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The manipulation of gene expression and the biosynthesis of Vitamin C, E and folate in light-and dark-germination of sweet corn seeds

Abstract

This study investigates the potential interrelationship between gene expression and biosynthesis of vitamin C, E and folate in sweet corn sprouts. Germination of sweet corn kernels was conducted in light and dark environments to determine if this relationship was regulated by photo-illumination. Results indicated that light and dark environments affected the DHAR, TMT and GTPCH expression and that these genes were the predominant genes of vitamin C, E and folate biosynthesis pathways respectively during the germination. Levels of vitamin C and folate increased during the germination of sweet corn seeds while vitamin E had a declining manner. Sweet corn sprouts had higher vitamin C and E levels as well as relevant gene expression levels in light environment while illumination had little influence on the folate contents and the gene expression levels during the germination. These results indicate that there might be a collaborative relationship between vitamin C and folate regulation during sweet corn seed germination, while an inhibitive regulation might exist between vitamin C and E.

Introduction

Vitamins are essential nutrients for all living creatures, they play a critical role in diverse metabolisms of living organisms. Lack of certain vitamins has been shown to induce a number of diseases, therefore governments use bio fortification of nutrients (mainly vitamins in plants) as a mechanism to improve the nutritional value of foods1. Over the past decade, the processes of synthesis of vitamins in plants have been investigated extensively from a plant molecular biology view point, and it is possible to increase the levels of vitamins in specific plants via gene technology2. As more and more pathways are understood, a more complex metabolism network has been shown to exist which indicates that these pathways may have interdependent regulations on each other3.

The biosynthetic pathways of vitamin C, E and folate (vitamin B9) in plants has been reviewed by a number of researchers4,5,6, their potential interdependent regulation is shown in Fig. 1. Vitamin C is a common compound existing in most living organisms and plays an important role in scavenging free radicals in living cells. The L-galactose pathway is the major pathway of vitamin C (L-ascorbic acid) biosynthesis in plants. This process begins with the phosphorylation of D-Glucose by hexokinase and ends with the epimerization of L-Galactono-1,4-lactone to L-Ascorbic acid by L-galactono-1,4-lactone dehydrogenase. Vitamin E consists of eight similar compounds: α-tocopherol, α-tocotrienol, β-tocopherol, β-tocotrienol, γ-tocopherol, γ-tocotrienol, δ-tocopherol and δ-tocotrienol. All of these compounds are lipid-soluble chemicals and are regarded as antioxidants. As Fig. 1 indicates, vitamin C and E work together in the cycle of ascorbic acid-glutathione-tocopherol, playing a role in eliminating free radicals on cell membrane7. The biosynthetic pathway of Vitamin E includes tocotrienol and tocopherol pathways. They both begin with L-tyrosine from shikimate pathway and end with series of methylation and cyclization. Folate, also called vitamin B9, is involved in DNA synthesis and thus it is critical for body development. Overall, the biosynthesis pathway of folate in plants is the assembly of a pterin, a p-aminobenzoate and polyglutamate tails in mitochondria6. Formation of p-aminobenzoate starts with chorismate which is one of the products of shikimate pathway, and ends in two steps in plastids8. Pterin synthesis firstly involves in the conversion of guanosine triphosphate to dihydroneopterin triphosphate via guanosine triphosphate cyclohydrolase I 9.

Figure 1
figure1

Pathways investigated in this study. (I) Vitamin E biosynthesis pathway. (II) Folate biosynthesis pathway. (III) Vitamin C biosynthesis pathway. (IV) Ascorbic acid-Glutathione-Tocopherol cycle. Letters indicates the catalyzing enzymes in the individual reactions and red letters refers to those enzymes studied in this paper: A, tyrosine aminotransferase; B, HPPD, 4-hydoxyphenyl-pruvate dioxygenase; C, DXPR, 1-deoxy-D-xylulose-5-phosphate reductase; D, HGGT, homogentisate geranylgeranyl transferase; E, I, MPBQ-MT, 2-methyl-6-phytyl-1,4-benzoquinol methyltransferase; F, TC, tocopherol/tocotrienol cyclase; G, TMT, tocopherol/tocotrienol methyltransferase; H, HPT, homogentisic acid phytyltransferase; J, GLDH, L-galactono-1,4-lactone dehydrogenase; K, APX, ascorbate peroxidase; L, MDHAR, monodehydroascorbate reductase; M, DHAR, dehydroascorbate reductase; N, GR, glutathione reductase; O, GTPCH, GTP cyclohydrolase; P, DHN aldolase; Q, HPPK, 6-hydroxymethyldihydropterin pyrophosphokinase; R, DHPS, dihydropteroate synthase; S, DHFS, dihydrofolate synthase; T, DHFR, dihydrofolate reductase; U, FPGS, folylpolyglutamate synthase; V, ADCS, aminodeoxychorismate synthase; W, aminodeoxychorismate lyase; X, GMP, GDP-mannose pyrophosphorylase; Y, GME, GDP-mannose-3,5-epimerase; Z, VTC2, GDP-L-galactose phosphorylase. Abbreviations: HPP, 4-hydoxyphenyl-pyruvate; HGA, homogentisic acid; GGDP, geranylgeranyl diphosphate; DDXP, 1-deoxy-D-xylulose-5-p; GGMB, 6-geranylgeranyl-2-methylbenzene-1,4-diol; GGDMB, geranylgeranyl-2,3-dimethylbenzene-1,4-diol; PDP, phytyldiphosphate; MPQ, 1-methyl-6-phytyl-1,4-benzoquinol; DMPQ, 2,3-dimenthyl-5-phytyl-1,4-benzoquinol; MDHA, monodehydroascorbate; DHA, dehydroascorbate; GSH, glutathione; GSSG, oxidized glutathione; NADP, nicotinamide adenine dinucleotide phosphate; NADPH, nicotinamide adenine dinucleotide phosphate; GTP, guanosine triphosphate; DHN-P, dihydroneopterin phosphate; DHN, dihydroneopterin; HMDHP, 6-hydroxymethyldihydropterin; HMDHP-P2, 6-hydroxymethyldihydropterin diphosphate; DHP, dihydropteroate; DHF, dihydrofolate; THF, tetrahydrofolate; ADC, aminodeoxychorismate; pABA, p-aminobenzoate.

