vascular development, apical dominance, stress tolerance and leaf senescence. Besides several mycorrhizal fungi reported to contribute to cytokinine levels of roots [40,41], production of these phytohormones has been well documented in the above-mentioned P. indica. In fact, relatively high levels of isopentenyladenine and cis-zeatins can be found in liquid cultures of this fungus, and accordingly the cytokinine levels are remarkably higher in roots of inoculated plants. Conversely, auxin levels are not influenced despite the ability by P. indica to produce this phytohormone as well, in connexion with the hypotesized conversion of some IAA into inactive compounds [42].

Finally, it must be mentioned that production of IAA, GA, abscisic acid and jasmonic acid in several combinations was observed by a pool of unidentified endophytic fungi recovered from five plants used in Indian ethnomedicine, Camellia caduca, Osbeckia chinensis, Osbeckia stellata, Potentilla fulgens, and Schima khasiana [43].

3. Compounds from Essential Oils

Essential oils of plants have a very varied chemical composition, including over 60 different kinds of volatile molecules which can be extracted by distillation and belong to two main groupings, terpenes and aromatic products. Besides contributing to the scent of plants, many of these compounds present interesting bioactive properties, ranging from antibiotic to antitumor effects [44]. The ability to produce such volatile antibiotics has stimulated to investigate several endophytic strains for their possible use in the so-called mycofumigation of foodstuffs [45,46,47]. Additional prospects for biotechnological applications reside in their use as flavoring agents in the food industry [48], and even as biofuels [49]. Not surprisingly, many compounds known from essential oils have been also found as secondary metabolites of endophytic fungi (Table 1), and novel molecules are more and more characterized as fermentation products of these strains, indicating their effective role in determining the mixture composition.

Table 1. Components * of essential oils of plants extracted from fungal endophytic strains.

**Table 1.** Components * of essential oils of plants extracted from fungal endophytic strains.
Compounds		Producing Species	Host Plants	Reference
Phenyl propanes
Asarone		Muscodor tigerii	Cinnamomum camphora	[50]
Eugenol		Annulohypoxylon stygium	not specified	[51]
Eugenol		Alternaria sp.	Rosa damascaena	[52]
Monoterpenes
Camphor		Nodulisporium sp.	Lagerstroemia loudoni	[47]
Carene		Meliniomyces variabilis	Pinus sylvestris	[53]
Carene		Nodulisporium sp.	L. loudoni	[47]
Cineole (eucalyptol)		Nodulisporium sp.	Persea indica	[54]
			L. loudoni	[47]
			Cassia fistula	[55]
Limonene		unknown Sordariomycetes	Mentha piperita	[56]
		Wickerhamomyces anomalus	Lactuca sativa	[57]
		Nodulisporium sp.	L. loudoni	[47]
		Nigrograna mackinnonii	Guazuma ulmifolia	[58]
Myrcene		W. anomalus	L. sativa	[57]
Myrcene		Nodulisporium sp.	L. loudoni	[47]
Ocimene		W. anomalus	L. sativa	[57]
Ocimene		Nodulisporium sp.	L. loudoni	[47]
Phellandrene		Muscodor fengyangensis	Actinidia chinensis, Pseudotaxus chienii	[59]
		Muscodor yucatanensis	Bursera simaruba	[60]
		unidentified strains	“weed grasses”	[61]
		Muscodor sp.	O. granulata	[62]
Pinane		Nodulisporium sp.	L. loudoni	[47]
Pinene		unknown Sordariomycetes	M. piperita	[56]
		M. variabilis, Phialocephala fortinii	P. sylvestris	[53]
		W. anomalus	L. sativa	[57]
		N. mackinnonii	G. ulmifolia	[58]
Sabinanes (thujanes)	Dihydroxysabinane	Phomopsis sp.	Camptotheca acuminata	[63]
	Sabinene (thujene)	Phomopsis sp.	Odontoglossum sp.	[64]
		W. anomalus	L. sativa	[57]
		Nodulisporium sp.	L. loudoni	[47]
Terpinene, terpineol		Nodulisporium sp.	L. loudoni	[47]
Terpinene, terpineol		N. mackinnonii	G. ulmifolia	[58]
Diterpenes
Abietadiene		Xylaria sp.	Cupressus lusitanica	[65]
Totarol		Xylaria sp.	C. lusitanica	[65]
Sesquiterpenes
Acoradiene		Phomopsis sp.	Odontoglossum sp.	[64]
Aristolene		M. yucatanensis	B. simaruba	[60]
Aromadendrene, isoledene		M. yucatanensis	B. simaruba	[60]
		Phoma sp.	Larrea tridentata	[66]
		Xylaria sp.	C. lusitanica	[65]
Bisabolene		M. fengyangensis	A. chinensis, P. chienii	[59]
Bisabolene		Xylaria sp.	C. lusitanica	[65]
Bisabolol		Muscodor kashayum	Aegle marmelos	[67]
Cadinanes	Cadalenes, calamenenes	Phomopsis cassiae	Cassia spectabilis	[68]
	Bombamalone D, calamenenes, dysodensiol D, indicumolide C	Phomopsis sp.	Pleioblastus amarus	[69]
	Cadinene, amorphene, muurolene	Phoma sp.	L. tridentata	[66]
	Cadinene, amorphene, muurolene	Xylaria sp.	C. lusitanica	[65]
	Cubenol	Xylaria sp.	C. lusitanica	[65]
Carotol		M. tigerii	C. camphora	[50]
Caryophyllane		Xylaria sp.	C. lusitanica	[65]
Caryophyllene (humulene)		Muscodor albus	Cinnamomum zeylanicum	[45]
		Muscodor albus	G. ulmifolia	[70]
		M. fengyangensis	A. chinensis, P. chienii	[59]
		M. yucatanensis	B. simaruba	[60]
		M. variabilis, P. fortinii	P. sylvestris	[53]
		Phoma sp.	L. tridentata	[66]
Isocaryophyllene		Muscodor sutura	Prestonia trifidi	[71]
Presilphiperfolanes		Xylaria sp.	Piper aduncum	[72]
Cedranes	Cedrene, cedrol	Xylaria sp.	C. lusitanica	[65]
Cedranes	Diepicedrene-1-oxide	M. fengyangensis	A. chinensis, P. chienii	[59]
Chamigrene		Phoma sp.	L. tridentata	[66]
Chamigrene		M. sutura	P. trifidi	[71]
Cuparene		unknown Sordariomycetes	M. piperita	[56]
Drimanes	Albicanol	Perenniporia tephropora	Taxus chinensis var. mairei	[73]
Drimanes	Hydroxyconfertifolin	Phomopsis sp.	Rhizophora stylosa	[74]
β-Elemene		Nodulisporium sp.	Cinnamomum loureirii	[46]
		M. yucatanensis	B. simaruba	[60]
		Penicillium baarnense, Penicillium frequentans	Curcuma zedoaria	[75]
Eremophilanes	Eremophilanolides	Xylaria sp.	Licuala spinosa	[76]
	Isopetasols	unidentified strain	Picea rubens	[77]
	Mairetolide A	Xylaria sp.	C. lusitanica	[78]
	Mairetolide F	Xylaria sp.	L. spinosa	[76]
	Valencene	M. albus	C. zeylanicum	[45]
			unidentified vine plant	[79]
			Oryza granulata	[62]
		Xylaria sp.	C. lusitanica	[78]
Eudesmanes, eudesmenes (selinenes)		Eutypella sp.	Etlingera littoralis	[80]
		Nodulisporium sp.	C. loureirii	[46]
		Phoma sp.	L. tridentata	[66]
		Xylaria sp.	C. lusitanica	[65]
Arundinols, arundinones		Microsphaeropsis arundinis	Ulmus macrocarpa	[81]
Capitulatin B, hydroxycapitulatin B		Nigrospora oryzae	Aquilaria sinensis	[82]
Farnesene		Xylaria sp.	C. lusitanica	[65]
Guaianes: guaiene, guaiol (champacol), aciphyllene, bulnesene, gurjunene		M. albus	unidentified vine plant	[79]
			C. zeylanicum	[45]
			Myristica fragrans	[83]
			G. ulmifolia	[70]
		Phoma sp.	L. tridentata	[66]
		Xylaria sp.	C. lusitanica	[65]
Himachalene		Phoma sp.	L. tridentata	[66]
Irones		Rhizopus oryzae	Iris germanica	[84]
Longicyclene		M. variabilis, P. fortinii	P. sylvestris	[53]
Longifolenes		M. yucatanensis	B. simaruba	[60]
		P. fortinii	P. sylvestris	[53]
		Xylaria sp.	C. lusitanica	[65]
Longipinene		Phoma sp.	L. tridentata	[66]
Occidentalol		Xylaria sp.	C. lusitanica	[65]
Thujopsanol, thujopsene		Xylaria sp.	C. lusitanica	[65]
Thujopsanol, thujopsene		M. sutura	P. trifidi	[71]
Ylangene		Phoma sp.	L. tridentata	[66]
Zingiberene		Xylaria sp.	C. lusitanica	[65]

* Not including fatty acids and their methyl esters.

Within the several groups of sesquiterpenes occurring in essential oils, the eremophilanes are particularly widespread among endophytic fungi, and many novel molecules of this series have been first discovered as their fermentation products (Table 2). It is quite interesting to note that eremophilanes include compounds with phytotoxic effects, such as phaseolinone and phomenone which are also known from an endophytic strain of Xylaria sp. from the matico tree (Piper aduncum) [72].

Table 2. Eremophilane compounds first characterized from endophytic fungal strains.

**Table 2.** Eremophilane compounds first characterized from endophytic fungal strains.
Compounds	Producing Species	Host Plants	Reference
Botryosphaeridione	Phoma sp.	Melia azedarach	[85]
Cupressolides A-B	Xylaria sp.	Cupressus lusitanica	[78]
Dihydroberkleasmin A	Pestalotiopsis photiniae	Podocarpus macrophyllus	[86]
Eremoxylarins A-B	xylariaceous fungus	not specified	[87]
MBJ-0011-13	Apiognomonia sp.	not specified	[88]
Periconianone B	Periconia sp.	Annona muricata	[89]
Pestalotiopsin A-B	P. photiniae	P. macrophyllus	[90]
Phomadecalins	Microdiplodia sp.	Pinus sp.	[91]
unnamed compounds	Xylaria sp.	Licuala spinosa	[76]
unnamed compounds	Xylaria sp.	mangrove plant	[92]
Xylarenones	Xylaria sp.	Torreya jackii	[93]
Xylarenones	Camarops sp	Alibertia macrophylla	[94,95]

Data introduced in the above tables are eventually incomplete, due to the ongoing addition of novel findings concerning the direct and indirect influence of endophytic fungi on the composition of essential oils, and ensuing effects on their biological activities. The resulting complex framework and the intriguing applicative perspectives are possibly indicative of the opportunity of a dedicated review for such a hot research topic. A recent one that can be cited here [96] is limited to sesquiterpenes, and not specifically addressed to fungal endophytes.

Another interesting finding on terpenoids from essential oils concerns a few such compounds, namely aristolene, guaiene and thujopsene, produced by strains of Daldinia spp. establishing symbiotic relationships with Xiphydria woodwasps on a number of tree species [97]. In a strict sense, these fungi cannot be considered endophytic since they are inoculated by the wasps and colonize the galleries excavated by their larvae. However, their belonging to the Xylariaceae, a group including Xylaria, Hypoxylon, Muscodor and Nodulisporium which are well-known for their endophytic habit, stimulates the appraisal of the ecological role held by these compounds in the identification of the host plant and the establishment of this particular symbiotic relationship, and to consider their possible relevance in other plant-insect interactions.

Finally, the effect of endophytic fungal strains in modifying the pattern of compounds in the essential oils of plants may have intriguing interactions with crop resistance/susceptibility toward pests. As an example, it has been observed that tomato plants harboring an unspecialized endophyte (Acremonium strictum), which remarkably influences composition of volatile compounds released by the host, are significantly preferred by adult whiteflies (Trialeurodes vaporariorum) [98], and for oviposition by the cotton bollworm (Helicoverpa armigera) [99]. Therefore, any factors influencing composition of essential oils may be considered in view of enhancing plant protection.

4. Other Terpenoids

Sesquiterpene lactones present some affinity with a few analog components of essential oils, such as guaianes and eudesmanes. Within this category, loliolide (Figure 1), first characterized from Lolium perenne [100], has been reported from a strain of Annulohypoxylon ilanense from the wood of a plant of Cinnamomum sp. [101]. Xanthatin (Figure 1), first isolated from cockleburs (Xanthium spp.) and characterized for its antimicrobial, anti-inflammatory, pro-apoptotic and trypanocidal properties [102,103], has been recovered from cultures of a strain of Paecilomyces sp. from Panax ginseng [104]. Moreover, dihydrocumambrin A (Figure 1), known as a secondary metabolite of Glebionis coronaria (=Chrysanthemum coronarium), has been recently extracted as a fermentation product of a strain of Lasiodiplodia (=Botryodiplodia) theobromae endophytic in leaves of Dracaena draco [105].

Figure 1. Structures of some terpenoids produced by endophytic fungi.

Ginkgolides are diterpenoid lactones known as secondary metabolites of G. biloba which are considered, particularly ginkgolide B, as prospect drugs based on documented antagonistic effects against the platelet-activating factor involved in a number of inflammatory disorders. Ginkgolides A-C and the related compound bilobalide (Figure 1) have been found as fermentation products of an endophytic strain of Fusarium oxysporum recovered from root bark of this living fossil tree [106].

More terpenoid compounds can be found in oleoresins of certain plants. Agathic acid is a diterpenoid representing the major component of the oleoresin of Agathis microstachya, an endangered species belonging to the Araucariaceae endemic to Queensland (Australia) [107], and more recently found in oleoresin of copaiba (Copaifera spp.) in the Amazon region [108]. It has been extracted from cultures of a strain of Botryosphaeria sp. endophytic in leaves of Maytenus hookeri, together with the related isocupressic acid which is commonly found in the needles of several coniferous species [109]. These compounds have been reported for an abortive effect on cows [110], while agathic acid is also known for some extent of trypanocidal activity [108].

Limonoids are tetranortriterpenes reported from members of Rutaceae and Meliaceae, among which the azadirachtins are best known and exploited for their insecticidal properties [111]. Azadirachtins A and B (Figure 2) have been recently extracted from cultures of a strain of Penicillium (Eupenicillium) parvum endophytic in the neem plant (Azadirachta indica) [112]. However, the importance of endophytes in the biosynthesis of these plant products may be more substantial, considering that an endophytic Penicillium strain from the chinaberry tree (Melia azedarach), which is another source of azadirachtin, has been reported to produce the austins [113], a series of meroterpenoids which may share the same biosynthetic pathway.

The structurally-related toosendanin (Figure 2) extracted from fruits and bark of Melia toosendan, possibly a synonym of M. azedarach which is used as an anti-helmintic remedy in the Chinese traditional medicine, has been also characterized with reference to its insecticidal effects deriving from antifeedant and growth regulatory properties [111]. Three unidentified strains endophytic in M. azedarach have been found to produce this compound [114], whose possible exploitation as an antitumor drug has been recently envisaged [115].

Figure 2. Structures of azadirachtins and toosendanin.

5. Coumarins

Additional metabolites occasionally found in essential oils, such as bergapten, can be ascribed to the coumarins, a heterogeneous class of natural products whose molecular structure is based on a benzopyran-2-one (Figure 3). These compounds are widespread in edible plants, therefore commonly assumed through dietary exposure, and considered interesting prospects for a pharmaceutical exploitation due to their antioxidant, anti-inflammatory, anticoagulant, antimicrobial, anticancer, antihypertensive, antihyperglycemic, and neuroprotective properties [116,117]. A number of these compounds primarily known from plants have recently started being reported as metabolites of endophytic fungi, such as coumarin found in extracts of strains of Alternaria spp., Penicillium spp. and Aspergillus flavus from the annual herb Crotalaria pallida [118].

Scopoletin (6-methoxy-7-hydroxycoumarin) is reported from several plants, where it is possibly involved in protection against pathogens due to its antimicrobial properties [119]. This compound has been isolated from a mangrove endophytic strain of Penicillium sp., together with bergapten and umbelliferone (7-hydroxycoumarin) [120]. Scopoletin, umbelliferone and 7-O-prenylumbelliferone, along with additional coumarins known from several plant species such as angelicin, brosiparin, columbianetin, jatamansinol, osthenol and seselin, have been recently extracted from cultures of an endophytic strain of A. ilanense [121]. Moreover, marmesin has been reported from a mangrovial endophytic strain of Fusarium sp. [122], while bergapten and meranzin have been extracted as fermentation products of a previously-mentioned isolate of L. theobromae from D. draco [105].

Within dihydroisocoumarins, mellein derives its name by a strain of Aspergillus melleus from which it was first characterized [123]. It is quite a common fungal metabolite, together with a number of derivatives [124]. However, several products in this series have been also directly reported from plants [125,126]. Examples of compounds produced by both plants and endophytic strains include 7-hydroxymellein extracted from cultures of a strain of Penicillium sp. associated to Alibertia macrophylla [127] and a strain of Xylaria cubensis derived from leaves of Litsea akoensis [128], and mellein itself from a strain of Nigrospora sp. from the benzoil tree (Moringa oleifera) [129]. Another xylariaceous fungus from fruits of the wingleaf soapberry (Sapindus saponaria) [130], and a strain of Annulohypoxylon squamulosum from Cinnamomum sp. [131] produced both compounds. Finally, a few mellein derivatives have been found together with isofraxidin (7-hydroxy-6,8-dimethoxycoumarin) as fermentation products of an endophytic strain of Annulohypoxylon bovei var. microspora from bark of Cinnamomum sp. [132].

Figure 3. Structures of coumarins produced by endophytic fungi.

6. Flavonoids

Commonly associated to coumarins for their fundamental antioxidant properties, flavonoids also display consistent anti-inflammatory, antibacterial, antiviral, antitumor, and vasodilatatory effects [133]. These polyphenolic compounds are widespread in plants where they represent a biochemical mechanism in pre- and post-infection resistance against pathogens [134]. Their structure consists of two benzene rings at either side of a 3-carbon ring, and multiple substitutions in this fundamental frame originate several classes of derivatives, such as flavones, isoflavones, flavonols, flavanones, catechins, and anthocyanins (Figure 4). Such a variation, and the concomitant occurrence of several compounds belonging to this class is the reason why many reports dealing with their production by endophytic fungal strains consider the total flavonoid content rather than every single product [135,136]. When a more detailed analysis is carried out, a complex pattern of metabolites in this series results; this is the case of a strain of A. ilanense producing kaempferol, quercetin, genkwanin, (+/−)-catechin, (−)-4′-hydroxy-5,7,3′-trimethoxyflavan-3-ol, tectochrysin (5-hydroxy-7-methoxyflavone), dimethylgalangin (3,7-dimethoxy-5-hydroxyflavone), and 5-hydroxy-3,6,7-trimethoxyflavone [121], and a strain of Fusarium sp. producing tectorigenin (6-methoxy-5,7,4′-trihydroxyisoflavone) and a few more isoflavones [122].

Figure 4. Structures of flavonoids produced by endophytic fungi.

Kaempferol has been more frequently mentioned as a fermentation product of endophytic fungi, such as a strain of Mucor fragilis from rhizomes of Sinopodophyllum hexandrum [137], a strain of Fusarium chlamydosporum from stem of Tylophora indica (Asclepiadaceae) [138], and a previously-mentioned unidentified strain from C. wenyujin [39]. It has been also found together with quercetin in the above-mentioned strain of A. squamulosum [131], and in a strain of A. bovei var. microspora together with kaempferitrin and luteolin [139]. A widespread plant metabolite with putative cancer chemopreventive and therapeutic properties [140], luteolin has been also reported as a secondary metabolite of an endophytic strain of A. fumigatus from the pigeon pea (Cajanus cajan), which itself is known as a source of this phytoestrogen [141].

Cajanol is another isoflavone from roots of C. cajan displaying antimicrobial properties, and pro-apoptotic activity resulting in assays against human breast cancer cells [142]. Endophytic strains of Hypocrea lixii from roots of C. cajan have also been reported to produce this compound in liquid cultures [143]. Another endophytic fungus from C. cajan, Chaetomium globosum, has been reported to produce apigenin (4′,5,7-trihydroxyflavone) [144]. Its glycosidic derivative vitexin (apigenin-8-C-β-d-glucopyranoside) has been found as a fermentation product of a strain of Colletotrichum sp. endophytic in G. biloba [145]. More glycosidic derivatives, namely apigenin-5-O-α-l-rhamnopyranosyl-(1→3)-β-d-glucopyranoside and euryanoside (apigenin-5-O-α-l-rhamnopyranosyl-(1→2)-(6″-O-acetyl)-β-d-glucopyranoside), have been detected as transformation products by a strain of Paraconiothyrium variabile endophytic in the Japanese plum yew (Cephalotaxus harringtonii) growing on crude extracts of the same plant, by which these compounds had been previously reported [146].

Rotenone is one of the oldest known bioactive plant metabolites, extracted from roots of tropical Leguminosae such as Lonchocarpus spp., Tephrosia spp., Mundulea spp., Dalbergia paniculata and Derris elliptica [147]. An unidentified Penicillium strain from the latter plant has been reported to produce this compound or a structural analog [148].

Silymarin is a bioactive extract of the fruits of milk thistle (Silybum marianum), containing seven flavolignans with reported antitumor and hepatoprotective properties [149,150]. Three of these compounds, silybin A, silybin B, and isosilybin A have been extracted as fermentation products of a strain of Aspergillus iizukae isolated from the leaves of S. marianum. Interestingly, flavonolignan synthesis attenuated after repeated subculturing of this strain, but could be resumed when autoclaved leaves of the host plant were added to the growth medium [151].

The chalcones (benzalacetophenones) are involved in flavonoid biosynthesis in plants through an isomerization process promoted by the enzyme chalcone flavanone isomerase [152]. These compounds exhibit notable bioactive properties [153], and significant anti-cancer effects [154]. An endophytic strain of Ceriporia lacerata has been found to produce 2′,4′-dihydroxy-6′-methoxy-3′,5′-dimethylchalcone first extracted from its host plant Cleistocalyx operculatus (=Eugenia operculata or Syzygium operculatum) [155].

