Article (Scientific journals)
Arabidopsis VTC2 encodes a GDP-L-galactose phosphorylase, the last unknown enzyme in the Smirnoff-Wheeler pathway to ascorbic acid in plants
Linster, Carole; Gomez, Tara A.; Christensen, Kathryn C. et al.
2007In Journal of Biological Chemistry, 282 (26), p. 18879-85
Peer Reviewed verified by ORBi
 

Files


Full Text
Linster_et_al_JBC_2007.pdf
Publisher postprint (678.8 kB)
Download

All documents in ORBilu are protected by a user license.

Send to



Details



Abstract :
[en] 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.
Disciplines :
Biochemistry, biophysics & molecular biology
Identifiers :
UNILU:UL-ARTICLE-2012-556
Author, co-author :
Linster, Carole  ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB)
Gomez, Tara A.
Christensen, Kathryn C.
Adler, Lital N.
Young, Brian D.
Brenner, Charles
Clarke, Steven G.
Language :
English
Title :
Arabidopsis VTC2 encodes a GDP-L-galactose phosphorylase, the last unknown enzyme in the Smirnoff-Wheeler pathway to ascorbic acid in plants
Publication date :
29 June 2007
Journal title :
Journal of Biological Chemistry
ISSN :
1083-351X
Publisher :
American Society for Biochemistry and Molecular Biology, Baltimore, United States - Maryland
Volume :
282
Issue :
26
Pages :
18879-85
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBilu :
since 26 December 2013

Statistics


Number of views
85 (4 by Unilu)
Number of downloads
102 (0 by Unilu)

Scopus citations®
 
159
Scopus citations®
without self-citations
150
WoS citations
 
146

Bibliography


Similar publications



Contact ORBilu