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Review

Fruit Development and Primary Metabolism in Apple

by
Verónica Tijero
*,
Francesco Girardi
and
Alessandro Botton
*
Department of Agronomy, Food, Natural Resources, Animals and Environment—DAFNAE, University of Padova, Agripolis, Viale dell’università 16-Legnaro, 35020 Padova, Italy
*
Authors to whom correspondence should be addressed.
Agronomy 2021, 11(6), 1160; https://0-doi-org.brum.beds.ac.uk/10.3390/agronomy11061160
Submission received: 30 April 2021 / Revised: 31 May 2021 / Accepted: 3 June 2021 / Published: 5 June 2021
(This article belongs to the Special Issue Recent Advances in Metabolic Processes and Metabolites of Agricultural Crops)
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Abstract

:
Apples (Malus domestica Borkh.) represent one of the most produced fruits worldwide, along with citrus and bananas. As high quality is an important trait for the consumer, many studies have focused on the research of new techniques to ensure and preserve the optimal organoleptic characteristics of this fruit. However, despite the huge number of studies on recent technological advances dealing with fruit final quality, less research has focused on the physiological aspects of apple development, including a variety of processes triggered after fertilization, such as photosynthesis, assimilation of carbohydrates, cell division, and cell enlargement, which determine apple final quality. In the present review, we summarize some of the most important changes and mechanisms linked to the primary metabolism of apples, as well as the effect of agronomic practices, such as fruit thinning, as key factors to improve apple quality and meet consumer demands, with the aim of amassing available information and suggesting future directions of research.

Graphical Abstract

1. Introduction

With more than 2500 species belonging to 90 different genera, the Rosaceae family is a very extended group, which comprises ornamental to edible crops. Within the latter, fleshy fruits have an economic importance given their nutritional contribution to a healthy diet; hence, there is high consumer demand [1]. Among the fleshy fruits belonging to the Rosaceae family, there are accessory fruits such as strawberry, stone fruits such as cherries, plums, apricots, or peaches, berries such as raspberries, and pomes such as apples and pears [2].
Apples (Malus domestica L. Borkh.) have an important economic impact worldwide. It is known that almost five million hectares of the worldwide area is harvested for apples, with approximately 17 million metric tons stemming from European production, representing 20% of the global production, which was approximately 90 million metric tons in 2019, becoming the fruit with the third largest production, behind citrus and bananas [3]. During their development, apples accumulate several compounds that are deemed valuable by consumers, such as sugars, organic acids, vitamins, fibers, and antioxidants [4]. The concentration of these compounds may vary depending on factors such as climate, genotype (i.e., cultivar), orchard management, harvest and storage conditions, and processing [5,6,7,8].
Due to its high importance, many studies have focused on developing new agricultural and biotechnological tools that may improve apple quality and maintain its freshness after harvest. Moreover, in the last few years, climate change has been a significant concern, causing production loss around the world. The use of different rootstocks, the exogenous application of agrochemicals during tree vegetation or reproduction, agronomic handling, edible coatings, and the employment of genetic resources are some examples of research topics currently studied [9,10].
The objective of this review was to summarize the main physiological aspects of primary metabolism in apple, such as photosynthesis and metabolite accumulation processes, as well as how they are affected by the application of agrochemicals during the first stages of apple development, when most of the final fruit’s quality at harvest is determined.

