Introduction

The tea plant [Camellia sinensis (L.) O. Kuntze] is an economically important crop. Its leaves and leaf buds are used to produce tea, one of the most important and widely consumed non-alcoholic beverages worldwide. Data from the Food and Agriculture Organization of the United Nations (FAO) (http://faostat3.fao.org) website indicated that approximately 2 240 594 ha of land in China was used to cultivate tea plants in 2016. Compounds from green tea could help prevent obesity1, cardiovascular disease2,3, and Alzheimer’s disease4.

Ascorbic acid (AsA), known as vitamin C, is present in plants and several animal species5,6. AsA is an organic compound with antioxidant properties7. In higher vascular plants, AsA has a vital role in physiological regulation, and it could be involved in the response to ozone, pathogen attack, and senescence8,9. Given these functions, AsA is an important organic compound in tea plants10. Ivanov et al.11 demonstrated that AsA from green tea extracts could inhibit atherogenesis. In rats, AsA derived from green tea could help protect against the toxic effects of orally ingested arsenic and improve cellular antioxidative effects12,13.

Four AsA biosynthesis pathways were identified in plants. These pathways include the l-galactose (l-Gal), l-gulose, d-galacturonate, and myo-inositol pathways14,15,16,17. l-galactose is an important precursor in the l-Gal pathway18,19. l-gulose and l-gulono-1,4-lactone are the main intermediates in the l-gulose pathway17,20. d-galacturonic acid is a key intermediate in the d-galacturonate pathway14. The d-glucuronate-mediated catalysis of myo-inositol into myo-inositol oxygenase (MIOX) is the key reaction of the myo-inositol pathway15,21. The l-Gal pathway might be the most validated and well-known AsA biosynthetic pathway in many plants22. Although the l-Gal pathway has a vital role in AsA biosynthesis in tea plants, other alternative pathways also participate in AsA biosynthesis in tea plants23. The l-Gal pathway is the dominant route of AsA biosynthesis in peach24, Arabidopsis25, carrot26, and celery27.

Abiotic stresses, including adverse temperature conditions, affect the distribution and levels of AsA in higher plants28. High and low temperatures induce ascorbate peroxidase (APX) gene expression in tea plants29. Low temperatures induce ascorbate peroxidase 3 (APX3) gene expression in Arabidopsis30. Furthermore, the expression levels of the APX gene are regulated by various abiotic stresses like salinity, intense light, and hydrogen peroxide (H2O2)31,32,33. Transgenic tobacco carrying the APX gene exhibit enhanced low- or high-temperature stress tolerance34. The AsA content of red and green transgenic tomato fruits carrying the dehydroascorbate reductase (DHAR) gene was increased, but the AsA content of green transgenic tomato fruit carrying the monodehydroascorbate reductase (MDHAR) gene was decreased35. Under chilling temperatures, MDHAR activity in tomato fruit was significantly correlated with AsA content36. In contrast, monodehydroascorbate reductase 3 activity was negatively related to AsA content in tomato leaves37. Transgenic tobacco plants carrying the DHAR gene from Arabidopsis showed improved Al-stress tolerance38. In addition, Arabidopsis overexpressing the rice DHAR gene showed enhanced tolerance to salt stress39.

In recent years, with the development of the tea industry and the expansion of tea cultivation areas, traditional artificial tea manufacturers have been replaced by machines. Large numbers of tea leaves are needed to meet the ever-increasing demands of the tea industry. Consequently, the storage and transportation of tea leaves have become important concerns in tea production. Transferring fresh tea leaves from the tea farm to the factory for processing takes several hours. Tea leaves are always stored away from heat to maintain freshness and prevent mold growth. Tea leaves are usually stored and transported under low- (4 °C) and room-temperature (25 °C) conditions. However, the high water content (~70%) in fresh tea leaves sometimes causes the internal temperature of tea leaves to rapidly increase to 38 °C during storage and transportation at room temperature. AsA is one of the important secondary metabolites in tea leaves. Different temperatures during the process of storage and transportation can affect the quality of fresh tea leaves, the flavor of processed tea, and AsA metabolism. The effects of different temperature conditions on the molecular mechanisms underlying the secondary metabolite production of tea leaves during storage and transportation remain unclear. AsA metabolism in tea leaves during storage and transportation requires study.