7. Xanthones and Quinones

With a number of pharmaceutical applications, xanthones (Figure 5) are structurally related to flavanoids, and also commonly recovered from both plant and fungal sources [156]. With reference to endophytic fungi, a mangrovial strain of Penicillium sp. has been found to produce 1,7-dihydroxyxanthone [120], primarily known for its antimalarial properties and reported as a secondary metabolite of plants such as Weddellina squamulosa (Podostemaceae) and several species in the Guttiferae [157,158].

Figure 5. Structures of xanthones produced by endophytic fungi.

Pinselin was initially characterized from a strain of Penicillium amarum, but later found to be identical to cassiollin reported from Cassia occidentalis [159]. This metabolite has been found as a fermentation product of a strain of Phomopsis sp. endophytic in rhizome of Paris polyphylla var. yunnanensis [160], together with additional xanthones including 6-O-methyl-2-deprenylrheediaxanthone B, previously extracted from bark of Garcinia vieillardii [161].

Fairly widespread as plant metabolites and widely used as dyes in the textile industry, anthraquinones are believed to contribute to the defense against pests and disease agents, based on their antifungal, antibacterial and insecticidal properties [162]. Several compounds in this class are also known from endophytic fungi (Figure 6). Emodin, physcion and citreorosein, found in several plant species such as rhubarb (Rheum spp.) [163], Cassia spp. [164], and Polygonum cuspidatum [165,166], are also produced by heterologous endophytic strains of Penicillium spp. (e.g., P. herquei, P. janthinellum) [167,168,169]. Emodin has been also reported from a strain of Talaromyces sp. from the mangrove Kandelia candel [170], while physcion was also extracted from cultures of an unidentified strain from the mangrove Avicennia marina [171], and of strains of A. fumigatus from Cynodon dactylon [172], and Aspergillus terreus from Opuntia ficus-indica [173]. Quinizarin known from roots of the madder plant (Rubia tinctorum) [174], has been reported as a secondary metabolite of a previously-mentioned unidentified strain from C. wenyujin [39]. Endocrocin, reported from roots of Rumex nepalensis [175], has recently been found to be produced by an endophytic strain of Pestalotia (Pestalotiopsis) acaciae [176]. Questinol and questin are known from Polygonum spp. [177] and again from Cassia spp. [164]. The former compound has been detected in the culture extracts of strains of Eurotium rubrum from the mangrove Hibiscus tiliaceus [178] and P. glabrum from pomegranate fruits [19], while the latter has been reported as a metabolite of an unidentified strain belonging to the Dothideomycetes from the Thai medicinal plant Leea rubra. This strain also produces the biosynthetically related chromone derivative eugenitin, previously extracted as a secondary metabolite of clove (Syzygium aromaticum), and its analog 6-hydroxymethyleugenitin [179]. A strain of Phoma sorghina endophytic in the medicinal plant Tithonia diversifolia [180] has been found to produce pachybasin and phomarin, known as secondary metabolites of species in the Scrophulariaceae, such as Digitalis spp. [181] and Isoplexis isabelliana [182], and 1,7-dihydroxy-3-methylanthraquinone, first extracted from leaves of Digitalis viridiflora [183]. Once again, the three latter compounds have been more recently extracted from cultures of a strain of Coniothyrium sp. endophytic in Salsola oppostifolia [184]. Finally, pachybasin has been also reported from an unidentified strain from the yellow moonshed (Arcangelisia flava) [185].

Hypericin, a secondary metabolite of St. John’s wort (Hypericum perforatum) and other congeneric species, has been extensively studied for its antidepressant, antiviral and antitumor properties. In combination with light the compound effectively induces apoptosis and/or necrosis of cancer cells, the reason why it has been exploited for the photodynamic therapy of cancer [186]. Hypericin has been found as a metabolic product of an endophytic strain of Thielavia subthermophila isolated from H. perforatum in India, together with the above-mentioned emodin considered as a possible precursor [187,188].

Figure 6. Structures of anthraquinones produced by endophytic fungi.

Sterequinone C, primarily extracted from bark of the Ayurvedic medicinal plant Stereospermum personatum [189], has been more recently found as a metabolite of an unidentified strain of Penicillium sp. from leaf of the mangrove Avicennia [120].

The tanshinones are diterpenoid quinones from roots and rhizomes of danshen (Salvia miltiorrhiza) and other Salvia spp. exerting antioxidant, anti-inflammatory and antitumor effects [190]. These compounds have been also extracted from endophytic strains of the same plant, particularly TR21 of Emericella foeniculicola [191], and D16 of Trichoderma atroviride [192]. Polysaccharides from the mycelium of the latter strain were found to elicit root growth and tanshinone production [193]. Moreover, a previously-mentioned strain of Paecilomyces sp. from P. ginseng has been found to produce isotanshinone [104].

Shikonin is a pigment of the Chinese therapeutic herb zicao (Lithospermum erythrorhizon) with a naphthoquinone structure, displaying interesting pharmacological activities based on its anti-inflammatory, antigonadotropic, anti-HIV and antitumor properties [194]. This compound has been recently recovered from extracts of an endophytic strain from roots of the old lady cactus (Mammillaria hahniana) [195]. Lapachol is another naphthoquinone derivative originally extracted from the bark of the lapacho tree (Handroanthus impetiginosus, syn. Tabebuia avellanedae), but later found in plants belonging to different botanical families. It is an active principle in lapacho used in ethnomedicine by indigenous populations of South America, and reported for a wide range of pharmacological activities [196]. Endophytic strains of Alternaria sp., A. alternata, A. niger and Penicillium sp. from the silver trumpet tree (Tabebuia argentea) have been found to produce this compound [197,198].

8. Lignans

Quite widespread as plant metabolites [199], the podophyllotoxins and related cyclolignans have been also characterized for their insecticidal effects [200,201]. However, the higher reputation for podophyllotoxin (Figure 7) and a few synthetic derivatives relies on their pharamacological applications, particularly as antitumor drugs [199,202]. These products have also been reported from an increasing number of endophytic fungi, such as Alternaria sp. from S. hexandrum [203] and Juniperus communis (=J. vulgaris) [204], Penicillium spp. from S. hexandrum, Diphylleia sinensis and Dysosma veitchii [203], Phialocephala fortinii from Podophyllum peltatum [205], Trametes hirsuta, Fusarium solani and M. fragilis from S. hexandrum [137,206,207], and F. oxysporum from Juniperus recurva [208]. Moreover, deoxypodophyllotoxin has been reported from a strain of A. fumigatus endophytic in J. communis [209].

Phillyrin (Figure 7) is another lignan displaying antioxidant, anti-inflammatory and antipyretic activities, known from Phyllirea and a number of medicinal plants such as Forsythia suspensa, a shrub used in Chinese traditional medicine [210]. An endophytic strain of Colletotrichum gloeosporioides from a fruit of this plant was found to produce phillyrin in liquid cultures [211]. Other lignans known from several plant species, such as sesamin, syringaresinol and ketopinoresinol (Figure 7), have been recently found as secondary metabolites of an endophytic strain of A. ilanense [121].

Figure 7. Structures of lignans produced by endophytic fungi.

9. Taxol and Taxanes

Taxol, also known as paclitaxel, is probably the most valuable compound in this review, at least considering its notoriety as the first billion-dollar anticancer drug. Temporarily set aside in chapter 4 concerning terpenoids, this diterpene compound presenting an unusual oxytane ring and a tricyclic core (Figure 8) was originally characterized from bark of the Pacific yew (Taxus brevifolia) [212], but later found in all other yew species [213]. Problems for an adequate pharmaceutical supplying were soon evident, and the need to find alternative sources lead to the discovery of the first endophytic fungal strain able to synthesize this compound, isolated from the inner bark of T. brevifolia and ascribed to the novel species Taxomyces andreanae [214]. This discovery was followed by an ongoing series of similar findings from yews, but also from other plants species, attaining to a provisional number of almost 100 reports of endophytic strains belonging to 72 fungal species from 32 different host plants, as listed in Table 3. However, these figures are underestimated, considering that we have not been able to check a number of reports from China and other Asian countries. Whether or not one or more of such strains can be effectively employed by the pharmaceutical industry is still under debate [1,215], and treating this theme goes beyond the scopes of this review. Nevertheless, there is no doubt that the issue of taxol production by endophytic fungi has stimulated a wide research activity concerning drugs and other reputed bioactive compounds extracted from plants, introducing new insights in the appreciation of the microbial component of biodiversity and the opportunity of its exploitation for human wellness.

Figure 8. Structures of taxol and baccatins.

Table 3. Endophytic fungi reported for production of taxol.

**Table 3.** Endophytic fungi reported for production of taxol.
Species	Host plants	Reference
Acremonium sp.	Taxus globosa	[216]
Alternaria sp.	Taxus cuspidata Ginkgo biloba Corylus avellana	[217] [218] [219]
Aspergillus candidus	Taxus × media	[220]
Aspergillus fumigatus	Podocarpus sp.	[221]
Aspergillus niger var. taxi	T. cuspidata	[222]
Aspergillus sp.	Taxus chinensis	[223]
Bartalinia robillardoides	Aegle marmelos	[224]
Botryosphaeria sp.	T. globosa	[216]
Botrytis sp.	T. chinensis var. mairei T. cuspidata	[225] [226]
Ceratobasidium sp.	T. chinensis	[223]
Chaetomella raphigera	Terminalia arjuna	[227]
Cladosporium cladosporioides	T. media	[228]
Cladosporium oxysporum	Moringa oleifera	[229]
Cladosporium tenuissimum	T. chinensis	[223]
Colletotrichum gloeosporioides	Justicia gendarussa Plumeria acutifolia T. media Tectona grandis M. oleifera	[230] [231] [232] [233] [234]
Colletotrichum sp.	Maguireothamnus speciosus	[235]
Coniothyrium diplodiella	T. chinensis	[223]
Didymostilbe sp.	T. chinensis var. mairei	[236]
Ectostroma sp.	T. chinensis var. mairei	[225]
Epacris sp.	T. chinensis	[223]
Fusarium arthrosporioides	T. cuspidata	[237]
Fusarium lateritium	Taxus baccata	[217]
Fusarium mairei	T. chinensis var. mairei	[238]
Fusarium oxysporum	Rhizophora annamalayana	[239]
Fusarium proliferatum	T. media	[232]
Fusarium redolens	Taxus wallichiana	[240]
Fusarium solani	Taxus celebica T. chinensis	[241] [242]
Fusarium sp.	T. wallichiana T. globosa	[243] [216]
Gliocladium sp.	T. baccata	[244]
Guignardia mangiferae	T. media	[232]
Gyromitra sp.	T. globosa	[216]
Lasiodiplodia theobromae	Morinda citrifolia T. baccata	[245] [246]
Metarhizium anisopliae	T. chinensis	[223]
Monochaetia sp.	T. baccata	[217]
Mucor rouxianus	T. chinensis	[247]
Mucor sp.	T. chinensis var. mairei	[248]
Nigrospora sp.	T. globosa	[216]
Nodulisporium sylviforme	T. cuspidata	[249]
Ozonium sp.	T. chinensis var. mairei	[250]
Paraconiothyrium brasiliense	T. chinensis	[223]
Paraconiothyrium sp.	T. media	[251]
Penicillium aurantiogriseum	C. avellana	[252]
Penicillium raistrickii	Taxus brevifolia	[253]
Penicillium sp.	Taxus yunnanensis (=T. wallichiana) T. globosa T. chinensis	[254] [216] [255]
Periconia sp.	Torreya grandifolia	[256]
Pestalotia bicilia	T. baccata	[217]
Pestalotia pauciseta	Cardiospermum helicacabum Tabebuia pentaphylla	[257] [258]
Pestalotiopsis guepinii	Wollemia nobilis	[259]
Pestalotiopsis microspora	T. cuspidata, T. wallichiana Taxodium distichum	[260] [261]
Pestalotiopsis neglecta	T. cuspidata	[262]
Pestalotiopsis sp.	W. nobilis Catharanthus roseus	[259] [263]
Pestalotiopsis terminaliae	T. arjuna	[264]
Pestalotiopsis versicolor	T. cuspidata	[262]
Pezicula sp.	T. chinensis	[223]
Phoma betae	G. biloba	[265]
Phomopsis sp.	G. biloba, Larix leptolepis, T. cuspidata T. chinensis	[266] [223]
Phyllosticta melochiae	Melochia corchorifolia	[267]
Phyllosticta sp.	Ocimum basilicum	[268]
Phyllosticta spinarum	Cupressus sp.	[269]
Pithomyces sp.	Taxus sumatrana	[216]
Rhizopus sp.	T. media	[270]
Seimatoantlerium nepalense	T. wallichiana	[271]
Sordaria sp.	T. chinensis	[223]
Sporormia minima	T. wallichiana	[272]
Stegolerium kukenani	Stegolepisguianensis	[273]
Stemphylium sedicola	T. baccata	[274]
Taxomyces andreanae	T. brevifolia	[214]
Taxomyces sp.	Taxus sp.	[275]
Trichoderma sp.	T. chinensis	[223]
Trichothecium sp.	T. wallichiana	[272]
Tubercularia sp.	T. mairei	[276]
Xylaria sp.	M. speciosus T. chinensis	[235] [223]

Another opportunity to obtain taxol is represented by a semisynthetic method starting from the structurally related taxane compounds baccatin III and 10-deacetylbaccatin III (Figure 8), which are more easily accessible for their occurrence in yew needles [277]. Besides a number of papers where these precursors are reported together with taxol (Table 3), specific references consider their production by endophytic strains from Taxus wallichiana, respectively Diaporthe phaseolorum [278] and Trichoderma sp. [279]. A more general biosynthetic ability concerning taxanes has been evidenced in a number of endophytic strains isolated from Taxus baccata which were not identified at the species level, ascribed to the genera Alternaria, Aspergillus, Beauveria, Epicoccum, Fusarium, Gelasinospora, Geotrichum, Phoma and Phomopsis [280]. Evidence as taxane producers has been also reported for strains of Cladosporium langeronii and Phomopsis sp. from Wollemia nobilis [281].

10. Quinoline Alkaloids

Camptothecin (CPT) is probably the best known representative of this group, whose importance and history as a plant-derived antitumor drug to be widely found as a secondary metabolite of endophytic fungi seems to retrace what just described for taxol. In fact, in the last decade, this compound, and its analogues 9-methoxycamptothecin (MCPT) and 10-hydroxycamptothecin (HCPT) (Figure 9), have been reported from a number of endophytes from Camptotheca acuminata and a few more trees in the unrelated botanical family of the Icacinaceae (Table 4).

The attempt to obtain CPT by fermentation has evidenced a fundamental problem which may affect the possible use of endophytic fungal strains for production of bioactive plant metabolites on a large scale. In fact, the loss of the biosynthetic ability has been documented in a number of strains of F. solani [282] and Aspergillus sp. [283]. This breakdown seems not to be related to the antibiotic properties of the compound, considering that resistance to CPT has been documented for a number of endophytic strains from C. acuminata [284], and it is intrinsic and not related to the biosynthetic aptitude [285]. On the other hand, production of camptothecins can be stimulated by exploiting the eliciting effects of a few organic and inorganic compounds, particularly salicylic acid which induced a higher HCPT yield by a strain of Xylaria sp. [286], and methyl jasmonate which increased CPT production by a strain of T. atroviride [283]. Furthermore, CPT production by a strain of F. solani from C. acuminata was notably increased by supplying an ethanolic extract of leaves of C. roseus containing strictosidine as a precursor in CPT biosynthesis, and even by ethanol itself [287].

Figure 9. Structures of quinoline alkaloids produced by endophytic fungi.

Table 4. Endophytic fungi producing camptothecin (CPT) and its analogues 9-methoxycamptothecin (MCPT) and 10-hydroxycamptothecin (HCPT).

**Table 4.** Endophytic fungi producing camptothecin (CPT) and its analogues 9-methoxycamptothecin (MCPT) and 10-hydroxycamptothecin (HCPT).
Compounds	Fungal Species	Host Plants	References
CPT	Entrophospora infrequens	Nothapodytes foetida	[288,289]
CPT	Neurospora sp.	N. foetida	[290]
CPT	Nodulisporium sp.	N. foetida	[291]
CPT, HCPT, MCPT	Fusarium solani	Camptotheca acuminata	[292]
CPT, HCPT, MCPT	F. solani	Apodytes dimidiata	[293]
CPT	Botryosphaeria parva	Nothapodytes nimmoniana	[294]
CPT	Diaporthe conorum	N. nimmoniana	[294]
CPT	Fusarium oxysporum	N. nimmoniana	[294]
CPT	Fusarium sacchari	N. nimmoniana	[294]
CPT	F. solani	N. nimmoniana	[294]
CPT	Fusarium sp.	N. nimmoniana	[294]
CPT	Fusarium subglutinans	N. nimmoniana	[294]
CPT	Fusarium verticillioides	N. nimmoniana	[294]
CPT	Galactomyces sp.	N. nimmoniana	[294]
CPT	Irpex lacteus	N. nimmoniana	[294]
CPT	Phomopsis sp.	N. nimmoniana	[294]
CPT	Unidentified strains	N. nimmoniana	[294]
HCPT	Xylaria sp.	C. acuminata	[286]
HCPT	Valsa mali	C. acuminata	[295]
CPT	Aspergillus spp.	C. acuminata	[283]
CPT	Trichoderma atroviride	C. acuminata	[283]
CPT, HCPT, MCPT	Alternaria alternata	Miquelia dentata	[296]
CPT, HCPT, MCPT	Fomitopsis sp.	M. dentata	[296]
CPT, HCPT, MCPT	Phomopsis sp.	M. dentata	[296]
CPT	F. oxysporum	N. foetida	[297]

A paramount pharmaceutical relevance also pertains to the cinchona-alkaloids (Figure 9) extracted from bark of quina trees (Cinchona sp.), representing fundamental drugs for malaria prophylaxis [298]. After reporting the first endophytic isolate (Diaporthe sp.) from Cinchona ledgeriana collected in Java (Indonesia) producing quinine, quinidine, cinchonidine, and cinchonine [299], additional 20 strains of Phomopsis sp., Schizophyllum sp., Penicillium sp., Fomitopsis sp., and Arthrinium sp. from the same source have been found to produce variable amounts of the these compounds [300,301].

Two more compounds in this class are to be considered in this review. Berberine (Figure 9) is a cardioprotective, antidiabetic, antibiotic and antitumor product known from several unrelated medicinal plants [302], which has been recently found as a secondary metabolite of a strain of F. solani from roots of the medicinal liana Coscinium fenestratum [303]. Sanguinarine (Figure 9), a benzylisoquinoline or benzophenanthridine alkaloid known from several plants belonging to the Papaveraceae, whose antimicrobial effects have been particularly exploited for toothpastes and mouthwashes [304], has been found to be produced by a strain of F. proliferatum from leaves of Macleaya cordata [305].

11. Other Alkaloids

The vinca-alkaloids (Figure 10) are a series of over a hundred bioactive products extracted from periwinkle (Catharanthus roseus) and the related Vinca species, mostly exploited in cancer chemotherapy based on their action on tubulin and microtubule organization [306]. Endophytic strains of Alternaria sp. [307] and F. oxysporum [308] from C. roseus respectively produced vinblastine and vincristine, while more recently another strain of the latter species has been found to produce both compounds [309], and to synthesize vincristine from vinblastine when the latter compound was added to the growth medium [310]. Finally, an unidentified strain from Vinca minor has been reported for production of vincamine [311].

Figure 10. Structures of vinca-alkaloids.

Caffeine, the methylxanthine alkaloid (Figure 11) from Coffea spp. well known as a psychoactive drug, has been evidenced in extracts of unidentified endophytic fungi recovered from the Indian ethnomedicinal plants Osbeckia chinensis, O. stellata and Potentilla fulgens [43].

Piperine (Figure 11) is an alkaloid of Piper longum and Piper nigrum known for its antimycobacterial, antihyperlipidemic, anti-inflammatory, immunoregulatory and antitumor properties [312,313,314]. This valuable compound has been extracted from liquid cultures of endophytic strains of Periconia sp. from P. longum [315], and Mycosphaerella sp. [316] and C. gloeosporioides [317] from P. nigrum.

Figure 11. Structures of miscellaneous alkaloids produced by endophytic fungi.

Aconitine is a diterpenoid alkaloid (Figure 11) extracted as a secondary metabolite of Aconitum species, displaying analgesic, anti-inflammatory and antitumor activity. It has been also found as a fermentation product of an endophytic strain of Cladosporium cladosporioides recovered from roots of Aconitum leucostomum [318].

Rohitukine is a chromane alkaloid (Figure 11) with anti-inflammatory, immunomodulatory and antitumor properties first characterized as a secondary metabolite of a few tropical plants, Amoora rohituka (=Aphanamixis polystachya) and Dysoxylum binectariferum (Meliaceae), Schumanniophyton (Tetrastigma) magnificum and Schumanniophyton (Assidora) problematicum (Rubiaceae) [319]. This compound has been recently reported as a fermentation product of endophytic strains of F. proliferatum, F. oxysporum and F. solani from D. binectariferum [320,321], and F. fujikuroi from A. rohituka [321].

Peimisine and peiminine are steroidal alkaloids (Figure 11) known to occur in bulbs of Fritillaria spp. used as in Chinese ethnomedicine for their expectorant effects. A strain of an undetermined Fusarium species endophytic in bulbs of Fritillaria unibracteata var. wabensis has been found to produce these compounds [322].

Swainsonine is a trihydroxy inolidizine alkaloid (Figure 11) acting as a glycosidase inhibitor which occurs in a number of plant species, such as Swainsona canescens, Ipomoea spp., Turbina cordata, Sida carpinifolia, and locoweeds (Astragalus and Oxytropis spp.) [323]. The latter are forage plants whose consumption by livestock is associated to the syndrome of locoism. It has been observed that a fungal endophytic species occurring in locoweeds, the vertically-transmitted Undifilum oxytropis [324,325], previously described as Embellisia sp. [326,327], is capable to produce swainsonine in vitro. Novel species of Undifilum, U. fulvum and U. cinereum, have been later reported for production of this compound, respectively in Astragalus lentiginosus and A. mollissimus [328], along with strains of an unidentified Undifilum sp. recovered from S. canescens in Australia [329]. Moreover, the compound was found to be produced by endophytic isolates of Fusarium tricinctum recovered from Oxytropis kansuensis and O. deflexa in China [330]. The inhibitory properties on α-mannosidase have been exploited for the development of swainsonine as an anticancer drug, which has been impaired by reason of undesirable side effects [331,332]. Finally, it is interesting to note that plants of A. lentiginosus and Oxytropis sericea germinated from the embryo, which is not colonized by endophytes, were found to be fungus free and did not contain swainsonine [333]. This evidence strongly supports the hypothesis that actually its occurrence in plants may entirely derive from biosynthesis by endophytic fungal strains.