Sweet corn (Zea mays L.) produces kernels which are high in sugar content and also contain a range of bioactive ingredients. It is often consumed as a fresh or canned vegetable and is widely consumed globally10. Researchers have investigated the potential of germinating kernels, and using these as sprouts, to enhance the nutritional value of the material as well as providing a novel food product for consumers11. However, few reports evaluate the effect of germination on the nutritional quality of sweet corn, and the role of gene expression in manipulating germination and the production of nutrients. Hashim and Fields12 found that germinated kernels contain higher levels of riboflavin and niacin compared to the non-germinated kernels. Lay and Fields13 also stated that germinated kernels had significantly higher contents of ascorbic acid. Obizoba14 studied how the nutritional profile of normal yellow corn varied during germination and concluded that 24 or 36 hours of sprouting produced optimal levels of bioactive nutrients. Despite these research reports, there remains a paucity of information regarding the gene expression occurring during germination and how this is associated with changes of vitamins in different stages of sweet corn seedling. In addition, the presence or absence of light is considered as an important factor during seed sprouting. Researchers have reported that light germinated corn had higher phenolic contents as well as antioxidant activity compared to germination conducted in the dark15.

This study focuses on the change of vitamin C, E and folate as well as the relative expression of associated key genes in four major stages of sweet corn sprouting. Stage 1 representing initial radical emergence (typically after 48 hours), stage 2 representing chitting of the corn (typically after 72 hours), stage 3 representing emergence of the shoot and development of the root (typically after 96 hours), stage 4 representing shoot and root elongation (typically after 130 hours). Evaluations were conducted on samples sprouted in both light and dark environments. The intentions of this study were to: study the change of three selected kinds of vitamins during different periods of sweet corn spout; explore the molecular mechanism which were related to these changes; determine the effect of light and dark processing on nutrient composition in different stages of sweet corn sprouting; provide an insight of the complex biosynthetic pathways of selected vitamins.

Results and Discussion

Moisture contents in sweet corn sprouts during light and dark germination

Moisture contents of germinating grains were determined according to the stages of sprout growth - For clarity, Fig. 2 illustrates the different stages of sprouting. The moisture contents of sweet corn sprouts in the four subsequent stages with light treatment were 53.51 ± 0.01%, 63.32 ± 0.02%, 63.80 ± 0.01% and 74.33 ± 0.01% respectively and those with dark treatment were 50.42 ± 0.02%, 58.41 ± 0.01%, 65.64 ± 0.02% and 70.27 ± 0.01% (n = 3). Moisture is required for seed germination16 and was used as a calibration factor in this study.

Figure 2
figure2

Sweet corn sprouts at different germination stages. Stage 1 representing initial radical emergence (typically after 48 hours); stage 2 representing chitting of the corn (typically after 72 hours); stage 3 representing emergence of the shoot and development of the root (typically after 96 hours); stage 4 representing shoot and root elongation with the appearance of euphylla (typically after 130 hours).

Vitamin C and relevant key gene expression in sweet corn sprouts during light and dark germination

Figure 3 demonstrates the changes of vitamin C. Overall, the contents of vitamin C increased during germination in both light and dark treatments. Three key genes (VTC2, GLDH, DHAR) affect the biosynthetic pathway of vitamin C4, 17, 18, the expression levels of these genes were studied and the results presented in Fig. 4. Compared to stage 1, the expression of DHAR gene in stage 4 of sprouting increased significantly (P < 0.05) from 186.9 ± 41.4 to 639.1 ± 81.8 and 162.3 ± 23.2 to 237.3 ± 70.4 under light and dark treatment respectively. The expressions of VTC2 and GLDH were observed to be different. For instance, in the light group, the level of VTC2 and GLDH mRNA had no significant difference during the sweet corn seed sprouting. However, the amounts of VTC2 and GLDH mRNA declined significantly (p < 0.05) in the dark treatment from 44.34 ± 5.40 to 16.06 ± 3.28 and 2.09 ± 0.23 to 1.01 ± 0.05 respectively. The data shows that DHAR gene was much more actively expressed than VTC2 and GLDH genes during sprouting.

Figure 3
figure3

Changes of vitamin C during sweet corn seed germination; Bars with different letter indicates significant difference (p < 0.05) exists within groups.

Figure 4
figure4

Changes of relative expression level of relevant genes in Vitamin C biosynthetic pathway during sweet corn seed germination; Bars with * and ** indicates significant difference at p < 0.05 and p < 0.01 respectively compared to stage 1. (a) Light treatment; (b) dark treatment.

Vitamin C works as an electron donor in animals and plants and is essential for repairing ROS (reactive oxygen species) damages in living cells19. Hence, vitamin C has become a standard to determine the nutritional quality of food. Our results illustrate that vitamin C levels increased during sprouting, specifically between the last two stages. Researchers have demonstrated previously that vitamin C was needed to scavenge the monolingual radicals during lignin biosynthesis in plant cells20. Therefore, as rapid growth of sweet corn sprouts occurred during the final two stages of sprouting, the rapid increase of vitamin C which was observed was reasonable. Similar phenomena have been recorded in soybean21 and mung bean22, 23 germination. For instance, Huang et al.23 reported that no vitamin C was found in non-germinated soybean and mung bean, whilst vitamin C increased during germination.

Previous research has indicated that vitamin C is generated by two ways: de novo synthesis from D-glucose, and the vitamin C recycling pathway called ascorbate-glutathione (AsA-GSH) cycle24. Three genes were selected in this study, two of which (VTC2, GLDH) were from L-galactose pathway and the other one (DHAR) was from the AsA-GSH cycle. It has been confirmed that L-galactose pathway is the main pathway to synthesize vitamin C in Arabidopsis25. VTC2 and GLDH are involved in the transformation of GDP-L-galactose to L-galactose-1-phosphate and L-galactono-1,4-lactoneto L-ascorbic acid respectively (Fig. 1). The AsA-GSH cycle contributes to scavenging free radicals and regulating the vitamin C level in plants. Our results indicated that the AsA pool was extremely active during the sprouting of sweet corn seeds and the AsA-GSH cycle was the predominant way to regulate the vitamin C amount in sweet corn sprouts as the vitamin C contents in different germinal stages changed in relation to variations in the expression level of DHAR (Figs 3 and 4). DHAR is a critical enzyme for maintaining sufficient amounts of vitamin C in plant tissues18. Numerous studies have stated that plants with higher DHAR levels performed higher tolerance to extreme conditions18, 26. Wang et al.27 reported that the expression level of DHAR was the highest among the detected genes during soya bean germination. Sytykiewicz17 highlighted that DHAR accumulated during maize germination. Therefore, it can be hypothesized that the accumulation of vitamin C during sweet corn seedling was mainly attributed to the expression of DHAR.

