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First published online February 24, 2002; 10.1104/pp.010640 Plant Physiol, March 2002, Vol. 128, pp. 1069-1076 The Priming of Amylose Synthesis in Arabidopsis Leaves1Institute of Plant Sciences, University of Bern, Altenbergrain 21, 3013 Bern, Switzerland (S.C.Z.); John Innes Centre, Colney Lane, Norwich NR4 7UH, United Kingdom (A.M.S.); and Institute of Cell and Molecular Biology, University of Edinburgh, Mayfield Road, Edinburgh EH9 3JH, United Kingdom (S.M.S.)
We investigated the mechanism of amylose synthesis in Arabidopsis
leaves using 14C-labeling techniques. First, we tested the
hypothesis that short malto-oligosaccharides (MOS) may act as primers
for granule-bound starch synthase I. We found increased amylose
synthesis in isolated starch granules supplied with
ADP[14C]glucose (ADP[14C]Glc) and MOS
compared with granules supplied with ADP[14C]Glc but no
MOS. Furthermore, using a MOS-accumulating mutant (dpe1), we found that more amylose was synthesized than
in the wild type, correlating with the amount of MOS in vivo. When
wild-type and mutant plants were tested in conditions where both lines
had similar MOS contents, no difference in amylose synthesis was
observed. We also tested the hypothesis that branches of amylopectin
might serve as the primers for granule-bound starch synthase I. In this model, elongated branches of amylopectin are subsequently cleaved to
form amylose. We conducted pulse-chase experiments, supplying a pulse
of ADP[14C]Glc to isolated starch granules or
14CO2 to intact plants, followed by a chase
period in unlabeled substrate. We detected no transfer of label from
the amylopectin fraction to the amylose fraction of starch either in
isolated starch granules or in intact leaves, despite varying the time course of the experiments and using a mutant line (sex4)
in which high-amylose starch is synthesized. We therefore find no
evidence for amylopectin-primed amylose synthesis in Arabidopsis. We
propose that MOS are the primers for amylose synthesis in Arabidopsis leaves.
1 This work was funded by the Biotechnology and Biological Science Research Council (BBSRC), UK (grant no. 208/D11090) and by the Gatsby Charitable Foundation. The John Innes Centre is funded by a competitive strategic grant from the BBSRC. * Corresponding author; e-mail sam.zeeman{at}ips.unibe.ch; fax 41-31-332-2059. © 2002 American Society of Plant Physiologists This article has been cited by other articles:
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