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STARCH SYNTHASE5, a Noncanonical Starch Synthase-Like Protein, Promotes Starch Granule Initiation in Arabidopsis.
Abt, Melanie R; Pfister, Barbara; Sharma, Mayank; Eicke, Simona; Bürgy, Léo; Neale, Isabel; Seung, David; Zeeman, Samuel C.
Affiliation
  • Abt MR; Institute of Molecular Plant Biology, Swiss Federal Institute of Technology in Zurich, 8092 Zurich, Switzerland.
  • Pfister B; Institute of Molecular Plant Biology, Swiss Federal Institute of Technology in Zurich, 8092 Zurich, Switzerland.
  • Sharma M; Institute of Molecular Plant Biology, Swiss Federal Institute of Technology in Zurich, 8092 Zurich, Switzerland.
  • Eicke S; Institute of Molecular Plant Biology, Swiss Federal Institute of Technology in Zurich, 8092 Zurich, Switzerland.
  • Bürgy L; Institute of Molecular Plant Biology, Swiss Federal Institute of Technology in Zurich, 8092 Zurich, Switzerland.
  • Neale I; Institute of Molecular Plant Biology, Swiss Federal Institute of Technology in Zurich, 8092 Zurich, Switzerland.
  • Seung D; Institute of Molecular Plant Biology, Swiss Federal Institute of Technology in Zurich, 8092 Zurich, Switzerland.
  • Zeeman SC; Institute of Molecular Plant Biology, Swiss Federal Institute of Technology in Zurich, 8092 Zurich, Switzerland szeeman@ethz.ch.
Plant Cell ; 32(8): 2543-2565, 2020 08.
Article in En | MEDLINE | ID: mdl-32471861
What determines the number of starch granules in plastids is an enigmatic aspect of starch metabolism. Several structurally and functionally diverse proteins have been implicated in the granule initiation process in Arabidopsis (Arabidopsis thaliana), with each protein exerting a varying degree of influence. Here, we show that a conserved starch synthase-like protein, STARCH SYNTHASE5 (SS5), regulates the number of starch granules that form in Arabidopsis chloroplasts. Among the starch synthases, SS5 is most closely related to SS4, a major determinant of granule initiation and morphology. However, unlike SS4 and the other starch synthases, SS5 is a noncanonical isoform that lacks catalytic glycosyltransferase activity. Nevertheless, loss of SS5 reduces starch granule numbers that form per chloroplast in Arabidopsis, and ss5 mutant starch granules are larger than wild-type granules. Like SS4, SS5 has a conserved putative surface binding site for glucans and also interacts with MYOSIN-RESEMBLING CHLOROPLAST PROTEIN, a proposed structural protein influential in starch granule initiation. Phenotypic analysis of a suite of double mutants lacking both SS5 and other proteins implicated in starch granule initiation allows us to propose how SS5 may act in this process.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Starch / Starch Synthase / Glycosyltransferases / Arabidopsis / Arabidopsis Proteins / Chloroplast Proteins Language: En Journal: Plant Cell Journal subject: BOTANICA Year: 2020 Document type: Article Affiliation country: Switzerland Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Starch / Starch Synthase / Glycosyltransferases / Arabidopsis / Arabidopsis Proteins / Chloroplast Proteins Language: En Journal: Plant Cell Journal subject: BOTANICA Year: 2020 Document type: Article Affiliation country: Switzerland Country of publication: United kingdom