“Longjing 43” is a typical tea plant cultivar widely cultivated for its high and stable production, and it is also used as a model for genetic and breeding research on tea plants40,41,42. This study was designed to investigate the effects of different temperatures on AsA metabolism in harvested tea leaves of “Longjing 43”. We performed an integrated transcriptome analysis and used isobaric tags for relative and absolute quantitation (iTRAQ) analysis to reveal the effects of high- (38 °C), low- (4 °C), and room-temperature (25 °C) treatments on the potential molecular mechanisms of AsA metabolism in Longjing 43 tea leaves. The differentially expressed proteins (DEPs) involved in AsA metabolism and the expression profiles of 18 genes related to AsA metabolism were identified. Furthermore, we discussed the morphological and anatomical characteristics and AsA distribution and level of tea leaves subjected to different temperature conditions. An understanding of the AsA levels and suitable storage and transportation conditions of tea leaves may provide guidance to the tea industry.

Materials and methods

Plant materials, growth conditions, and temperature treatments

One-year-old tea plant cuttings (C. sinensis cv. “Longjing 43”) were cultivated in an artificial climate chamber at Nanjing Agricultural University, Nanjing, China (32°02′ N, 118°50′ E). The soil type used for tea plant growth contained a mixture of peat, vermiculite, and perlite (3:2:1, v/v). Thirty clonally propagated tea plants were grown under an artificial climate chamber condition (25 °C for 16 h during daytime, 18 °C for 8 h during the dark, 150 μmol/m2/s light intensity, and 75% relative humidity). Tea leaves were collected as previously described41, laid flat, and wilted for approximately 4 h under different temperature treatments (4, 38, and 25 °C) on 27 September 2016. One bud and two leaves were collected from each sample. The sample for each treatment was picked from 10 tea plants, mixed, and divided into three biological replicates. Samples wilted for 4 h under 25 °C were used as the control. The tea leaves were used for RNA isolation and AsA content determination.

Dynamic changes in AsA levels

The oxalic acid method was performed as previously described for the determination of AsA levels in tea leaves23. Briefly, each fresh sample (200 mg) was homogenized in 4 mL of 1.0% (w/v) oxalic acid (24094A, Shanghai, Adamas, China) and centrifuged at 10 000 × g for 10 min at 4 °C. The reaction solution was used to assay AsA content using reversed-phase high-performance liquid chromatography (RP-HPLC). A Shimadzu LC-20A series (Shimadzu Co., Kyoto, Japan) with a Hedera ODS-2 C18 analytical column (250 mm × 4.6 mm i.d., 5 μm nominal particle size) was used for chromatographic separation analysis at 254 nm. Methyl alcohol (MS#1922-801, TEDIA, Susong, China) was used as mobile phase A, and 0.1% (w/v) oxalic acid was used as mobile phase B. The ratio of mobile phase A to B was 5%:95%. Finally, the AsA level was determined by injecting 20 μL of filtrate into the RP-HPLC system and recorded as mg/100 g fresh weight (FW).

Cytological–anatomical structure and AsA distribution analysis

Paraffin-embedded sections of tea leaves were analyzed using a previously described method with some modifications to investigate the cytological–anatomical structures and AsA distribution in tea leaves43. Briefly, leaves, including major veins, were cut into sections with dimensions of 2.5 mm × 2.5 mm. Subsequently, the excised leaf sections were fixed in FAA solution (ethanol:formalin:acetic acid, 90:5:5, v:v:v) (Servicebio, Wuhan, China). After 20 min of deparaffinization with xylene (20641F, Shanghai, Adamas, China) and 40 min of dehydration with ethanol (73537S, Shanghai, Adamas, China), the sections were stained for 1–2 h with 1% safranin O solution (59222C, Shanghai, Adamas, China) and washed with tap water. The sections were dehydrated with 50% ethanol solution (v/v) for 1 min, 70% ethanol solution (v/v) for 1 min, and 80% ethanol solution (v/v) for 1 min. Subsequently, the samples were stained with 0.5% fast green solution (39722B, Shanghai, Adamas, China) for 30–60 s. The sections were dried at 60 °C and washed for 5 min with xylene. Finally, the sections were sealed with neutral balsam for further analysis.

