Metabolic and transcriptional elucidation of the carotenoid biosynthesis pathway in peel and flesh tissue of loquat fruit during on-tree development

Carotenoids are the main colouring substances found in orange-fleshed loquat fruits. The aim of this study was to unravel the carotenoid biosynthetic pathway of loquat fruit (cv. ‘Obusa’) in peel and flesh tissue during distinct on-tree developmental stages through a targeted analytical and molecular approach. Substantial changes regarding colour parameters, both between peel and flesh and among the different developmental stages, were monitored, concomitant with a significant increment in carotenoid content. Key genes and individual compounds that are implicated in the carotenoid biosynthetic pathway were further dissected with the employment of molecular (RT-qPCR) and advanced analytical techniques (LC-MS). Results revealed significant differences in carotenoid composition between peel and flesh. Thirty-two carotenoids were found in the peel, while only eighteen carotenoids were identified in the flesh. Trans-lutein and trans-β-carotene were the major carotenoids in the peel; the content of the former decreased with the progress of ripening, while the latter registered a 7.2-fold increase. However, carotenoid profiling of loquat flesh indicated trans-β-cryptoxanthin, followed by trans-β-carotene and 5,8-epoxy-β-carotene to be the most predominant carotenoids. High amounts of trans-β-carotene in both tissues were supported by significant induction in a chromoplast-specific lycopene β-cyclase (CYCB) transcript levels. PSY1, ZDS, CYCB and BCH were up-regulated and CRTISO, LCYE, ECH and VDE were down-regulated in most of the developmental stages compared with the immature stage in both peel and flesh tissue. Overall, differential regulation of expression levels with the progress of on-tree fruit development was more evident in the middle and downstream genes of carotenoid biosynthetic pathway. Carotenoid composition is greatly affected during on-tree loquat development with striking differences between peel and flesh tissue. A link between gene up- or down-regulation during the developmental stages of the loquat fruit, and how their expression affects carotenoid content per tissue (peel or flesh) was established.


Background
Loquat (Eriobotrya japonica Lindl) is a member of the Rosaceae family that is commercially cultivated in many countries [1][2][3], being highly appreciated for its light, refreshing taste [2,4]. Therefore, although initially considered as an underutilized crop, nowadays loquat can gain added value as it is available during late winterearly spring period [5]. The loquat tree has three flushes of growth per year, and the principal tree growth can be separated into 8 distinct developmental stages [2]. In particular, under Mediterranean weather conditions, the tree blooms between October and early November and its fruit develops through winter, ripening from early February until May. Fruit is usually consumed fresh, but it is also known to be used processed into jam, jelly, wine, syrup, and juice. It is also known that the leaves, flowers and fruits are traditionally used in Chinese medicine since they are linked with healthpromoting properties [1,6].
Carotenoids play an important role in loquat, as they affect organoleptic characteristics and health properties of the fruit. In particular, carotenoids are the main pigments in loquat and impact flavor acceptability, since they are precursors of important volatile flavor compounds [7]. Regarding nutraceutical properties of fruit carotenoids, a significant number of studies depicted their beneficial effect to the promotion of health, including the prevention and/or treatment of chronic and cardiovascular diseases [8]. In particular, fruits rich in carotenoids are directly connected to the prevention of inflammation and cataract [1,9,10] and are also known to enhance immune responses [1,9,11]. Carotenoid profile in loquat is influenced by maturity stage, environmental and most promptly genetic factors. Loquat cultivars have been segregated to white-and red-fleshed [10,12]. However, segregation of loquat cultivars based on their flesh color can be confusing, since additionally the terms yellow-and orange-fleshed are being used. White-fleshed cultivars have a creamy, pale yellow color, while the terms red-and orange-fleshed can be considered as synonymous. The latter type cultivars have higher carotenoid concentrations than the lighter coloured ones [1,5,9,10,12].
The carotenoid biosynthetic pathway is controlled by the presence of the key enzyme PSY (Fig. 1, [10,11,13,[15][16][17]). Regarding loquat fruit, Fu et al. [10] investigated the mechanism underlying the differentiation of carotenoids in a red-fleshed (cv. 'Luoyangqing') and a white-fleshed (cv. 'Baisha') cultivar; differences in carotenoid accumulation in the two cultivars were linked with the differential expression of PSYI, CYCB, and BCH genes. The aim of the current study was to monitor the carotenoid composition in peel and flesh tissue of 'Obusa' fruits, an orange-fleshed cultivar, in correlation with the progress of fruit maturity. Towards this aim, high-resolution temporal expression profiles of carotenoid biosynthetic genes in both tissues were determined by RT-qPCR and linked with individual carotenoids, quantified by LC-MS.