2. Fruit as a Photosynthetic Organ

Photosynthesis in leaves is one of the most studied processes in plant science, considering that it is a key mechanism allowing the growth and development of different organs, whereby plants convert sunlight energy into biochemical energy [11]; however, photosynthesis is not only specific to foliar organs. Several studies have reported potential carbon assimilation in other tissues, such as seeds, petioles, stems, or fruits [12,13]. Concerning fleshy fruit, photosynthesis may be limited to the first stages of fruit development, when the fruit is still green and immature [14].
Similar to leaves, young apples have a photosynthetic system with active chloroplasts, which are located at the level of the hypodermal and inner perivascular green tissues, exhibiting a flat and elongated structure with stacked thylakoids forming a hypergranum, but which are smaller and fewer than those found in leaves [15,16]. Photosynthetic pigments (chlorophyll a and b and carotenoids β-carotene, lutein, violaxanthin, and neoxanthin) are also found in both the skin (peel) and the cortex (pulp) of apples, but they are less concentrated and irregularly distributed [17]. Although chlorophyll content gradually decreases as the apple develops, these pigments may accept light energy for photosynthesis, as shown in chlorophyll fluorescence images of young apples where the operating efficiency of photosystem II (Fq’/Fm’) indicates functional photosynthetic electron transport [12].
There are two potential major sources of CO2 available for the photosynthetic process in fruits. The first is atmospheric CO2 that diffuses through the stomata and is assimilated by the ribulose-1,5-biphosphate carboxylase, or Rubisco, to produce sugars, as occurs in foliar tissues. However, young apples not only have a determined number of stomata per fruit that remains constant since flower development, but they are fewer than can be found in leaves [16]. Secondly, apple fruits can accumulate about 1–8% of CO2 from mitochondrial respiration. This CO2 is fixed and refixed in a malate-CO2 shuttle by the phosphoenolpyruvate carboxylase (PEPc). As PEPc light-dependent activity surpasses Rubisco and is correlated with higher chlorophyll content, it is similar to the carbon assimilation mechanism of C4/CAM plants [18]. The downregulation of chlorophyll biosynthesis genes in tomato was correlated with a reduction in photosynthetic rate, but fruit size and metabolite levels remained unaltered, suggesting that fruit photosynthesis is not essential for growth and development, as the main source of photoassimilates is leaves. However, a delay in seed development was observed, which suggests an important role of CO2 (re)fixation from fruit photosynthesis [19]. The rates of CO2 assimilation in immature apples, as in tomatoes, are lower than in leaves, which means that the CO2 fixed in the peel also has little effect on growth and development in this crop [20,21]. Similarly to tomato, this suggests that apple photosynthesis may be mainly used to support seed development and accumulate malate via the malate-CO2 shuttle.