The influence of light and dark treatment on vitamin C and relevant gene expression in sweet corn sprout was also studied. Previously Davey et al.28 reviewed the relationship between light, hexose and germination in detail. Significant differences existed in vitamin C contents as well as the gene expression. Figure 3 indicates that sweet corn seeds sprouted in the dark environment tended to have lower vitamin C level than in light environment. An increase of expression level of VTC2 and GLDH during sweet corn germination occurred in the light environment while a significant (p < 0.05) decrease was observed in the dark environment (Fig. 4). D-glucose is the original material to vitamin C de novo synthesis, photosynthesis provides sufficient ingredients for the L-galactose pathway, causing higher level of expression of VTC2 and GLDH and thus higher level of vitamin C. Gallie18 claimed that high light levels increased the production of ROS in plants. This observation might explain the higher expression level of DHAR in light germination, something that also agrees with previous research on the importance of DHAR to plant cells under different stress17, 18, 20, 24, 26, 28, 29.

Vitamin E and relevant key gene expression in sweet corn sprouts during light and dark germination

Levels of α-tocopherol, α-tocotrienol, β-tocopherol, γ-tocopherol, γ-tocotrienol, δ-tocopherol, δ-tocotrienol as well as total vitamin E are presented in Table 1. Total vitamin E levels dropped significantly in the light samples from 9.08 ± 0.01 to 6.72 ± 0.38, 4.36 ± 0.03 and 4.31 ± 0.08 mg/100 g DW during the progressive stages of sprouting. A similar decrease was also observed in the dark environment. In light and dark groups, there was no significant difference of β-tocopherol content throughout sprouting, while the other six detected compounds declined during the germination stages with the highest levels in the initial stage of sprouting. γ-tocotrienol was the most abundant vitamin E compound in sweet corn seed sprouts, followed by α-tocopherol, γ-tocopherol, α-tocotrienol, δ-tocotrienol, δ-tocopherol and β-tocopherol. The amounts of δ-tocopherol, α-tocopherol and γ-tocopherol accounted for more than 80% of the total vitamin E in sweet corn sprouts. The contribution rate of δ-tocotrienol decreased during stage 1 and 2 of sprouting from 23% to 21% and 20% to 16% in light and dark treatment respectively, but increased between stage 3 and 4 from 18% to 26% and 16% to 20% in light and dark treatment respectively. The situation of γ-tocotrienol was opposite to that of δ-tocotrienol with its contribution rate increasing in the first three stages but decreasing in the final stage in both the light and dark groups.

Table 1 Change of Vitamin E profiles in sweet corn during germination.

To better understand the molecular mechanism behind these changes, five key-coding genes (HPT, TC, TMT, DXPR and HPPD) from the vitamin E biosynthetic pathway30,31,32 were selected for further investigation and their expression levels in sweet corn sprouts were evaluated (Fig. 5). TMT was the dominant gene among the five detected genes with the highest expression level. In light environment, the expression level of TMT was constant until stage 3 of sprouting and after that, it underwent a significant (p < 0.05) decrease from 1966 ± 127 to 1418 ± 118 between the last stages. The expression level of TMT in dark environment declined from 485.9 ± 56.2 to 346.4 ± 21.6 folds during stage 1 and 2, and then increased to 442.1 ± 66.9 folds at stage 3. DXPR was the second predominant gene in this study whose expression levels performed a typical U-curve during the sprouting stages in both light and dark groups. The expression level of HPT increased significantly (p < 0.05) during the light sprouting while showed little change during dark germination. TC and HPPD presented the lowest expression level in sweet corn sprouts. Overall, all the five selected genes tended to have higher expression levels in light seedling of sweet corn than the dark.

Figure 5
figure5

Changes of relative expression level of relevant genes in Vitamin E biosynthetic pathway during sweet corn seed germination; Bars with * and ** indicates significant difference at p < 0.05 and p < 0.01 respectively compared to stage 1. (a) Light treatment; (b) dark treatment.

Vitamin E, including tocopherols and tocotrienols, are lipo-antioxidants in living organisms protecting cells against various oxidative stresses30. Sattler et al.32 reported that vitamin E was accumulated in seeds and critical for seed germination. However, few researchers have studied the vitamin E production during sweet corn sprouting. To our knowledge, most studies illustrate an increasing pattern of vitamin E contents during seed germination, including soya bean27, maize33 and sesame34. However, Kim et al.35 reported that decreased vitamin E level were observed in germinated rice. Bellani et al.36 showed different changing manners of tocopherols in different parts of radish seeds during germination with vitamin E contents in aged radish seeds decreased during a 24-hour-germination.

Our study showed a decreasing pattern of vitamin E in sweet corn sprouts. This phenomenon indicated that the consumption rate of vitamin E exceeded the production rate in sweet corn sprouts during germination causing rapidly decline of vitamin E levels. The reasons for this are currently unknown. We observed a significant (p < 0.05) increase of α-tocopherol in light conditions during the 2nd and 3rd stage of sprouting. This could be explained by the presence of green areas on the sprouts at these stages (tocopherols are synthesized by photosynthetic organisms)32. On the other hand, our study indicated that γ-tocotrienol was the main vitamin E in sweet corn sprouts. Researchers have confirmed that tocotrienols are the major isomers of vitamin E in different kinds of seeds, such as rice and wheat30, 31. The degree of seed dormancy might be another factor that influences the vitamin E composition in seeds. Numerous reports have documented the importance of vitamin E to seed quiescence and longevity32 as well as germination37. As a result, tocotrienols might play an important role in maintaining seed vigor during dormancy38.

Homogentisic acid (HGA) is the core compound in biosynthetic pathway of vitamin E. It can be involved in the biosynthesis of tocopherols as well as tocotrienols by reacting with phytyldiphosphate (PDP) and geranylgeranyl diphosphate (GGDP) respectively39. Many researchers have studied 4-hydoxyphenyl-pruvate dioxygenase (HPPD) expression and illustrated an over-expression of HPPD may induce increases in vitamin E in barley, tobacco seeds and potato tubers40. Naqvi et al.41 found that synchronous expression of HPPD and 2-methyl-6-phytyl-1,4-benzoquinol methyltransferase (MPBQ-MT) tripled the tocopherol level in corn kernels. MPBQ-MT is involved in downstream regulation of tocopherol biosynthesis.

