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PLANT PHYSIOLOGY
Article
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PLANT PHYSIOLOGY
Article . 2017 . Peer-reviewed
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MPG.PuRe
Article . 2017
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Starch Synthase 4 and Plastidal Phosphorylase Differentially Affect Starch Granule Number and Morphology

Authors: Irina Malinova; Saleh Alseekh; Regina Feil; Alisdair R. Fernie; Otto Baumann; Mark Aurel Schöttler; John E. Lunn; +1 Authors

Starch Synthase 4 and Plastidal Phosphorylase Differentially Affect Starch Granule Number and Morphology

Abstract

The process of starch granule formation in leaves of Arabidopsis (Arabidopsis thaliana) is obscure. Besides STARCH SYNTHASE4 (SS4), the PLASTIDIAL PHOSPHORYLASE (PHS1) also seems to be involved, since dpe2-1/phs1a double mutants lacking both PHS1 and the cytosolic DISPROPORTIONATING ENZYME2 (DPE2) displayed only one starch granule per chloroplast under normal growth conditions. For further studies, a dpe2-1/phs1a/ss4 triple mutant and various combinations of double mutants were generated and metabolically analyzed with a focus on starch metabolism. The dpe2-1/phs1a/ss4 mutant revealed a massive starch excess phenotype. Furthermore, these plants grown under 12 h of light/12 h of dark harbored a single large and spherical starch granule per plastid. The number of starch granules was constant when the light/dark regime was altered, but this was not observed in the parental lines. With regard to growth, photosynthetic parameters, and metabolic analyses, the triple mutant additionally displayed alterations in comparison with ss4 and dpe2-1/phs1a The results clearly illustrate that PHS1 and SS4 are differently involved in starch granule formation and do not act in series. However, SS4 appears to exert a stronger influence. In connection with the characterized double mutants, we discuss the generation of starch granules and the observed formation of spherical starch granules.

Country
Germany
Keywords

Light, Arabidopsis Proteins, Arabidopsis, Glycogen Debranching Enzyme System, Starch, Plant Leaves, Microscopy, Electron, Starch Synthase, Mutation, Plastids, Protein Tyrosine Phosphatases, Institut für Biochemie und Biologie

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
50
Top 10%
Top 10%
Top 10%
bronze