Fruit material and experimental design
Loquat fruits cv. 'Obusa' were harvested at ca. 10-day intervals, between March 30th and May 14th (Fig. 2), from a commercial orchard (Episkopi, Lemesos, Cyprus), owned by the first author. For each developmental stage, 30 uniform fruits were selected based on size and colour; such fruit were divided into three 10-fruit sublots, representing the biological replications. Fruit were initially used for the determination of physical dimensions and colour and subsequently for molecular and analytical analysis, as described below. The developmental stages were defined using the BBCH scale [2].
For the molecular analysis, fresh samples of both peel and flesh were flash frozen in liquid nitrogen and maintained at −80°C until needed. For the determination of carotenoid profiles, samples were freeze-dried (Freeze Dryer-Christ Alpha 1-4 LD plus).

Quality attributes
Physical dimensions of fruit were determined with the employment of an analytical grader and an electronic calibre (IS11112, Insize). The colour parameters CIE L* (brightness or lightness; 0 = black, 100 = white), a* (−a* = greenness, +a* = redness) and b* (−b* = blueness, +b* = yellowness) were measured at the peel and at the flesh tissue per fruit with a chroma meter (CR-400, Konica Minolta).

Spectrophotometric determination of carotenoid and chlorophyll content
Twenty mL of acetone-hexane (4:6, v/v) were added to 100 mg of lyophilised plant material and thoroughly mixed. Upon separation of the two phases, the absorbance was determined in the supernatant at 453, 505, 645 and 663 nm. Based on Nagata and Yamashita equations, total carotenoids, chlorophyll-a and chlorophyll-b contents were determined [18].

LC-MS analysis of loquat carotenoids
The carotenoid analysis was carried out using an Agilent 1200 HPLC equipped with a photodiode array detector and a single quadrupole mass spectrometer detector in series (6120 Quadrupole, Agilent Technologies, Santa Clara, CA, USA). Chromatographic separation was performed on a reverse-phase Poroshell 120 EC-C 18 column (100 mm × 3 mm, 2.7 μm particle size) (Agilent Technologies) operating at 32°C. Water with 0.05 M ammonium acetate and acetonitrile: methanol (70: 30) were used as mobile phases A and B, respectively, with a flow rate of 0.7 mL min −1 . The linear gradient started with 60% of solvent B in A, reaching 100% solvent B at 20 min; this was maintained up to 35 min. The initial conditions were re-established at 36 min and kept under isocratic conditions up to 40 min. Injection volume was 5 μL. Detection and quantification of all carotenoids and carotenoid esters were carried out in UV-vis at 450 nm (Additional file 1: Figure S1).
The identification of carotenoids in loquat was carried out on an Agilent 1100 HPLC system equipped with a photodiode array and an ion trap mass spectrometer detector (Agilent Technologies, Waldbronn, Germany). The mass detector was a Bruker ion trap spectrometer (model HCT Ultra) equipped with an APCI (Atmospheric Pressure Chemical Ionization). The mass spectrometer parameters were as follows: positive ion mode (APCI +); source temperature, 350°C; probe temperature, 450°C, corona voltage, 4.0 kV; The full scan mass covered the range from m/z 100 up to m/z 1200 and the target mass was adjusted to 350. Collision-induced fragmentation experiments were performed in the ion trap using helium as the collision gas, with voltage ramping cycles from 0.3 up to 2 V. Mass spectrometry data were acquired in the positive mode, and the MS n was carried out in the automatic mode. The identification of the peaks was performed by the extracted ion-chromatograms of the ion current at m/z values corresponding to the [M-H] + ions of the individually investigated compounds, as well as their fragmentation. Furthermore, to confirm the identification of the carotenoids and obtain a more reliable identification, samples were analyzed with the Agilent 1290 Infinity UPLC system coupled to a quadrupole (Q-TOF) mass spectrometer (6550 Accurate-Mass QTOF, Agilent Technologies) using an electrospray interface with jet stream technology. The chromatographic separation was developed under the same conditions, as described above. The optimal conditions for the electrospray interface were as follows: gas temperature: 300°C, drying gas 11 L/min, nebulizer 65 psi, sheath gas temperature 400°C, sheath gas flow 12 L/min. Spectra were acquired in the m/z range of 100-1100, in a positive mode and with an acquisition rate of 1.5 spectra in MS, maintaining a mass resolution over 50,000 for the mass range used. Internal mass calibration by the simultaneous acquisition of reference ions and mass drift compensation was used for obtaining low mass errors. Q-TOF MS data were processed using the Mass Hunter Qualitative Analysis software (version B.06.00). For quantification, β-apo-8′-carotenal was used as an internal standard. Lutein, β-carotene and violaxanthin (Sigma, St Louis, MO, USA) in a concentration range of 5-100 μg.mL −1 were used to quantify compounds in three different groups, hydroxycarotenoids, carotenes, and epoxycarotenoids, respectively. Neoxanthin, neochrome, β-cryptoxanthin epoxides and β-carotene epoxides were estimated as violaxanthin. β-Cryptoxanthin was quantitated as lutein. The cis-isomers were quantitated with the calibration curve of the all-trans isomers. Concentrations were expressed as micrograms of pigment per 100 g of sample fresh weight (μg 100 g −1 F.W.).