We selected HPT as our focus as it is involved in the formation of tocopherol/tocotrienol cyclase (TC) and tocopherol/tocotrienol methyltransferase (TMT) are both needed in tocopherol and tocotrienol pathway triggering cyclization and methylation in downstream regulation respectively. Wang et al.27 reported the expression levels of HPPD, MPBQ-MT, TC and TMT exhibited irregular changes during germination but reached peak levels at 3 days after germination of soya beans, with MPBQ-MT being the predominant gene. However, the expression levels of genes in our study declined during germination. In addition, the results indicated that methylation was extremely active in sweet corn sprouts, because the expression level of TMT was much higher than other genes. Thus, we speculate that high levels of γ-tocopherol, γ-tocotrienol, δ-tocopherol or δ-tocotrienol was accumulated in sweet corn seed because these four isomers are methylated by TMT transforming to α-tocopherol, α-tocotrienol, β-tocopherol or β-tocotrienol respectively at the end of the vitamin E biosynthetic pathway. The speculation was based on the observations regarding the amounts of γ-tocotrienol being larger than any isomers in sweet corn sprouts. Although vitamin E and C are both antioxidants in living plant cells, they seemed to exhibit different metabolic mechanisms during sweet corn germination. Vitamin C could be mass synthesized during germination of sweet corn while vitamin E would be largely consumed which might be vast accumulated during sweet corn kernel maturation.

Exposure to a dark environment seemed to inhibit the expression level of the coding genes leading to smaller amounts of vitamin E in sweet corn sprouts. Several research have investigated the influence of light on vitamin E in plants42, 43 and shown that light could enhance the level of vitamin E as well gene expression possibly as a defense mechanism44. Therefore, the concentration of vitamin E as well as its relevant gene expression in sweet corn sprouts are light related.

Folate and relevant key gene expression in sweet corn sprouts during light and dark germination

The effect of light and dark treatment on folate contents during sweet corn sprouting is presented in Fig. 6. In our studies, we characterized the folate content as free folate (the folate readily extracted without any enzymatic or thermal treatment) and bound folate (representing the difference between the folate recorded from extraction following thermal and enzymatic extraction – total folate content- and that which was readily extracted – free folate content). The free folate in light group increased during the first two stages of sprouting and then declined during the following stages of sprouting. The free folate in the dark group decreased until last stage of sprouting before increasing.

Figure 6
figure6

Changes of Folates during sweet corn seed germination; Bars with different letter indicates significant difference (p < 0.05) exists within groups. (a) Light treatment; (b) dark treatment. Free means readily extracted folate, which is obtained by free-enzyme extraction after autoclaving.

The relative expression levels of six key-encoding genes of folate biosynthesis pathway6, 45 at different stages of sprouting with light and dark treatments are shown in Fig. 7. In the light group, GTP cyclohydrolase (GTPCH) was the most active gene among the six selected genes, but no significant change of expression level was observed during sprouting. 6-hydroxymethyldihydropterin pyrophosphokinase (HPPK) was the second most abundant gene with expression levels increasing significantly (p < 0.05) during the first two stages of sprouting and then remaining unchanged from stage 2 to 4. The relative expression level of folylpolyglutamate synthase (FPGS) had no significant change until stage 3 after which it increased significantly (p < 0.05). Dihydrofolate synthase (DHFS) was inactive during the germination with no significant change of its relative expression levels. The relative expression level of aminodeoxychorismate synthase (ADCS) and dihydrofolate reductase (DHFR) increased significantly (p < 0.05) during sprouting. In the dark environment, GTPCH was also the most active gene among the six selected genes but its relative expression level decreased dramatically (p < 0.05) from stage onwards. Unlike the light group, DHFS was the second predominant gene and its relative expression level exhibited no significant change until the third stage of sprouting while it increased to the later stages. HPPK possessed a lower relative expression level amongst the other genes and was inactive during germination with the dark treatment. The relative expression level of DHFR remained unchanged during the former three stages and increased dramatically (p < 0.05) at stage 4. FPGS displayed a much lower relative expression level with light treatment, but its relative expression level increased significantly (p < 0.05) from stage 2 to 3 and remained unchanged at the next stages. ADCS was inactive during the germination with no significant change of its relative expression levels.

Figure 7
figure7

Changes of relative expression level of relevant genes in folate biosynthetic pathway during sweet corn seed germination; Bars with * and ** indicates significant difference at p < 0.05 and p < 0.01 respectively compared to stage 1. (a) Light treatment; (b) dark treatment.

Folate is a general term for a series of compounds playing a critical role in transferring one-carbon unit45. Hefni and Witthöft46 found that germination resulted in a four-to-six-times increase in folate contents in wheat and rye seeds. Shohag et al.47 also reported two-to-four-fold increase occurred during legume seed germination. However, we found no articles reporting the situation in sweet corn seeds. In general, the total folate content increased in sweet corn seed sprouts during germination. Anukul et al.48 illustrated that folate polyglutamylation was required in the development of rice seeds. Folate are actively involved in the formation of amino acids as well as DNA; highly active during the germination9, 49. Folate have been found to be related with improving stress resistance of plants50. Interestingly, a peak was observed during the light germination at stage 2 but not in the dark group. Given the fact that light was the only variable in the test, it was reasonable to consider light as a regulating factor of folate biosynthesis during the sprouting of sweet corn seeds. Previously researchers have reported illumination enhanced total folate contents in lettuce51 and other crops. However, few researchers have studied the expression of relevant genes under light stimulus52.

It has been reported that folates are usually combined and bonded with different compounds forming food matrixes53, 54. Results indicated a reduction in free folate content of the sweet corn sprouts during germination. This suggests that the free folate gradually became conjugated in a compound matrix during the germination. In addition, we found that the contribution rate of free folate to the total amount of folate present in the sprouts declined over time from 38% to 33%, 24%, 14% in light environment and 32% to 26%, 11%, 16% in dark environment.

Six genes from different branches of folate biosynthetic pathway were chosen to understand the changing pattern of folate during sweet corn seed germination. GTPCH is involved in the formation of the pterin ring (Fig. 1) with researchers confirming that GTPCH was a rate-limiting enzyme manipulating the activity of folate pathway in Arabidopsis thaliana 55. It has been reported that GTPCH transcript could be found in various tissues of wheats56 and over-expression of GTPCH led to increase of folate contents in crops57, 58. Our results showed that GTPCH was the predominant gene among the six selected genes with the highest expression level. The levels of GTPCH gene relative expression in sweet corn sprouts during the germination in both light and dark groups was highly consistent with the variations observed in total folate content. This observation indicates that the transcript level of GTPCH may determine the amounts of total folate in sweet corn sprouts56, 58.