12. 3-Nitropropionic Acid

Analogous for its effects in livestock intoxication, 3-nitropropionic acid (NPA) is a secondary metabolite involved in the nitrification process in Leguminosae [334], particularly of the genera Hippocrepis, Lotus, Scorpiurus and Securigera, and the species Astragalus falcatus and Coronilla viminalis [335]. The fact that the latter are the only species in the respective genera to be reported to produce this compound has raised the interrogative if it is actually produced by associated endophytic microrganinsms. In fact NPA is mainly known as a toxin from a number of fungal species [336,337,338], and mentioned as a product of endophytic fungi such as Melanconium betulinum from birches in Germany [339], and a number of Phomopsis species, including P. phaseoli (= Diaporthe phaseolorum) from an unidentified rainforest tree of Guyana [339], and P. longicolla from Trichilia elegans in Brazil [340]. Isolates of Phomopsis spp. from crêpe ginger (Costus sp.) in Costa Rica and from Thai medicinal plants also produce this compound, together with a few strains of unidentified species from the latter source [335,341].

13. Saponines

Saponines are glycosides where the sugar moiety is bound through a glycosidic linkage to an aglycone (sapogenin) which can be a triterpenoid or a steroid compound. Generally considered as antinutritional factors, these products have been recently re-evaluated for their nutraceutical properties deriving from consistent anticholesterolemic effects and inhibition of sugar and ethanol absorption. Additional antibiotic, antitumor and immunomodulatory properties have also been reported [342]. Saponins are known to occur in many taxonomically unrelated plants, but there is an increasing evidence that their production is also widespread among endophytic fungi. Again such a biosynthetic ability may represent an aspect of the mutualistic relationships established in view of plant defense, considering that some plant pathogens are reported to have developed saponin-detoxifying enzymes as a virulence factor [343]. To this regard, production of saponins has been recently documented for strains of Aspergillus sp. from Salvadora oleoides [344] and Justicia beddomei [345], Aspergillus sp., Bulgaria sp. and Sirococcus conigenus from Potentilla fulgens [346], A. niger and F. oxysporum from Crotalaria pallida [347], A. alternata, A. niger and Penicillium sp. from Loranthus sp. [348], A. alternata, A. flavus, A. niger, Colletotrichum gleosporioides and Trichoderma sp. from Tabebuia argentea [197], Cochliobolus lunatus (anamorph Curvularia lunata) from Boswellia ovalifoliolata, and Monochaetia karstenii (=Pestalotiopsis maculans) and Phyllosticta sp. from Shorea thumbuggaia [349], Aspergillus neoniveus (=Fennellia nivea) from Typhonium divaricatum [350], A. alternata, A. flavus, A. niger, Cladosporium sp., Penicillium sp., Phomopsis sp. and Trichoderma sp. from Aegle marmelos [351], A. niger, A. terreus, Aspergillus sp., Aspergillus tubingensis, Coprinopsis cinerea, C. lunata and Fusarium sp. from Eugenia jambolana [352], Aspergillus awamori and again C. gleosporioides from Rauwolfia serpentina [353].

More particularly, the ginsenosides (Figure 12), previously characterized from plants in the genus Panax, have been extracted from cultures of root endophytic strains of Penicillium sp., Dictyochaeta sp. and Camarosporium sp. from Aralia elata [354], and of Fusarium sp., Aspergillus sp. and Verticillium sp. from P. ginseng [355]. However, the ability by endophytic strains of F. oxysporum, Fusarium sp. and Nodulisporium sp. from Panax notoginseng to transform ginsenosides to yield additional analog compounds [356] demonstrates that endophytic fungi directly contribute to the particular pattern of these compounds occurring in plant tissues.

Figure 12. Structures of saponines produced by endophytic fungi.

A similar effect has been documented for an endophytic strain of Fusarium sp. from Dioscorea nipponica which was able to increase diosgenin content in its liquid cultures added with a rhizome extract of the host plant [357]. Diosgenin is a steroidal sapogenin (Figure 12) known as a secondary metabolite of a number of plant species, particularly the yams (Dioscorea spp.). It is an important precursor for production of semi-synthetic steroids, such as corticosteroids, progesterone and other steroidal drugs, and displays a number of important pharmacological effects [358]. This valuable compound is also produced by endophytic strains of Cephalosporium sp. and Paecilomyces sp. from P. polyphylla var. yunnanensis [359,360]. In vitro cell culturing represents an alternative means for production of this drug, considering that natural populations of one of the most important sources, the yellow ginger (Dioscorea zingiberensis), are decreasing due to overexploitation, and agricultural production is problematic by reason of the 3–4 years required for obtaining mature rhizomes. Oligosaccharides and polysaccharides extracted from an endophytic strain (Dzf17) of F. oxysporium have been found to elicit growth and diosgenin production in cell cultures of D. zingiberensis [361,362]. The same effect was also observed when both cell cultures and seedlings were treated with beauvericin produced by an endophytic strain of Fusarium redolens from the same plant species [363].

Gymnemagenin, a triterpenoid sapogenin (Figure 12) extracted from the renowned anti-diabetic herb Gymnema sylvestre, has been found as a fermentation product of an endophytic strain of Penicillium oxalicum recovered from leaves of this plant in India [364].

14. Miscellaneous Compounds

Resveratrol (Figure 13) is a stilbene phytoalexin produced by many plants in response to biotic and abiotic injuries, and a reputed nutraceutical based on its antioxidant properties [365]. A number of endophytic strains from Vitis vinifera, Vitis quinquangularis, and P. cuspidatum belonging to the genera Alternaria, Aspergillus, Botryosphaeria, Cephalosporium, Geotrichum, Mucor and Penicillium were found to be able to produce this compound; however, only a Alternaria strain retained this capability after repeated culturing cycles [366]. Another leaf strain of Alternaria, together with root strains of F. solani, F. oxysporum and F. proliferatum from C. cajan, have been found to produce cajaninstilbene acid (Figure 13), a related antioxidant compound originally characterized from the host plant [367].

Figure 13. Structures of miscellaneous compounds produced by endophytic fungi.

Mainly used as a food additive, curcumin (Figure 13) is a diarylheptanoid compound of turmeric (Curcuma longa) with potential pharmaceutical applications [368], which has been recently found as a fermentation product of a previously-mentioned endophytic strain from C. wenyujin [39].

Falcarinol, also known as carotatoxin or panaxynol (Figure 13), is a fatty alcohol reported from several unrelated plant species such as carrots (Daucus carota) and other Apiaceae, red ginseng (P. ginseng), ivies (Hedera spp.) and other Araliaceae. It is considered a natural pesticide protecting roots from fungal diseases, and displayed some extent of activity against certain types of cancer [369]. Production of this compound has been reported by a strain of Paecilomyces sp. from P. ginseng [104].

Myrtucommulones are acylphloroglucinol compounds extracted from myrtle (Myrtus communis) and related plants in the Myrtaceae considered as prospect pharmaceuticals based on consistent antibacterial, antimalarial, antioxidant, anti-inflammatory and antitumor properties. So far 13 analogues (myrtucommulones A-M) have been characterized from plant sources, and the production of myrtucommulone A (Figure 13) and D has been recently reported from a myrtle endophytic strain of Neofusicoccum australe (teleomorph Botryosphaeria australis) [370].

Finally, the widespread pentacyclic triterpenoid compound ursolic acid, also known as prunol or malol, and reported for its anticancer and cardioprotective properties [371], has been recently found in extracts of a cited endophytic strain of A. stygium [51].

15. Future Perspectives

Data considered in this review highlight a continuously increasing number of plant-derived bioactive products also occurring as secondary metabolites of endophytic fungal strains. Therefore, it is quite easy to foresee that the finding of additional such compounds is under way and may disclose further applicative opportunities. As an example, the reported production of colchatetralene, a structural analog of colchicine, by an endophytic strain (Aspergillus sp.) from seeds of Gloriosa superba [372] has paved the way for the possible production of this important drug by a microbial agent. Moreover, indications have been reported concerning the possible production of the secoiridoid glycoside gentiopicrin and of the cardiotonic drug digoxin by endophytic fungal strains, respectively from Gentiana macrophylla [373] and Digitalis lanata [374], and more circumstantiated studies are expected for these important compounds.

Within the above-considered categories, volatile compounds from essential oils particularly represent a mine to be dug more in depth. In fact benzophenone derivatives, which are biosinthetically related to xanthones and known as main components of the scent of species in a few botanical families such as Clusiaceae, Gentianaceae, Moraceae, Polygalaceae, Rosaceae and Thymelaceae, are also widespread secondary metabolites of fungi [375]. Therefore, it would not be surprising if additional compounds previously reported from plants are also evidenced as fermentation products of endophytic strains [376,377,378].

The likely finding by endophytic strains has been also anticipated for asperphenamate, a phenylalanine derivative recently attracting attention for its antitumor properties. In fact this compound was first characterized from Aspergillus flavipes and a number of fungi which are also known for their endophytic habit. Therefore, its subsequently observed occurrence in many botanically unrelated plant species is considered to possibily derive by the biosynthetic ability of endophytic fungal strains [379]. Besides the above-mentioned case of swainsonine, a more direct proof that some plant metabolites can be actually produced by their associated endophytic fungi has been provided by the finding of the mycotoxin alternariol, along with the related compounds altenusin and alternariol 5-O-methyl ether, in foliar extracts of the medicinal plant Polygonum senegalense harboring an Alternaria strain [380]. The latter compound had been also extracted from Anthocleista djalonensis, a tree used in traditional medicine in West Africa [381].

Further investigational opportunities arise from the ability by endophytic fungi to modify plant metabolites into novel bioactive compounds, and actually several examples of such a kind of biochemical interaction have been reported so far. A strain of Xylaria sp. associated with Cinchona pubescens was found to be able to convert the above-mentioned Cinchona alkaloids into their 1-N-oxides [382]. Strains of Diaporthe spp. from the tea plant (Camellia sinensis) and from rhizome of C. longa respectively performed the stereoselective oxidation of (+)-catechin and (–)-epicatechin into the corresponding 3,4-cis-dihydroflavan derivatives [383,384], and the conversion of curcumin into a few colorless hydroderivatives [385]. Moreover, an unidentified strain from yellow moonshed (Archangelisia flava) has been reported to convert berberine into its 7-N-oxide derivative [386].

On the other end, endophytic fungi may also have a role in degradation of plant metabolites. As an example, a strain of Phomopsis liquidambari from the stem of Chinese bishopwood (Bischofia polycarpa) has been showed to degrade the phytoestrogen luteolin and additional phenolic compounds such as phenanthrene [387], introducing the possible employment of endophytic fungal strains in bioremediation [388].

However, there is no doubt that in the future the most intriguing research hint concerns the genetic bases of production of bioactive metabolites by these closely associated but phylogenetically unrelated organisms. Although a negationist point of view has been advanced concerning taxol biosynthesis by endophytes [389], taken as a whole the over 300 cases mentioned in this review concerning homologous and heterologous endophytic strains producing plant bioactive compounds represent a compelling evidence that these micorganisms and their host plants interact at some level in the biosynthetic process. The main hypothesis is that these interactions may lead to horizontal gene transfers or genetic recombinations, from the plant to its endophytic counterpart and/or vice-versa, originating novel specialized strains able to accumulate certain metabolites in the host tissues [186], which would be a good reason to explain why in the end a mutualistic relationship is established. The fact that most of these compounds have been originally extracted from plants has generated a somehow misleading preconception that it is the endophytic microbe that for some reasons acquires the ability to produce a given plant metabolite. However, actually, the finding of taxol and other bioactive products from endophytic strains of plants which themselves are not reported as a source of the same compound could be considered as an indication that a reverse influence may be more likely. On the other hand, investigations concerning complex diterpenoid compounds, such as gibberellins and again taxol, have shown that the biosynthetic pathways in plant and endophytes may differ at some level [5,251], which is a clue for an independent development of the subtended genetic traits. However, in the end, the problem is again preconceptual, since it cannot be excluded that such a variation in the biosynthetic scheme may also exist within the categories of both plants and associated endophytes.

An even more complex situation could result if further evidence is provided that synthesis of bioactive metabolites in fungi is in turn influenced by other associated microbes. This is the case of rhizoxin which has been found to be actually synthesized by an endosymbiotic bacterium (Burkholderia rhizoxinica) residing in the cytosol of the rice fungal pathogen Rhizopus microsporus [390,391]. Moreover, such a kind of provision may well occur in endophytic fungi, considering that a widespread presence of endohyphal bacteria resulted in a survey on Ascomycetous endophytes of Cupressaceae [392]. Moreover, a role of giant linear plasmids in the synthesis of antibiotic compounds in Streptomyces has been proposed since over 25 years [393]. If eventually confirmed for other metabolites, the role of these “third parties” could represent the means through which the biosynthetic abilities are interchanged between plants and their associated endophytes, and also explain why in a few cases this property is lost after repeated subculturing. This latter undesired aspect, which is reported to impair an efficient employment of endophytic fungi by the pharmaceutical industry, might also be consequential to more subtle events at the gene level, considering that the plant-endophyte interaction may involve promotion of gene transcriptions. Coherent with this possibility are the elicitating properties observed by endophytes on the synthesis of a number of bioactive plant products, with a few cases previously mentioned in this review [193,361,362]. Finally, an intriguing elicitating function may also characterize other cohabiting endophytic strains not directly capable to produce a given metabolite, as shown in the case of strains of Alternaria sp. and Phomopsis sp. which consistently increased taxol synthesis by a taxol-producer Paraconiothyrium sp. from Taxus x media in co-cultures [394].

Quite clearly, the complex evolving scenario outlined in this paper is introductory to further advances in the elucidation of the genetic and biochemical bases of the synthesis of bioactive compounds, and the reflecting biocenotic interactions among plants, their associated endophytes and other involved microorganisms. New acquisitions in these fields will be fundamental in order to exploit microbial strains for a large-scale production of plant-derived drugs in controlled fermentative processes.

Acknowledgments

This paper has been prepared within the agreement among the Council for Agricultural Research and Economics, the Department of Environmental Biological and Pharmaceutical Sciences and Technologies, and the non-profit company WWF-Oasi, for the study of fungal endophytes associated to forest plants at the Astroni Nature Reserve.

Author Contributions

Authors contributed equally to this review.

Conflicts of Interest

The authors declare no conflict of interest.