RNA extraction, cDNA synthesis and quantitative real-time RT-PCR analysis
Total RNA was extracted from three bulked biological replicates of loquat fruit material for each developmental stage (S1-S6) according to a modified cetyltrimethylammonium bromide (CTAB) protocol developed by Gambino et al. [20]. Next, RNA integrity was confirmed spectrophotometrically (Nanodrop 1000 Spectrophotometer, Thermo Scientific) followed by gel electrophoresis and samples were treated with RNase-free DNase (Cat. No. NU01a, HT Biotechnology LTD, England) to remove total gDNA, as elsewhere described [21].
Total RNA (0.5 μg) was reverse transcribed using the PrimeScript™ RT reagent Kit (Takara Bio, Japan), according to the manufacturer's protocol (Takara Bio, Japan). Subsequently, quantitative real-time RT-PCR was performed with BioRad IQ5 real-time PCR cycler (BioRad, USA). In total, three biological replicates were analyzed for each developmental stage for both loquat peel and flesh. The reaction mixture consisted of 4 μL cDNA in reaction buffer (15-fold diluted first-strand cDNA for all genes except for VDE and LCYE that were diluted 5-fold), 0.5 μL of each primer (10 pmol/μL) and 5 μL Sensi-FAST™ SYBR ® & Fluorescein mix 2× (Bioline). The total reaction volume was 10 μL. The initial denaturation step was at 95°C for 5 min, followed by 40 cycles of amplification [95°C for 30 s, annealing temperature (Ta o C) for 30 s, and 72°C for 30 s] and a final elongation stage at 72°C for 5 min. Gene amplification cycle was followed by a melting curve run, carrying out 61 cycles with 0.5°C increment from 65 to 95°C. The annealing temperature of previously published primers for loquat carotenoid biosynthetic genes (58 to 65°C) is shown in Additional file 1: Table S1. Loquat's actin gene was used as a housekeeping reference gene (EjACT).

Statistical analyses
Statistical analyses were carried out by comparing the averages of each developmental stage based on the analysis of variance (one way ANOVA) according to Duncan's multiple way test with a significance level of 5% (P ≤ 0,05), using the SPSS v.17.0 statistical analysis software package.
The relative quantification and statistical analysis of gene expression levels was performed with the REST-XL software, using the pairwise fixed reallocation randomization test [22]. Gene expression levels were normalized against the EjACT housekeeping reference gene; the initial developmental stage (S1) both for peel and flesh tissue was used for calibration.