ADCS catalyzes the reaction of choirmate and glutamine providing the material for p-aminobenzoate (pABA) synthesis. This process takes place in plastids45 where photosynthesis also happen. Therefore, there might be some links between the activity of ADCS and light, as we observed that in light environment the relative expression level of ADCS increased, while in the dark the expression level of ADCS was lower. HPPK, usually combined with dihydropteroate synthase (DHPS), is involved in the production of dihydropteroate (DHP). Navarrete et al.59 investigated the role of HPPK/DHPS in Arabidopsis thaliana and found that besides taking part in folate synthesis, cytosolic HPPK/DHPS had a role in stress tolerance. Previous research has illustrated that illumination could induce various free radicals in plant cells18, 28, 44. Hence, the relative expression level of HPPK seemed to be light-related60 (Fig. 6). DHFS, DHFR and FPGS are encoding genes for synthesis of dihydrofolate (DHF), tetrahydrofolate (THF) and polyglutamylated folate respectively involved in downstream regulation of folate biosynthesis (Fig. 1). In general, all of their relative expression levels increased in different degrees, which could be explained by the requirement of nucleotide synthesis during sweet corn seed germination60. However, their relative expression levels had a significant (p < 0.05) increase with the dark treatments. Meng et al.49 suggested that FPGS was necessary for seed reserve accumulation and hypocotyl elongation in Arabidopsis under dark conditions. It is possible that the same phenomenon also occurred in sweet corn sprouts under dark environment. The extra function of FPGS compared to the light triggered the significant (p < 0.05) increase of the activity of DHFS and DHFR because of their interdependent relationship6.

Potential interrelationships of the biosynthesis of vitamin C, E and folate in sweet corn sprouts

Indirect connections among vitamin metabolisms in plants exist and researchers have confirmed the relationship of N metabolism and folate biosynthesis in atdfb-3 mutants49. Our study tried to provide an insight of the potential interdependent relationships among vitamin C, E and folate and the main breakthrough point would be their common role in biotic stress resistance in plants. A synergistic relationship between vitamin C and folate during the germination of sweet corn seeds was observed during this study, with both the levels of vitamin C and total folate increasing during germination. However, we also suggest that the active biosynthesis of folate may inhibit the activity of L-galactose pathway in sweet corn sprouts. GTP is needed in both pathways (Fig. 1). Therefore, high expression level of GTPCH and extremely low expression level of GLDH were detected in our experiment. Critical role of vitamin C in plant cell expansion and division, root growth and elongation have been reviewed thoroughly28. Gorelova et al.45 reviewed the metabolism of folate and illustrated accelerated total NADPH synthesis in animals and possibly also plants. Since NADPH is involved in ascorbate-glutathione cycle, which play an important part in ROS removal by reducing monodehydroascorbate into ascorbic acid. Folate accumulation in sweet corn sprouts might lead to accumulation of NADPH and thus contribute to the accumulation of ascorbic acid.

On the other hand, total vitamin E contents decreased over time with the increase of vitamin C in our study. This result contradicts the result from Wang et al.27, which reported the simultaneous increase of vitamin C and E in soya bean seed germination. Nevertheless, α-tocopherol can be regenerated from α-chromanoxy radical in ascorbate-glutathione cycle where vitamin C is oxidized to MDHA 4. Excessive vitamin C might generate extra α-tocopherol within cells, which would in turn trigger negative feedback to vitamin E biosynthesis. Therefore, vitamin C was supposed to compete or even inhibit the biosynthesis of vitamin E during the sweet corn seed germination.

In conclusion, the results revealed the changing pattern of vitamin C, E and folate during the germination of sweet corn sprouts in both light and dark environments as well as illustrating the molecular mechanisms behind these changes by studying the relevant key-encoding genes of these biosynthetic pathways. Further research is required to elaborate on these relationships. Such further study could involve the study of more genes as well as the determination of the levels of enzymatic pathways to disclose the activity of the whole metabolic pathways of different vitamins during sweet corn seed germination. In addition, genetic technologies, such as transgenic technology and gene knockout techniques could be applied to deeper study the interrelationship among different vitamins.

Materials and Methods

Sample preparation

Sweet corn seeds were obtained from crop research institute of Guangdong academy of agricultural science, Guangzhou, China). Intact seeds were selected by hand and then immersed in 75% alcohol for 1 min for sterilization. The seeds were soaked in distilled water for 2 hours. Next, the moistened seeds were divided into two groups and placed into glass containers with wet degreasing cotton and filter paper beneath. Each group was performed in triplicate. Both the light and dark groups were kept in an artificial climate chamber (PQX-330A-22A, Life Technology, Ningbo, Zhejiang, China) with temperature of 20 °C and illumination of 35000 LX. The dark group was wrapped with silver paper to avoid illumination. The cotton and filter paper were rewetted every 24 hours and the lamps were kept on during the experiment. Samples were collected at four different stages as shown in Fig. 2: Stage 1 representing initial radical emergence (typically after 48 hours), stage 2 representing chitting of the corn (typically after 72 hours), stage 3 representing emergence of the shoot and development of the root (typically after 96 hours), stage 4 representing shoot and root elongation (typically after 130 hours). About 50 seeds were used for germination in each container and about 6–7 seeds (typically 2 g) were collected for experiments. The collected samples were treated with liquid nitrogen and ground into flour. The samples were then stored at −80 °C until analysis.

Measurement of moisture content

The moisture content was measured by the oven-drying method modified in our lab21. Samples (1 g) were placed in an oven at 105 °C until constant weight. The moisture of the sample was expressed as percent of dry weight (DW) in triplicate with data reported as mean ± SD (n = 3).

RNA isolation, cDNA synthesis and quantitative real-time PCR analysis of relative gene expression

The extraction of RNA and subsequent cDNA conversion were carried out by Hipure Plant RNA Mini Kit (Megen, Guangzhou, China) and PrimeScriptTM RT Reagent Kit with gDNA Eraser (Takara Biotechnology, Dalian, China) according to the instruction booklets from the producers. Obtained RNA and cDNA were kept at −80 °C and −20 °C respectively until required for analysis. Real-time PCR was prepared using SYBP® Premix Ex TaqTM Kit (Takara Biotechnology, Dalian, China) and accomplished by LightCycler® 480 Real-Time PCR System (F. Hoffmann-La Roche Ltd, Switzerland). The ACTIN (GRMZM2G126010) was selected as the reference gene61 and the primers used in this study were listed in Supplemental Table 1. PCR conditions were programmed as 95 °C for 3 min and 40 cycles of 95 °C for 5 s, 56 °C for 30 s, 72 °C for 30 s. Melt curve analysis was carried out following each real-time PCR operation. The efficiencies of the primers used were about 20. The concentration of mRNA was quantities before converting and so did cDNA before running RT-PCR. Cycle threshold (Ct) values were obtained after each operation which were around 17–22 and relative expression was calculated using the 2−ΔΔCt method. Results are shown as mean ± SD (n = 3).