To observe the distribution of AsA in tea leaves, the acidic–alcoholic AgNO3 method was used in accordance with the procedure described by Chinoy44. In this method, samples were immersed in a mixture solution composed of distilled water:ethanol:acetic acid (29:66:10, v:v:v). Leaf samples were vacuumized for 1 h in 5% AgNO3 (N#A4769, Shanghai, Adamas, China) (silver nitrate:mixture solution, w/v) and stored for 24 h at 4 °C. Subsequently, excess residue was washed off for 20 min with 70% ethanol solution containing 5% ammonium acetate (72564A, Shanghai, Adamas, China). Finally, samples were analyzed as paraffin sections without safranin O/fast green staining.

Total RNA isolation and cDNA reverse transcription

Total RNA was extracted from three samples in accordance with the instructions included with the Quick RNA isolation Kit (Aidlab, Beijing, China). RNA extraction was performed with RNase-free DNaseI (TaKaRa, Dalian, China) to eliminate genomic DNA contamination. The extracted RNA concentration of each sample was calculated using a Nanodrop 2000 spectrophotometer (Thermo Scientific, Wilmington, DE, USA). The first-strand cDNA of each sample was synthesized in accordance with the instructions included with the PrimeScript RT reagent kit (TaKaRa, Dalian, China). The synthetized cDNA of each sample was diluted 18 times and used as template for quantitative real-time PCR (qRT-PCR) amplification. The experiments were repeated as three independent biological samples.

Protein extraction, labeling, liquid chromatography-tandem mass spectrometry analysis and data analysis

Lysis solution [9 M urea, 4% 3-[(3-cholamidopropyl) dimethylammonio]-1-propane sulfonate, 1% dithiothreitol, and 1% immobilized pH gradient buffer (GE Healthcare)] was used to extract protein from each sample. The mixture was centrifuged at 15 000 rpm for 15 min after 1 h of incubation at 30 °C. Dissolution buffer (AB Sciex, Foster City, CA, USA) was used to dissolve the total protein from each sample, and each sample was labeled using an iTRAQ Reagent-8 plex Multiplex Kit (AB Sciex). The labeled sample was separated by liquid chromatography (LC) with an Eksigent nanoLC-Ultra 2D system (AB SCIEX).

LC fractions were analyzed with a Triple TOF 5600 mass spectrometer (AB SCIEX) under the following conditions: ion spray voltage, 2.5 kV; nebulizer gas pressure, 5 PSI; curtain gas pressure, 30 PSI; and interface heater temperature, 150 °C. The information-dependent acquisition mode was applied for 35 product ion scans (2+ to 5+) above a threshold ion count of 150 in the mass spectrometry survey scan. The dynamic exclusion duration was 18 s. The data for iTRAQ protein were analyzed using Protein Pilot Software Version 4.0 against the database Uniprot_grape.

Database search for DEPs, qRT-PCR, and protein–protein interaction analysis

The DEPs involved in the AsA recycling pathway in tea leaves subjected to different temperature treatments were identified using iTRAQ-based quantitative proteomics41. The protein–protein interaction (PPI) prediction was performed using the search tool for the retrieval of interacting genes/proteins (STRING) (Version 10.0, http://string-db.org/)45. Additionally, the interaction networks of proteins and AsA were constructed using STITCH (search tool for interacting chemicals; http://stitch.embl.de/)46.

Gene expression analysis through qRT-PCR

The 18 AsA metabolism-related genes were identified by searching the known amino-acid sequences from carrot against tea plant genomic or transcriptomic database using Bioedit software26,47,48,49. The primers (Table 1) used in the qRT-PCR analysis were designed using Primer Premier 6.0 software. The CsTBP gene is a stable reference gene that has been used in the gene expression analysis of tea plants40. Here the CsTBP gene was used as the reference gene for normalizing the expression levels of AsA metabolism-related genes in different samples. A Bio-Rad iQ5 platform (Bio-Rad, Hercules, CA, USA) system was used for the qRT-PCR analysis, which was performed using SYBR Premix Ex Taq (Tli RNaseH Plus; TaKaRa, Dalian, China) in accordance with the manufacturer’s protocol. Each reaction volume of 15 μL contained 7.2 μL of deionized water, 5.5 μL of SYBR Premix Ex Taq (Tli RNaseH Plus; TaKaRa, Dalian, China), 1.5 μL of diluted cDNA strands, and 0.4 μL of each primer. The thermal cycling conditions of qRT-PCR were as follows: 95 °C for 30 s; 40 cycles at 95 °C for 5 s; and 55 °C for 25 s. The transcript abundance measurements of each reaction were repeated as three independent biological samples.

