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Published on October 1, 2004; 10.1104/pp.104.047712

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Received June 7, 2004
Returned for revision July 5, 2004
Accepted July 5, 2004

Activation of Photosynthesis and Resistance to Photoinhibition in Cyanobacteria within Biological Desert Crust

Yariv Harel , Itzhak Ohad , and Aaron Kaplan *

Department of Plant and Environmental Sciences, The Hebrew University of Jerusalem, Jerusalem, 91014, Israel; Minerva Arid Ecosystems Research Center, The Hebrew University of Jerusalem, Jerusalem, 91014, Israel
Department of Biological Chemistry, The Hebrew University of Jerusalem, Jerusalem, 91014, Israel; Minerva, Avron-Evenari Center of Photosynthesis Research, The Hebrew University of Jerusalem, Jerusalem, 91014, Israel
Department of Plant and Environmental Sciences, The Hebrew University of Jerusalem, Jerusalem, 91014, Israel; Minerva Arid Ecosystems Research Center, The Hebrew University of Jerusalem, Jerusalem, 91014, Israel; Minerva, Avron-Evenari Center of Photosynthesis Research, The Hebrew University of Jerusalem, Jerusalem, 91014, Israel

* Corresponding author; email: aaronka{at}vms.huji.ac.il.

Filamentous cyanobacteria are the main primary producers in biological desert sand crusts. The cells are exposed to extreme environmental conditions including temperature, light, and diurnal desiccation/rehydration cycles. We have studied the kinetics of activation of photosynthesis during rehydration of the cyanobacteria, primarily Microcoleus sp., within crust samples collected in the Negev desert, Israel. We also investigated their susceptibility to photoinhibition. Activation of the photosynthetic apparatus, measured by fluorescence kinetics, thermoluminescence, and low temperature fluorescence emission spectra, did not require de novo protein synthesis. Over 50% of the photosystem II (PSII) activity, assembled phycobilisomes, and photosystem I (PSI) antennae were detected within less than 5 min of rehydration. Energy transfer to PSII and PSI by the respective antennae was fully established within 10 to 20 min of rehydration. The activation of a fraction of PSII population (about 20%-30%) was light and temperature-dependent but did not require electron flow to plastoquinone [was not inhibited by 3-(3,4-dichlorophenyl)-1,1-dimethylurea]. The cyanobacteria within the crusts are remarkably resistant to photoinhibition even in the absence of protein synthesis. The rate of PSII repair increased with light intensity and with time of exposure. Consequently, the extent of photoinhibition in high-light-exposed crusts reached a constant, relatively low, level. This is in contrast to model organisms such as Synechocystis sp. strain PCC 6803 where PSII activity declined continuously over the entire exposure to high illumination. Ability of the crust's organisms to rapidly activate photosynthesis upon rehydration and withstand photoinhibition under high light intensity may partly explain their ability to survive in this ecosystem.




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