3. Accumulation of Carbohydrates and Other Primary Metabolites

To reach the optimal commercial quality, fruits on the tree must be able to increase their size, especially during the first stages of development, as well as accumulate sugars and other metabolites important to consumers. Throughout its development, apple experiences different stages from a physiological point of view, in which can be categorized as (1) cell division, (2) cell expansion that partially overlaps with cell division and is continuous until the harvest time, (3) maturation, and (4) fruit ripening, representing important stages where the fruit undergoes structural and biochemical changes that result in the conversion of a green and nonpalatable fruit into a high quality and nutritional fruit (Figure 1A) [1,22,23].
Apples show a simple sigmoid curve growth pattern with an exponential initial growth phase, followed by linear growth, based on an expolinear equation that involves fruit diameter [26,27,28] (Figure 1A). During the early developmental stages of apple, sugars are essential to provide the energy needed by the fruitlets in order to endure cell division and subsequent cell expansion; therefore, apple fruitlets become a strong sink organ [29]. Regulated by the sink strength, photoassimilates are translocated from the mother tree to the fruitlet tissues via the apoplast [30]. However, during the reproductive season, young growing shoots are stronger sinks than fruits, causing an extreme competition for tree resources; as a consequence, the tree is not able to support all growing fruitlets, thus inducing the natural abscission of weaker ones [31,32]. This phenomenon, often called “June drop” or simply “physiological fruit drop”, is not sufficient to achieve a suitable fruit load, thus leading to two main issues: (i) poor fruit quality at harvest, and (ii) alternate bearing (reviewed by Costa et al. [33]). For this reason, most apple cultivars need to be thinned manually, mechanically, or chemically to improve their final quality by indirectly modifying, among other factors, the content of primary metabolites (Table 1). Such operations must be carried out early in the season, i.e., at bloom or at fruitlet stage, and the chemical option is currently the gold standard for growers due to its lower cost and better management of application time.
Outside of mechanical thinning and the use of some caustic agents (i.e., ATS, ammonium thiosulphate), most thinning agents make use of active ingredients with hormone-like activity, such as ethephon (an ethylene releaser), naphthaleneacetic acid (NAA), naphthaleneacetamide (NAD), and the cytokinin-like 6-benzyladenine (BA). Metamitron, a photosynthesis inhibitor, has also been recently released as a thinning agent [33], thus providing growers with new chemical tools that can be applied according to their thinning strategy, i.e., using several thinners at different times in order to achieve an optimal fruit load.
The physiological mechanisms on which the different thinners rely have been deeply investigated, especially with respect to BA and metamitron. While the former stimulates shoot growth and bud outbreak with little direct effect on the fruitlets, metamitron inhibits photosystem II, causing nutritional stress in both cases, thereby enhancing the strong competition for assimilates between the vegetative and reproductive sinks. This new condition is perceived by the weaker fruitlets and, as a result, a complex network is activated at the cortex and seeds of apple fruitlets, in which sugars, mainly sucrose and trehalose, work as the primary signaling molecules. During sugar starvation, there is an accumulation of reactive oxygen species (ROS) molecules, especially hydrogen peroxide (H2O2), which interact with the phytohormones involved in this process, including ethylene and abscisic acid (ABA), thus inducing seed abortion and a subsequent activation of the abscission zone [33,46,47].
In addition to bloom or fruitlet thinners, there are a few agronomical practices that can be performed to indirectly modify the content of primary metabolites and further improve the apple’s final quality, including some “cosmetic” practices addressed to improve the appearance of fruits and summer pruning (Table 1).
Even though the application of agrochemicals is a common practice, there are no health concerns with respect to their usage due to the following reasons: (i) they are mainly applied shortly after full bloom, and the preharvest interval (PHI) is largely respected, as, in most cases, apples are picked after at least 3 months following treatment; (ii) most of the active ingredients are closely similar to endogenous hormones and, consequently, are easily metabolized by both the target trees and the surrounding environment, thus also ruling out any environmental concerns [48,49,50].
