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Phosphorylation of C6- and C3-positions of glucosyl residues in starch is catalysed by distinct dikinases.

Authors :
Ritte G
Heydenreich M
Mahlow S
Haebel S
Kötting O
Steup M
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.

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