Abstract

An Arabidopsis double knock-out mutant lacking cytosolic disproportionating enzyme 2 (DPE2) and the plastidial phosphorylase (PHS1) revealed a dwarf-growth phenotype, reduced starch content, an uneven distribution of starch within the plant rosette, and a reduced number of starch granules per chloroplast under standard growth conditions. In contrast, the wild type contained 5–7 starch granules per chloroplast. Mature and old leaves of the double mutant were essentially starch free and showed plastidial disintegration. Several analyses revealed that the number of starch granules per chloroplast was affected by the dark phase. So far, it was unclear if it was the dark phase per se or starch degradation in the dark that was connected to the observed decrease in the number of starch granules per chloroplast. Therefore, in the background of the double mutant dpe2/phs1, a triple mutant was generated lacking the initial starch degrading enzyme glucan, water dikinase (GWD). The triple mutant showed improved plant growth, a starch-excess phenotype, and a homogeneous starch distribution. Furthermore, the number of starch granules per chloroplast was increased and was similar to wild type. However, starch granule morphology was only slightly affected by the lack of GWD as in the triple mutant and, like in dpe2/phs1, more spherical starch granules were observed. The characterized triple mutant was discussed in the context of the generation of starch granules and the formation of starch granule morphology.

Highlights

  • Transitory starch metabolism is a central process in the plant life cycle

  • Analysis of the GWD protein was performed by SDS-PAGE, Starch granule number per chloroplast in dpe2/phs1 is dependent on initiation of starch degradation western blotting, and immunodetection as described by Mahlow et al [12]

  • The absence of disproportionating enzyme 2 (DPE2) and PHS1 was confirmed by native PAGE and subsequent activity staining

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Summary

Introduction

Transitory starch metabolism is a central process in the plant life cycle. Many aspects of the synthesis and degradation of starch granules remain obscure. Neither the physicochemical mechanism nor the proteins involved in the initiation and formation of the starch granules have been identified. Arabidopsis wild-type chloroplasts contain a strictly regulated number of starch granules, with 5–7 granules per chloroplast [1]. A significant alteration of the number of starch granules per chloroplast was observed in plants lacking soluble starch synthase 4 (SS4; [2]). In this mutant, only one starch granule per chloroplast was detected.

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