Extraction and Determination of Vitamin C

Vitamin C content in sweet corn sprouts was extracted by 0.1% oxalic acid solution and determined by HPLC-PAD system (Waters Corp, Milford, MA, USA). About 0.2 g ground sample was dissolved in 0.1% oxalic acid solution and treated by Bioruptor® sonication system (Diagenode Inc. USA) for 60 seconds. And then the mixture was brought to centrifugation. The upper liquid was collected and filtrated for the HPLC detection at the wave length of 245 nm. The HPLC conditions were: symmetry shield RP18 column (150 mm × 4.6 mm × 5 μm) with the temperature of 30 °C; methanol/oxalic acid (5:95, v/v) as affluent phase with the flow rate of 1.0 mL/min. Ascorbic acid was used as calibration. Data is expressed as milligram per 100 grams of dry weight sample (mean ± SD, n = 3).

Extraction and Determination of Vitamin E

Extraction of vitamin E in sweet corn sprouts was conducted by the modified method described previously62. The determination of Vitamin E in sweet corn sprouts was carried out by a FL-HPLC system with a Waters 2475 Multi λ Fluorescence Detector at an excitation wavelength of 290 nm and an emission wavelength of 330 nm. The elution phase consisting of hexanes/isopropyl alcohol/acetic acid (99.05:0.85:0.1, v/v/v) with the flow rate of 1.0 mL/min was pumped by a Waters 515 HPLC Pump through a silica column (ZORBAX RX-SIL 4.6 × 250 mm, 5 μm, Agilent Technologies Inc., California, USA). The injection volume of extract samples was 20 μL. Identification of vitamin E was accomplished by the comparison of retention time between samples and standards. The quantification was carried out by standard curves. The outcomes were reported as milligram per 100 grams of dry weight sample (mean ± SD, n = 3).

Extraction of Free and Total Folate

The extraction of folate was accomplished by the method used before63 and modified in our lab. For extraction of free folate, 0.5 g sample was mixed well with 10 mL disodium hydrogen phosphate in 15 mL centrifuge tube and then the mixture was sterilized by autoclaving the samples at 115 °C for 15 min. After cooling down, the solution was filtrated by vacuum filtration. The filtrate was collected and stored at −20 °C until determination. For extraction of total folate, 0.5 g sample was mixed well with 9.4 mL disodium hydrogen phosphate in 15 mL centrifuge tube and then the mixture was sterilized at 115 °C for 15 min. After the solution cooled down, 0.1 mL α-amylase (1.5 U/mg), 0.1 mL papain (≥6000 U/100 mg) and 0.4 mL chicken pancreas solution were added subsequently. After sufficient mix, the mixture was digested at 37 °C for 16 h with adequate shaking. After digestion, the tubes were placed in a boiling water for 3 min to inactive enzymes. Tubes were centrifuged and the total folate extracts were obtained by collecting the liquid through needle filter heads. Total folate extracts were kept at −20 °C until use.

Determination of Folate Content

The determination of folate in sweet corn sprouts was carried out by standard assays53, 54. Briefly, each culture tube was prepared by 4.8 mL Milli-Q water, 5 mL DifcoTM Folic Acid Assay Medium (Sparks, MD, USA) and 0.2 mL folate extract. And then the tubes were sterilized at 121 °C for 20 min. After the tubes were cooled down, 50 μL enterococcus hirae (ATCC® 8043TM, American Type Culture Collection, Manassas, VA, USA) suspension was added aseptically to each tube. Tubes were incubated at 37 °C for 19 h. When the incubation was finished, the tubes were brought to a 4 °C refrigerator for 15 min to stop the bacterial reproduction. Finally, the absorbance at 660 nm was read and recorded. The calculation was performed by a standard curve made by folic acid (Sigma, St. Louis, MO, USA). The results were reported as microgram of folic acid per 100 grams of dry weight sample (mean ± SD, n = 3).

Statistics analysis

Statistics analysis was performed by OriginPro 2016 (OriginLab Corporation, Northampton, MA, USA). The differences among the sweet corn sprouts were determined by Tukey’s multiple comparison test (p < 0.05) with SPSS software 13.0 (SPSS Inc., Chicago, 1 L, USA).

References

  1. 1.

    Simons, M. & Bertr, Hirel. Nitrogen-use efficiency in maize (Zea mays L.): from ‘omics’ studies to metabolic modelling. Journal of Experimental Botany 65, 5657–5671 (2014).

  2. 2.

    Kusano, M. & Fukushima, A. Current challenges and future potential of tomato breeding using omics approaches. Breeding Science 63, 31–41 (2013).

  3. 3.

    Colmsee, C. et al. OPTIMAS-DW: a comprehensive transcriptomics, metabolomics, ionomics, proteomics and phenomics data resource for maize. BMC Plant Biology 12, 1–10 (2012).

  4. 4.

    Smirnoff, N. & Wheeler, G. L. Ascorbic acid in plants: biosynthesis and function. Critical Reviews in Plant Sciences 35, 291–314 (2000).

  5. 5.

    Dellapenna, D. & Pogson, B. J. Vitamin synthesis in plants: Tocopherols and Carotenoids. Annual Review of Plant Biology 57, 711–738 (2006).

  6. 6.

    Hanson, A. D. & Gregory, J. F. Folate biosynthesis, turnover, and transport in plants. Annual Review of Plant Biology 62, 105 (2011).

  7. 7.

    Noctor, G. & Foyer, C. H. Ascorbate and glutathione: Keeping Active Oxygen Under Control. Annual Review of Plant Biology 49, 249 (1998).

  8. 8.

    Basset, G. J. et al. Folate synthesis in plants: the last step of the p-aminobenzoate branch is catalyzed by a plastidial aminodeoxychorismate lyase. Plant Journal for Cell & Molecular Biology 40, 453–461 (2004).

  9. 9.