In apples, cell division is generally completed 3–4 weeks after pollination [26]. During this short period of time, the carbohydrates produced in the leaf mesophyll and translocated to the immature fruits are sorbitol and sucrose. The loading of both sugars into a complex formed between the companion cell and the sieve element (SE–CC) follows the symplasmic pathway (Figure 2) [51,52]. However, specific transporters for sorbitol (SOT) and sucrose (SUT) located on the plasma membrane allow these sugars to enter the cell parenchyma through apoplasmic unloading [30,53]. To meet the energy requirements for cell division, sorbitol, the major carbohydrate transported into young apples and other fruits from the Rosaceae family [54,55,56], is converted into fructose by sorbitol dehydrogenase (SDH) [57]. On the other hand, sucrose conversion into fructose and glucose has two different routes: (1) regulated by the sucrose synthase (SUSY) enzyme, located in the cytoplasm, and (2) regulated by cell-wall invertase (CWINV), situated at the cell-wall space, where hexose transporters (HT) transfer the products from the conversion into the cytosol [30]. Consequently, these two hexoses are phosphorylated by fructokinase (FK), specific for fructose, and hexokinase (HK), specific for glucose. The two products obtained from this process are rapidly metabolized, as fructose 6-phosphate enters the glycolysis/TCA cycle to produce energy, while glucose 6-phosphate (G6P) is later used for starch synthesis as storage [58]. G6P transmembrane transporters located at the plastid membrane were found to show a high expression around 40 days after full bloom (DAFB), facilitating G6P import from the cytosol into plastids, where synthesis and accumulation of starch takes place, as several enzymes involved in starch formation, such as starch synthase, starch branching enzyme, and ADP glucose pyrophosphorylase were also co-expressed with G6P transporters [16,24,59]. As a result, G6P accumulation is decreased during apple development (Figure 1B, Table 2). In addition, cell vacuoles also store sugars that have not been metabolized, such as fructose, glucose, and sucrose, by transporting them into the vacuole space through some tonoplast transporters, e.g., MdSUT4.1, which is significantly associated with sucrose accumulation in apple vacuoles [53,60].
As fruit development progresses over time, apples continue to accumulate a high amount of sugars within vacuoles, thus generating an osmotic pressure that stimulates a high influx of water. This compartmentation of sugars is important for inducing turgor pressure, which is the main force controlling cell enlargement [61]. Previous studies have shown that isolated vacuoles from immature apple flesh presented a higher turgor pressure than vacuoles from mature apples, as vacuoles from immature fruits contained 706 mM of total sugars (mostly fructose and glucose) in comparison to 67 mM of total sugars accumulated in the apoplast [62], while the content of total sugars in vacuoles from mature fruits was 937 mM compared to 440 mM of total sugars in the apoplast [54]. Therefore, this indicates that, during the early development of apples, there is active cell division that requires a high input of energy from the photoassimilates, sorbitol and sucrose, produced by leaf photosynthesis, which are translocated and rapidly metabolized in immature apple fruits, as a high expression of the enzymes SDH, CWINV, SUSY, FK, and HK was observed on “Greensleeves” apples [58]. Afterward, fruits start to accumulate sugars (Figure 1B, Table 2) into vacuoles, causing a high turgor pressure that is translated into active cell enlargement and, consequently, an increase in fruit growth that continues over time throughout the development of apples. In fact, one of the main sugars highly accumulated in vacuoles is fructose, due to the coordinated actions of three factors: (1) an elevated fructose supply generated from sorbitol and sucrose conversion by SDH, SUSY, and INV enzymes, (2) a decrease in FK expression and activity during cell expansion, which implies that less fructose is metabolized as the fruit continues to develop and more is available for accumulation, and (3) the upregulation of tonoplast transporters, which actively transport fructose from the cytoplasm into vacuoles during apple growth [24,57,63].
In addition to the major sugars present in apple primary metabolism, trehalose 6-phosphate (T6P; Table 2), which is a precursor product of trehalose biosynthesis and a promoter of plant growth [64], has been found in “Gala” apple [65]. T6P showed low concentration levels during apple development, but it was positively correlated with sorbitol, suggesting the possible regulation of a different starch accumulation pathway. However, further investigation is needed to unravel the role of T6P in sugar metabolism [65,66].
