Characterization of the 32,000 dalton chloroplast membrane protein. III. Probing its biological function in Spirodela [oligorrhiza]

The rapidly turning over, photoinduced thylakoid protein, P-32000, is the main pulse-labeled membrane polypeptide in the chloroplasts of Spirodela oligorrhiza, yet little is known of its physiological function. Two hypotheses are tested: that P-32000 synthesis is necessary for thylakoid biogenesis;...

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Veröffentlicht in:Plant physiology (Bethesda) 1979-11, Vol.64 (5), p.828-832
Hauptverfasser: Weinbaum, Steven A., Gressel, Jonathan, Avi Reisfeld, Edelman, Marvin
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Sprache:eng
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Zusammenfassung:The rapidly turning over, photoinduced thylakoid protein, P-32000, is the main pulse-labeled membrane polypeptide in the chloroplasts of Spirodela oligorrhiza, yet little is known of its physiological function. Two hypotheses are tested: that P-32000 synthesis is necessary for thylakoid biogenesis; that it directly participates in photosynthesis. Spirodela cultures were dissected into expanding and fully mature tissue. Fronds from both developmental stages transcribed a 0.5 × 106 dalton RNA likely to be the message for P-32000. As to the protein itself. synthesis occurred in both types of tissue but was considerably enhanced in the fully mature state. Thus, a purely transient, developmental function for P-32000 during thylakoid biogenesis appears ruled out. Low concentrations of D-threo-chloramphenicol severely suppressed P-32000 synthesis but not its turnover. As a result, fronds depleted in P-32000 were obtained. However, photoassimilation of CO2 remained at 86% of normal in tissue > 80% depleted of P-32000. Thus, P-32000 did not appear to be rate-limiting, suggesting that it does not serve as a direct, integral part of the photosynthetic pathway.
ISSN:0032-0889
1532-2548
DOI:10.1104/pp.64.5.828