References

Kusari, S.; Spiteller, M. Are we ready for industrial production of bioactive plant secondary metabolites utilizing endophytes? Nat. Prod. Rep. 2011, 28, 1203–1207. [Google Scholar] [CrossRef] [PubMed]
Schulz, B.; Boyle, C.; Draeger, S.; Römmert, A.K.; Krohn, K. Endophytic fungi: A source of novel biologically active secondary metabolites. Mycol. Res. 2002, 106, 996–1004. [Google Scholar] [CrossRef]
Manici, L.M.; Kelderer, M.; Caputo, F.; Mazzola, M. Auxin-mediated relationships between apple plants and root inhabiting fungi: Impact on root pathogens and potentialities of growth-promoting populations. Plant Pathol. 2015, 64, 843–851. [Google Scholar] [CrossRef]
Kawaide, H. Biochemical and molecular analyses of gibberellin biosynthesis in fungi. Biosci. Biotechnol. Biochem. 2006, 70, 583–590. [Google Scholar] [CrossRef] [PubMed]
Bömke, C.; Tudzynski, B. Diversity, regulation, and evolution of the gibberellin biosynthetic pathway in fungi compared to plants and bacteria. Phytochemistry 2009, 70, 1876–1893. [Google Scholar] [CrossRef] [PubMed]
Khan, A.L.; Hussain, J.; Al-Harrasi, A.; Al-Rawahi, A.; Lee, I.J. Endophytic fungi: Resource for gibberellins and crop abiotic stress resistance. Crit. Rev. Biotechnol. 2015, 35, 62–74. [Google Scholar] [CrossRef] [PubMed]
Yabuta, T.; Hayashi, T. Biochemical studies on Bakanae fungus of rice. Part 3. Physiological action of gibberellin on plants. J. Agric. Chem. Soc. Jpn. 1939, 15, 403–413. [Google Scholar]
Porter, J.K.; Bacon, C.W.; Cutler, H.G.; Arrendale, R.F.; Robbins, J.D. In vitro auxin production by Balansia epichloe. Phytochemistry 1985, 24, 1429–1431. [Google Scholar] [CrossRef]
De Battista, J.P.; Bacon, C.W.; Severson, R.; Plattner, R.D.; Bouton, J.H. Indole acetic acid production by the fungal endophyte of tall fescue. Agron. J. 1990, 82, 878–880. [Google Scholar] [CrossRef]
Yue, Q.; Miller, C.J.; White, J.F.; Richardson, M.D. Isolation and characterization of fungal inhibitors from Epichloë festucae. J. Agric. Food Chem. 2000, 48, 4687–4692. [Google Scholar] [CrossRef] [PubMed]
Malinowski, D.P.; Belesky, D.P. Ecological importance of Neotyphodium spp. grass endophytes in agroecosystems. Grassland Sci. 2006, 52, 1–14. [Google Scholar] [CrossRef]
Schardl, C.L. Fungal endophytes in Lolium and Festuca species. In Molecular Breeding of Forage and Turf; Yamada, T., Spangenberg, G., Eds.; Springer: New York, NY, USA, 2009; pp. 285–298. [Google Scholar]
Di Menna, M.E.; Finch, S.C.; Popay, A.J.; Smith, B.L. A review of the Neotyphodium lolii/Lolium perenne symbiosis and its associated effects on animal and plant health, with particular emphasis on ryegrass staggers. N. Z. Vet. J. 2012, 60, 315–328. [Google Scholar] [CrossRef] [PubMed]
Ek, M.; Ljungquist, P.O.; Stenström, E. Indole-3-acetic acid production by mycorrhizal fungi determined by gas chromatography-mass spectrometry. New Phytol. 1983, 94, 401–407. [Google Scholar] [CrossRef]
Barroso, J.; Chaves Neves, H.; Pais, M.S. Production of indole-3-ethanol and indole-3-acetic acid by the mycorrhizal fungus of Ophrys lutea (Orchidaceae). New Phytol. 1986, 103, 745–749. [Google Scholar] [CrossRef]
Rudawska, M.; Bernillon, J.; Gay, G. Indole compounds released by the ectendomycorrhizal fungal strain MrgX isolated from a pine nursery. Mycorrhiza 1992, 2, 17–23. [Google Scholar] [CrossRef]
Lu, H.; Zou, W.X.; Meng, J.C.; Hu, J.; Tan, R.X. New bioactive metabolites produced by Colletotrichum sp., an endophytic fungus in Artemisia annua. Plant Sci. 2000, 151, 67–73. [Google Scholar] [CrossRef]
Bhagobaty, R.K.; Joshi, S.R. Promotion of seed germination of green gram and chick pea by Penicillium verruculosum RS7PF, a root endophytic fungus of Potentilla fulgens L. Adv. Biotechnol. 2009, 8, 7–15. [Google Scholar]
Hammerschmidt, L.; Wray, V.; Lin, W.; Kamilova, E.; Proksch, P.; Aly, A.H. New styrylpyrones from the fungal endophyte Penicillium glabrum isolated from Punica granatum. Phytochem. Lett. 2012, 5, 600–603. [Google Scholar] [CrossRef]
Nassar, A.H.; El-Tarabily, K.A.; Sivasithamparam, K. Promotion of plant growth by an auxin-producing isolate of the yeast Williopsis saturnus endophytic in maize (Zea mays L.) roots. Biol. Fertil. Soils 2005, 42, 97–108. [Google Scholar] [CrossRef]
Sirrenberg, A.; Göbel, C.; Grond, S.; Czempinski, N.; Ratzinger, A.; Karlovsky, P.; Santos, P.; Feussner, I.; Pawlowski, K. Piriformospora indica affects plant growth by auxin production. Physiol. Plant. 2007, 131, 581–589. [Google Scholar] [CrossRef] [PubMed]
Verma, S.; Varma, A.; Rexer, K.-H.; Hassel, A.; Kost, G.; Sarbhoy, A.; Bisen, P.; Bütehorn, B.; Franken, P. Piriformospora indica, gen. et sp. nov., a new root-colonizing fungus. Mycologia 1998, 90, 896–903. [Google Scholar] [CrossRef]
Qiang, X.; Weiss, M.; Kogel, K.H.; Schäfer, P. Piriformospora indica—A mutualistic basidiomycete with an exceptionally large plant host range. Mol. Plant Pathol. 2012, 13, 508–518. [Google Scholar] [CrossRef] [PubMed]
Xin, G.; Glawe, D.; Doty, S.L. Characterization of three endophytic, indole-3-acetic acid-producing yeasts occurring in Populus trees. Mycol. Res. 2009, 113, 973–980. [Google Scholar] [CrossRef] [PubMed]
Dai, C.C.; Yu, B.Y.; Li, X. Screening of endophytic fungi that promote the growth of Euphorbia pekinensis. Afr. J. Biotechnol. 2008, 7, 3505–3510. [Google Scholar]
Waqas, M.; Khan, A.L.; Kang, S.M.; Kim, Y.H.; Lee, I.J. Phytohormone-producing fungal endophytes and hardwood-derived biochar interact to ameliorate heavy metal stress in soybeans. Biol. Fertil. Soils 2014, 50, 1155–1167. [Google Scholar] [CrossRef]
Waqas, M.; Khan, A.L.; Kamran, M.; Hamayun, M.; Kang, S.M.; Kim, Y.H.; Lee, I.J. Endophytic fungi produce gibberellins and indoleacetic acid and promotes host-plant growth during stress. Molecules 2012, 17, 10754–10773. [Google Scholar] [CrossRef] [PubMed]
Khan, A.L.; Hamayun, M.; Kang, S.M.; Kim, Y.H.; Jung, H.Y.; Lee, J.H.; Lee, I.J. Endophytic fungal association via gibberellins and indole acetic acid can improve plant growth under abiotic stress: An example of Paecilomyces formosus LHL10. BMC Microbiol. 2012, 12, 3. [Google Scholar] [CrossRef] [PubMed]
Rim, S.O.; Lee, J.H.; Choi, W.Y.; Hwang, S.K.; Suh, S.J.; Lee, I.J.; Rhee, I.K.; Kim, J.G. Fusarium proliferatum KGL0401 as a new gibberellin-producing fungus. J. Microbiol. Biotechnol. 2005, 15, 809–814. [Google Scholar]
Tsavkelova, E.A.; Bömke, C.; Netrusov, A.I.; Weiner, J.; Tudzynski, B. Production of gibberellic acids by an orchid-associated Fusarium proliferatum strain. Fungal Genet. Biol. 2008, 45, 1393–1403. [Google Scholar] [CrossRef] [PubMed]
Hamayun, M.; Khan, S.A.; Kim, H.-Y.; Chaudhary, M.F.; Hwang, Y.-H.; Shin, D.-H.; Kim, I.-K.; Lee, B.-H.; Lee, I.-J. Gibberellin production and plant growth enhancement by newly isolated strain of Scolecobasidium tshawytschae. J. Microbiol. Biotechnol. 2009, 19, 560–565. [Google Scholar] [PubMed]
Khan, S.A.; Hamayun, M.; Yoon, H.; Kim, H.Y.; Suh, S.J.; Hwang, S.K.; Kim, J.M.; Lee, I.J.; Choo, Y.S.; Yoon, U.H.; et al. Plant growth promotion and Penicillium citrinum. BMC Microbiol. 2008, 8, 231. [Google Scholar] [CrossRef] [PubMed]
Khan, S.A.; Hamayun, M.; Kim, H.Y.; Yoon, H.J.; Seo, J.C.; Choo, Y.S.; Lee, I.J.; Kim, S.D.; Rhee, I.K.; Kim, J.G. A new strain of Arthrinium phaeospermum isolated from Carex kobomugi Ohwi is capable of gibberellin production. Biotechnol. Lett. 2009, 31, 283–287. [Google Scholar] [CrossRef] [PubMed]
Hamayun, M.; Khan, S.A.; Ahmad, N.; Tang, D.S.; Kang, S.M.; Na, C.I.; Sohn, E.Y.; Hwang, Y.H.; Shin, D.H.; Lee, B.H.; et al. Cladosporium sphaerospermum as a new plant growth-promoting endophyte from the roots of Glycine max (L.) Merr. World J. Microbiol. Biotechnol. 2009, 25, 627–632. [Google Scholar] [CrossRef]
Hamayun, M.; Khan, S.A.; Khan, M.A.; Khan, A.L.; Kang, S.; Kim, S.K.; Joo, G.J.; Lee, I.L. Gibberellin production by pure cultures of a new strain of Aspergillus fumigatus. World J. Microbiol. Biotechnol. 2009, 25, 1785–1792. [Google Scholar] [CrossRef]
Khan, A.L.; Hamayun, M.; Kim, Y.H.; Kang, S.M.; Lee, I.J. Ameliorative symbiosis of endophyte (Penicillium funiculosum LHL06) under salt stress elevated plant growth of Glycine max L. Plant Physiol. Biochem. 2011, 49, 852–861. [Google Scholar] [CrossRef] [PubMed]
Khan, A.L.; Hamayun, M.; Kim, Y.H.; Kang, S.M.; Lee, J.H.; Lee, I.J. Gibberellins producing endophytic Aspergillus fumigatus sp. LH02 influenced endogenous phytohormonal levels, isoflavonoids production and plant growth in salinity stress. Proc. Biochem. 2011, 46, 440–447. [Google Scholar] [CrossRef]
Hamayun, M.; Khan, S.A.; Iqbal, I.; Ahmad, B.; Lee, I.J. Isolation of a gibberellin-producing fungus (Penicillium sp. MH7) and growth promotion of crown daisy (Chrysanthemum coronarium). J. Microbiol. Biotechnol. 2010, 20, 202–207. [Google Scholar] [CrossRef] [PubMed]
Yan, J.; Qi, N.; Wang, S.; Gadhave, K.; Yang, S. Characterization of secondary metabolites of an endophytic fungus from Curcuma wenyujin. Curr. Microbiol. 2014, 69, 740–744. [Google Scholar] [CrossRef] [PubMed]
Crafts, C.B.; Miller, C.O. Detection and identification of cytokinins produced by mycorrhizal fungi. Plant Physiol. 1974, 54, 586–588. [Google Scholar] [CrossRef] [PubMed]
Barker, S.J.; Tagu, D. The roles of auxins and cytokinins in mycorrhizal symbioses. J. Plant Growth Regul. 2000, 19, 144–154. [Google Scholar] [PubMed]
Vadassery, J.; Ritter, C.; Venus, Y.; Camehl, I.; Varma, A.; Shahollari, B.; Novák, O.; Strnad, M.; Ludwig-Müller, J.; Oelmüller, R. The role of auxins and cytokinins in the mutualistic interaction between Arabidopsis and Piriformospora indica. Mol. Plant Microbe Interact. 2008, 21, 1371–1383. [Google Scholar] [CrossRef] [PubMed]
Bhagobaty, R.K.; Joshi, S.R. Metabolite profiling of endophytic fungal isolates of five ethno-pharmacologically important plants of Meghalaya, India. J. Metabolomics Syst. Biol. 2011, 2, 20–31. [Google Scholar]
Bakkali, F.; Averbeck, S.; Averbeck, D.; Idaomar, M. Biological effects of essential oils—A review. Food Chem. Toxicol. 2008, 46, 446–475. [Google Scholar] [CrossRef] [PubMed]
Strobel, G.A.; Dirkse, E.; Sears, J.; Markworth, C. Volatile antimicrobials from Muscodor albus, a novel endophytic fungus. Microbiology 2001, 147, 2943–2950. [Google Scholar] [CrossRef] [PubMed]
Park, M.S.; Ahn, J.; Choi, G.J.; Choi, Y.H.; Jang, K.S.; Kim, J.C. Potential of the volatile-producing fungus Nodulisporium sp. CF016 for the control of postharvest diseases of apple. Plant Pathol. J. 2010, 26, 253–259. [Google Scholar] [CrossRef]
Suwannarach, N.; Kumla, J.; Bussaban, B.; Nuangmek, W.; Matsui, K.; Lumyong, S. Biofumigation with the endophytic fungus Nodulisporium spp. CMU-UPE34 to control postharvest decay of citrus fruit. Crop Prot. 2013, 45, 63–70. [Google Scholar] [CrossRef]
Abrahão, M.R.; Molina, G.; Pastore, G.M. Endophytes: Recent developments in biotechnology and the potential for flavor production. Food Res. Int. 2013, 52, 367–372. [Google Scholar] [CrossRef]
Bohlmann, J.; Keeling, C.I. Terpenoid biomaterials. Plant J. 2008, 54, 656–669. [Google Scholar] [CrossRef] [PubMed]
Saxena, S.; Meshram, V.; Kapoor, N. Muscodor tigerii sp. nov.—Volatile antibiotic producing endophytic fungus from the Northeastern Himalayas. Ann. Microbiol. 2015, 67, 47–57. [Google Scholar] [CrossRef]
Cheng, M.J.; Wu, M.D.; Chen, J.J.; Cheng, Y.C.; Hsieh, M.T.; Hsieh, S.Y.; Yuan, G.F.; Su, Y.S. Secondary metabolites from the endophytic fungus Annulohypoxylon stygium BCRC 34024. Chem. Nat. Compd. 2014, 50, 237–241. [Google Scholar] [CrossRef]
Kaul, S.; Wani, M.; Dhar, K.L.; Dhar, M.K. Production and GC-MS trace analysis of methyl eugenol from endophytic isolate of Alternaria from rose. Ann. Microbiol. 2008, 58, 443–445. [Google Scholar] [CrossRef]
Bäck, J.; Aaltonen, H.; Hellén, H.; Kajos, M.K.; Patokoski, J.; Taipale, R.; Pumpanen, J.; Heinonsalo, J. Variable emissions of microbial volatile organic compounds (MVOCs) from root-associated fungi isolated from Scots pine. Atmos. Environ. 2010, 44, 3651–3659. [Google Scholar] [CrossRef]
Tomsheck, A.R.; Strobel, G.A.; Booth, E.; Geary, B.; Spakowicz, D.; Knighton, B.; Floerchinger, C.; Sears, J.; Liarzi, O.; Ezra, D. Hypoxylon sp., an endophyte of Persea indica, producing 1,8-cineole and other bioactive volatiles with fuel potential. Microb. Ecol. 2010, 60, 903–914. [Google Scholar] [CrossRef] [PubMed]
Nigg, J.; Strobel, G.; Knighton, W.B.; Hilmer, J.; Geary, B.; Riyaz-Ul-Hassan, S.; Harper, J.K.; Valenti, D.; Wang, Y. Functionalized para-substituted benzenes as 1,8-cineole production modulators in an endophytic Nodulisporium species. Microbiology 2014, 160, 1772–1782. [Google Scholar] [CrossRef] [PubMed]
Mucciarelli, M.; Camusso, W.; Maffei, M.; Panicco, P.; Bicchi, C. Volatile terpenoids of endophyte-free and infected peppermint (Mentha piperita L.): Chemical partitioning of a symbiosis. Microb. Ecol. 2007, 54, 685–696. [Google Scholar] [CrossRef] [PubMed]
Gao, J.; Xu, A.Q.; Tang, X.K. Isolation, identification and volatile compound analysis of an aroma-producing endophytic yeast from romaine lettuce. Food Sci. 2011, 23, 33. [Google Scholar]
Shaw, J.J.; Spakowicz, D.J.; Dalal, R.S.; Davis, J.H.; Lehr, N.A.; Dunican, B.F.; Orellana, E.A.; Narváez-Trujillo, A.; Strobel, S.A. Biosynthesis and genomic analysis of medium-chain hydrocarbon production by the endophytic fungal isolate Nigrograna mackinnonii E5202H. Appl. Microbiol. Biotechnol. 2015, 99, 3715–3728. [Google Scholar] [CrossRef] [PubMed]
Zhang, C.L.; Wang, G.P.; Mao, L.J.; Komon-Zelazowska, M.; Yuan, Z.L.; Lin, F.C.; Druzhinina, I.S.; Kubicek, C.P. Muscodor fengyangensis sp. nov. from southeast China: Morphology, physiology and production of volatile compounds. Fungal Biol. 2010, 114, 797–808. [Google Scholar] [CrossRef] [PubMed]
Macías-Rubalcava, M.L.; Hernández-Bautista, B.E.; Oropeza, F.; Duarte, G.; González, M.C.; Glenn, A.E.; Hanlin, R.T.; Anaya, A.L. Allelochemical effects of volatile compounds and organic extracts from Muscodor yucatanensis, a tropical endophytic fungus from Bursera simaruba. J. Chem. Ecol. 2010, 36, 1122–1131. [Google Scholar] [CrossRef] [PubMed]
Ting, A.S.Y.; Mah, S.W.; Tee, C.S. Identification of volatile metabolites from fungal endophytes with biocontrol potential towards Fusarium oxysporum f. sp. cubense race 4. Am. J. Agric. Biol. Sci. 2010, 5, 177–182. [Google Scholar] [CrossRef]
Yuan, Z.L.; Su, Z.Z.; Mao, L.J.; Peng, Y.Q.; Yang, G.M.; Lin, F.C.; Zhang, C.L. Distinctive endophytic fungal assemblage in stems of wild rice (Oryza granulata) in China with special reference to two species of Muscodor (Xylariaceae). J. Microbiol. 2011, 9, 15–23. [Google Scholar] [CrossRef] [PubMed]
Lin, T.; Lin, X.; Lu, C.; Hu, Z.; Huang, W.; Huang, Y.; Shen, Y. Secondary metabolites of Phomopsis sp. XZ-26, an endophytic fungus from Camptotheca acuminata. Eur. J. Org. Chem. 2009, 18, 2975–2982. [Google Scholar] [CrossRef]
Singh, S.K.; Strobel, G.A.; Knighton, B.; Geary, B.; Sears, J.; Ezra, D. An endophytic Phomopsis sp. possessing bioactivity and fuel potential with its volatile organic compounds. Microb. Ecol. 2011, 61, 729–739. [Google Scholar] [CrossRef] [PubMed]
Santos Filho, F.C.; da Silva Amaral, L.; Rodrigues-Filho, E. Composition of essential oils from Cupressus lusitanica and a Xylariaceous fungus found on its leaves. Biochem. Syst. Ecol. 2011, 39, 485–490. [Google Scholar] [CrossRef]
Strobel, G.; Singh, S.K.; Riyaz-Ul-Hassan, S.; Mitchell, A.M.; Geary, B.; Sears, J. An endophytic/pathogenic Phoma sp. from creosote bush producing biologically active volatile compounds having fuel potential. FEMS Microbiol. Lett. 2011, 320, 87–94. [Google Scholar] [CrossRef] [PubMed]
Meshram, V.; Kapoor, N.; Saxena, S. Muscodor kashayum sp. nov.—A new volatile anti-microbial producing endophytic fungus. Mycology 2013, 4, 196–204. [Google Scholar] [CrossRef] [PubMed]
Silva, G.H.; Teles, H.L.; Zanardi, L.M.; Marx Young, M.C.; Eberlin, M.N.; Hadad, R.; Pfenning, L.H.; Costa-Neto, C.M.; Castro-Gamboa, I.; da Silva Bolzani, V.; et al. Cadinane sesquiterpenoids of Phomopsis cassiae, an endophytic fungus associated with Cassia spectabilis (Leguminosae). Phytochemistry 2006, 67, 1964–1969. [Google Scholar] [CrossRef] [PubMed]
Guo, F.; Yang, S.X.; Liu, L.; Wang, Y. Chemical constituents and their toxic activity from the endophytic fungus Phomopsis sp. KY-12, isolated from Pleioblastus amarus. Nat. Prod. Res. Dev. 2014, 26, 1389–1392. [Google Scholar]
Strobel, G.A.; Kluck, K.; Hess, W.M.; Sears, J.; Ezra, D.; Vargas, P.N. Muscodor albus E-6, an endophyte of Guazuma ulmifolia making volatile antibiotics: Isolation, characterization and experimental establishment in the host plant. Microbiology 2007, 153, 2613–2620. [Google Scholar] [CrossRef] [PubMed]
Kudalkar, P.; Strobel, G.; Riyaz-Ul-Hassan, S.; Geary, B.; Sears, J. Muscodor sutura, a novel endophytic fungus with volatile antibiotic activities. Mycoscience 2012, 53, 319–325. [Google Scholar] [CrossRef]
Silva, G.H.; de Oliveira, C.M.; Teles, H.L.; Pauletti, P.M.; Castro-Gamboa, I.; Silva, D.H.S.; da Silva Bolzani, V.; Young, M.C.M.; Costa-Neto, C.M.; Pfenning, L.H.; et al. Sesquiterpenes from Xylaria sp., an endophytic fungus associated with Piper aduncum (Piperaceae). Phytochem. Lett. 2010, 3, 164–167. [Google Scholar] [CrossRef]
Wu, L.S.; Hu, C.L.; Han, T.; Zheng, C.J.; Ma, X.Q.; Rahman, K.; Qin, L.P. Cytotoxic metabolites from Perenniporia tephropora, an endophytic fungus from Taxus chinensis var. mairei. Appl. Microbiol. Biotechnol. 2013, 97, 305–315. [Google Scholar] [CrossRef] [PubMed]
Zang, L.Y.; Wei, W.; Guo, Y.; Wang, T.; Jiao, R.H.; Ng, S.W.; Tan, R.X.; Ge, H.M. Sesquiterpenoids from the mangrove-derived endophytic fungus Diaporthe sp. J. Nat. Prod. 2012, 75, 1744–1749. [Google Scholar] [CrossRef] [PubMed]
Xuan, Q.; Zhang, L.Q.; Yang, J.; Li, Y.P. β-Elemene from Curcuma zedoaria endophytic fungus. Nat. Prod. Res. Dev. 2011, 23, 473–475. [Google Scholar]
Isaka, M.; Chinthanom, P.; Boonruangprapa, T.; Rungjindamai, N.; Pinruan, U. Eremophilane-type sesquiterpenes from the fungus Xylaria sp. BCC 21097. J. Nat. Prod. 2010, 73, 683–687. [Google Scholar] [CrossRef] [PubMed]
Sumarah, M.W.; Puniani, E.; Sørensen, D.; Blackwell, B.A.; Miller, J.D. Secondary metabolites from anti-insect extracts of endophytic fungi isolated from Picea rubens. Phytochemistry 2010, 71, 760–765. [Google Scholar] [CrossRef] [PubMed]
Amaral, L.S.; Rodrigues-Filho, E. Two novel eremophilane sesquiterpenes from an endophytic xylariaceous fungus isolated from leaves of Cupressus lusitanica. J. Braz. Chem. Soc. 2010, 21, 1446–1450. [Google Scholar] [CrossRef]
Atmosukarto, I.; Castillo, U.; Hess, W.M.; Sears, J.; Strobel, G. Isolation and characterization of Muscodor albus I-41.3 s, a volatile antibiotic producing fungus. Plant Sci. 2005, 169, 854–861. [Google Scholar] [CrossRef]
Isaka, M.; Palasarn, S.; Lapanun, S.; Chanthaket, R.; Boonyuen, N.; Lumyong, S. γ-Lactones and ent-eudesmane sesquiterpenes from the endophytic fungus Eutypella sp. BCC 13199. J. Nat. Prod. 2009, 72, 1720–1722. [Google Scholar] [CrossRef] [PubMed]
Luo, J.; Liu, X.; Li, E.; Guo, L.; Che, Y. Arundinols A-C and arundinones A and B from the plant endophytic fungus Microsphaeropsis arundinis. J. Nat. Prod. 2013, 76, 107–112. [Google Scholar] [CrossRef] [PubMed]
Li, D.; Chen, Y.; Pan, Q.; Tao, M.; Zhang, W. A new eudesmane sesquiterpene from Nigrospora oryzae, an endophytic fungus of Aquilaria sinensis. Rec. Nat. Prod. 2014, 8, 330–333. [Google Scholar]
Sopalun, K.; Strobel, G.A.; Hess, W.M.; Worapong, J. A record of Muscodor albus, an endophyte from Myristica fragrans in Thailand. Mycotaxon 2003, 88, 239–247. [Google Scholar]
Zhang, L.; Gu, S.; Shao, H.; Wei, R. Isolation, determination and aroma product characterization of fungus producing irone. Mycosystema 1999, 18, 49–54. [Google Scholar]
Zhang, L.; Wang, S.Q.; Li, X.J.; Zhang, A.L.; Zhang, Q.; Gao, J.M. New insight into the stereochemistry of botryosphaeridione from a Phoma endophyte. J. Mol. Struct. 2012, 1016, 72–75. [Google Scholar] [CrossRef]
Yang, X.L.; Zhang, S.; Zhu, H.J.; Luo, D.Q. Dihydroberkleasmin A: A new eremophilane sesquiterpenoid from the fermentation broth of the plant endophytic fungus Pestalotiopsis photiniae. Molecules 2011, 16, 1910–1916. [Google Scholar] [CrossRef] [PubMed]
Shiono, Y.; Murayama, T. New eremophilane-type sesquiterpenoids, eremoxylarins A and B from xylariaceous endophytic fungus YUA-026. Z. Naturforsch. B 2005, 60, 885–890. [Google Scholar] [CrossRef]
Kawahara, T.; Itoh, M.; Izumikawa, M.; Sakata, N.; Tsuchida, T.; Shin-ya, K. Three eremophilane derivatives, MBJ-0011, MBJ-0012 and MBJ-0013, from an endophytic fungus Apiognomonia sp. f24023. J. Antibiot. 2013, 66, 299–302. [Google Scholar] [CrossRef] [PubMed]
Zhang, D.; Ge, H.; Zou, J.H.; Tao, X.; Chen, R.; Dai, J. Periconianone A, a new 6/6/6 carbocyclic sesquiterpenoid from endophytic fungus Periconia sp. with neural anti-inflammatory activity. Org. Lett. 2014, 16, 1410–1413. [Google Scholar] [CrossRef] [PubMed]
Yang, X.L.; Zhang, S.; Zhu, H.J.; Luo, D.Q.; Gao, X.Y. Eremophilane-type sesquiterpenoids from the fermentation broth of plant endophytic fungus Pestalotiopsis photiniae isolated from the Chinese Podocarpaceae plant Podocarpus macrophyllus. Helv. Chim. Acta 2011, 94, 1463–1469. [Google Scholar] [CrossRef]
Hatakeyama, T.; Koseki, T.; Murayama, T.; Shiono, Y. Eremophilane sesquiterpenes from the endophyte Microdiplodia sp. KS 75-1 and revision of the stereochemistries of phomadecalins C and D. Phytochem. Lett. 2010, 3, 148–151. [Google Scholar] [CrossRef]
Song, Y.; Wang, J.; Huang, H.; Ma, L.; Wang, J.; Gu, Y.; Liu, L.; Lin, Y. Four eremophilane sesquiterpenes from the mangrove endophytic fungus Xylaria sp. BL321. Mar. Drugs 2012, 10, 340–348. [Google Scholar] [CrossRef] [PubMed]
Hu, Z.Y.; Li, Y.Y.; Huang, Y.J.; Su, W.J.; Shen, Y.M. Three new sesquiterpenoids from Xylaria sp. NCY2. Helv. Chim. Acta 2008, 91, 46–52. [Google Scholar] [CrossRef]
De Oliveira, C.M.; Silva, G.H.; Regasini, L.O.; Flausino, O., Jr.; López, S.N.; Abissi, B.M.; Gomes de Souza Berlinck, R.; Durães Sette, L.; Costa Bonugli-Santos, R.; Rodrigues, A.; et al. Xylarenones C-E from an endophytic fungus isolated from Alibertia macrophylla. J. Nat. Prod. 2011, 74, 1353–1357. [Google Scholar] [CrossRef] [PubMed]
Gubiani, J.R.; Zeraik, M.L.; Oliveira, C.M.; Ximenes, V.F.; Nogueira, C.R.; Fonseca, L.M.; Sila, D.H.S.; da Silva Bolzani, V.; Araujo, A.R. Biologically active eremophilane-type sesquiterpenes from Camarops sp., an endophytic fungus isolated from Alibertia macrophylla. J. Nat. Prod. 2014, 77, 668–672. [Google Scholar] [CrossRef] [PubMed]