Table 1 qRT-PCR primer sequences of genes related to AsA biosynthetic and recycling pathways in tea leaves
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Statistical analysis

Experiments on water loss, AsA contents, and expression levels of AsA metabolism-related genes were performed with three independent samples. Data were analyzed using the Statistical Package for Social Sciences (SPSS) statistics version 17.0 (SPSS, Inc., Chicago, IL, USA). Differences in the expression levels of AsA metabolism-related genes, water levels, and AsA contents were detected using Duncan’s multiple-range test at a P < 0.05 probability level. Data are presented as the mean ± standard deviation.

Results

Morphological changes and weight loss exhibited by tea leaves subjected to different temperature treatments

The morphological changes and weight losses exhibited by tea leaves subjected to different temperature treatments were investigated. The remnant percentages of tea leaves were 90.01%, 84.67%, and 73.33% at 4, 25, and 38 °C, respectively (Fig. 1).

Fig. 1: Effects of temperature treatments on the water loss of tea leaves.
figure 1

Error bars represent the standard deviation among three independent replicates. Data are presented as the mean ± SD of three independent replicates. Different lowercase letters indicate significant differences at P < 0.05 based on three biological repetitions

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AsA levels of tea leaves

The AsA levels of tea leaves were measured using RP-HPLC. The standard curve for AsA concentration was constructed prior to sample measurement (Fig. S1). The AsA levels of tea leaves under different temperature treatments differed significantly (Fig. 2a). Figure 2b shows the HPLC profiles of AsA in tea leaves subjected to different temperature treatments. Among the three treatments, the highest AsA level (41.06 mg/100 g) was recorded after 4 °C treatment, and the lowest level (33.09 mg/100 g) was recorded after 38 °C treatment. The AsA level in tea leaves subjected to 25 °C treatment was 36.77 mg/100 g.

Fig. 2: AsA contents and AsA RP-HPLC profiles of tea leaves under different temperature treatments.
figure 2

a AsA contents of tea leaves under different temperature treatments. b AsA RP-HPLC profiles of tea leaves under different temperature treatments. Error bars represent the standard deviation among three independent replicates. Data for AsA content are presented as the mean ± SD of three independent replicates. Different lowercase letters indicate significant differences at P < 0.05 based on three biological repetitions

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Fig. 3: Distribution of AsA in tea leaves under different temperature treatments.
figure 3

a Control group. b Cool acidic–alcoholic AgNO3 treatment group. Epidermis (Ep), spongy tissue (St), phloem (P), and xylem (X) are marked in the figure. The scale bar represents a length of 50 μm

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AsA distribution in tea leaves

Cytological–anatomical structure analysis was performed to elucidate the effects of different temperature treatments on the AsA level and distribution in tea leaves. The bioactive AsA levels in tea leaves significantly changed under high- and low-temperature treatments (Fig. 3a, b). As inferred from the distribution of black spots throughout the leaves, the highest AsA levels were observed in leaves subjected to 4 °C treatment. The lowest AsA content was observed in leaves subjected to 38 °C treatment. AsA was mainly distributed in the spongy tissue of tea leaves that received 4 and 25 °C treatments, and it was rarely distributed in the xylem of tea leaves that received 38 °C treatment.

Identification of the DEPs in the AsA recycling pathway in tea leaves

The DEPs of tea leaves that received different temperature treatments were analyzed using iTRAQ (Fig. 4; Table 2). In this study, two AsA metabolism-related proteins were identified in leaves subjected to 4 °C treatment: CsAPX1 (Table S1) and CsDHAR2 (Table S2). The CsAPX1 protein was also identified in leaves treated with 38 °C (Table S3). These AsA metabolism-related proteins were differentially expressed in tea leaves under different temperature treatments. Under 4 °C treatment, the expression level of CsDHAR2 was lower than CsAPX1.