Results and discussion
Qualitative attributes  Table S2). Maximum fruit size and weight was recorded at stage S5, which coincides with the optimum maturity stage for harvest.
Colour parameters in the flesh ranged between 52.12-74.32 for L*, −11.51-10.67 for a* and 30.75-36.67 for b*. The corresponding values for L * , a * , b * parameters in the peel were 45.65-64.99, −17.66-12.42 and 28.20-49. 19 (Additional file 1: Table S3). Previous study in loquat cultivars indicated that the a*/b* chroma ratio receive negative values in immature fruits, around zero for pale yellow-colored fruits, and positive values for orangecolored loquat fruits; thus higher ratio can be linked with higher carotenoid accumulation [1]. In our study, the a*/b* ratio in the flesh received negative values at stages S1-S3, implying the green colour, the S4 value indicates the colour break and the S5 and S6 had the higher values. Similarly, the a*/b* ratio was lower in the peel during the first three early stages (−0.60 to −0.20), close to zero in the breaker stage, while it received positive values during the last maturation stages (0.24-0.29) (Additional file 1: Table S3). Overall, the a*/b* ratio can be linked with total carotenoid accumulation and its transient increase with the progress of on-tree development, in accordance with previous studies [1,16].

Carotenoid and chlorophyll contents
Initially, a rapid colorimetric assay was employed to screen carotenoid and chlorophyll contents. Total carotenoids varied between 0.8-6.1 and 0.1-5.9 mg 100 g −1 FW β-carotene equivalents in the peel and in the flesh, respectively (data not shown). The highest concentrations in Chl a and Chl b were found in the peel tissue at the immature green stage (18.0 and 12.1 mg 100 g −1 FW, respectively), while their contents were substantially lower in the flesh (0.6 and 0.5 mg 100 g −1 FW at S1 stage, respectively) and degraded thereafter with the progress of on-tree ripening. During ripening of fleshy fruits chloroplasts turn into chromoplasts; this process encompass a transient increase of carotenoids and degradation of chlorophylls [23]. Chl a is a blue-green coloured pigment and is less stable than the yellowgreen Chl b.

Identification of carotenoids in loquat fruit using LC-MS
Carotenoids in the peel and in the flesh were identified and quantified (Table 1, Additional file 1: Figure S1). Thirty-two carotenoids were detected by HPLC-DAD and LC-MS techniques. Peak identification was based on their relative retention time values, their UV-Vis spectra, their mass spectra, information from the literature and comparison with authentic standards when possible. Table 1 summarizes the identification data for each carotenoid, including chromatographic and spectroscopic values.
All-trans-neoxanthin (peak 1) showed a characteristic UV-visible spectrum. The molecular mass of neoxanthin was confirmed by the protonated molecule at m/z 601 and by consecutive losses of three hydroxyl groups from the protonated molecule, at m/z 583, 565 and 547, verified by MS/MS. The UV-visible absorption spectrum of neochrome (peak 2) showed λmax at 397, 420 and 448 nm with high spectral fine structure (%III/II 90); these values are in agreement with previous studies in loquat [9]. All-trans-violaxanthin (peak 3) was identified by comparison with the authentic standard. The protonated molecule at m/z 601, and the fragments at m/z 583 and 565, due to the losses of hydroxyl groups and at m/z 221, all formed from 601 at both MS/MS and in-source fragmentations. Peak 8 was tentatively identified as cis-violaxanthin with a mass spectrum, lower λmax and spectral fine structure values similar to those of peak 3. β-diepoxy cryptoxanthin, peak 7 and 32 (only in flesh in S5 and S6)] showed the [M + H] + at m/z 585. The second order MS experiments revealed a fragment at m/z 567 due to the loss of water and the ions at m/z 221 and at m/z 205 characteristic of the epoxide group with one ion located in a ring with a hydroxyl group and another one in an unsubstituted ring respectively. All trans-lutein was identified by comparison with an authentic standard. All trans-lutein (peak 10) and cis-lutein (peak 19) showed characteristic UV-visible spectra, with a hypsochromic shift of 8 nm for the cis isomer. The identification of both lutein isomers was confirmed by their mass spectra with the protonated molecule at m/z 569 and fragments at m/z 551 and m/z 533 due to the loss of one and two hydroxyl group respectively. The MS/MS showed, in addition, the presence of fragments at m/z 477 resulting from the loss of toluene ([M + H-92] + ) from the polyene chain. In APCI-MS, the fragment with m/z 551 presented a higher intensity than the protonated molecular ion (m/z 569). Peaks 17 and 18 were identified as mono-epoxides of β-cryptoxanthin considering their UV-vis and MS characteristics by the comparison with literature data [9,24]. The mass spectra of both epoxides presented the protonated molecule at m/z 569 and fragment ion at m/z 551 due to the loss of a hydroxyl group. Peak 17 was designated as 5′,6′-epoxy-β-cryptoxanthin due to the presence of the mass fragment at m/z 205 that is consistent with the location of one epoxide group in the unsubstituted ring whilst peak 18 showed the mass fragment at m/z 221, indicating that the epoxide groups were in a ring with a hydroxyl group. β-Apo-8′-carotenal was identified as peak 21 (internal standard). The mass spectra presented the protonated molecule at m/z 417. Ions of m/z 399 and 389 were detected corresponding to the loss of water and carbon monoxide respectively. Elimination of toluene from the protonated molecule was observed at m/z 325. The use of an internal standard was recommended to estimate the losses during the extraction process. Saponification with potassium hydroxide has been an integral part of carotenoid analyses. Kimura et al. [25] showed that β-apo-8′-carotenal was completely transformed to citranaxanthin (peak 22), apparently by aldol condensation with acetone. The conversion percentage from β-apo-8′-carotenal to citranaxanthin was 98% and their sum was considered for quantification. The identification of citranaxanthin was confirmed on the basis of its protonated molecule at m/z 457 [26] and its characteristic UV-vis spectrum [27]. Due to the presence of the same chromophore, β-cryptoxanthin (peak 26) and β-carotene have similar UV-visible spectra. As expected, the protonated molecule was detected at m/z 553 and the MS/MS revealed the presence of fragment ions at m/z 551 and 461 corresponding to the losses of the hydroxyl group and toluene. 5,8-epoxy-β-carotene (peak 30) could not be identified by its UV-visible spectral characteristics. Mass spectra highlighted the protonated molecule at m/z 553 and the MS/MS showed the presence of fragment ions at m/z 551 and 461 corresponding to the losses of the hydroxyl group and toluene, respectively, and at m/z 221 that corresponds to the location of the epoxide group in the 3-hydroxy-β-ring. The mass spectra of beta-carotene, peak 31, showed the protonated molecule at m/z 537 and a fragment ion in the MS/MS at m/z 444, corresponding to the loss of the toluene from the polyene chain.