Kramer, R.; Abraham, W.R. Volatile sesquiterpenes from fungi: What are they good for? Phytochem. Rev. 2012, 11, 15–37. [Google Scholar] [CrossRef]
Pažoutová, S.; Follert, S.; Bitzer, J.; Keck, M.; Surup, F.; Šrůtka, P.; Holuša, J.; Stadler, M. A new endophytic insect-associated Daldinia species, recognised from a comparison of secondary metabolite profiles and molecular phylogeny. Fungal Divers. 2013, 60, 107–123. [Google Scholar] [CrossRef]
Vidal, S. Changes in suitability of tomato for whiteflies mediated by a non-pathogenic endophytic fungus. Entomol. Experim. Appl. 1996, 80, 272–274. [Google Scholar] [CrossRef]
Jallow, M.F.; Dugassa-Gobena, D.; Vidal, S. Influence of an endophytic fungus on host plant selection by a polyphagous moth via volatile spectrum changes. Arthropod Plant Interact. 2008, 2, 53–62. [Google Scholar] [CrossRef]
Hodges, R.; Porte, A.L. The structure of loliolide: A terpene from Lolium perenne. Tetrahedron 1964, 20, 1463–1467. [Google Scholar] [CrossRef]
Wu, M.D.; Cheng, M.J.; Chen, I.S.; Su, Y.S.; Hsieh, S.Y.; Chang, H.S.; Chang, C.W.; Yuan, G.F. Phytochemical investigation of Annulohypoxylon ilanense, an endophytic fungus derived from Cinnamomum species. Chem. Biodivers. 2013, 10, 493–505. [Google Scholar] [CrossRef] [PubMed]
Ginesta-Peris, E.; Garcia-Breijo, F.J.; Primo-Yúfera, E. Antimicrobial activity of xanthatin from Xanthium spinosum L. Lett. Appl. Microbiol. 1994, 18, 206–208. [Google Scholar] [CrossRef]
Nibret, E.; Youns, M.; Krauth-Siegel, R.L.; Wink, M. Biological activities of xanthatin from Xanthium strumarium leaves. Phytother. Res. 2011, 25, 1883–1890. [Google Scholar] [CrossRef] [PubMed]
Xu, L.L.; Han, T.; Wu, J.Z.; Zhang, Q.Y.; Zhang, H.; Huang, B.K.; Rahman, K.; Qin, L.P. Comparative research of chemical constituents, antifungal and antitumor properties of ether extracts of Panax ginseng and its endophytic fungus. Phytomedicine 2009, 16, 609–616. [Google Scholar] [CrossRef] [PubMed]
Zaher, A.M.; Moharram, A.M.; Davis, R.; Panizzi, P.; Makboul, M.A.; Calderón, A.I. Characterisation of the metabolites of an antibacterial endophyte Botryodiplodia theobromae Pat. of Dracaena draco L. by LC–MS/MS. Nat. Prod. Res. 2015, 29. [Google Scholar] [CrossRef]
Cui, Y.; Yi, D.; Bai, X.; Sun, B.; Zhao, Y.; Zhang, Y. Ginkgolide B produced endophytic fungus (Fusarium oxysporum) isolated from Ginkgo biloba. Fitoterapia 2012, 83, 913–920. [Google Scholar] [CrossRef] [PubMed]
Carman, R.M.; Marty, R.A. Diterpenoids. IX. Agathis microstachya oleoresin. Aust. J. Chem. 1966, 19, 2403–2406. [Google Scholar] [CrossRef]
Izumi, E.; Ueda-Nakamura, T.; Veiga V.F., Jr.; Pinto, A.C.; Nakamura, C.V. Terpenes from Copaifera demonstrated in vitro antiparasitic and synergic activity. J. Med. Chem. 2012, 55, 2994–3001. [Google Scholar] [CrossRef] [PubMed]
Yuan, L.; Zhao, P.J.; Ma, J.; Lu, C.H.; Shen, Y.M. Labdane and tetranorlabdane diterpenoids from Botryosphaeria sp. MHF, an endophytic fungus of Maytenus hookeri. Helv. Chim. Acta 2009, 92, 1118–1125. [Google Scholar] [CrossRef]
Gardner, D.R.; Panter, K.E.; Stegelmeier, B.L. Implication of agathic acid from Utah juniper bark as an abortifacient compound in cattle. J. Appl. Toxicol. 2010, 30, 115–119. [Google Scholar] [CrossRef] [PubMed]
Isman, M.B. Botanical insecticides, deterrents, and repellents in modern agriculture and an increasingly regulated world. Annu. Rev. Entomol. 2006, 51, 45–66. [Google Scholar] [CrossRef] [PubMed]
Kusari, S.; Verma, V.C.; Lamshoeft, M.; Spiteller, M. An endophytic fungus from Azadirachta indica A. Juss. that produces azadirachtin. World J. Microbiol. Biotechnol. 2012, 28, 1287–1294. [Google Scholar] [CrossRef]
Dos Santos, R.M.G.; Rodrigues-Fo, E. Meroterpenes from Penicillium sp. found in association with Melia azedarach. Phytochemistry 2002, 61, 907–912. [Google Scholar]
Wang, Q.; Fu, Y.; Gao, J.; Wang, Y.; Li, X.; Zhang, A. Preliminary isolation and screening of the endophytic fungi from Melia azedarach L. Acta Agric. Boreali-Occident. Sin. 2007, 16, 224–227. [Google Scholar]
Man, S.; Gao, W.; Wei, C.; Liu, C. Anticancer drugs from traditional toxic Chinese medicines. Phytother. Res. 2012, 26, 1449–1465. [Google Scholar] [CrossRef] [PubMed]
Pal, S.; Chatare, V.; Pal, M. Isocoumarin and its derivatives: An overview on their synthesis and applications. Curr. Org. Chem. 2011, 15, 782–800. [Google Scholar] [CrossRef]
Venugopala, K.N.; Rashmi, V.; Odhav, B. Review on natural coumarin lead compounds for their pharmacological activity. BioMed Res. Int. 2013. [Google Scholar] [CrossRef] [PubMed]
Umashankar, T.; Govindappa, M.; Ramachandra, Y.L. In vitro antioxidant and antimicrobial activity of partially purified coumarins from fungal endophytes of Crotalaria pallida. Int. J. Curr. Microbiol. Appl. Sci. 2014, 3, 58–72. [Google Scholar]
Gnonlonfin, G.B.; Sanni, A.; Brimer, L. Review scopoletin—A coumarin phytoalexin with medicinal properties. Crit. Rev. Plant Sci. 2012, 31, 47–56. [Google Scholar] [CrossRef]
Huang, Z.; Yang, J.; Cai, X.; She, Z.; Lin, Y. A new furanocoumarin from the mangrove endophytic fungus Penicillium sp. (ZH16). Nat. Prod. Res. 2012, 26, 1291–1295. [Google Scholar] [CrossRef] [PubMed]
Cheng, M.J.; Wu, M.D.; Chen, J.J.; Hsieh, S.Y.; Yuan, G.F.; Chen, I.S.; Chang, C.W. Secondary metabolites from the endophytic fungus of Annulohypoxylon ilanense. Chem. Nat. Compd. 2013, 49, 523–525. [Google Scholar] [CrossRef]
Huang, Z.; Yang, J.; She, Z.; Lin, Y. Isoflavones from the mangrove endophytic fungus Fusarium sp. (ZZF41). Nat. Prod. Commun. 2010, 5, 1771–1773. [Google Scholar] [PubMed]
Nishikawa, E. Biochemisty of filamentous fungi. II. A metabolic product of Aspergillus melleus Yukawa. Part I. Bull. Agric. Chem. Soc. Jpn. 1933, 9, 107–109. [Google Scholar] [CrossRef]
Krohn, K.; Bahramsari, R.; Flörke, U.; Ludewig, K.; Kliche-Spory, C.; Michel, A.; Aust, H.-J.; Draeger, S.; Schulz, B.; Antus, S. Dihydroisocoumarins from fungi: Isolation, structure elucidation, circular dichroism and biological activity. Phytochemistry 1997, 45, 313–320. [Google Scholar] [CrossRef]
Das, A.J. Moringa oleifera (Lamm.): A plant with immense importance. J. Biol. Act. Prod. Nat. 2012, 2, 307–315. [Google Scholar] [CrossRef]
Chacón-Morales, P.; Amaro-Luis, J.M.; Bahsas, A. Isolation and characterization of (+)-mellein, the first isocoumarin reported in Stevia genus. Avan. Quim. 2013, 8, 145–151. [Google Scholar]
Oliveira, C.M.; Regasini, L.O.; Silva, G.H.; Pfenning, L.H.; Young, M.C.M.; Berlinck, R.G.S.; Bolzani, V.S.; Araujo, A.R. Dihydroisocoumarins produced by Xylaria sp. and Penicillium sp., endophytic fungi associated with Piper aduncum and Alibertia macrophylla. Phytochem. Lett. 2011, 4, 93–96. [Google Scholar] [CrossRef]
Fan, N.W.; Chang, H.S.; Cheng, M.J.; Hsieh, S.Y.; Liu, T.W.; Yuan, G.F.; Chen, I.S. Secondary metabolites from the endophytic fungus Xylaria cubensis. Helv. Chim. Acta 2014, 97, 1689–1699. [Google Scholar] [CrossRef]
Zhao, J.H.; Zhang, Y.L.; Wang, L.W.; Wang, J.Y.; Zhang, C.L. Bioactive secondary metabolites from Nigrospora sp. LLGLM003, an endophytic fungus of the medicinal plant Moringa oleifera Lam. World J. Microbiol. Biotechnol. 2012, 28, 2107–2112. [Google Scholar] [CrossRef] [PubMed]
Amaral, L.S.; Murgu, M.; Rodrigues-Fo, E.; de Souza, A.Q.; de Moura Sarquis, M.I. A saponin tolerant and glycoside producer xylariaceous fungus isolated from fruits of Sapindus saponaria. World J. Microbiol. Biotechnol. 2008, 24, 1341–1348. [Google Scholar] [CrossRef]
Cheng, M.J.; Wu, M.D.; Yuan, G.F.; Chen, Y.L.; Su, Y.S.; Hsieh, M.T.; Chen, I.S. Secondary metabolites and cytotoxic activities from the endophytic fungus Annulohypoxylon squamulosum. Phytochem. Lett. 2012, 5, 219–223. [Google Scholar] [CrossRef]
Cheng, M.J.; Wu, M.D.; Hsieh, S.Y.; Hsieh, M.T.; Chen, I.S.; Yuan, G.F. Constituents of the endophytic fungus Annulohypoxylon boveri var. microspora BCRC 34012. Helv. Chim. Acta 2011, 94, 1108–1114. [Google Scholar] [CrossRef]
Calderón-Montaño, J.M.; Burgos-Morón, E.; Pérez-Guerrero, C.; López-Lázaro, M. A review on the dietary flavonoid kaempferol. Mini Rev. Med. Chem. 2011, 11, 298–344. [Google Scholar] [CrossRef]
Treutter, D. Significance of flavonoids in plant resistance and enhancement of their biosynthesis. Plant Biol. 2005, 7, 581–591. [Google Scholar] [CrossRef] [PubMed]
Huang, W.Y.; Cai, Y.Z.; Hyde, K.D.; Corke, H.; Sun, M. Biodiversity of endophytic fungi associated with 29 traditional Chinese medicinal plants. Fungal Divers. 2008, 33, 61–75. [Google Scholar]
Qiu, M.; Xie, R.S.; Shi, Y.; Zhang, H.; Chen, H.M. Isolation and identification of two flavonoid-producing endophytic fungi from Ginkgo biloba L. Ann. Microbiol. 2010, 60, 143–150. [Google Scholar] [CrossRef]
Huang, J.X.; Zhang, J.; Zhang, X.R.; Zhang, K.; Zhang, X.; He, X.R. Mucor fragilis as a novel source of the key pharmaceutical agents podophyllotoxin and kaempferol. Pharm. Biol. 2014, 52, 1237–1243. [Google Scholar] [CrossRef] [PubMed]
Chaturvedi, P.; Gajbhiye, S.; Roy, S.; Dudhale, R.; Chowdhary, A. Determination of kaempferol in extracts of Fusarium chlamydosporum, an endophytic fungi of Tylophora indica (Asclepeadaceae) and its anti-microbial activity. J. Pharm. Biol. Sci. 2014, 9, 51–55. [Google Scholar]
Cheng, M.J.; Wu, M.D.; Hsieh, S.Y.; Su, Y.S.; Chen, I.S.; Yuan, G.F. Secondary metabolites from the endophytic fungus Annulohypoxylon boveri var. microspora BCRC 34012. Chem. Nat. Compd. 2011, 47, 536–540. [Google Scholar] [CrossRef]
Lopez-Lazaro, M. Distribution and biological activities of the flavonoid luteolin. Mini Rev. Med. Chem. 2009, 9, 31–59. [Google Scholar] [CrossRef] [PubMed]
Zhao, J.; Ma, D.; Luo, M.; Wang, W.; Zhao, C.; Zu, Y.; Fu, Y.; Wink, M. In vitro antioxidant activities and antioxidant enzyme activities in HepG2 cells and main active compounds of endophytic fungus from pigeon pea [Cajanus cajan (L.) Millsp.]. Food Res. Int. 2014, 56, 243–251. [Google Scholar] [CrossRef]
Luo, M.; Liu, X.; Zu, Y.; Fu, Y.; Zhang, S.; Yao, L.; Efferth, T. Cajanol, a novel anticancer agent from pigeonpea [Cajanus cajan (L.) Millsp.] roots, induces apoptosis in human breast cancer cells through a ROS-mediated mitochondrial pathway. Chem. Biol. Interact. 2010, 188, 151–160. [Google Scholar] [CrossRef] [PubMed]
Zhao, J.; Li, C.; Wang, W.; Zhao, C.; Luo, M.; Mu, F.; Fu, Y.; Zu, Y.; Yao, M. Hypocrea lixii, novel endophytic fungi producing anticancer agent cajanol, isolated from pigeon pea (Cajanus cajan [L.] Millsp.). J. Appl. Microbiol. 2013, 115, 102–113. [Google Scholar] [PubMed]
Gao, Y.; Zhao, J.; Zu, Y.; Fu, Y.; Liang, L.; Luo, M.; Wang, W.; Efferth, T. Antioxidant properties, superoxide dismutase and glutathione reductase activities in HepG2 cells with a fungal endophyte producing apigenin from pigeon pea [Cajanus cajan (L.) Millsp.]. Food Res. Int. 2012, 49, 147–152. [Google Scholar] [CrossRef]
Zhou, S.L.; Wang, M.X.; Chen, S.L. Two compounds from the endophytic Colletotrichum sp. of Ginkgo biloba. Nat. Prod. Commun. 2011, 6, 1131–1132. [Google Scholar]
Tian, Y.; Amand, S.; Buisson, D.; Kunz, C.; Hachette, F.; Dupont, J.; Nay, B.; Prado, S. The fungal leaf endophyte Paraconiothyrium variabile specifically metabolizes the host-plant metabolome for its own benefit. Phytochemistry 2014, 108, 95–101. [Google Scholar] [CrossRef] [PubMed]
Haller, H.L.; Goodhue, L.D.; Jones, H.A. The constituents of Derris and other rotenone-bearing plants. Chem. Rev. 1942, 30, 33–48. [Google Scholar] [CrossRef]
Hu, M.Y.; Zhong, G.H.; Sun, Z.T.; Sh, G.; Liu, H.M.; Liu, X.Q. Insecticidal activities of secondary metabolites of endophytic Pencillium sp. in Derris elliptica Benth. J. Appl. Entomol. 2005, 129, 413–417. [Google Scholar] [CrossRef]
Davis-Searles, P.R.; Nakanishi, Y.; Kim, N.-C.; Graf, T.N.; Oberlies, N.H.; Wani, M.C.; Wall, M.E.; Agrawal, R.; Kroll, D.J. Milk thistle and prostate cancer: Differential effects of pure flavonolignans from Silybum marianum on antiproliferative end points in human prostate carcinoma cells. Cancer Res. 2005, 65, 4448–4457. [Google Scholar] [CrossRef] [PubMed]
Jayaraj, R.; Deb, U.; Bhaskar, A.S.; Prasad, G.B.; Rao, P.V. Hepatoprotective efficacy of certain flavonoids against microcystin induced toxicity in mice. Environ. Toxicol. 2007, 22, 472–479. [Google Scholar] [CrossRef] [PubMed]
El-Elimat, T.; Raja, H.A.; Graf, T.N.; Faeth, S.H.; Cech, N.B.; Oberlies, N.H. Flavonolignans from Aspergillus iizukae, a fungal endophyte of milk thistle (Silybum marianum). J. Nat. Prod. 2014, 77, 193–199. [Google Scholar] [CrossRef] [PubMed]
Dao, T.T.H.; Linthorst, H.J.M.; Verpoorte, R. Chalcone synthase and its functions in plant resistance. Phytochem. Rev. 2011, 10, 397–412. [Google Scholar] [CrossRef] [PubMed]
Patil, C.B.; Mahajan, S.K.; Katti, S.A. Chalcone: A versatile molecule. J. Pharm. Sci. Res. 2009, 1, 11–22. [Google Scholar]
Sahu, N.K.; Balbhadra, S.S.; Choudhary, J.; Kohli, D.V. Exploring pharmacological significance of chalcone scaffold: A review. Curr. Med. Chem. 2012, 19, 209–225. [Google Scholar] [CrossRef] [PubMed]
Wang, J.; Yao, L.Y.; Lu, Y.H. Ceriporia lacerata DMC1106, a new endophytic fungus: Isolation, identification, and optimal medium for 2′,4′-dihydroxy-6′-methoxy-3′,5′-dimethylchalcone production. Biotechnol. Bioprocess Eng. 2013, 18, 669–678. [Google Scholar] [CrossRef]
Negi, J.S.; Bisht, V.K.; Singh, P.; Rawat, M.S.M.; Joshi, G.P. Naturally occurring xanthones: Chemistry and biology. J. Appl. Chem. 2013. [Google Scholar] [CrossRef]
Nagem, T.J.; de Oliveira, F.F. Xanthones and other constituents of Vismia parviflora. J. Braz. Chem. Soc. 1997, 8, 505–508. [Google Scholar] [CrossRef]
Kato, L.; Alves de Oliveira, C.M.; Vencato, I.; Lauriucci, C. Crystal structure of 1,7-dihydroxyxanthone from Weddellina squamulosa Tul. J. Chem. Crystall. 2005, 35, 23–26. [Google Scholar] [CrossRef]
Law, K.K.; Chan, T.L.; Tam, S.W.; Shatin, N.T. Synthesis of pinselic acid and pinselin. J. Org. Chem. 1979, 44, 4452–4453. [Google Scholar] [CrossRef]
Yang, H.Y.; Gao, Y.H.; Niu, D.Y.; Yang, L.Y.; Gao, X.M.; Du, G.; Hu, Q.F. Xanthone derivatives from the fermentation products of an endophytic fungus Phomopsis sp. Fitoterapia 2013, 91, 189–193. [Google Scholar] [CrossRef] [PubMed]
Hay, A.E.; Aumond, M.C.; Mallet, S.; Dumontet, V.; Litaudon, M.; Rondeau, D.; Richomme, P. Antioxidant xanthones from Garcinia vieillardii. J. Nat. Prod. 2004, 67, 707–709. [Google Scholar] [CrossRef] [PubMed]
Gessler, N.N.; Egorova, A.S.; Belozerskaya, T.A. Fungal anthraquinones. Appl. Biochem. Microbiol. 2013, 49, 85–99. [Google Scholar] [CrossRef]
Danielsen, K.; Aksnes, D.W.; Francis, G.W. NMR study of some anthraquinones from rhubarb. Magn. Reson. Chem. 1992, 30, 359–360. [Google Scholar] [CrossRef]
Dave, H.; Ledwani, L. A review on anthraquinones isolated from Cassia species and their applications. Indian J. Nat. Prod. Res. 2012, 3, 291–319. [Google Scholar]
Jayasuriya, H.; Koonchanok, N.M.; Geahlen, R.L.; McLaughlin, J.L.; Chang, C.J. Emodin, a protein tyrosine kinase inhibitor from Polygonum cuspidatum. J. Nat. Prod. 1992, 55, 696–698. [Google Scholar] [CrossRef] [PubMed]
Leu, Y.L.; Hwang, T.L.; Hu, J.W.; Fang, J.Y. Anthraquinones from Polygonum cuspidatum as tyrosinase inhibitors for dermal use. Phytother. Res. 2008, 22, 552–556. [Google Scholar] [CrossRef] [PubMed]
Marinho, A.M.R.; Rodrigues-Filho, E.; Moitinho, M.L.R.; Santos, L.S. Biologically active polyketides produced by Penicillium janthinellum isolated as an endophytic fungus from fruits of Melia azedarach. J. Braz. Chem. Soc. 2005, 16, 280–283. [Google Scholar] [CrossRef]
Wang, F.W.; Hou, Z.M.; Wang, C.R.; Li, P.; Shi, D.H. Bioactive metabolites from Penicillium sp., an endophytic fungus residing in Hopea hainanensis. World J. Microbiol. Biotechnol. 2008, 24, 2143–2147. [Google Scholar] [CrossRef]
Marinho, A.M.R.; Marinho, P.S.B.; Santos, L.S.; Rodrigues Filho, E.; Ferreira, I.C.P. Active polyketides isolated from Penicillium herquei. Anais Acad. Bras. Ciências 2013, 85, 909–912. [Google Scholar] [CrossRef] [PubMed]
Liu, F.; Cai, X.L.; Yang, H.; Xia, X.K.; Guo, Z.Y.; Yuan, J.; Li, M.F.; She, Z.G.; Lin, Y.C. The bioactive metabolites of the mangrove endophytic fungus Talaromyces sp. ZH-154 isolated from Kandelia candel (L.) Druce. Planta Med. 2010, 76, 185–189. [Google Scholar] [CrossRef] [PubMed]
Zhu, F.; Lin, Y.C.; Zhou, S.N. Anthraquinone derivatives isolated from marine fungus #2526 from the South China Sea. Chin. J. Org. Chem. 2004, 24, 1114–1117. [Google Scholar]
Liu, J.Y.; Song, Y.C.; Zhang, Z.; Wang, L.; Guo, Z.J.; Zou, W.X.; Tan, R.X. Aspergillus fumigatus CY018, an endophytic fungus in Cynodon dactylon as a versatile producer of new and bioactive metabolites. J. Biotechnol. 2004, 114, 279–287. [Google Scholar] [CrossRef] [PubMed]
Wu, S.H.; Chen, Y.W.; Qin, S.; Huang, R. A new spiroketal from Aspergillus terreus, an endophytic fungus in Opuntia ficusindica Mill. J. Basic Microbiol. 2008, 48, 140–142. [Google Scholar] [CrossRef] [PubMed]
Derksen, G.C.H.; Van Beek, T.A. Rubia tinctorum L. Stud. Nat. Prod. Chem. 2002, 26, 629–684. [Google Scholar]
Gautam, R.; Karkhile, K.V.; Bhutani, K.K.; Jachak, S.M. Anti-inflammatory, cyclooxygenase (COX)-2, COX-1 inhibitory, and free radical scavenging effects of Rumex nepalensis. Planta Med. 2010, 76, 1564–1569. [Google Scholar] [CrossRef] [PubMed]
Yang, X.L.; Awakawa, T.; Wakimoto, T.; Abe, I. Induced production of novel prenyldepside and coumarins in endophytic fungi Pestalotiopsis acaciae. Tetrahedron Lett. 2013, 54, 5814–5817. [Google Scholar] [CrossRef]
Ogwuru, N.; Adamczeski, M. Bioactive natural products derived from Polygonum species of plants: Their structures and mechanisms of action. Stud. Nat. Prod. Chem. 2000, 22, 607–642. [Google Scholar]
Li, D.L.; Li, X.M.; Li, T.G.; Dang, H.Y.; Proksch, P.; Wang, B.G. Benzaldehyde derivatives from Eurotium rubrum, an endophytic fungus derived from the mangrove plant Hibiscus tiliaceus. Chem. Pharm. Bull. 2008, 56, 1282–1285. [Google Scholar] [CrossRef] [PubMed]
Chomcheon, P.; Wiyakrutta, S.; Sriubolmas, N.; Ngamrojanavanich, N.; Mahidol, C.; Ruchirawat, S.; Kittakoop, P. Metabolites from the endophytic mitosporic Dothideomycete sp. LRUB20. Phytochemistry 2009, 70, 121–127. [Google Scholar] [CrossRef] [PubMed]
Borges, W.D.S.; Pupo, M.T. Novel anthraquinone derivatives produced by Phoma sorghina, an endophyte found in association with the medicinal plant Tithonia diversifolia (Asteraceae). J. Braz. Chem. Soc. 2006, 17, 929–934. [Google Scholar] [CrossRef]
Imre, S.; Sar, S.; Thomson, R.H. Anthraquinones in Digitalis species. Phytochemistry 1976, 15, 317–320. [Google Scholar] [CrossRef]
Arrebola, M.L.; Ringbom, T.; Verpoorte, R. Anthraquinones from Isoplexis isabelliana cell suspension cultures. Phytochemistry 1999, 52, 1283–1286. [Google Scholar] [CrossRef]
Imre, S. Flavone and anthraquinone dyes from Digitalis species. I. isolation of a new anthraquinone dye from Digitalis viridiflora leaves. Phytochemistry 1969, 8, 315. [Google Scholar] [CrossRef]
Sun, P.; Huo, J.; Kurtan, T.; Mandi, A.; Antus, S.; Tang, H.; Draeger, S.; Schulz, B.; Hussain, H.; Krohn, K.; et al. Structural and stereochemical studies of hydroxyanthraquinone derivatives from the endophytic fungus Coniothyrium sp. Chirality 2013, 25, 141–148. [Google Scholar] [CrossRef] [PubMed]
Wulansari, D.; Jamal, Y.; Agusta, A. Pachybasin, a major metabolite from culture broth of endophytic Coelomyceteous AFKR-18 fungus isolated from a yellow moonsheed plant, Arcangelisia flava (L.) Merr. Hayati J. Biosci. 2014, 21, 95–100. [Google Scholar] [CrossRef]
Karioti, A.; Bilia, A.R. Hypericins as potential leads for new therapeutics. Int. J. Mol. Sci. 2010, 11, 562–594. [Google Scholar] [CrossRef] [PubMed]
Kusari, S.; Lamshöft, M.; Zühlke, S.; Spiteller, M. An endophytic fungus from Hypericum perforatum that produces hypericin. J. Nat. Prod. 2008, 71, 159–162. [Google Scholar] [CrossRef] [PubMed]
Kusari, S.; Zühlke, S.; Kosuth, J.; Čellárová, E.; Spiteller, M. Light-independent metabolomics of endophytic Thielavia subthermophila provides insight into microbial hypericin biosynthesis. J. Nat. Prod. 2009, 72, 1825–1835. [Google Scholar] [CrossRef]
Kumar, U.S.; Aparna, P.; Rao, R.J.; Rao, T.P.; Rao, J.M. 1-Methyl anthraquinones and their biogenetic precursors from Stereospermum personatum. Phytochemistry 2003, 63, 925–929. [Google Scholar] [CrossRef]
Zhang, Y.; Jiang, P.; Ye, M.; Kim, S.H.; Jiang, C.; Lü, J. Tanshinones: Sources, pharmacokinetics and anti-cancer activities. Int. J. Mol. Sci. 2012, 13, 13621–13666. [Google Scholar] [CrossRef] [PubMed]
Ma, C.; Jiang, D.; Wei, X. Mutation breeding of Emericella foeniculicola TR21 for improved production of tanshinone IIA. Proc. Biochem. 2011, 46, 2059–2063. [Google Scholar] [CrossRef]
Ming, Q.L.; Han, T.; Li, W.; Zhang, Q.Y.; Zhang, H.; Zheng, C.J.; Huang, F.; Rahman, K.; Qin, L.P. Tanshinone IIA and tanshinone I production by Trichoderma atroviride D16, an endophytic fungus in Salvia miltiorrhiza. Phytomedicine 2012, 19, 330–333. [Google Scholar] [CrossRef] [PubMed]
Ming, Q.; Su, C.; Zheng, C.; Jia, M.; Zhang, Q.; Zhang, H.; Rahman, K.; Han, T.; Qin, L. Elicitors from the endophytic fungus Trichoderma atroviride promote Salvia miltiorrhiza hairy root growth and tanshinone biosynthesis. J. Exp. Bot. 2013, 64, 5687–5694. [Google Scholar] [CrossRef] [PubMed]
Chen, X.; Yang, L.; Zhang, N.; Turpin, J.A.; Buckheit, R.W.; Osterling, C.; Oppenheim, J.J.; Zack Howard, O.M. Shikonin, a component of Chinese herbal medicine, inhibits chemokine receptor function and suppresses human immunodeficiency virus type 1. Antimicrob. Agents Chemother. 2003, 47, 2810–2816. [Google Scholar] [CrossRef] [PubMed]
Movahhedin, N.; Albadry, M.; Hamann, T. Isolation and characterization of cytotoxic compounds from endophytes of an endangered American cactus, Mammillaria hahniana. Planta Med. 2014, 80, PD136. [Google Scholar] [CrossRef]
Epifano, F.; Genovese, S.; Fiorito, S.; Mathieu, V.; Kiss, R. Lapachol and its congeners as anticancer agents: A review. Phytochem. Rev. 2014, 13, 37–49. [Google Scholar] [CrossRef]
Sadananda, T.S.; Nirupama, R.; Chaithra, K.; Govindappa, M.; Chandrappa, C.P.; Vinay Raghavendra, B. Antimicrobial and antioxidant activities of endophytes from Tabebuia argentea and identification of anticancer agent (lapachol). J. Med. Plants Res. 2011, 5, 3643–3652. [Google Scholar]
