Please use this identifier to cite or link to this item: https://doi.org/10.1007/BF00408244
Title: The kinetics of photoinhibition and its recovery in the red alga Porphyridium cruentum
Authors: Lee, Y.K. 
Vonshak, A.
Keywords: Biomass
O2 evolution
Photoinhibition
Photosynthesis
Porphyridium cruentum
Recovery
Issue Date: Oct-1988
Citation: Lee, Y.K., Vonshak, A. (1988-10). The kinetics of photoinhibition and its recovery in the red alga Porphyridium cruentum. Archives of Microbiology 150 (6) : 529-533. ScholarBank@NUS Repository. https://doi.org/10.1007/BF00408244
Abstract: When Porphyridium cruentum cells were illuminated with high fluence rate between 1900 and 4800 μmol photons m-2s-1, a decrease in the photosynthetic activity of the cells was observed. Within the time frame of 20 min, and under the fluence rates studied, the sum of photons to be absorbed by cells (mg of chlorophyll (Chl), sufficient to initiate photoinhibition was calculated to be 9235.8 μmol. The minimal specific light absorption rate to initiate photoinhibition in P. cruentum ranges between 2.29 and 4.26 μmol photons s-1 mg-1 chl.a. There was a linear relationship between the specific rate of photoinhibition and the specific light absorption rate. A photon number of 2.56×104 μmol mg-1 chl.a photoinhibited photosynthesis instantaneously. At 15°C, no photoinhibitory effect was observed at 2300 μmol photons m-2 s-1 even after 45 min of illumination. At the other extreme of 35°C, 84% inhibition of photosynthetic activity was observed within 10 min of exposure to 2300 μmol photons m-2 s-1. Between 20 and 30°C, the photoinhibitory effect was comparable. Photoinhibited P. cruentum cells recovered readily when transferred to low light (90 μmol photons m-2 s-1) and darkness, and the specific rate of recovery was independent of the light intensity to which the cells were exposed, during the photoinhibitory treatment. © 1988 Springer-Verlag.
Source Title: Archives of Microbiology
URI: http://scholarbank.nus.edu.sg/handle/10635/130069
ISSN: 03028933
DOI: 10.1007/BF00408244
Appears in Collections:Staff Publications

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