Carotenoid composition in loquat fruit
Results revealed great differences in carotenoid composition between peel and flesh. In particular, 32 carotenoids were found in loquat peel, while only eighteen carotenoids were identified in the flesh. Except for qualitative differences, the concentration of carotenoids was significantly higher in the peel than in the flesh. This was not the case when total carotenoids were determined spectrophotometrically, indicating the limitations of such colorimetric assays. Chromatograms also revealed that the major carotenoids in peel were trans-lutein and trans-β-carotene. The concentration of trans-lutein decreased with the progress of ripening from 1621.5 to 688.4 μg 100 g −1 FW. On the other hand, trans-β-carotene content increased drastically from 151.9 to 1096.9 μg 100 g −1 FW. The biosynthesis of some carotenoids such as trans-β-cryptoxanthin, 5,8-epoxy-β-carotene, β-diepoxy-cryptoxanthin and cisviolaxanthin has also been monitored (Fig. 3, Additional file 1: Table S4). Conversely, trans-neoxanthin and transneochrome decreased or remained stable with the progress of on-tree fruit development in the peel, while they were not detected in the flesh during the last developmental stages. The carotenoid profiling of loquat flesh was found to be quite different from the peel. The most abundant carotenoid in mature fruits was trans-β-cryptoxanthin, followed by trans-β-carotene, compounds 18 and 31, and 5,8-epoxy-β-carotene (peak 30) ( Table 1, Fig. 3, Additional file 1: Table S4). An increment in the concentration of all carotenoids during on-tree development except for transneoxanthin, trans-neochrome and trans-lutein was found (Fig. 3, Additional file 1: Table S4). Overall, a great effect of the developmental stage on the carotenoid composition was revealed.
The carotenoid quantification in our study proved that the peel had higher carotenoid concentrations than the flesh, except for β-diepoxy-cryptoxanthin which was found from the 3rd until the 6th maturity stage in the peel, ranging from 15.0 ± 0.8 to 21.2 ± 1.7 μg 100 g −1 FW, as well as in flesh during the last maturity stages (S5 and S6) at 17.6 ± 1.2 and 21.4 ± 1.8 μg 100 g −1 FW, respectively (Fig. 3, Additional file 1: Table S4). Trans-neoxanthin and trans-neochrome appeared throughout all developmental stages in the peel as well as in the first 4 maturation stages in the flesh. On the other hand, trans-violaxanthin increased in the peel with the progress of ontree ripening (15.6 ± 2.5 to 25.2 ± 4.6 μg 100 g −1 FW), while it was detected in the flesh during the last stages (S4-S6) with progressive increase (from 12.5 ± 0.2 to 21.5 ± 1.6 μg 100 g −1 FW). Similar findings and trend were observed for cis-violaxanthin which ranged from 16.2 ± 2.5 to 23.2 ± 3.0 μg 100 g −1 FW in the peel, being detectable in the flesh from S4 stage onwards (12.3 ± 0.1 to 19.1 ± 1.5 μg 100 g −1 FW). 5′,6′-Epoxyβ-cryptoxanthin and cis-lutein were detected exclusively in the peel throughout all developmental stages (Fig. 3). Intriguingly, trans-lutein in the peel registered the highest contents during the initial developmental stages and went descending thereafter, meanwhile it was found in detectable amounts in the flesh only at stages 1 and 2, yet substantially lower compared to the peel. Citranaxanthin and phytoene have also been identified, although they were not quantified (Table 1).