Channabasava, R.; Govindappa, M. First report of anticancer agent, lapachol producing endophyte, Aspergillus niger of Tabebuia argentea and its in vitro cytotoxicity assays. Bangladesh J. Pharmacol. 2014, 9, 129–139. [Google Scholar] [CrossRef]
Gordaliza, M.; Garcı́a, P.A.; Miguel del Corral, J.M.; Castro, M.A.; Gómez-Zurita, M.A. Podophyllotoxin: Distribution, sources, applications and new cytotoxic derivatives. Toxicon 2004, 44, 441–459. [Google Scholar] [CrossRef]
Inamori, Y.; Kubo, M.; Tsujibo, H.; Ogawa, M.; Baba, K.; Kozawa, M.; Fujita, E. The biological activities of podophyllotoxin compounds. Chem. Pharm. Bull. 1986, 34, 3928–3932. [Google Scholar] [CrossRef] [PubMed]
Gao, R.; Gao, C.; Tian, X.; Yu, X.; Di, X.; Xiao, H.; Zhang, X. Insecticidal activity of deoxypodophyllotoxin, isolated from Juniperus sabina L, and related lignans against larvae of Pieris rapae L. Pest Manag. Sci. 2004, 60, 1131–1136. [Google Scholar] [CrossRef] [PubMed]
You, Y. Podophyllotoxin derivatives: Current synthetic approaches for new anticancer agents. Curr. Pharm. Design 2005, 11, 1695–1717. [Google Scholar] [CrossRef]
Yang, X.; Guo, S.; Zhang, L.; Shao, H. Select of producing podophyllotoxin endophytic fungi from podophyllin plant. Nat. Prod. Res. Dev. 2003, 15, 419–422. [Google Scholar]
Lu, L.; He, J.; Yu, X.; Li, G.; Zhang, X. Studies on isolation and identification of endophytic fungi strain SC13 from harmaceutical plant Sabina vulgaris Ant. and metabolites. Acta Agric. Boreali-Occident. Sin. 2006, 15, 85–89. [Google Scholar]
Eyberger, A.L.; Dondapati, R.; Porter, J.R. Endophyte fungal isolates from Podophyllum peltatum produce podophyllotoxin. J. Nat. Prod. 2006, 69, 1121–1124. [Google Scholar] [CrossRef] [PubMed]
Puri, S.C.; Nazir, A.; Chawla, R.; Arora, R.; Riyaz-ul-Hasan, S.; Amna, T.; Ahmed, B.; Verma, V.; Singh, S.; Sagar, R.; et al. The endophytic fungus Trametes hirsuta as a novel alternative source of podophyllotoxin and related aryl tetralin lignans. J. Biotechnol. 2006, 122, 494–510. [Google Scholar] [CrossRef] [PubMed]
Nadeem, M.; Ram, M.; Alam, P.; Ahmad, M.M.; Mohammad, A.; Al-Qurainy, F.; Khan, S.; Abdin, M.Z. Fusarium solani, P1, a new endophytic podophyllotoxin-producing fungus from roots of Podophyllum hexandrum. Afr. J. Microbiol. Res. 2012, 6, 2493–2499. [Google Scholar]
Kour, A.; Shawl, A.S.; Rehman, S.; Sultan, P.; Qazi, P.H.; Suden, P.; Khajuria, R.K.; Verma, V. Isolation and identification of an endophytic strain of Fusarium oxysporum producing podophyllotoxin from Juniperus recurva. World J. Microbiol. Biotechnol. 2008, 24, 1115–1121. [Google Scholar] [CrossRef]
Kusari, S.; Lamshöft, M.; Spiteller, M. Aspergillus fumigatus Fresenius, an endophytic fungus from Juniperus communis L. Horstmann as a novel source of the anticancer pro-drug deoxypodophyllotoxin. J. Appl. Microbiol. 2009, 107, 1019–1030. [Google Scholar] [CrossRef] [PubMed]
Kong, P.; Zhang, L.; Guo, Y.; Lu, Y.; Lin, D. Phillyrin, a natural lignan, attenuates tumor necrosis factor α-mediated insulin resistance and lipolytic acceleration in 3T3-L1 adipocytes. Planta Med. 2014, 80, 880–886. [Google Scholar] [CrossRef] [PubMed]
Zhang, Q.; Wei, X.; Wang, J. Phillyrin produced by Colletotrichum gloeosporioides, an endophytic fungus isolated from Forsythia suspensa. Fitoterapia 2012, 83, 1500–1505. [Google Scholar] [CrossRef] [PubMed]
Wani, M.C.; Taylor, H.L.; Wall, M.E.; Coggon, P.; McPhail, A.T. Plant antitumor agents. VI. Isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia. J. Am. Chem. Soc. 1971, 93, 2325–2327. [Google Scholar] [PubMed]
Vidensek, N.; Lim, P.; Campbell, A.; Carlson, C. Taxol content in bark, wood, root, leaf, twig and seedling from several Taxus species. J. Nat. Prod. 1990, 53, 1609–1610. [Google Scholar] [CrossRef] [PubMed]
Stierle, A.; Strobel, G.; Stierle, D. Taxol and taxane production by Taxomyces andreanae, an endophytic fungus of pacific yew. Science 1993, 260, 214–216. [Google Scholar] [CrossRef] [PubMed]
Kusari, S.; Singh, S.; Jayabaskaran, C. Rethinking production of Taxol^® (paclitaxel) using endophyte biotechnology. Trends Biotechnol. 2014, 32, 304–311. [Google Scholar] [CrossRef] [PubMed]
Soca-Chafre, G.; Rivera-Orduña, F.N.; Hidalgo-Lara, M.E.; Hernandez-Rodriguez, C.; Marsch, R.; Flores-Cotera, L.B. Molecular phylogeny and paclitaxel screening of fungal endophytes from Taxus globosa. Fungal Biol. 2011, 115, 143–156. [Google Scholar] [CrossRef] [PubMed]
Strobel, G.A.; Hess, W.M.; Ford, E.; Sidhu, R.S.; Yang, X. Taxol from fungal endophytes and the issue of biodiversity. J. Ind. Microbiol. 1996, 17, 417–423. [Google Scholar] [CrossRef]
Kim, S.U.; Strobel, G.A.; Ford, E. Screening of taxol-producing endophytic fungi from Ginkgo biloba and Taxus cuspidata in Korea. Agric. Chem. Biotechnol. 1999, 42, 97–99. [Google Scholar]
Michalczyk, A.; Cieniecka-Rosłonkiewicz, A.; Cholewińska, M. Plant endophytic fungi as a source of paclitaxel. Herba Pol. 2014, 60, 22–33. [Google Scholar]
Zhang, P.; Zhou, P.-P.; Yu, L.-J. An endophytic taxol-producing fungus from Taxus x media, Aspergillus candidus MD3. FEMS Microbiol. Lett. 2009, 293, 155–159. [Google Scholar] [CrossRef] [PubMed]
Sun, D.; Ran, X.; Wang, J. Isolation and identification of a taxol-producing endophytic fungus from Podocarpus. Acta Microbiol. Sin. 2008, 48, 589–595. [Google Scholar]
Zhao, K.; Ping, W.; Li, Q.; Hao, S.; Zhao, L.; Gao, T.; Zhou, D. Aspergillus niger var. taxi, a new species variant of taxol-producing fungus isolated from Taxus cuspidata in China. J. Appl. Microbiol. 2009, 107, 1202–1207. [Google Scholar]
Liu, K.; Ding, X.; Deng, B.; Chen, W. Isolation and characterization of endophytic taxol-producing fungi from Taxus chinensis. J. Ind. Microbiol. Biotechnol. 2009, 36, 1171–1177. [Google Scholar] [CrossRef] [PubMed]
Gangadevi, V.; Muthumary, J. Taxol, an anticancer drug produced by an endophytic fungus Bartalinia robillardoides Tassi, isolated from a medicinal plant, Aegle marmelos Correa ex Roxb. World J. Microbiol. Biotechnol. 2008, 24, 717–724. [Google Scholar] [CrossRef]
Hu, K.; Tan, F.; Tang, K.; Zhu, S.; Wang, W. Isolation and screening of endophytic fungi synthesizing taxol from Taxus chinensis var. mairei. J. Southwest China Norm. Univ. (Nat. Sci. Ed.) 2006, 31, 134–137. [Google Scholar]
Zhao, K.; Zhao, L.; Jin, Y.; Wei, H.; Ping, W.; Zhou, D. Isolation of a taxol-producing endophytic fungus and inhibiting effect of the fungus metabolites on HeLa cell. Mycosystema 2008, 27, 735–744. [Google Scholar]
Gangadevi, V.; Muthumary, J. A novel endophytic taxol-producing fungus Chaetomella raphigera isolated from a medicinal plant, Terminalia arjuna. Appl. Biochem. Biotechnol. 2009, 158, 675–684. [Google Scholar] [CrossRef] [PubMed]
Zhang, P.; Zhou, P.P.; Yu, L.J. An endophytic taxol-producing fungus from Taxus media, Cladosporium cladosporioides MD2. Curr. Microbiol. 2009, 59, 227–232. [Google Scholar] [CrossRef] [PubMed]
Raj, K.G.; Manikandan, R.; Arulvasu, C.; Pandi, M. Anti-proliferative effect of fungal taxol extracted from Cladosporium oxysporum against human pathogenic bacteria and human colon cancer cell line HCT 15. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 2015, 138, 667–674. [Google Scholar]
Gangadevi, V.; Muthumary, J. Isolation of Colletotrichum gloeosporioides, a novel endophytic taxol-producing fungus from the leaves of a medicinal plant, Justicia gendarussa. Mycol. Balc. 2008, 5, 1–4. [Google Scholar]
Nithya, K.; Muthumary, J. Growth studies of Colletotrichum gloeosporioides (Penz.) Sacc.—A taxol producing endophytic fungus from Plumeria acutifolia. Indian J. Sci. Technol. 2009, 2, 14–19. [Google Scholar]
Xiong, Z.Q.; Yang, Y.Y.; Zhao, N.; Wang, Y. Diversity of endophytic fungi and screening of fungal paclitaxel producer from Anglojap yew, Taxus x media. BMC Microbiol. 2013, 13, 71. [Google Scholar] [CrossRef] [PubMed]
Senthilkumar, N.; Murugesan, S.; Mohan, V.; Muthumary, J. Taxol producing fungal endophyte, Colletotrichum gleospoiroides (Penz.) from Tectona grandis L. Curr. Biotica 2013, 7, 8–15. [Google Scholar]
Raj, K.G.; Rajapriya, P.; Muthumary, J.; Pandi, M. Molecular identification and characterization of the taxol-producing Colletotrichum gloeosporioides from Moringa oleifera Linn. In Microbial Diversity and Biotechnology in Food Security; Kharwar, R.N., Upadhyay, R., Dubey, N., Raghuwanshi, R., Eds.; Springer India: New Delhi, India, 2014; pp. 111–120. [Google Scholar]
Strobel, G.A.; Ford, E.; Li, J.-Y.; Sears, J.; Sidhu, R.S.; Hess, W.M. Seimatoantlerium tepuiense gen. nov., a unique epiphytic fungus producing taxol from the Venezuelan Guyana. Syst. Appl. Microbiol. 1999, 22, 426–433. [Google Scholar] [CrossRef]
Wang, Y.; Tang, K. A new endophytic taxol- and baccatin III-producing fungus isolated from Taxus chinensis var. mairei. Afr. J. Biotechnol. 2011, 10, 16379–16386. [Google Scholar]
Li, C.-T.; Li, Y.; Wang, Q.-J.; Sung, C.-K. Taxol production by Fusarium arthrosporioides isolated from yew, Taxus cuspidata. J. Med. Biochem. 2008, 27, 454–458. [Google Scholar] [CrossRef]
Xu, F.; Tao, W.; Chang, L.; Guo, L. Strain improvement and optimization of the media of taxol-producing fungus Fusarium mairei. Biochem. Eng. J. 2006, 31, 67–73. [Google Scholar] [CrossRef]
Elavarasi, A.; Rathna, G.S.; Kalaiselvam, M. Taxol producing mangrove endophytic fungi Fusarium oxysporum from Rhizophora annamalayana. Asian Pac. J. Trop. Biomed. 2012, 2, S1081–S1085. [Google Scholar] [CrossRef]
Garyali, S.; Reddy, M.S. Taxol production by an endophytic fungus, Fusarium redolens, isolated from Himalayan yew. J. Microbiol. Biotechnol. 2013, 23, 1372–1380. [Google Scholar] [CrossRef] [PubMed]
Chakravarthi, B.V.S.K.; Das, P.; Surendranath, K.; Karande, A.A.; Jayabaskaran, C. Production of paclitaxel by Fusarium solani isolated from Taxus celebica. J. Biosci. 2008, 33, 259–267. [Google Scholar] [CrossRef] [PubMed]
Deng, B.W.; Liu, K.H.; Chen, W.Q.; Ding, X.W.; Xie, X.C. Fusarium solani, Tax-3, a new endophytic taxol-producing fungus from Taxus chinensis. World J. Microbiol. Biotechnol. 2009, 25, 139–143. [Google Scholar] [CrossRef]
Gogoi, D.K.; Deka Boruah, H.P.; Saikia, R.; Bora, T.C. Optimization of process parameters for improved production of bioactive metabolite by a novel endophytic fungus Fusarium sp. DF2 isolated from Taxus wallichiana of North East India. World J. Microbiol. Biotechnol. 2008, 24, 79–87. [Google Scholar] [CrossRef]
Sreekanth, D.; Syed, A.; Sarkar, S.; Sarkar, D.; Santhakumari, B.; Ahmad, A.; Khan, I. Production, purification and characterization of taxol and 10DAB III from a new endophytic fungus Gliocladium sp. isolated from the Indian yew tree, Taxus baccata. J. Microbiol. Biotechnol. 2009, 19, 1342–1347. [Google Scholar] [CrossRef] [PubMed]
Pandi, M.; Kumaran, R.S.; Choi, Y.-K.; Kim, H.J.; Muthumary, J. Isolation and detection of taxol, an anticancer drug produced from Lasiodiplodia theobromae, an endophytic fungus of the medicinal plant Morinda citrifolia. Afr. J. Biotechnol. 2011, 10, 1428–1435. [Google Scholar]
Venkatachalam, R.; Subban, K.; Paul, M.J. Taxol from Botryodiplodia theobromae (BT 115)-an endophytic fungus of Taxus baccata. J. Biotechnol. 2008, 136, S189–S190. [Google Scholar] [CrossRef]
Miao, Z.; Wang, Y.; Yu, X.; Guo, B.; Tang, K. A new endophytic taxane production fungus from Taxus chinensis. Appl. Biochem. Microbiol. 2009, 45, 81–86. [Google Scholar] [CrossRef]
Zhou, X.; Zheng, W.; Zhu, H.; Tang, K. Identification of a taxol-producing endophytic fungus EFY-36. Afr. J. Biotechnol. 2009, 8, 2623–2625. [Google Scholar]
Zhao, K.; Zhou, D.P.; Ping, W.X.; Ge, J. Study on the preparation and regeneration of protoplast from taxol-producing fungus Nodulisporium sylviforme. Nat. Sci. 2004, 2, 52–59. [Google Scholar]
Guo, B.H.; Wang, Y.C.; Zhou, X.W.; Hu, K.; Tan, F.; Miao, Z.Q.; Tang, K.X. An endophytic taxol-producing fungus BT2 isolated from Taxus chinensis var. mairei. Afr. J. Biotechnol. 2006, 5, 875–877. [Google Scholar]
Soliman, S.S.M.; Tsao, R.; Raizada, M.N. Chemical inhibitors suggest endophytic fungal paclitaxel is derived from both mevalonate and non-mevalonate-like pathways. J. Nat. Prod. 2011, 74, 2497–2504. [Google Scholar] [CrossRef] [PubMed]
Yang, Y.; Zhao, H.; Barrero, R.A.; Zhang, B.; Sun, G.; Wilson, I.W.; Xie, F.; Walker, K.D.; Parks, J.W.; Bruce, R.; et al. Genome sequencing and analysis of the paclitaxel-producing endophytic fungus Penicillium aurantiogriseum NRRL 62431. BMC Genomics 2014, 15, 69. [Google Scholar] [CrossRef] [PubMed]
Stierle, A.; Stierle, D.; Stierle, S. Bioactive compounds from four endophytic Penicillium sp. of a northwest pacific yew tree. Nat. Prod. Chem. 2000, 24, 933–977. [Google Scholar]
Liu, J.J.; Gong, H.X.; Yang, D.L.; Chen, S.J.; Yang, L. Study on endophytic fungi producing taxol isolated from Taxus yunnanensis. Prog. Mod. Biomed. 2006, 6, 53–55. [Google Scholar]
Wang, Y.; Ma, Z.; Hu, F.; Fan, M.; Li, Z. Isolation and screening of endophytic fungi producing taxol from Taxus chinensis of Huangshan. Nat. Prod. Res. Dev. 2014, 26, 1624–1627. [Google Scholar]
Li, J.Y.; Sidhu, R.S.; Ford, E.J.; Long, D.M.; Hess, W.M.; Strobel, G.A. The induction of taxol production in the endophytic fungus—Periconia sp. from Torreya grandifolia. J. Ind. Microbiol. Biotechnol. 1998, 20, 259–264. [Google Scholar] [CrossRef]
Gangadevi, V.; Murugan, M.; Muthumary, J. Taxol determination from Pestalotiopsis pauciseta, a fungal endophyte of a medicinal plant. Chin. J. Biotechnol. 2008, 24, 1433–1438. [Google Scholar] [CrossRef]
Vennila, R.; Thirunavukkarasu, S.V.; Muthumary, J. In-vivo studies on anticancer activity of taxol isolated from an endophytic fungus Pestalotiopsis pauciseta Sacc. VM1. Asian J. Pharm. Clin. Res. 2010, 3, 30–34. [Google Scholar]
Strobel, G.A.; Hess, W.M.; Li, J.-Y.; Ford, E.; Sears, J.; Sidhu, R.S.; Summerell, B. Pestalotiopsis guepinii, a taxol-producing endophyte of the Wollemi pine, Wollemia nobilis. Aust. J. Bot. 1997, 45, 1073–1082. [Google Scholar] [CrossRef]
Strobel, G.; Yang, X.; Sears, J.; Kramer, R.; Sidhu, R.S.; Hess, W.M. Taxol from Pestalotiopsis microspora, an endophytic fungus of Taxus wallachiana. Microbiology 1996, 142, 435–440. [Google Scholar] [CrossRef] [PubMed]
Li, J.; Strobel, G.; Sidhu, R.; Hess, W.M.; Ford, E.J. Endophytic taxol producing fungi from bald cypress Taxodium distichum. Microbiology 1996, 142, 2223–2226. [Google Scholar] [CrossRef] [PubMed]
Kumaran, R.S.; Kim, H.J.; Hur, B.-K. Taxol promising fungal endophyte, Pestalotiopsis species isolated from Taxus cuspidata. J. Biosci. Bioeng. 2010, 110, 541–546. [Google Scholar]
Srinivasan, K.; Muthumary, J. Taxol production from Pestalotiopsis sp. an endophytic fungus isolated from Catharanthus roseus. J. Ecobiotechnol. 2009, 1, 28–31. [Google Scholar]
Gangadevi, V.; Muthumary, J. Taxol production by Pestalotiopsis terminaliae, an endophytic fungus of Terminalia arjuna (arjun tree). Biotechnol. Appl. Biochem. 2009, 52, 9–15. [Google Scholar] [CrossRef] [PubMed]
Kumaran, R.S.; Choi, Y.K.; Lee, S.; Jeon, H.J.; Jung, H.; Kim, H.J. Isolation of taxol, an anticancer drug produced by the endophytic fungus, Phoma betae. Afr. J. Biotechnol. 2014, 11, 950–960. [Google Scholar]
Kumaran, R.S.; Hur, B.-K. Screening of species of the endophytic fungus Phomopsis for the production of the anticancer drug taxol. Biotechnol. Appl. Biochem. 2009, 54, 21–30. [Google Scholar] [CrossRef] [PubMed]
Kumaran, R.S.; Muthumary, J.; Hur, B.-K. Isolation and identification of taxol, an anticancer drug from Phyllosticta melochiae Yates, an endophytic fungus of Melochia corchorifolia L. Food Sci. Biotechnol. 2008, 17, 1246–1253. [Google Scholar]
Gangadevi, V.; Muthumary, J. Endophytic fungal diversity from young, mature and senescent leaves of Ocimum basilicum L. with special reference to taxol production. Indian J. Sci. Technol. 2007, 1, 1–12. [Google Scholar]
Kumaran, R.S.; Muthumary, J.; Hur, B.-K. Production of taxol from Phyllosticta spinarum, an endophytic fungus of Cupressus sp. Eng. Life Sci. 2008, 8, 438–446. [Google Scholar] [CrossRef]
Li, T.; Zhang, Z.; Zhang, P.; Wang, C.; Liu, B.; Liu, T.; Fu, C.; Yu, L. Isolation and identification of a taxol-producing endophytic fungus identified from Taxus media. Agric. Sci. Technol. Hunan 2010, 11, 38–40. [Google Scholar]
Bashyal, B.; Li, J.Y.; Strobel, G.; Hess, W.M.; Sidhu, R. Seimatoantlerium nepalense, an endophytic taxol producing coelomycete from Himalayan yew (Taxus wallachiana). Mycotaxon 1999, 72, 33–42. [Google Scholar]
Shrestha, K.; Strobel, G.A.; Shrivastava, S.P.; Gewali, M.B. Evidence for paclitaxel from three new endophytic fungi of Himalayan yew of Nepal. Planta Med. 2001, 67, 374–376. [Google Scholar] [CrossRef] [PubMed]
Strobel, G.A.; Hess, W.M.; Baird, G.; Ford, E.; Li, J.Y.; Sidhu, R.S. Stegolerium kukenani gen. et sp. nov. an endophytic, taxol producing fungus from the Roraima and Kukenan tepuis of Venezuela. Mycotaxon 2001, 78, 353–361. [Google Scholar]
Mirjalili, M.H.; Farzaneh, M.; Bonfill, M.; Rezadoost, H.; Ghassempour, A. Isolation and characterization of Stemphylium sedicola SBU-16 as a new endophytic taxol-producing fungus from Taxus baccata grown in Iran. FEMS Microbiol. Lett. 2012, 328, 122–129. [Google Scholar] [CrossRef] [PubMed]
Wan, B.; Li, A.M.; Wang, X.L. Separation of a fungus producing taxol. Sci. China Ser. C. 2001, 44, 156–160. [Google Scholar] [CrossRef] [PubMed]
Wang, J.; Li, G.; Lu, H.; Zheng, Z.; Huang, Y.; Su, W. Taxol from Tubercularia sp. strain TF5, an endophytic fungus of Taxus mairei. FEMS Microbiol. Lett. 2000, 193, 249–253. [Google Scholar] [CrossRef] [PubMed]
Appendino, G. The phytochemistry of the yew tree. Nat. Prod. Rep. 1995, 12, 349–360. [Google Scholar] [CrossRef] [PubMed]
Zaiyou, J.; Li, M.; Guifang, X.; Xiuren, Z. Isolation of an endophytic fungus producing baccatin III from Taxus wallichiana var. mairei. J. Ind. Microbiol. Biotechnol. 2013, 40, 1297–1302. [Google Scholar] [CrossRef] [PubMed]
Li, Y.; Yang, J.; Zhou, X.; Zhao, W.; Jian, Z. Isolation and identification of a 10-deacetyl baccatin-III-producing endophyte from Taxus wallichiana. Appl. Biochem. Biotechnol. 2015, 175, 2224–2231. [Google Scholar] [CrossRef] [PubMed]
Caruso, M.; Colombo, A.L.; Fedeli, L.; Pavesi, A.; Quaroni, S.; Saracchi, M.; Ventrella, G. Isolation of endophytic fungi and actinomycetes taxane producers. Ann. Microbiol. 2000, 50, 3–14. [Google Scholar]
Staniek, A.; Woerdenbag, H.J.; Kayser, O. Screening the endophytic flora of Wollemia nobilis for alternative paclitaxel sources. J. Plant Interact. 2010, 5, 189–195. [Google Scholar] [CrossRef]
Kusari, S.; Zühlke, S.; Spiteller, M. Effect of artificial reconstitution of the interaction between the plant Camptotheca acuminata and the fungal endophyte Fusarium solani on camptothecin biosynthesis. J. Nat. Prod. 2011, 74, 764–775. [Google Scholar] [CrossRef] [PubMed]
Pu, X.; Qu, X.; Chen, F.; Bao, J.; Zhang, G.; Luo, Y. Camptothecin-producing endophytic fungus Trichoderma atroviride LY357: Isolation, identification, and fermentation conditions optimization for camptothecin production. Appl. Microbiol. Biotechnol. 2013, 97, 9365–9375. [Google Scholar] [CrossRef] [PubMed]
Liu, W.; Reinscheid, U.M. Camptothecin-resistant fungal endophytes of Camptotheca acuminata. Mycol. Prog. 2004, 3, 189–192. [Google Scholar] [CrossRef]
Kusari, S.; Košuth, J.; Čellárová, E.; Spiteller, M. Survival-strategies of endophytic Fusarium solani against indigenous camptothecin biosynthesis. Fungal Ecol. 2011, 4, 219–223. [Google Scholar] [CrossRef]
Liu, K.; Ding, X.; Deng, B.; Chen, W. 10-Hydroxycamptothecin produced by a new endophytic Xylaria sp., M20, from Camptotheca acuminata. Biotechnol. Lett. 2010, 32, 689–693. [Google Scholar] [CrossRef] [PubMed]
Venugopalan, A.; Srivastava, S. Enhanced camptothecin production by ethanol addition in the suspension culture of the endophyte, Fusarium solani. Bioresour. Technol. 2015, 188, 251–257. [Google Scholar] [CrossRef] [PubMed]
Puri, S.C.; Verma, V.; Amna, T.; Qazi, G.N.; Spiteller, M. An endophytic fungus from Nothapodytes foetida that produces camptothecin. J. Nat. Prod. 2005, 68, 1717–1719. [Google Scholar] [CrossRef] [PubMed]
Amna, T.; Puri, S.C.; Verma, V.; Sharma, J.P.; Khajuria, R.K.; Musarrat, J.; Spiteller, M.; Qazi, G.N. Bioreactor studies on the endophytic fungus Entrophospora infrequens for the production of an anticancer alkaloid camptothecin. Can. J. Microbiol. 2006, 52, 189–196. [Google Scholar] [CrossRef] [PubMed]
Rehman, S.; Shawl, A.S.; Kour, A.; Andrabi, R.; Sudan, P.; Sultan, P.; Verma, V.; Qazi, G.N. An endophytic Neurospora sp. from Nothapodytes foetida producing camptothecin. Appl. Biochem. Microbiol. 2008, 44, 203–209. [Google Scholar] [CrossRef]
Rehman, S.; Shawl, A.S.; Kour, A.; Sultan, P.; Ahmad, K.; Khajuria, R.; Qazi, G.N. Comparative studies and identification of camptothecin produced by an endophyte at shake flask and bioreactor. Nat. Prod. Res. 2009, 23, 1050–1057. [Google Scholar] [CrossRef] [PubMed]
Kusari, S.; Zühlke, S.; Spiteller, M. An endophytic fungus from Camptotheca acuminata that produces camptothecin and analogues. J. Nat. Prod. 2009, 72, 2–7. [Google Scholar] [CrossRef]
Shweta, S.; Zuehlke, S.; Ramesha, B.T.; Priti, V.; Kumar, P.M.; Ravikanth, G.; Spiteller, M.; Vasudeva, R.; Shaanker, R.U. Endophytic fungal strains of Fusarium solani, from Apodytes dimidiata E. Mey. ex Arn (Icacinaceae) produce camptothecin, 10-hydroxycamptothecin and 9-methoxycamptothecin. Phytochemistry 2010, 71, 117–122. [Google Scholar] [CrossRef] [PubMed]
Gurudatt, P.S.; Priti, V.; Shweta, S.; Ramesha, B.T.; Ravikanth, G.; Vasudeva, R.; Amna, T.; Deepika, S.; Ganeshaiah, K.N.; Uma Shaanker, R.; et al. Attenuation of camptothecin production and negative relation between hyphal biomass and camptothecin content in endophytic fungal strains isolated from Nothapodytes nimmoniana Grahm (Icacinaceae). Curr. Sci. 2010, 98, 1006–1010. [Google Scholar]
Min, C.; Wang, X. Isolation and identification of the 10-hydroxycamptothecin-producing endophytic fungi from Camptotheca acuminata Decne. Acta Bot. Boreal.-Occident. Sin. 2009, 29, 614–617. [Google Scholar]
Shweta, S.; Gurumurthy, B.R.; Ravikanth, G.; Ramanan, U.S.; Shivanna, M.B. Endophytic fungi from Miquelia dentata Bedd., produce the anti-cancer alkaloid, camptothecine. Phytomedicine 2013, 20, 337–342. [Google Scholar] [CrossRef] [PubMed]
Musavi, S.F.; Dhavale, A.; Balakrishnan, R.M. Optimization and kinetic modeling of cell-associated camptothecin production from an endophytic Fusarium oxysporum NFX06. Prep. Biochem. Biotechnol. 2015, 45, 158–172. [Google Scholar] [CrossRef] [PubMed]