Organic acids are also accumulated into apple cell vacuoles, playing an important role in fruit acidity and its final organoleptic quality [67]. Around 85–90% of total organic acids in apples are represented by malic acid, while acetic acid, oxalic acid, fumaric acid, and citric acid are also found but in minor proportions inside the cell vacuole [62]. There are two pathways used to synthesize malate, the predominant form of malic acid (Figure 3). In the first one, phosphoenolpyruvate (PEP), derived from sugar metabolism during the early stages of apple development, is converted into oxaloacetate (OAA) at the cytoplasm by PEPc, a cytosolic enzyme responsible for the carboxylation of PEP. Then, OAA is reduced to malate (a reversible conversion) by the cytosolic NAD-dependent malate dehydrogenase [68,69,70,71]. In the second one, malate is produced in the mitochondria through the TCA cycle, where CO2 from mitochondrial respiration must be fixed, as fruits fix little CO2 from fruit photosynthesis via Rubisco [16,71]. It has been suggested that cytosolic conversion of OAA into malate is the most likely route for its synthesis, as PEPc is highly expressed during “Greensleeves” apple development [24].
As the fruit continues to metabolize sugars, the malate level is increased and accumulates in the vacuole thanks to the malate transporters localized at the tonoplast, activated by the MYB transcription factors MdMYB1/10 and MdMYB73, which also regulate the activation of the two primary proton pumps, the vacuolar H+-ATPase and the vacuolar pyrophosphatase, both playing an important role in determining fruit acidity [68,72,73]. The highest levels of malate were observed 60 days after bloom in low-acid and high-acid apple genotypes from a cross population of “Toko” and “Fuji”. As the apple continues to grow, malate levels subsequently decrease (Figure 1B, Table 2) and the activity of NADP-dependent malic enzyme increases, which is in charge of malate degradation [69,70]. By the end of apple development, there is an accumulation of soluble sugars not only due to the decrease in malate content, but also due to the hydrolyzation of the accumulated starch, which provides fructose, glucose, and sucrose [4,74].
Alongside malate, other organic acids from the TCA cycle such as succinic acid, fumaric acid, and citric acid (Figure 3) also present higher concentrations in immature apples; however, as cell expansion begins, their levels decrease throughout apple development [25,75]. In contrast, ascorbic acid is accumulated at a mature stage, as well as tartaric acid (Figure 1B, Table 2) [25]. Although the concentration of ascorbic acid in apples is low, compared with other fruits such as kiwifruits or blackcurrant [76], it has been reported that apple peel contains more ascorbic acid than the flesh in “Gala” apples, and that it is synthesized from the galactose pathway [77]. Ascorbic acid is a well-known antioxidant and cofactor for several enzymes, and a higher concentration of this organic acid may suggest an antioxidant role during the last stages of apple development, as a response to the increased production of ROS due to high light and high temperature, possibly causing a disorder on apple peel called sunburn [78,79].
Primary metabolism also comprises the accumulation of amino acids which are the constituents of many key proteins associated with fruit development. Amino-acid biosynthesis is linked to carbohydrate metabolism (Figure 3); thus, aromatic amino acids such as phenylalanine, tyrosine and tryptophan are obtained from the shikimate pathway, in which PEP from glycolysis is the main substrate, while F6P is the initial precursor for histidine, formed after a series of reactions starting from phosphoribosylpyrophosphate [80,81]. Moreover, pyruvate is the substrate of branched-chain amino acids valine and leucine, as well as for alanine biosynthesis, while glycine, cysteine, and serine are formed from 3-phosphoglycerate, also from the glycolysis process [82]. Intermediates from the TCA cycle are also involved in the synthesis of amino acids (Figure 3), mainly OAA, which is the precursor of aspartic acid and all its derived amino acids, such as lysine, threonine, methionine, isoleucine, and asparagine, whereas 2-oxo-glutarate is the precursor for glutamic acid, the base for the synthesis of glutamine, arginine, and proline [82,83]. Studies in “Honeycrisp”, “Pinova”, and “Greensleeves” apple cultivars showed different levels of amino acids throughout fruit development (Figure 1B, Table 2) [24,25,75]. More than 80 proteins related to amino-acid biosynthesis derived from glycolysis and the TCA cycle were found, mostly dehydrogenases, synthases, and kinases specific for each amino acid [24]. During the early stages of apple development, tyrosine, methionine, phenylalanine, and arginine show a higher accumulation after 84 DAFB, while fruit cells are expanding; however, after reaching their maximum, their levels decrease as the fruit continues to develop. On the other hand, amino acids such as asparagine, threonine, cysteine, glutamine, lysine, aspartic acid, histidine, and glutamic acid exhibit an increasing accumulation trend throughout apple development, reaching their peak at a mature stage. Lastly, the quantification of leucine, alanine, proline, serine, valine, tryptophan, isoleucine, and other amino acids showed minimum levels and a tendency to decrease during the developmental cycle. Many amino acids are precursors of several secondary metabolites, such as phenylpropanoids, while others, e.g., asparagine, can be a storage form for free amino acids, as previously suggested [75].