Gene expression profiles
With the aim to shed light on the carotenoid biosynthetic pathway in loquat fruit, the expression profile of thirteen known genes of the carotenoid pathway was analyzed, showing differential expression patterns in the peel and the flesh tissue (Fig. 4, Additional file 1: Tables  S5-S6 and Figures S2-S3). For gene expression analyses, each tissue was examined individually, considering S1 stage as the calibrator of the tissue tested (peel or flesh).
Middle and downstream genes of the carotenoid biosynthetic pathway (CYCB, LCYE, BCH, ECH and VDE) showed clear differentiation in their expression levels among S2-S6 developmental stages compared with the remaining genes. In both peel and flesh, PSY1, ZDS,  Table S4 CYCB, and BCH were significantly up-regulated in most of the developmental stages compared with the S1 stage respectively, whereas CRTISO, LCYE, ECH and VDE were generally down-regulated. PDS was significantly up-regulated at the S6 stage in the peel, while it was significantly suppressed at the S3 stage in the flesh tissue. ZDS presented an increase in expression levels between the S3 and S5 stage in peel, though the increase was at the S4 and S6 stage in flesh tissue. Non statistically significant changes in expression levels of DXS, DXR (both involved in MEP pathway) and LCYB were monitored in the peel in comparison with the S1 stage; in flesh DXR followed the same trend whereas, DXS presented an accumulation at the S3 and LCYB transcript levels decreased gradually through stages S4-S6 which could account for the low or non-detectable trans-lutein findings in the flesh (Figs. 1, 3 and 4). ZEP expression levels presented highest suppression at the S6 stage in peel, contrarily to flesh profile where it was up-regulated at the S3-S5 stages.
BCH and CYCB transcript levels were substantially up-regulated with the progress of on-tree fruit development both in the peel and in the flesh, registering the highest values at the last stage for both tissues (Fig. 4, Additional file 1: Tables S5, S6). Notably in flesh tissue, a 8.1-and 11.0-fold increase of CYCB and BCH transcripts during the last stage compared to the initial stage was recorded, respectively. PSY1 presented statistically significant increases at the S3, S4 and S6 stages of the peel and throughout all stages in the flesh (S2-S6); the most prominent gene regulation in the flesh was found at the S3 and S5 stages (Additional file 1: Table S6).
Contrarily, CRTISO, LCYE, ECH and VDE demonstrated overall a down-regulation expression pattern in both peel and flesh tissue. CRTISO was down-regulated at stages S3-S5 in peel; a similar trend was monitored in the flesh (S3-S6 stages). ECH had similar expression pattern (suppression) for both peel and flesh from stage S3 onwards. LCYE was down-regulated in peel throughout the five developmental stages; the most abundant decrease (128 fold change) was registered at the S5 stage. Interestingly, in flesh the decrease was registered at the S2 stage and remained undetected thereafter. VDE expression levels were repressed throughout S3 to S6 stages in peel and throughout all developmental stages in flesh. In both peel and flesh, VDE presented a substantial suppression at the S5 stages (36.8 and 49.5 fold change, respectively) compared with S1 stage.
Notably, PSY1, known to catalyse the first step in the carotenoid formation [14], expression levels depicted a general up-regulation with the progress of on-tree fruit development both in the peel and in the flesh; however the highest transcript values in flesh tissue were monitored at S3 and S5 stages, not concomitant with total carotenoid accumulation. In another fleshy fruit (apple), Ampomah-Dwamena et al. [28] also postulated that PSY1 expression levels had no direct correlation with carotenoid content in different genotypes. On the other hand, PDS, an upstream pathway gene, presented statistically significantly higher transcript levels only in the peel at the last developmental stage (S6); PDS expression levels have been correlated with high-and low-carotenoid content apple cultivars [28].
