Volume 71, Issue 1 pp. 103-109
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Cytochrome b6/f Complex as an Indigenous Photodynamic Generator of Singlet Oxygen in Thylakoid Membranes

Hwa-Jin Suh

Hwa-Jin Suh

Department of Agricultural Chemistry, College of Agriculture and Life Sciences, Seoul National University, Suwon, Korea

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Chang Sook Kim

Chang Sook Kim

Department of Agricultural Chemistry, College of Agriculture and Life Sciences, Seoul National University, Suwon, Korea

Current address: Harmful Algal Biology Division, National Fisheries Research and Development Institute, Pusan, 619-900, Korea.

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Jin Jung

Corresponding Author

Jin Jung

Department of Agricultural Chemistry, College of Agriculture and Life Sciences, Seoul National University, Suwon, Korea

*To whom correspondence should be addressed at: Department of Agricultural Chemistry, College of Agriculture and Life Sciences, Seoul National University, Suwon, 441-744, Korea. Fax: +82 331 293 8608; [email protected]Search for more papers by this author
First published: 01 May 2007
Citations: 7

ABSTRACT

Possible association of photodynamic sensitization by cytochrome b6/f complex (cyt b6/f) via singlet oxygen (1O2) mechanism with photoinhibition damage to photosystem II (PS II) was studied using such subthylakoid preparations as photosystem I (PS I) particles, PS II core complex and cyt b6/f from spinach leaves. Upon exposure to bright light, PS II core complex lost photosynthetic electron transport activity to a certain extent, whose spectral dependence implied that pheophytin a is likely involved in photoinactivation of PS II core complex in itself. The presence of PS I particles exerted virtually no effect on PS II core photoinactivation. However, the inclusion of cyt b6/f in samples resulted in a marked exacerbation of the photoinactivation, particularly in UV-A and blue light. Such effect of cyt b6/f was suppressed by azide and enhanced by the medium deuteration. Photogeneration of 1O2 from cyt b6/f was confirmed by ESR and spectrophotometry, chemically trapping 1O2. Action spectra for both 1O2 photoproduction and PS II core photoinactivation by cyt b6/f bore a close resemblance to each other, seemingly carrying the absorption characteristics of the Rieske Fe-S protein. A complex deficient in the Rieske protein prepared from intact cyt b6/f showed virtually no generation of 1O2 in light, whereas an efficient photoformation of 1O2 was seen in the Rieske protein preparation. The results suggest that cyt b6/f, rather specifically the Rieske center, may play a prominent role in photoinhibition processes through type II photosensitization in thylakoids.

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