4. Future Perspectives and Conclusions

In this review, we aimed to describe the most important pathways and compounds either involved in or derived from primary metabolism, which is important for many developing fruits, as it provides the basis of final fruit size and quality. Considering its importance, research is focused on improving fruit quality and extending shelf-life to fulfil consumers’ high standards, as apples are one of the most produced fruits worldwide. With the release of the apple genome sequence in 2010 [84], many molecular advances have been achieved in recent years, improving apple breeding programs and the comprehension of the most important physiological processes, with relevant positive effects in terms of knowledge transfer to the productive sector, especially with regard to agronomic practices (i.e., thinning and optimization of harvest date). Many studies have demonstrated the effect of these agronomic practices on final fruit quality in terms of primary metabolite content, even though these positive effects are most likely achieved through indirect mechanisms.
The literature is not very exhaustive when it comes to fruit physiology during apple development on the tree, as most studies have sectorially focused on the very beginning of development, i.e., flowering, fruit set, and fruitlet stage, on the later stages, i.e., ripening, or on the postharvest phase, without any semblance of continuity. As an example, we found that the latest review on apple photosynthesis was about 30 years ago [16], despite photosynthesis being a key process not only for fruit development but also for the ignition of primary metabolism. Considering the technological improvements made in the last decades (e.g., in measuring gas exchanges at the orchard, tree, and single organ level), this topic deserves more detailed investigations, as several questions are still unanswered.
When we think about fruit final quality, this concept is always linked to secondary metabolism and its various products, such as volatiles, flavonoids, or terpenoids. However, it is during the early stages of development, when primary metabolites such as sugars, organic acids, and amino acids play an important role, that most of the final fruit quality is determined, as many significant secondary metabolites are produced by primary metabolites that are the main substrate for many reactions. Within secondary metabolism, plant hormones play a crucial role in apple final quality. In addition to ethylene, the main phytohormone involved in the ripening process for climacteric fruits such as apples, many other hormones are involved such as auxins, cytokinins, or gibberellins, which are common plant growth regulators, or even jasmonates. Although some of these plant growth regulators are used in exogenous treatments such as agrochemicals for horticultural procedures, little is known about how these treatments may directly affect primary metabolism. Therefore, the interplay between different hormones and primary metabolism should be further investigated, representing an important advance in the research of apple physiology, from which future agronomical practices can be inspired.
In conclusion, apple development is a complex process that requires further research focusing on physiological aspects for a full understanding, involving subprocesses ranging from cellular modifications to genetic reprogramming, as well as fruit photosynthesis and climate sensory, sugar, and hormonal signaling.

