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Phosphorylation of C6- and C3-positions of glucosyl residues in starch is catalysed by distinct dikinases.
- Source :
-
FEBS letters [FEBS Lett] 2006 Sep 04; Vol. 580 (20), pp. 4872-6. Date of Electronic Publication: 2006 Aug 10. - Publication Year :
- 2006
-
Abstract
- Glucan, water dikinase (GWD) and phosphoglucan, water dikinase (PWD) are required for normal starch metabolism. We analysed starch phosphorylation in Arabidopsis wild-type plants and mutants lacking either GWD or PWD using (31)P NMR. Phosphorylation at both C6- and C3-positions of glucose moieties in starch was drastically decreased in GWD-deficient mutants. In starch from PWD-deficient plants C3-bound phosphate was reduced to levels close to the detection limit. The latter result contrasts with previous reports according to which GWD phosphorylates both C6- and C3-positions. In these studies, phosphorylation had been analysed by HPLC of acid-hydrolysed glucans. We now show that maltose-6-phosphate, a product of incomplete starch hydrolysis, co-eluted with glucose-3-phosphate under the chromatographic conditions applied. Re-examination of the specificity of the dikinases using an improved method demonstrates that C6- and C3-phosphorylation is selectively catalysed by GWD and PWD, respectively.
- Subjects :
- Arabidopsis Proteins genetics
Glucans chemistry
Glucose chemistry
Nuclear Magnetic Resonance, Biomolecular
Phosphorylation
Phosphotransferases (Paired Acceptors) genetics
Recombinant Proteins genetics
Recombinant Proteins metabolism
Starch chemistry
Arabidopsis Proteins metabolism
Glucans metabolism
Glucose metabolism
Phosphotransferases (Paired Acceptors) metabolism
Starch metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0014-5793
- Volume :
- 580
- Issue :
- 20
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 16914145
- Full Text :
- https://doi.org/10.1016/j.febslet.2006.07.085