Fig. 4
figure 4

Expression profiles of DEPs in the AsA recycling pathway in tea leaves under different temperature treatments

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Table 2 DEP information for AsA metabolism-related proteins in tea leaves under high- and low-temperature treatments
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Gene expression profiles of AsA metabolism-related genes in tea leaves

The expression levels of genes involved in AsA biosynthetic and recycling pathways in tea leaves under different temperature treatments were detected to explore the effects of temperature on the expression profiles of the genes of interest (Fig. 5). Genes involved in the AsA biosynthetic and recycling pathways were identified by referring to the tea plant transcriptome database.

Fig. 5: qRT-PCR analysis of the expression levels of genes involved in AsA biosynthesis and recycling pathways in tea leaves under different temperature treatments.
figure 5

a Genes involved in the AsA biosynthetic pathway. b Genes involved in the AsA recycling pathway. Phosphomannose mutase (CsPMM), GDP-l-galactose phosphorylase (CsGGP), l-galactose dehydrogenase (CsGalDH), phosphoglucose isomerase 1 (CsPGI1), phosphoglucose isomerase 2 (CsPGI2), phosphomannose isomerase (CsPMI), l-galactono-1,4-lactone dehydrogenase (CsGalLDH), GDP-d-mannose pyrophosphorylase (CsGMP), GDP-d-mannose-3ʹ,5ʹ-epimerase (CsGME), l-galactose-1-P phosphatase (CsGPP), d-galacturonate reductase (CsGalUR), myo-inositol oxygenase (CsMIOX), glutathione reductase (CsGR), dehydroascorbate reductase 1 (CsDHAR1), dehydroascorbate reductase 2 (CsDHAR2), ascorbate peroxidase (CsAPX), ascorbate oxidase (CsAO), and monodehydroascorbate reductase (CsMDHAR). Error bars represent the standard deviation among the three independent replicates. Data are presented as the mean ± SD of three independent replicates. Different lowercase letters indicate significant differences at P < 0.05 based on three biological replicates

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The expression levels of five genes (CsGalDH, CsPGI1, CsPGI2, CsGMP, and CsGME) involved in the AsA biosynthetic pathway were upregulated under low-temperature (4 °C) treatment relative to room-temperature (25 °C) treatment. The expression levels of 10 genes (CsPMM, CsGGP, CsGalDH, CsPGI1, CsPGI2, CsGalLDH, CsGMP, CsGME, CsGalUR, and CsMIOX) were downregulated under high-temperature (38 °C) treatment compared to room-temperature treatment. In addition, the expression levels of CsGPP and CsPMI were significantly upregulated under high-temperature treatment compared to under room-temperature treatment. Among the genes involved in the AsA recycling pathway, the expression levels of four genes (CsDHAR1, CsAPX, CsAO, and CsMDHAR) were downregulated under high-temperature treatment, and two genes (CsDHAR2 and CsAO) were upregulated under low-temperature treatment compared to room-temperature treatment. CsAPX and CsMIOX expression levels were suppressed under high- or low-temperature treatments.

PPI analysis

STRING was used to construct the PPI networks of AsA metabolism DEPs in both C. sinensis (NCBI Taxonomy ID: 542762) under different temperature treatments and Arabidopsis (NCBI Taxonomy ID: 3702). Sequence similarity analysis indicated that AsA metabolism-related proteins in tea plants corresponded to those in Arabidopsis thaliana (Table S4). STRING was applied to construct a PPI network between the AsA metabolism-related proteins of tea plants and those of Arabidopsis (Fig. 6). The results indicated that CsAPX interacts with CsDHAR1 and CsDHAR2. CsDHAR1 and TPI are coexpressed. TPI is a protein involved in gluconeogenesis. In addition, CsDHAR2 and GR are coexpressed. Subsequently, STITCH was used to analyze the known and predicted interaction networks of chemicals, proteins, and AsA (Fig. 7). AsA interacts with some chemical compounds, including erythorbic acid, diphosphopyridine nucleotide, sodium ascorbate, ascorbate radical, dehydroascorbic acid, and hydrogen peroxide.

