Mutants of Arabidopsis Lacking a Chloroplastic Isoamylase Accumulate Phytoglycogen and an Abnormal Form of Amylopectin

Author:

Wattebled Fabrice1,Dong Ying1,Dumez Sylvain1,Delvallé David1,Planchot Véronique1,Berbezy Pierre1,Vyas Darshna1,Colonna Paul1,Chatterjee Manash1,Ball Steven1,D'Hulst Christophe1

Affiliation:

1. Unité de Glycobiologie Structurale et Fonctionnelle, Unité Mixte de Recherche 8576 Centre National de la Recherche Scientifique, Université des Sciences et Technologies de Lille, 59655 Villeneuve d'Ascq cedex, France (F.W., Y.D., S.D., D.D., S.B., C.D.); Unité de Recherche sur les Biopolymères, Intéractions et Assemblages, Institut National de la Recherche Agronomique Centre de Nantes, 4431

Abstract

Abstract Mutant lines defective for each of the four starch debranching enzyme (DBE) genes (AtISA1, AtISA2, AtISA3, and AtPU1) detected in the nuclear genome of Arabidopsis (Arabidopsis thaliana) were produced and analyzed. Our results indicate that both AtISA1 and AtISA2 are required for the production of a functional isoamylase-type of DBE named Iso1, the major isoamylase activity found in leaves. The absence of Iso1 leads to an 80% decrease in the starch content in both lines and to the accumulation of water-soluble polysaccharides whose structure is similar to glycogen. In addition, the residual amylopectin structure in the corresponding mutant lines displays a strong modification when compared to the wild type, suggesting a direct, rather than an indirect, function of Iso1 during the synthesis of amylopectin. Mutant lines carrying a defect in AtISA3 display a strong starch-excess phenotype at the end of both the light and the dark phases accompanied by a small modification of the amylopectin structure. This result suggests that this isoamylase-type of DBE plays a major role during starch mobilization. The analysis of the Atpu1 single-mutant lines did not lead to a distinctive phenotype. However, Atisa2/Atpu1 double-mutant lines display a 92% decrease in starch content. This suggests that the function of pullulanase partly overlaps that of Iso1, although its implication remains negligible when Iso1 is present within the cell.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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