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Review
. 2013:2013:795964.
doi: 10.1155/2013/795964. Epub 2013 Jan 17.

L-ascorbic Acid: a multifunctional molecule supporting plant growth and development

Affiliations
Review

L-ascorbic Acid: a multifunctional molecule supporting plant growth and development

Daniel R Gallie. Scientifica (Cairo). 2013.

Abstract

L-Ascorbic acid (vitamin C) is as essential to plants as it is to animals. Ascorbic acid functions as a major redox buffer and as a cofactor for enzymes involved in regulating photosynthesis, hormone biosynthesis, and regenerating other antioxidants. Ascorbic acid regulates cell division and growth and is involved in signal transduction. In contrast to the single pathway responsible for ascorbic acid biosynthesis in animals, plants use multiple pathways to synthesize ascorbic acid, perhaps reflecting the importance of this molecule to plant health. Given the importance of ascorbic acid to human nutrition, several technologies have been developed to increase the ascorbic acid content of plants through the manipulation of biosynthetic or recycling pathways. This paper provides an overview of these approaches as well as the consequences that changes in ascorbic acid content have on plant growth and function. Discussed is the capacity of plants to tolerate changes in ascorbic acid content. The many functions that ascorbic acid serves in plants, however, will require highly targeted approaches to improve their nutritional quality without compromising their health.

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Figures

Figure 1
Figure 1
l-Ascorbic acid biosynthetic pathways in plants and animals. Reactions 1–8 represent the pathway in animals and reactions 9–24 represent the pathways in plants. Enzymes in each pathway are 1, phosphoglucomutase; 2, UDP-glucose pyrophosphorylase; 3, UDP-glucose dehydrogenase; 4, glucuronate-1-phosphate uridylyltransferase; 5, glucuronate 1-kinase; 6, glucuronate reductase; 7, aldonolactonase (aka. gluconolactonase); 8, gulono-1,4-lactone oxidase or dehydrogenase; 9, glucose-6-phosphate isomerase; 10, mannose-6-phosphate isomerase; 11, phosphomannose mutase; 12, GDP-mannose pyrophosphorylase (mannose-1-phosphate guanylyltransferase) (VTC1); 13, GDP-mannose-3′, 5′-epimerase; 14, GDP-l-galactose phosphorylase (VTC2 and VTC5); 15, l-galactose-1-phosphate phosphatase (VTC4); 16, l-galactose dehydrogenase; 17, l-galactono-1,4-lactone dehydrogenase; 18, methylesterase; 19, d-galacturonate reductase; 20, aldonolactonase; 21, phosphodiesterase; 22, sugar phosphatase; 23, l-gulose dehydrogenase; 24, myo-inositol oxygenase. Adapted from Agius et al. [35].
Figure 2
Figure 2
Role of DHAR and MDAR in l -ascorbic acid recycling. Asc is synthesized from l-galactono-1,4-lactone by l-galactono-1,4-lactone dehydrogenase (GLDH). When Asc is oxidized to monodehydroascorbate (MDHA), it can be reduced to Asc by monodehydroascorbate reductase (MDAR) or it can disproportionate non-enzymatically to Asc and dehydroascorbate (DHA). DHA spontaneously hydrolyzes to 2,3-diketogulonic acid unless salvaged by dehydroascorbate reductase (DHAR) which uses glutathione (GSH) as the reductant. Oxidized glutathione (GSSG) is reduced by glutathione reductase (GR) using NADPH as the reductant.

References

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