Fig. 6: PPI of proteins in the AsA metabolic pathway.
figure 6

a Proteins involved in the AsA biosynthetic pathway. b Proteins involved in the AsA recycling pathway. Associations among proteins shared by tea plants and Arabidopsis jointly contribute to a common function

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Fig. 7: Interaction network of chemicals, proteins, and AsA in Arabidopsis.
figure 7

The image presents a comprehensive view. Thick lines represent strong associations. Protein–protein interactions are shown in gray. Chemical–protein interactions are shown in green. Chemical–chemical interactions are shown in red

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Discussion

Effects of temperature on the morphology and weight loss of tea leaves

High or low temperatures have various effects on plant morphology. For example, low temperature helps prevent the postharvest weight loss of fruits during storage50. By contrast, high temperature accelerates the postharvest weight loss of sugarcane cultivars during storage51. In this study, we found that different temperature treatments resulted in the postharvest weight loss of tea leaves. Postharvest weight loss often accompanies postharvest physiological deterioration in sweet cherry52. Temperature elevations during storage might promote the physiological deterioration of broccoli buds53. High temperature could cause cellular dehydration in plants54. The cell membrane mediates the selective transport of ions and organic molecules from the external environment55 and receives temperature stress signals56. It also maintains the shape of the cell by anchoring the cytoskeleton. Cell membrane damage causes cellular dehydration, which might affect weight loss in tea leaves at high temperatures.

Effects of temperature on AsA level and distribution in tea leaves

External factors like sunlight, temperature, relative humidity, oxidative stress, and pollution influence AsA distribution and levels in plants57,58. In this study, the effects of different temperature conditions on the AsA level and distribution in tea leaves were detected and analyzed. AsA levels in tea leaves under low-temperature treatment are higher than those in tea leaves under room- or high-temperature treatment. AsA levels in sea buckthorn leaves and stems decreased with increasing temperature59. Temperature stress could affect the contents of antioxidant and lipid peroxidation enzymes60. Because AsA is an antioxidant, its levels could also be influenced by temperature stress9. Cold stress increases the AsA content of pepper (Capsicum annuum L.)61. A similar finding was observed for Cistus clusii under field conditions and a Mediterranean climate62.

Considerable evidence from different studies suggested that the AsA distribution differs across plant species. For example, AsA is mainly distributed in the mesocarp, septum, and loculi of ripening tomato fruits63 and in the vascular tissues and peel of apple fruits64. In plants, AsA is negligibly distributed in vacuoles and is mainly located in the cytoplasm65,66. However, in this study, we found that AsA mainly localizes in the mesophyll cells in tea leaves.

Effects of temperature on the expression levels of AsA metabolism-related genes in tea leaves

Gene expression in most plants is affected by abiotic stress, including high or low temperature stress67,68. In most plants, the gene expression levels involved in AsA metabolism are related to abiotic stress69,70. Although AsA metabolism-related genes were detected and identified in tea plants on the basis of transcriptome data and the expression of AsA metabolism-related genes in response to temperature stress was analyzed23,29, the expression patterns of AsA metabolism-related genes in tea leaves under different temperature stresses remain unclear.

In apple leaves, the expression levels of APX, DHAR, and GR decreased after 4 h of continuous high-temperature treatment71. In this study, we found that the expression levels of the CsAPX and CsDHAR1 genes decreased and CsGR increased under treatment with 38 °C. Exposing tomatoes after harvest to temperatures from 12 to 3 °C for 56 h inhibits GME1 expression28. Similarly, we found that exposing tea leaves to temperatures of 25 to 38 °C for 4 h decreased CsGME expression. In A. Actinidia eriantha. GGP expression was inhibited after heat treatment (42 °C) relative to normal conditions (25 °C)72. Here CsGGP expression was reduced after treatment at 38 °C compared to treatment at 25 °C.

In harvested tomato, GPP is the only AsA biosynthetic gene that was affected by 4 °C treatment. Its expression level peaked after 3 h of treatment and decreased to virtually undetectable levels after 1 h of treatment at 40 °C. High temperature induced CsGPP expression in the tea plant, and CsGPP transcript abundance was negatively correlated with AsA levels in tea leaves. GPP expression was closely associated with AsA levels during tomato ripening73. GPP is an enzyme that converts l-galactose-1-P to l-ascorbate. Shade significantly induced GPP1 expression in ripe red tomato fruits. GPP1 expression was correlated with AsA levels in tomato leaves and fruits74. These findings implied that CsGPP has important associations with AsA levels in tea leaves.

