| Literature DB >> 17462988 |
Carole L Linster1, Tara A Gomez, Kathryn C Christensen, Lital N Adler, Brian D Young, Charles Brenner, Steven G Clarke.
Abstract
The first committed step in the biosynthesis of L-ascorbate from D-glucose in plants requires conversion of GDP-L-galactose to L-galactose 1-phosphate by a previously unidentified enzyme. Here we show that the protein encoded by VTC2, a gene mutated in vitamin C-deficient Arabidopsis thaliana strains, is a member of the GalT/Apa1 branch of the histidine triad protein superfamily that catalyzes the conversion of GDP-L-galactose to L-galactose 1-phosphate in a reaction that consumes inorganic phosphate and produces GDP. In characterizing recombinant VTC2 from A. thaliana as a specific GDP-L-galactose/GDP-D-glucose phosphorylase, we conclude that enzymes catalyzing each of the ten steps of the Smirnoff-Wheeler pathway from glucose to ascorbate have been identified. Finally, we identify VTC2 homologs in plants, invertebrates, and vertebrates, suggesting that a similar reaction is used widely in nature.Entities:
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Year: 2007 PMID: 17462988 PMCID: PMC2556065 DOI: 10.1074/jbc.M702094200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157