Andrade-Neto, V.F.; Brandão, M.G.L.; Stehmann, J.R.; Oliveira, L.A.; Krettli, A.U. Antimalarial activity of Cinchona-like plants used to treat fever and malaria in Brazil. J. Ethnopharmacol. 2003, 87, 253–256. [Google Scholar] [CrossRef]
Maehara, S.; Simanjuntak, P.; Kitamura, C.; Ohashi, K.; Shibuya, H. Cinchona alkaloids are also produced by an endophytic filamentous fungus living in Cinchona plant. Chem. Pharm. Bull. 2011, 59, 1073–1074. [Google Scholar] [CrossRef] [PubMed]
Maehara, S.; Simanjuntak, P.; Kitamura, C.; Ohashi, K.; Shibuya, H. Bioproduction of Cinchona alkaloids by the endophytic fungus Diaporthe sp. associated with Cinchona ledgeriana. Chem. Pharm. Bull. 2012, 60, 1301–1304. [Google Scholar] [CrossRef] [PubMed]
Maehara, S.; Simanjuntak, P.; Maetani, Y.; Kitamura, C.; Ohashi, K.; Shibuya, H. Ability of endophytic filamentous fungi associated with Cinchona ledgeriana to produce Cinchona alkaloids. J. Nat. Med. 2013, 67, 421–423. [Google Scholar] [CrossRef] [PubMed]
Sun, Y.; Xun, K.; Wang, Y.; Chen, X. A systematic review of the anticancer properties of berberine, a natural product from Chinese herbs. Anti-Cancer Drugs 2009, 20, 757–769. [Google Scholar] [CrossRef] [PubMed]
Vinodhini, D.; Agastian, P. Berberine production by endophytic fungus Fusarium solani from Coscinium fenestratum. Int. J. Biol. Pharm. Res. 2013, 4, 1239–1245. [Google Scholar]
Grenby, T.H. The use of sanguinarine in mouthwashes and toothpaste compared with some other antimicrobial agents. Br. Dent. J. 1995, 178, 254–258. [Google Scholar] [CrossRef] [PubMed]
Wang, X.; Min, C.; Ge, M.; Zuo, R. An endophytic sanguinarine-producing fungus from Macleaya cordata, Fusarium proliferatum BLH51. Curr. Microbiol. 2014, 68, 336–341. [Google Scholar] [CrossRef] [PubMed]
Hadfield, J.A.; Ducki, S.; Hirst, N.; McGown, A.T. Tubulin and microtubules as targets for anticancer drugs. Prog. Cell Cycle Res. 2002, 5, 309–325. [Google Scholar]
Guo, B.; Li, H.; Zhang, L. Isolation of a fungus producting vinblastine. J. Yunnan Univ. (Nat. Sci.) 1997, 20, 214–215. [Google Scholar]
Zhang, L.; Guo, B.; Li, H.; Zeng, S.; Shao, H.; Gu, S.; Wei, R. Preliminary study on the isolation of endophytic fungus of Catharanthus roseus and its fermentation to produce products of therapeutic value. Chin. Tradit. Herb. Drugs 1999, 31, 805–807. [Google Scholar]
Kumar, A.; Patil, D.; Rajamohanan, P.R.; Ahmad, A. Isolation, purification and characterization of vinblastine and vincristine from endophytic fungus Fusarium oxysporum isolated from Catharanthus roseus. PLoS ONE 2013, 8, e71805. [Google Scholar] [CrossRef] [PubMed]
Kumar, A.; Ahmad, A. Biotransformation of vinblastine to vincristine by the endophytic fungus Fusarium oxysporum isolated from Catharanthus roseus. Biocatal. Biotransform. 2013, 31, 89–93. [Google Scholar] [CrossRef]
Yin, H.; Sun, Y.H. Vincamine-producing endophytic fungus isolated from Vinca minor. Phytomedicine 2011, 18, 802–805. [Google Scholar] [CrossRef] [PubMed]
Sunila, E.S.; Kuttan, G. Immunomodulatory and antitumor activity of Piper longum Linn. and piperine. J. Ethnopharmacol. 2004, 90, 339–346. [Google Scholar] [CrossRef] [PubMed]
Maneesai, P.; Norman, S.; Krongkarn, C. Piperine is anti-hyperlipidemic and improves endothelium-dependent vasorelaxation in rats on a high cholesterol diet. J. Physiol. Biomed. Sci. 2012, 25, 27–30. [Google Scholar]
Huan, Q.U.; Min, L.V.; Hui, X.U. Piperine: Bioactivities and structural modifications. Mini Rev. Med. Chem. 2015, 15, 145–156. [Google Scholar]
Verma, V.C.; Lobkovsky, E.; Gange, A.C.; Singh, S.K.; Prakash, S. Piperine production by endophytic fungus Periconia sp. isolated from Piper longum L. J. Antibiot. 2011, 64, 427–431. [Google Scholar] [CrossRef] [PubMed]
Chithra, S.; Jasim, B.; Anisha, C.; Mathew, J.; Radhakrishnan, E.K. LC-MS/MS based identification of piperine production by endophytic Mycosphaerella sp. PF13 from Piper nigrum. Appl. Biochem. Biotechnol. 2014, 173, 30–35. [Google Scholar] [CrossRef] [PubMed]
Chithra, S.; Jasim, B.; Sachidanandan, P.; Jyothis, M.; Radhakrishnan, E.K. Piperine production by endophytic fungus Colletotrichum gloeosporioides isolated from Piper nigrum. Phytomedicine 2014, 21, 534–540. [Google Scholar] [CrossRef] [PubMed]
Yang, K.; Liang, J.; Li, Q.; Kong, X.; Chen, R.; Jin, Y. Cladosporium cladosporioides XJ-AC03, an aconitine-producing endophytic fungus isolated from Aconitum leucostomum. World J. Microbiol. Biotechnol. 2013, 29, 933–938. [Google Scholar] [CrossRef] [PubMed]
Khadem, S.; Marles, R.J. Chromone and flavonoid alkaloids: Occurrence and bioactivity. Molecules 2012, 17, 191–206. [Google Scholar] [CrossRef] [PubMed]
Kumara, P.M.; Soujanya, K.N.; Ravikanth, G.; Vasudeva, R.; Ganeshaiah, K.N.; Shaanker, R.U. Rohitukine, a chromone alkaloid and a precursor of flavopiridol, is produced by endophytic fungi isolated from Dysoxylum binectariferum Hook.f and Amoora rohituka (Roxb). Wight & Arn. Phytomedicine 2014, 21, 541–546. [Google Scholar] [PubMed]
Kumara, P.M.; Zuehlke, S.; Priti, V.; Ramesha, B.T.; Shweta, S.; Ravikanth, G.; Vasudeva, R.; Santhoshkumar, T.R.; Spiteller, M.; Uma Shaanker, R. Fusarium proliferatum, an endophytic fungus from Dysoxylum binectariferum Hook.f, produces rohitukine, a chromane alkaloid possessing anti-cancer activity. Antonie Van Leeuwenhoek 2012, 101, 323–329. [Google Scholar] [CrossRef] [PubMed]
Pan, F.; Hou, K.; Gao, F.; Hu, B.; Chen, Q.; Wu, W. Peimisine and peiminine production by endophytic fungus Fusarium sp. isolated from Fritillaria unibracteata var. wabensis. Phytomedicine 2014, 21, 1104–1109. [Google Scholar] [CrossRef] [PubMed]
Cook, D.; Gardner, D.R.; Pfister, J.A. Swainsonine-containing plants and their relationship to endophytic fungi. J. Agric. Food Chem. 2014, 62, 7326–7334. [Google Scholar] [CrossRef] [PubMed]
Pryor, B.M.; Creamer, R.; Shoemaker, R.A.; McLain-Romero, J.; Hambleton, S. Undifilum, a new genus for endophytic Embellisia oxytropis and parasitic Helminthosporium bornmuelleri on legumes. Botany 2009, 87, 178–194. [Google Scholar] [CrossRef]
Cook, D.; Gardner, D.R.; Grum, D.; Pfister, J.A.; Ralphs, M.H.; Welch, K.D.; Green, B.T. Swainsonine and endophyte relationships in Astragalus mollissimus and Astragalus lentiginosus. J. Agric. Food Chem. 2011, 59, 1281–1287. [Google Scholar] [CrossRef] [PubMed]
Braun, K.; Romero, J.; Liddell, C.; Creamer, R. Production of swainsonine by fungal endophytes of locoweed. Mycol. Res. 2003, 107, 980–988. [Google Scholar] [CrossRef] [PubMed]
Ralphs, M.H.; Creamer, R.; Baucom, D.; Gardner, D.R.; Welsh, S.L.; Graham, J.D.; Hart, C.; Cook, D.; Stegelmeier, B.L. Relationship between the endophyte Embellisia spp. and the toxic alkaloid swainsonine in major locoweed species (Astragalus and Oxytropis). J. Chem. Ecol. 2008, 34, 32–38. [Google Scholar] [CrossRef] [PubMed]
Baucom, D.L.; Romero, M.; Belfon, R.; Creamer, R. Two new species of Undifilum, fungal endophytes of Astragalus (locoweeds) in the United States. Botany 2012, 90, 866–875. [Google Scholar] [CrossRef] [PubMed]
Grum, D.S.; Cook, D.; Baucom, D.; Mott, I.W.; Gardner, D.R.; Creamer, R.; Allen, J.G. Production of the alkaloid swainsonine by a fungal endophyte in the host Swainsona canescens. J. Nat. Prod. 2013, 76, 1984–1988. [Google Scholar] [CrossRef] [PubMed]
Lu, H.; Chen, J.; Lu, W.; Ma, Y.; Zhao, B.; Wang, J. Isolation and identification of swainsonine-producing fungi found in locoweeds and their rhizosphere soil. Afr. J. Microbiol. Res. 2012, 6, 4959–4969. [Google Scholar]
Chen, S.; Zhao, B.; Gao, R.; Li, R. The progress in research of swainsonine immunogenicity and anticancer-activity. Nat. Prod. Res. Dev. 2003, 16, 66–70. [Google Scholar]
Fiaux, H.; Kuntz, D.A.; Hoffman, D.; Janzer, R.C.; Gerber-Lemaire, S.; Rose, D.R.; Juillerat-Jeanneret, L. Functionalized pyrrolidine inhibitors of human type II α-mannosidases as anti-cancer agents: Optimizing the fit to the active site. Bioorg. Med. Chem. 2008, 16, 7337–7346. [Google Scholar] [CrossRef] [PubMed]
Oldrup, E.; McLain-Romero, J.; Padilla, A.; Moya, A.; Gardner, D.; Creamer, R. Localization of endophytic Undifilum fungi in locoweed seed and influence of environmental parameters on a locoweed in vitro culture system. Botany 2010, 88, 512–521. [Google Scholar] [CrossRef]
Hipkin, C.R.; Simpson, D.J.; Wainwright, S.J.; Salem, M.A. Nitrification by plants that also fix nitrogen. Nature 2004, 430, 98–101. [Google Scholar] [CrossRef] [PubMed]
Chomcheon, P.; Wiyakrutta, S.; Sriubolmas, N.; Ngamrojanavanich, N.; Isarangkul, D.; Kittakoop, P. 3-Nitropropionic acid (3-NPA), a potent antimycobacterial agent from endophytic fungi: Is 3-NPA in some plants produced by endophytes? J. Nat. Prod. 2005, 68, 1103–1105. [Google Scholar] [CrossRef] [PubMed]
Bush, M.T.; Touster, O.; Brockman, J.E. The production of beta-nitropropionic acid by a strain of Aspergillus flavus. J. Biol. Chem. 1951, 188, 685–693. [Google Scholar] [PubMed]
Hershenhorn, J.; Vurro, M.; Zonn, M.C.; Stierle, A.; Strobel, G. Septoria cirsii, a potential biocontrol agent of Canada thistle and its phytotoxin—β-nitropropionic acid. Plant Sci. 1993, 94, 227–234. [Google Scholar] [CrossRef]
Wei, D.-L.; Chang, S.-C.; Lin, S.-C.; Doong, M.-L.; Jong, S.-C. Production of 3-nitropropionic acid by Arthrinium species. Curr. Microbiol. 1994, 28, 1–5. [Google Scholar] [CrossRef]
Schwarz, M.; Köpcke, B.; Weber, R.W.; Sterner, O.; Anke, H. 3-Hydroxypropionic acid as a nematicidal principle in endophytic fungi. Phytochemistry 2004, 65, 2239–2245. [Google Scholar] [CrossRef] [PubMed]
Flores, A.C.; Pamphile, J.A.; Sarragiotto, M.H.; Clemente, E. Production of 3-nitropropionic acid by endophytic fungus Phomopsis longicolla isolated from Trichilia elegans A. JUSS ssp. elegans and evaluation of biological activity. World J. Microbiol. Biotechnol. 2013, 29, 923–932. [Google Scholar] [PubMed]
Elsässer, B.; Krohn, K.; Flörke, U.; Root, N.; Aust, H.J.; Draeger, S.; Schulz, B.; Antus, S.; Kurtán, T. X-ray structure determination, absolute configuration and biological activity of phomoxanthone A. Eur. J. Org. Chem. 2005, 21, 4563–4570. [Google Scholar] [CrossRef]
Netala, V.R.; Ghosh, S.B.; Bobbu, P.; Anitha, D.; Tartte, V. Triterpenoid saponins: A review on biosynthesis, applications and mechanism of their action. Int. J. Pharm. Pharm. Sci. 2014, 7, 24–28. [Google Scholar]
Osbourn, A. Saponins and plant defence—A soap story. Trends Plant Sci. 1996, 1, 4–9. [Google Scholar] [CrossRef]
Dhankhar, S.; Kumar, S.; Dhankhar, S.; Yadav, J.P. Antioxidant activity of fungal endophytes isolated from Salvadora oleoides Decne. Int. J. Pharm. Pharm. Sci. 2012, 4, 381–385. [Google Scholar]
Prabavathy, D.; Nachiyar, C. Cytotoxic potential and phytochemical analysis of Justicia beddomei and its endophytic Aspergillus sp. Asian J. Pharm. Clin. Res. 2013, 6, 159–161. [Google Scholar]
Nath, A.; Joshi, S.R. Bioactivity assessment of endophytic fungi associated with the ethnomedicinal plant Potentilla fulgens. World J. Pharm. Res. 2013, 2, 2596–2607. [Google Scholar]
Govindappa, M.; Bharath, N.; Shruthi, H.B.; Santoyo, G. In vitro antioxidant activity and phytochemical screening of endophytic extracts of Crotalaria pallida. Free Radic. Antioxid. 2011, 1, 79–86. [Google Scholar] [CrossRef]
Govindappa, M.; Channabasava, R.; Sowmya, D.V.; Meenakshi, J.; Shreevidya, M.R.; Lavanya, A.; Santoyo, G.; Sadananda, T.S. Phytochemical screening, antimicrobial and in vitro anti-inflammatory activity of endophytic extracts from Loranthus sp. Pharmacognosy J. 2011, 3, 82–90. [Google Scholar] [CrossRef]
Pragathi, D.; Vijaya, T.; Mouli, K.C.; Anitha, D. Diversity of fungal endophytes and their bioactive metabolites from endemic plants of Tirumala hills-Seshachalam biosphere reserve. Afr. J. Biotechnol. 2013, 12, 4317–4323. [Google Scholar]
Saraswaty, V.; Srikandace, Y.; Simbiyani, N.A.; Setiyanto, H.; Udin, Z. Antioxidant activity and total phenolic content of endophytic fungus Fennellia nivea NRRL 5504. Pakistan J. Biol. Sci. 2013, 16, 1574–1578. [Google Scholar] [CrossRef]
Karunai Selvi, B.; Balagengatharathilagam, P. Isolation and screening of endophytic fungi from medicinal plants of Virudhunagar district for antimicrobial activity. Int. J. Sci. Nat. 2014, 5, 147–155. [Google Scholar]
Yadav, M.; Yadav, A.; Yadav, J.P. In vitro antioxidant activity and total phenolic content of endophytic fungi isolated from Eugenia jambolana Lam. Asian Pac. J. Trop. Med. 2014, 7, S256–S261. [Google Scholar] [CrossRef]
Nath, A.; Chattopadhyay, A.; Joshi, S.R. Biological activity of endophytic fungi of Rauwolfia serpentina Benth: An ethnomedicinal plant used in folk medicines in Northeast India. Proc. Natl. Acad. Sci. India Sect. B Biol. Sci. 2015, 85, 233–240. [Google Scholar] [CrossRef]
Wu, H.; Yang, H.; You, X.; Li, Y. Isolation and characterization of saponin-producing fungal endophytes from Aralia elata in Northeast China. Int. J. Mol. Sci. 2012, 13, 16255–16266. [Google Scholar] [CrossRef] [PubMed]
Wu, H.; Yang, H.; You, X.; Li, Y. Diversity of endophytic fungi from roots of Panax ginseng and their saponin yield capacities. SpringerPlus 2013, 2, 107. [Google Scholar] [CrossRef] [PubMed]
Luo, S.L.; Dang, L.Z.; Li, J.F.; Zou, C.G.; Zhang, K.Q.; Li, G.H. Biotransformation of saponins by endophytes isolated from Panax notoginseng. Chem. Biodivers. 2013, 10, 2021–2031. [Google Scholar] [CrossRef] [PubMed]
Ding, C.H.; Du, X.W.; Xu, Y.; Xu, X.M.; Mou, J.C.; Yu, D.; Wu, J.K.; Meng, F.J.; Liu, Y.; Wang, W.L.; et al. Screening for differentially expressed genes in endophytic fungus strain 39 during co-culture with herbal extract of its host Dioscorea nipponica Makino. Curr. Microbiol. 2014, 69, 517–524. [Google Scholar] [CrossRef] [PubMed]
Patel, K.; Gadewar, M.; Tahilyani, V.; Patel, D.K. A review on pharmacological and analytical aspects of diosgenin: A concise report. Nat. Prod. Bioprospect. 2012, 2, 46–52. [Google Scholar] [CrossRef]
Zhou, L.; Cao, X.; Yang, C.; Wu, X.; Zhang, L. Endophytic fungi of Paris polyphylla var. yunnanensis and steroid analysis in the fungi. Nat. Prod. Res. Dev. 2004, 16, 198–200. [Google Scholar]
Cao, X.; Li, J.; Zhou, L.; Xu, L.; Li, J.; Zhao, J. Determination of diosgenin content of the endophytic fungi from Paris polyphylla var. yunnanensis by using an optimum ELISA. Nat. Prod. Res. Dev. 2007, 19, 1020–1023. [Google Scholar]
Zhang, R.; Li, P.; Xu, L.; Chen, Y.; Sui, P.; Zhou, L.; Li, J. Enhancement of diosgenin production in Dioscorea zingiberensis cell culture by oligosaccharide elicitor from its endophytic fungus Fusarium oxysporum Dzf17. Nat. Prod. Commun. 2009, 4, 1459–1462. [Google Scholar] [PubMed]
Li, P.; Mou, Y.; Shan, T.; Xu, J.; Li, Y.; Lu, S.; Zhou, L. Effects of polysaccharide elicitors from endophytic Fusarium oxysporium Dzf17 on growth and diosgenin production in cell suspension culture of Dioscorea zingiberensis. Molecules 2011, 16, 9003–9016. [Google Scholar] [CrossRef] [PubMed]
Yin, C.; Li, P.; Li, H.; Xu, L.; Zhao, J.; Shan, T.; Zhou, L.G. Enhancement of diosgenin production in Dioscorea zingiberensis seedling and cell cultures by beauvericin from the endophytic fungus Fusarium redolens Dzf2. J. Med. Plants Res. 2011, 5, 6550–6554. [Google Scholar]
Parthasarathy, R.; Sathiyabama, M. Gymnemagenin-producing endophytic fungus isolated from a medicinal plant Gymnema sylvestre R. Br. Appl. Biochem. Biotechnol. 2014, 172, 3141–3152. [Google Scholar] [CrossRef] [PubMed]
Pangeni, R.; Sahni, J.K.; Ali, J.; Sharma, S.; Baboota, S. Resveratrol: Review on therapeutic potential and recent advances in drug delivery. Expert Opin. Drug Deliv. 2014, 11, 1285–1298. [Google Scholar] [CrossRef] [PubMed]
Shi, J.; Zeng, Q.; Liu, Y.; Pan, Z. Alternaria sp. MG1, a resveratrol-producing fungus: Isolation, identification, and optimal cultivation conditions for resveratrol production. Appl. Microbiol. Biotechnol. 2012, 95, 369–379. [Google Scholar] [CrossRef] [PubMed]
Zhao, J.; Fu, Y.; Luo, M.; Zu, Y.; Wang, W.; Zhao, C.; Gu, C. Endophytic fungi from pigeon pea (Cajanus cajan (L.) Millsp.) produce antioxidant cajaninstilbene acid. J. Agric. Food Chem. 2012, 60, 4314–4319. [Google Scholar] [CrossRef]
Hatcher, H.; Planalp, R.; Cho, J.; Torti, F.M.; Torti, S.V. Curcumin: From ancient medicine to current clinical trials. Cell. Mol. Life Sci. 2008, 65, 1631–1652. [Google Scholar] [CrossRef] [PubMed]
Hansen, S.L.; Purup, S.; Christensen, L.P. Bioactivity of falcarinol and the influence of processing and storage on its content in carrots (Daucus carota L). J. Sci. Food Agric. 2003, 83, 1010–1017. [Google Scholar] [CrossRef]
Nicoletti, R.; Ferranti, P.; Caira, S.; Misso, G.; Castellano, M.; Di Lorenzo, G.; Caraglia, M. Myrtucommulone production by a strain of Neofusicoccum australe endophytic in myrtle (Myrtus communis). World J. Microbiol. Biotechnol. 2014, 30, 1047–1052. [Google Scholar] [CrossRef] [PubMed]
Liu, J. Pharmacology of oleanolic acid and ursolic acid. J. Ethnopharmacol. 1995, 49, 57–68. [Google Scholar] [CrossRef]
Budhiraja, A.; Nepali, K.; Sapra, S.; Gupta, S.; Kumar, S.; Dhar, K.L. Bioactive metabolites from an endophytic fungus of Aspergillus species isolated from seeds of Gloriosa superba Linn. Med. Chem. Res. 2013, 22, 323–329. [Google Scholar] [CrossRef]
Yin, H.; Zhao, Q.; Sun, F.M.; An, T. Gentiopicrin-producing endophytic fungus isolated from Gentiana macrophylla. Phytomedicine 2009, 16, 793–797. [Google Scholar] [CrossRef] [PubMed]
Kaul, S.; Ahmed, M.; Zargar, K.; Sharma, P.; Dhar, M.K. Prospecting endophytic fungal assemblage of Digitalis lanata Ehrh. (foxglove) as a novel source of digoxin: A cardiac glycoside. 3 Biotech 2013, 3, 335–340. [Google Scholar] [CrossRef]
Wu, S.B.; Long, C.; Kennelly, E.J. Structural diversity and bioactivities of natural benzophenones. Nat. Prod. Rep. 2014, 31, 1158–1174. [Google Scholar] [CrossRef] [PubMed]
Wang, F.W.; Ye, Y.H.; Ding, H.; Chen, Y.X.; Tan, R.X.; Song, Y.C. Benzophenones from Guignardia sp. IFB-E028, an endophyte on Hopea hainanensis. Chem. Biodivers. 2010, 7, 216–220. [Google Scholar] [CrossRef] [PubMed]
Asai, T.; Otsuki, S.; Sakurai, H.; Yamashita, K.; Ozeki, T.; Oshima, Y. Benzophenones from an endophytic fungus, Graphiopsis chlorocephala, from Paeonia lactiflora cultivated in the presence of an NAD+-dependent HDAC inhibitor. Org. Lett. 2013, 15, 2058–2061. [Google Scholar] [CrossRef] [PubMed]
Luo, H.; Li, X.M.; Li, C.S.; Wang, B.G. Diphenyl ether and benzophenone derivatives from the marine mangrove-derived fungus Penicillium sp. MA-37. Phytochem. Lett. 2014, 9, 22–25. [Google Scholar] [CrossRef]
Frisvad, J.C.; Houbraken, J.; Popma, S.; Samson, R.A. Two new Penicillium species Penicillium buchwaldii and Penicillium spathulatum, producing the anticancer compound asperphenamate. FEMS Microbiol. Lett. 2013, 339, 77–92. [Google Scholar] [CrossRef] [PubMed]
Aly, A.H.; Edrada-Ebel, R.; Indriani, I.D.; Wray, V.; Müller, W.E.; Totzke, F.; Zirrgiebel, U.; Schächtele, C.; Kubbutat, M.H.G.; Lin, W.H.; et al. Cytotoxic metabolites from the fungal endophyte Alternaria sp. and their subsequent detection in its host plant Polygonum senegalense. J. Nat. Prod. 2008, 71, 972–980. [Google Scholar] [CrossRef] [PubMed]
Onocha, P.A.; Okorie, D.A.; Connolly, J.D.; Roycroft, D.S. Monoterpene diol, iridoid glucoside and dibenzo-α-pyrone from Anthocleista djalonensis. Phytochemistry 1995, 40, 1183–1189. [Google Scholar] [CrossRef]
Shibuya, H.; Kitamura, C.; Maehara, S.; Nagahata, M.; Winarno, H.; Simanjuntak, P.; Kim, H.-S.; Wataya, Y.; Ohashi, K. Transformation of Cinchona alkaloids into 1-N-oxide derivatives by endophytic Xylaria sp. isolated from Cinchona pubescens. Chem. Pharm. Bull. 2003, 51, 71–74. [Google Scholar] [CrossRef] [PubMed]
Agusta, A.; Maehara, S.; Ohashi, K.; Simanjuntak, P.; Shibuya, H. Stereoselective oxidation at C-4 of flavans by the endophytic fungus Diaporthe sp. isolated from a tea plant. Chem. Pharm. Bull. 2005, 53, 1565–1569. [Google Scholar] [CrossRef] [PubMed]
Shibuya, H.; Agusta, A.; Ohashi, K.; Maehara, S.; Simanjuntak, P. Biooxidation of (+)-catechin and (−)-epicatechin into 3, 4-dihydroxyflavan derivatives by the endophytic fungus Diaporthe sp. isolated from a tea plant. Chem. Pharm. Bull. 2005, 53, 866–867. [Google Scholar] [CrossRef] [PubMed]
Maehara, S.; Ikeda, M.; Haraguchi, H.; Kitamura, C.; Nagoe, T.; Ohashi, K.; Shibuya, H. Microbial conversion of curcumin into colorless hydroderivatives by the endophytic fungus Diaporthe sp. associated with Curcuma longa. Chem. Pharm. Bull. 2011, 59, 1042–1044. [Google Scholar] [CrossRef] [PubMed]
Agusta, A.; Wulansari, D.; Nurkanto, A.; Fathoni, A. Biotransformation of protoberberine alkaloids by the endophytic fungus Coelomycetes AFKR-3 isolated from yellow moonsheed plant (Archangelisia flava (L.) Merr.). Proc. Chem. 2014, 13, 38–43. [Google Scholar] [CrossRef]
Wang, H.W.; Zhang, W.; Su, C.L.; Zhu, H.; Dai, C.C. Biodegradation of the phytoestrogen luteolin by the endophytic fungus Phomopsis liquidambari. Biodegradation 2015, 26, 197–210. [Google Scholar] [CrossRef] [PubMed]
Chen, Y.; Wang, H.W.; Li, L.; Dai, C.C. The potential application of the endophyte Phomopsis liquidambari to the ecological remediation of long-term cropping soil. Appl. Soil Ecol. 2013, 67, 20–26. [Google Scholar] [CrossRef]
Heinig, U.; Scholz, S.; Jennewein, S. Getting to the bottom of taxol biosynthesis by fungi. Fungal Divers. 2013, 60, 161–170. [Google Scholar] [CrossRef]
Partida-Martinez, L.P.; Hertweck, C. Pathogenic fungus harbours endosymbiotic bacteria for toxin production. Nature 2005, 437, 884–888. [Google Scholar] [CrossRef] [PubMed]
Partida-Martinez, L.P.; Groth, I.; Schmitt, I.; Richter, W.; Roth, M.; Hertweck, C. Burkholderia rhizoxinica sp. nov. and Burkholderia endofungorum sp. nov., bacterial endosymbionts of the plant-pathogenic fungus Rhizopus microsporus. Int. J. Syst. Evol. Microbiol. 2007, 57, 2583–2590. [Google Scholar] [CrossRef] [PubMed]
Hoffman, M.T.; Arnold, A.E. Diverse bacteria inhabit living hyphae of phylogenetically diverse fungal endophytes. Appl. Environ. Microbiol. 2010, 76, 4063–4075. [Google Scholar] [CrossRef] [PubMed]
Kinashi, H.; Shimaji, M.; Sakai, A. Giant linear plasmids in Streptomyces which code for antibiotic biosynthesis genes. Nature 1987, 328, 454–456. [Google Scholar] [CrossRef] [PubMed]
Soliman, S.S.; Raizada, M.N. Interactions between co-habitating fungi elicit synthesis of taxol from an endophytic fungus in host Taxus plants. Front. Microbiol. 2013, 4, 3. [Google Scholar] [CrossRef] [PubMed]