AO is a crucial enzyme in AsA accumulation. Previous studies hinted that the levels of AO expression and of AsA are linked. For example, suppressing AO expression increased AsA levels in harvested tomato fruits after drought treatment75. In this study, we found that CsAO expression is positively correlated with AsA levels in tea leaves. Transgenic Arabidopsis plants carrying the CuZnSOD and APX genes showed improved abiotic stress tolerance76. In tea leaves, CsAPX expression was higher at 25 °C than at 4 °C. APX mRNA abundance in harvested potato tubers was higher at 20 °C than at 5 °C77.

DEPs of proteins related to AsA metabolism-related proteins in tea leaves

iTRAQ technology enhanced the precision and reliability of the quantitative analysis of human, animal, and plant proteins78,79,80. The proteomics approach enabled the functional analysis of proteins related to AsA metabolism in plants81,82. iTRAQ-based quantitative proteomics analysis showed that drought treatment decreased the expression levels of APX and AO proteins in the leaves of cultivated tobacco83. iTRAQ analysis indicated that APX activity decreased from 0 to 12 h but increased from 12 to 96 h during postharvest physiological deterioration84. In addition, metabolic proteome analysis showed that the protein abundance of APX1 decreased in the embryo-surrounding tissues of wheat in response to high salt stress85. The protein abundance of SlGalLDH in the young leaves and harvested fruit of four transgenic tomato lines was lower than in the young leaves and harvested fruit of control plants86. Protein gel blot analysis illustrated that the positive protein signals of LetAPX in four transgenic tomato lines were stronger than in wild-type lines87. Proteomic analysis has revealed that APX1 plays a major role in response to drought and heat stress in Arabidopsis88. The VTC2 protein appears to exhibit a dual function in green tomato tissues73. The VTC2 protein shares high similarity with the CsGGP protein. These findings suggest that the function of CsGGP protein might be like the VTC2 protein. iTRAQ-based analysis identified that APX3 and DHAR proteins were expressed during the early or late postharvest physiological deterioration of M. esculenta at 27 °C84.

In this study, iTRAQ-based analysis indicated that CsAPX1 and CsDHAR2 proteins were expressed in tea leaves after 4 h of 4 °C treatment and that the CsAPX1 protein was expressed in tea leaves after 4 h of treatment at 38 °C. Treatment at 38 and 4 °C upregulated CsAPX1 and CsDHAR2 protein expression. Our findings implied that CsAPX1 and CsDHAR2 proteins were involved in AsA recycling pathways in tea leaves. Previous studies also showed that the DHAR1 protein localizes to plant peroxisomes and chloroplasts89,90. The APX protein localizes to the cytosol, chloroplast, and peroxisomes91. AsA content and distribution are closely associated with chloroplasts92,93. In the AsA-GSH cycle of chloroplasts, APX can scavenge H2O2, DHAR, and MDHAR, and it can catalyze the regeneration of AsA94,95. Consequently, these results indicated that CsAPX1 and CsDHAR2 proteins could be involved in the AsA recycling pathway in tea leaves subjected to different temperature treatments.

Conclusions

Numerous studies on the regulatory mechanisms underlying the postharvest quality of various crops were conducted. This study investigated the effects of different temperature treatments on AsA metabolism in tea leaves (Fig. 8). AsA content and distribution in tea leaves subjected to different temperature treatments were investigated. qRT-PCR and iTRAQ were utilized to analyze the expression patterns of proteins and genes related to the AsA metabolic pathway. The results indicated that AsA is mainly distributed in mesophyll cells in tea leaves. High or low temperatures modulate the expression levels of the CsAPX and CsDHAR2 genes. iTRAQ revealed that high and low temperatures upregulated CsAPX1 and CsDHAR2 protein expression. Therefore, CsAPX1 and CsDHAR2 proteins might play important roles in AsA recycling in tea leaves. The data provided by this study will help provide additional insight on the investigation of AsA levels in tea leaves and provide a foundation for strategies to enhance tea product quality and flavor.

Fig. 8
figure 8

Flow chart of the effects of different temperature treatments on AsA in tea leaves

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