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Plant Physiology 100:1142-1149 (1992)
© 1992 American Society of Plant Biologists

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Environmental and Stress Physiology

Photoacclimation in the Red Alga Porphyridium cruentum1

Changes in Photosynthetic Enzymes, Electron Carriers, and Light-Saturated Rate of Photosynthesis as a Function of Irradiance and Spectral Quality

Francis X. Cunningham, Jr., Avigad Vonshak and Elisabeth Gantt

Department of Botany, University of Maryland, College Park, Maryland 20742, Microalgal Biotechnology Laboratory, The Jacob Blaustein Institute for Desert Research, Ben-Gurion University of the Negev, Sede-Boker Campus, Israel 84990

Acclimation of the photosynthetic apparatus to changes in the light environment was studied in the unicellular red alga Porphyridium cruentum (American Type Culture Collection No. 50161). Absolute or relative amounts of four photosynthetic enzymes and electron carriers were measured, and the data were compared with earlier observations on light-harvesting components (F.X. Cunningham, Jr., R.J. Dennenberg, L. Mustárdy, P.A. Jursinic, E. Gantt [1989] Plant Physiol 91: 1179-1187; F.X. Cunningham, Jr., R.J. Dennenberg, P.A. Jursinic, E. Gantt [1990] Plant Physiol 93: 888-895) and with measurements of photosynthetic capacity. Pmax, the light-saturated rate of photosynthesis on a chlorophyll (Chl) basis, increased more than 4-fold with increase in growth irradiance from 6 to 280 µeinsteins·m–2·s–1. Amounts of ferredoxin-NADP+ reductase, ribulose-1,5-bisphosphate carboxylase, and cytochrome f increased in parallel with Pmax, whereas numbers of the light-harvesting complexes (photosystem [PS] I, PSII, and phycobilisomes) changed little, and ATP synthase increased 7-fold relative to Chl. The calculated minimal turnover time for PSII under the highest irradiance, 5 ms, was thus about 4-fold faster than that calculated for cultures grown under the lowest irradiance (19 ms). A change in the spectral composition of the growth light (irradiance kept constant at 15 µeinsteins·m–2·s–1) from green (absorbed predominantly by the phycobilisome antenna of PSII) to red (absorbed primarily by the Chl antenna of PSI) had little effect on the amounts of ribulose-1,5-bisphosphate carboxylase, ATP synthase, and phycobilisomes on a Chl, protein, or thylakoid area basis. However, the number of PSI centers declined by 40%, cytochrome f increased by 40%, and both PSII and ferredoxin-NADP+ reductase increased approximately 3-fold on a thylakoid area basis. The substantial increase in ferredoxin-NADP+ reductase under PSI light is inconsistent with a PSI-mediated reduction of NADP as the sole function of this enzyme. Our results demonstrate a high degree of plasticity in content and composition of thylakoid membranes of P. cruentum.


1 This research was supported in part by grant No. DE-FG05-90ER20007 from the U.S. Department of Energy.




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Copyright © 1992 by the American Society of Plant Biologists