    Jiang, L. et al. The mitochondrial folylpolyglutamate synthetase gene is required for nitrogen utilization during early seedling development in arabidopsis. Plant physiology 161, 971–989 (2013).

  10. 10.

    Singh, I., Langyan, S. & Yadava, P. Sweet Corn and Corn-Based Sweeteners. Sugar Tech. 16, 144–149 (2014).

  11. 11.

    Rehal, J. Enhancement of Attributes of Cereals by Germination and Fermentation: A Review. Critical Reviews in Food Science and Nutrition 55, 1575–1589 (2015).

  12. 12.

    Hashim, N. & Fields, M. L. Vitamin B, relative nutritive value and palatability of germinated corn (Zea mays L.). Pertanika (1979).

  13. 13.

    Lay, M. G. & Fields, M. L. Nutritive Value of Germinated Corn and Corn Fermented After Germination. Journal of Food Science 46, 1069–1073 (2010).

  14. 14.

    Obizoba, I. C. The effects of varying sprouting periods on the nutritional quality of normal yellow corn (Zea mays). Plant Foods for Human Nutrition 40, 73–81 (1990).

  15. 15.

    Randhir, R. & Shetty, K. Developmental stimulation of total phenolics and related antioxidant activity in light- and dark-germinated corn by natural elicitors. Process Biochemistry 40, 1721–1732 (2005).

  16. 16.

    Jain, A., Srinivasan, K., Yadav, R. P. & Mishra, A. Effect of moisture content on in vitro regeneration of embryonic axis explants of cowpea (Vigna unguiculata L.). Legume. Research 40, 74–79 (2017).

  17. 17.

    Sytykiewicz, H. Expression Patterns of Genes Involved in Ascorbate-Glutathione Cycle in Aphid-Infested Maize (Zea mays L.) Seedlings. International Journal of Molecular Sciences 17, 1–30 (2016).

  18. 18.

    Gallie, D. R. The role of l-ascorbic acid recycling in responding to environmental stress and in promoting plant growth. Journal of Experimental Botany 64, 433–443 (2013).

  19. 19.

    Cruzrus, E., Amaya, I., Sánchezsevilla, J. F., Botella, M. A. & Valpuesta, V. Regulation of L-ascorbic acid content in strawberry fruits. Journal of Experimental Botany 62, 4191–4201 (2011).

  20. 20.

    Otter, T. & Polle, A. The Influence of Apoplastic Ascorbate on the Activities of Cell Wall-Associated Peroxidase and NADH Oxidase in Needles of Norway Spruce (Picea abies L.). Plant & Cell Physiology 35, 1231–1238 (1994).

  21. 21.

    Wang, H. et al. Effect of germination on lignan biosynthesis, and antioxidant and antiproliferative activities in flaxseed (Linum usitatissimum L.). Food Chemistry 205, 170–177 (2016).

  22. 22.

    Guo, X., Li, T., Tang, K. & Liu, R. H. Effect of germination on phytochemical profiles and antioxidant activity of mung bean sprouts (Vigna radiata). Journal of Agricultural & Food Chemistry 60, 11050–11055 (2012).

  23. 23.

    Huang, X., Cai, W. & Xu, B. Kinetic changes of nutrients and antioxidant capacities of germinated soybean (Glycine max L.) and mung bean (Vigna radiata L.) with germination time. Food Chemistry 143, 268–276 (2014).

  24. 24.

    Li, Z. et al. Transcriptional profile of genes involved in ascorbate glutathione cycle in senescing leaves for an early senescence leaf (esl) rice mutant. Journal of Plant Physiology 176, 1–15 (2015).

  25. 25.

    Conklin, P. L. et al. Arabidopsis thaliana VTC4 encodes L-galactose-1-P phosphatase, a plant ascorbic acid biosynthetic enzyme. Journal of Biological Chemistry 281, 15662–15670 (2006).

  26. 26.

    Liu, Y. J. et al. Gene families of maize glutathione-ascorbate redox cycle respond differently to abiotic stresses. Journal of Plant Physiology 169, 183–192 (2012).

  27. 27.

    Wang, L. et al. The dynamic changes of ascorbic acid, tocopherols and antioxidant activity during germination of soya bean (Glycine max). International Journal of Food Science & Technology 50, 2367–2374 (2015).

  28. 28.

    Davey, M. W. et al. Plant L-ascorbic acid: chemistry, function, metabolism, bioavailability and effects of processing. Journal of the Science of Food & Agriculture 80, 825–860 (2000).

  29. 29.

    Gatzek, S., Wheeler, G. L. & Smirnoff, N. Antisense suppression of l -galactose dehydrogenase in Arabidopsis thaliana provides evidence for its role in ascorbate synthesis and reveals light modulated l -galactose synthesis. The Plant journal: for cell and molecular biology 30, 541–553 (2002).

  30. 30.

    Cahoon, E. B. et al. Metabolic redesign of vitamin E biosynthesis in plants for tocotrienol production and increased antioxidant content. Nature Biotechnology 21, 1082–1087 (2003).

  31. 31.

    Siles, L., Cela, J. & Munnébosch, S. Vitamin E analyses in seeds reveal a dominant presence of tocotrienols over tocopherols in the Arecaceae family 95, 207–214 (2013).

  32. 32.

    Sattler, S. E., Gilliland, L. U., Magallaneslundback, M., Pollard, M. & Dellapenna, D. Vitamin E is essential for seed longevity and for preventing lipid peroxidation during germination. Plant Cell 16, 1419–1432 (2004).

  33. 33.

    Hiran, P., Kerdchoechuen, O. & Laohakunjit, N. Combined effects of fermentation and germination on nutritional compositions, functional properties and volatiles of maize seeds. Journal of Cereal Science 71, 207–216 (2016).

  34. 34.

    Taeshik, H., Sungjin, P. & Lo, Y. M. Effects of germination on chemical composition and functional properties of sesame (Sesamum indicum L.) seeds. Bioresource Technology 100, 1643–1647 (2009).

  35. 35.

    Kim, M. Y. et al. Changes of phenolic-acids and vitamin E profiles on germinated rough rice (Oryza sativa L.) treated by high hydrostatic pressure. Food Chemistry 217, 106–111 (2017).

  36. 36.

    Bellani, L. M., Salvini, L., Dell’Aquila, A. & Scialabba, A. Reactive oxygen species release, vitamin E, fatty acid and phytosterol contents of artificially aged radish (Raphanus sativus L.) seeds during germination. Acta Physiologiae Plantarum 34, 1789–1799 (2012).

  37. 37.