Trans-lutein presented appreciably high accumulation in the first four stages in the peel with a reduction at ripe and over-ripe stages, while detectable amounts in the flesh were registered only during the initial developmental stages, as chloroplasts began to develop into chromoplasts. This decrease can be attributed to the fact that (1) LCYE was markedly down-regulated throughout the developmental stages in both peel and flesh compared to corresponding per tissue immature stage (notably not detectable transcripts during S3-S6 of flesh was monitored), (2) LCYB was down-regulated over the last developmental stages in flesh (S4-S6) and (3) ECH mRNA expression was generally down-regulated both in the peel and in the flesh (S3-S6). Fu et al. [10] noted that lutein is showing a transient decrease in the flesh of loquat cultivars with the progress of on-tree fruit . Relative mRNA abundance was evaluated by real-time RT-PCR using three biological repeats. Up-regulation is indicated in green; down-regulation is indicated in red. A diagonal line in a box indicates a statistically significant value (P ≤ 0.05). A scale of colour intensity is presented as a legend. The first developmental stage (S1) both for the peel and the flesh was used for calibrating gene exeression values. Actual relative expression levels are shown in Additional file 1: Tables S5-S6 and Figs. S2-S3 development, whereas there is no connection with BCH expression which appears to be up-regulated especially in the red-fleshed cultivar 'Luoyangqing'. An up-regulation of BCH gene expression was also monitored in our study in a similar flesh-type loquat cultivar. Ampomah-Dwamena et al. [28] showed a close correlation between LCYE expression and carotenoid content in apple fruit skin. This was not the case with the flesh; suggesting that down-regulation of LCYE is consistent with lower trans-lutein concentrations in the flesh.
Contrarily, the high BCH expression values registered in the flesh at the last two stages can be linked with the transient carotenoid accumulation of trans-β-cryptoxanthin in these stages, concomitant with higher mRNA expression of CYCB and non-detectable LCYE transcripts (Stages S3-S6). These findings are in accordance with Fu et al. [10], where the BCH values for the red-fleshed cultivar 'Luoyangqing' showed a transient increase at the breaker stage. In addition, CYCB expression levels were also higher after the S4 stage. Kato et al. [11] stated that the decrease of LCYE gene expression in Citrus fruits is related with higher contents of β-carotene as the ε, β-branch of the carotenoid pathway shifts to the β, βbranch during transition from immature to mature stage. Zhao et al. [16] found that BCH is responsible for high β-cryptoxanthin content in persimmon fruit, in accordance with findings in other loquat cultivars [29]. The latter study suggests a direct link between the synthesis and accumulation of β-cryptoxanthin and the abundant expression of BCH. The transient increase of trans-β-carotene towards the S6 peel stage can also be linked with the up-regulation of CYCB and down-regulation of LCYE, as elsewhere described [10]. Zhang et al. [29] also links the higher β-carotene level in loquat peel with the abundant increase of PSY1, as well as CYCB and BCH mRNA expression levels.
VDE expression which leads to violaxanthin biosynthesis is significantly suppressed in almost all stages, both in the flesh and in the peel compared with the calibrator (S1 stage) (thus expecting very little violaxanthin); in the case of ZEP, which converts violaxanthin back to precursor molecules such as zeaxanthin, the main trend is that it is induced in several stages in the flesh. This is in accordance with metabolite levels, as both cis-and trans-violaxanthin are at appreciable low concentrations and/or non-detectable during several stages in the flesh (Figs. 3, 4; Additional file 1: Table S4).