Author Contributions

A.B. conceptualized the review; V.T. and A.B. participated in manuscript preparation; F.G. revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the University of Padova Uni-Impresa call 2018 and by DOR (grants no. 1989001/19, 2018552/20, and 2182278/21) and BIRD (grant no. 209593/20) projects.

Conflicts of Interest

The authors declare no conflict of interest.

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Agronomy 11 01160 g001 550
Figure 1. Apple growth curve (dashed line), highlighting main processes and primary metabolites. (A) Simple sigmoid growth pattern based on an expolinear equation for apple. The main physiological processes and events accompanying apple development are indicated. (B) Heatmap showing the time course progression of the levels of some of the most important sugars, organic acids, and amino acids found in apple at four developmental stages (27, 84, 125, and 165 DAFB). Levels were elaborated from references [24,25] and are reported as log2 of the foldchange, keeping the first value equal to 1. GLU, glucose; FRU, fructose; SUC, sucrose; SOR, sorbitol; G6P, glucose-6-phosphate; T6P, trehalose-6-phosphate; MA, malic acid; CA, citric acid; SA, succinic acid; TA, tartaric acid; AA, ascorbic acid.
Figure 1. Apple growth curve (dashed line), highlighting main processes and primary metabolites. (A) Simple sigmoid growth pattern based on an expolinear equation for apple. The main physiological processes and events accompanying apple development are indicated. (B) Heatmap showing the time course progression of the levels of some of the most important sugars, organic acids, and amino acids found in apple at four developmental stages (27, 84, 125, and 165 DAFB). Levels were elaborated from references [24,25] and are reported as log2 of the foldchange, keeping the first value equal to 1. GLU, glucose; FRU, fructose; SUC, sucrose; SOR, sorbitol; G6P, glucose-6-phosphate; T6P, trehalose-6-phosphate; MA, malic acid; CA, citric acid; SA, succinic acid; TA, tartaric acid; AA, ascorbic acid.
Agronomy 11 01160 g001
Agronomy 11 01160 g002 550
Figure 2. Sugar metabolism in apple. Sorbitol and sucrose are the photoassimilates unloaded to cell fruits via apoplasmic unloading from the sieve element–companion cell complex (SE-CC). With their respective cell-wall transporter, these compounds enter the parenchyma cell where they are converted into hexoses (fructose and glucose), which are phosphorylated by fructokinase and hexokinase, respectively, to enter glycolysis/TCA cycle, with the objective of satisfying the energetic requirements for apple growth. The cytoplasm is divided according to (A) high sugar metabolism that produces energy, starch for storage, and malate used to (re)fix the mitochondrial CO2 via the malate-CO2 shuttle, as well as for accumulation, and (B) slower sugar metabolism that starts to accumulate sucrose, fructose, and glucose inside the vacuoles. In red letters, the enzymes are abbreviated as follows: SDH, sorbitol dehydrogenase; SUSY, sucrose synthase; FK, fructokinase; HK, hexokinase. Sugar transporters are abbreviated as follows: SOT, sorbitol transporter; SUT, sucrose transporter; HT, hexose transporter.
Figure 2. Sugar metabolism in apple. Sorbitol and sucrose are the photoassimilates unloaded to cell fruits via apoplasmic unloading from the sieve element–companion cell complex (SE-CC). With their respective cell-wall transporter, these compounds enter the parenchyma cell where they are converted into hexoses (fructose and glucose), which are phosphorylated by fructokinase and hexokinase, respectively, to enter glycolysis/TCA cycle, with the objective of satisfying the energetic requirements for apple growth. The cytoplasm is divided according to (A) high sugar metabolism that produces energy, starch for storage, and malate used to (re)fix the mitochondrial CO2 via the malate-CO2 shuttle, as well as for accumulation, and (B) slower sugar metabolism that starts to accumulate sucrose, fructose, and glucose inside the vacuoles. In red letters, the enzymes are abbreviated as follows: SDH, sorbitol dehydrogenase; SUSY, sucrose synthase; FK, fructokinase; HK, hexokinase. Sugar transporters are abbreviated as follows: SOT, sorbitol transporter; SUT, sucrose transporter; HT, hexose transporter.
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Figure 3. A general description of organic acid and amino-acid metabolism pathway during apple development, which involves glycolysis and the TCA cycle. Red arrows indicate the expected route of malate formation, accumulation, and degradation in apples. Blue boxes and arrows mark the diverse biosynthesis pathways of the different amino acids. In red letters, the enzymes are abbreviated as follows: PEPc, phosphoenolpyruvate carboxylase; cMDH, NAD-dependent malate dehydrogenase; NADP-ME, NADP-dependent malic enzymes; FK, fructokinase; HK, hexokinase.
Figure 3. A general description of organic acid and amino-acid metabolism pathway during apple development, which involves glycolysis and the TCA cycle. Red arrows indicate the expected route of malate formation, accumulation, and degradation in apples. Blue boxes and arrows mark the diverse biosynthesis pathways of the different amino acids. In red letters, the enzymes are abbreviated as follows: PEPc, phosphoenolpyruvate carboxylase; cMDH, NAD-dependent malate dehydrogenase; NADP-ME, NADP-dependent malic enzymes; FK, fructokinase; HK, hexokinase.
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Table
Table 1. Main agronomic practices that can indirectly affect the primary metabolite content of apples at harvest.
Table 1. Main agronomic practices that can indirectly affect the primary metabolite content of apples at harvest.
Agronomic PracticeTiming 1Details 2Effects at HarvestReference
Thinning63–65/69–71mechanical, ethephon, ATS↑SSC, ↑acidity[34,35,36]
69–726-BA, NAA, NAD, metamitron↑SSC, ↑acidity[36,37,38,39]
Cosmetics 369–71
63–65		GA4, GA7
GA3		↑acidity
↓acidity		[40,41]
Summer pruning76–77-↑SSC[42,43]
Ripening delay81–851-MCP↓starch hydrolysis[44]
1 Phenological stages as reported by the BBCH scale [45]. 2 Technique or chemical. 3 Treatments to improve the appearance (color, shape, etc.). ATS, ammonium thiosulfate; SSC, soluble solid content; 6-BA, 6-benzyladenine; NAA, naphthaleneacetic acid; NAD, naphthaleneacetamide; 1-MCP, 1-methylcyclopropene.
Table
Table 2. Primary metabolites analyzed using different techniques. This table is based on the most recent resources with the highest amounts of metabolites quantified in the same experiment. G6P, glucose-6-phosphate; T6P, trehalose-6-phosphate.
Table 2. Primary metabolites analyzed using different techniques. This table is based on the most recent resources with the highest amounts of metabolites quantified in the same experiment. G6P, glucose-6-phosphate; T6P, trehalose-6-phosphate.
MetabolitesAnalysis TechniquesReferences
GlucoseGC–MS 1
UPLC–ESI-MS/MS 2		[24]
[25]
FructoseGC–MS[24,25]
SucroseGC–MS
UPLC–ESI-MS/MS		[24]
[25]
SorbitolGC–MS
UPLC–ESI-MS/MS		[24]
[25]
G6PGC–MS
UPLC–ESI-MS/MS		[24]
[25]
T6PUPLC–ESI-MS/MS[25]
Organic acidsGC–MS
UPLC–ESI-MS/MS		[24]
[25]
Amino acidsHPLC 3
UPLC–ESI-MS/MS		[24]
[25]
1 Gas chromatography–mass spectrometry. 2 Ultraperformance liquid chromatography–electrospray tandem mass spectrometry. 3 High-performance liquid chromatography.
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Tijero, V.; Girardi, F.; Botton, A. Fruit Development and Primary Metabolism in Apple. Agronomy 2021, 11, 1160. https://0-doi-org.brum.beds.ac.uk/10.3390/agronomy11061160

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Tijero V, Girardi F, Botton A. Fruit Development and Primary Metabolism in Apple. Agronomy. 2021; 11(6):1160. https://0-doi-org.brum.beds.ac.uk/10.3390/agronomy11061160

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Tijero, Verónica, Francesco Girardi, and Alessandro Botton. 2021. "Fruit Development and Primary Metabolism in Apple" Agronomy 11, no. 6: 1160. https://0-doi-org.brum.beds.ac.uk/10.3390/agronomy11061160

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