    Farahani, H. A. Effect of vitamin E on seedling growth in parsley (Petroselinum sativum L.). African Journal of Microbiology Research 6, 5934–5939 (2012).

  38. 38.

    Falk, J. & Munnébosch, S. Tocochromanol functions in plants: antioxidation and beyond. Journal of Experimental Botany 61, 1549–1566 (2010).

  39. 39.

    Shutu, X. et al. Dissecting tocopherols content in maize (Zea mays L.), using two segregating populations and high-density single nucleotide polymorphism markers. BMC Plant Biology 12(201), 1–14 (2012).

  40. 40.

    Jiang, J. et al. P-hydroxyphenylpyruvate dioxygenase from Medicago sativa is involved in vitamin E biosynthesis and abscisic acid-mediated seed germination. Scientific Reports 7(40625), 1–15 (2017).

  41. 41.

    Naqvi, S. et al. Simultaneous expression of Arabidopsis ρ-hydroxyphenylpyruvate dioxygenase and MPBQ methyltransferase in transgenic corn kernels triples the tocopherol content. Transgenic Research 20, 177–181 (2010).

  42. 42.

    Kobayashi, N. & Dellapenna, D. Tocopherol metabolism, oxidation and recycling under high light stress in Arabidopsis. Plant Journal 55, 607–618 (2008).

  43. 43.

    Tang, Y. L., Ren, W. W., Zhang, L. & Tang, K. X. Molecular cloning and characterization of a tocopherol cyclase gene from Lactuca sativa (Asteraceae). Genetics & Molecular Research Gmr 10, 693–702 (2011).

  44. 44.

    Lushchak, V. I. & Semchuk, N. M. Tocopherol biosynthesis: chemistry, regulation and effects of environmental factors. Acta Physiologiae Plantarum 34, 1607–1628 (2012).

  45. 45.

    Gorelova, V., Ambach, L., Rebeille, F. & Stove, C. & Van der Straeten, D. Folates in Plants: Research Advances and Progress in Crop Biofortification. Frontiers in Chemistry 5, 1–20 (2017).

  46. 46.

    Hefni, M. & Witthöft, C. M. Effect of germination and subsequent oven-drying on folate content in different wheat and rye cultivars. Journal of Cereal Science 56, 374–378 (2012).

  47. 47.

    Shohag, M. J., Wei, Y. & Yang, X. Changes of folate and other potential health-promoting phytochemicals in legume seeds as affected by germination. Journal of Agricultural & Food Chemistry 60, 9137–9143 (2012).

  48. 48.

    Anukul, N. et al. Folate Polyglutamylation is Required for Rice Seed Development. Rice 3, 181–193 (2010).

  49. 49.

    Meng, H. et al. Arabidopsis plastidial folylpolyglutamate synthetase is required for seed reserve accumulation and seedling establishment in darkness. Plos One 9, 1–14 (2014).

  50. 50.

    Wittek, F. et al. Folic acid induces salicylic acid-dependent immunity in Arabidopsis and enhances susceptibility to Alternaria brassicicola. Molecular Plant Pathology 16, 616 (2015).

  51. 51.

    Długosz-Grochowska, O., Kołton, A. & Wojciechowska, R. Modifying folate and polyphenol concentrations in Lamb’s lettuce by the use of LED supplemental lighting during cultivation in greenhouses. Journal of Functional Foods 26, 228–237 (2016).

  52. 52.

    Stutte, G. W. Commercial transition to LEDs: A Pathway to Higher Value Products? Ashs Conference (2014).

  53. 53.

    American Assn. of Analytical Chemists (AOAC). Total Folates in Cereals and Cereal Foods Microbiological Assay-Trienzyme Procedure AOAC Official Method (2004.05).

  54. 54.

    Iyer, R. & Tomar, S. K. Folate: a functional food constituent. Journal of Food Science 74, R114–122 (2009).

  55. 55.

    Hossain, T. et al. Enhancement of folates in plants through metabolic engineering. Proceedings of the National Academy of Sciences of the United States of America 101, 5158–5163 (2004).

  56. 56.

    Shaner, M. I., Don, B. & Robertj, H. GTP cyclohydrolase 1 expression and folate accumulation in the developing wheat seed. Journal of Cereal Science 48, 503–512 (2008).

  57. 57.

    Naqvi, S. et al. Transgenic Multivitamin Corn through Biofortification of Endosperm with Three Vitamins Representing Three Distinct Metabolic Pathways. Proceedings of the National Academy of Sciences of the United States of America 106, 7762–7767 (2009).

  58. 58.

    Nunes, A. C., Kalkmann, D. C. & Aragão, F. J. Folate biofortification of lettuce by expression of a codon optimized chicken GTP cyclohydrolase I gene. Transgenic Research 18, 661–667 (2009).

  59. 59.

    Navarrete, O. et al. A folate independent role for cytosolic HPPK/DHPS upon stress in Arabidopsis thaliana. Phytochemistry 73, 23–33 (2012).

  60. 60.

    Jabrin, S., Ravanel, S., Douce, R. & Rébeillé, F. One-Carbon Metabolism in Plants. Regulation of Tetrahydrofolate Synthesis during Germination and Seedling Development. Plant Physiology 131, 1431–1439 (2003).

  61. 61.

    Galli, V., da Silva Messias, R. & dos Anjos e Silva, S. D. Selection of reliable reference genes for quantitative real-time polymerase chain reaction studies in maize grains. Plant Cell Reports 32, 1869–1877 (2013).

  62. 62.

    Okarter, N., Liu, C.-S., Sorrells, M. E. & Liu, R. H. Phytochemical content and antioxidant activity of six diverse varieties of whole wheat. Food Chemistry 119, 249–257 (2010).

  63. 63.

    Pandrangi, S. & LaBorde, L. F. Optimization of microbiological assay of folic acid and determination of folate content in spinach. International Journal of Food Science and Technology 39, 525–532 (2004).

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Acknowledgements

Authors are greatly thankful to National Natural Science Foundation of China (31501765), Science and Technology Planning Project of Guangdong Province-China (2016B020233004) for financial support.

Author information

X.G., F.L. and C.S.B. conceived and designed the experiments; F.L., N.X. and L.X. performed the experiments; S.Y. and W.H. determined vitamin C by HPLC analysis; F.L. and N.X. analyzed the data; X.G. and J.H. contributed chemicals and materials; F.L., C.S.B. and X.G. interpreted the data and wrote the draft manuscript all authors reviewed the manuscript.

Correspondence to Xinbo Guo.

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