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Nicoletti, R.; Fiorentino, A. Plant Bioactive Metabolites and Drugs Produced by Endophytic Fungi of Spermatophyta. Agriculture 2015, 5, 918-970. https://0-doi-org.brum.beds.ac.uk/10.3390/agriculture5040918

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Nicoletti R, Fiorentino A. Plant Bioactive Metabolites and Drugs Produced by Endophytic Fungi of Spermatophyta. Agriculture. 2015; 5(4):918-970. https://0-doi-org.brum.beds.ac.uk/10.3390/agriculture5040918

Chicago/Turabian Style

Nicoletti, Rosario, and Antonio Fiorentino. 2015. "Plant Bioactive Metabolites and Drugs Produced by Endophytic Fungi of Spermatophyta" Agriculture 5, no. 4: 918-970. https://0-doi-org.brum.beds.ac.uk/10.3390/agriculture5040918

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Plant Bioactive Metabolites and Drugs Produced by Endophytic Fungi of Spermatophyta

Abstract

1. Introduction

2. Phytohormones

3. Compounds from Essential Oils

4. Other Terpenoids

5. Coumarins

6. Flavonoids

7. Xanthones and Quinones

8. Lignans

9. Taxol and Taxanes

10. Quinoline Alkaloids

11. Other Alkaloids

12. 3-Nitropropionic Acid

13. Saponines

14. Miscellaneous Compounds

15. Future Perspectives

Acknowledgments

Author Contributions

Conflicts of Interest

References

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