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Plastidial phosphorylase is required for normal starch synthesis in Chlamydomonas reinhardtii

  • Among the three distinct starch phosphorylase activities detected in Chlamydomonas reinhardtii, two distinct plastidial enzymes (PhoA and PhoB) are documented while a single extraplastidial form (PhoC) displays a higher affinity for glycogen as in vascular plants. The two plastidial phosphorylases are shown to function as homodimers containing two 91-kDa (PhoA) subunits and two 110-kDa (PhoB) subunits. Both lack the typical 80-amino-acid insertion found in the higher plant plastidial forms. PhoB is exquisitely sensitive to inhibition by ADP-glucose and has a low affinity for malto-oligosaccharides. PhoA is more similar to the higher plant plastidial phosphorylases: it is moderately sensitive to ADP-glucose inhibition and has a high affinity for unbranched malto-oligosaccharides. Molecular analysis establishes that STA4 encodes PhoB. Chlamydomonas reinhardtii strains carrying mutations at the STA4 locus display a significant decrease in amounts of starch during storage that correlates with the accumulation of abnormally shaped granulesAmong the three distinct starch phosphorylase activities detected in Chlamydomonas reinhardtii, two distinct plastidial enzymes (PhoA and PhoB) are documented while a single extraplastidial form (PhoC) displays a higher affinity for glycogen as in vascular plants. The two plastidial phosphorylases are shown to function as homodimers containing two 91-kDa (PhoA) subunits and two 110-kDa (PhoB) subunits. Both lack the typical 80-amino-acid insertion found in the higher plant plastidial forms. PhoB is exquisitely sensitive to inhibition by ADP-glucose and has a low affinity for malto-oligosaccharides. PhoA is more similar to the higher plant plastidial phosphorylases: it is moderately sensitive to ADP-glucose inhibition and has a high affinity for unbranched malto-oligosaccharides. Molecular analysis establishes that STA4 encodes PhoB. Chlamydomonas reinhardtii strains carrying mutations at the STA4 locus display a significant decrease in amounts of starch during storage that correlates with the accumulation of abnormally shaped granules containing a modified amylopectin structure and a high amylose content. The wild-type phenotype could be rescued by reintroduction of the cloned wild-type genomic DNA, thereby demonstrating the involvement of phosphorylase in storage starch synthesis.zeige mehrzeige weniger

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Metadaten
Verfasserangaben:David DauvilleeORCiD, Vincent ChochoisORCiD, Martin SteupORCiDGND, Sophie Haebel, Nora EckermannGND, Gerhard RitteGND, Jean-Philippe RalORCiD, Christophe ColleoniORCiD, Glenn HicksGND, Fabrice Wattebled, Philippe Deschamps, Luc Lienard, Laurent Cournac, Jean-Luc Putaux, Danielle Dupeyre, Steven G. Ball
DOI:https://doi.org/10.1111/j.1365-313X.2006.02870.x
ISSN:0960-7412
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/17018036
Titel des übergeordneten Werks (Englisch):The plant journal
Verlag:Blackwell
Verlagsort:Oxford
Publikationstyp:Wissenschaftlicher Artikel
Sprache:Englisch
Datum der Erstveröffentlichung:13.09.2006
Erscheinungsjahr:2006
Datum der Freischaltung:29.05.2020
Freies Schlagwort / Tag:(glycogen) starch phosphorylase; Chlamydomonas; amylopectin; starch
Band:48
Ausgabe:2
Seitenanzahl:12
Erste Seite:274
Letzte Seite:285
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Peer Review:Referiert
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