Mechanism of inhibition and decoupling of oxygen evolution from electron transfer in photosystem II by fluoride, ammonia and acetate
Ca2+ extraction from oxygen-evolving complex (OEC) of photosystem II (PSII) is accompanied by decoupling of oxygen evolution/electron transfer processes [Semin et al. Photosynth. Res. 98 (2008) 235] and appearance of a broad EPR signal at g=2 (split “S3” signal) what can imply the relationship betwe...
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Veröffentlicht in: | Journal of photochemistry and photobiology. B, Biology Biology, 2016-05, Vol.158, p.145-153 |
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Sprache: | eng |
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Zusammenfassung: | Ca2+ extraction from oxygen-evolving complex (OEC) of photosystem II (PSII) is accompanied by decoupling of oxygen evolution/electron transfer processes [Semin et al. Photosynth. Res. 98 (2008) 235] and appearance of a broad EPR signal at g=2 (split “S3” signal) what can imply the relationship between these effects. Split signal have been observed not only in Ca-depleted PSII but also in PSII membranes treated by fluoride anions, sodium acetate, and NH4Cl. Here we investigated the question: can such compounds induce the decoupling effect during treatment of PSII like Ca2+ extraction does? We found that F−, sodium acetate, and NH4Cl inhibit O2 evolution in PSII membranes more effectively than the reduction of artificial electron acceptor 2,6-dichlorophenolindophenol, i.e. the action of these compounds is accompanied by decoupling of these processes in OEC. Similarity of effects observed after Ca2+ extraction and F−, CH3COO− or NH4Cl treatments suggests that these compounds can inactivate function of Ca2+. Such inactivation could originate from disturbance of the network of functionally active hydrogen bonds around OEC formed with participation of Ca2+. This inhibition effect is observed in the region of low concentration of inhibitors. Increasing of inhibitor concentration is accompanied by appearance of other sites of inhibition.
•Treatment of PSII by F−, NH4Cl, acetate results in appearance of split EPR signal and decoupling effect.•We imply that these inhibitors disturb the hydrogen bond network around Ca2+.•All investigated inhibitors have other inhibition sites at higher concentrations. |
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ISSN: | 1011-1344 1873-2682 |
DOI: | 10.1016/j.jphotobiol.2016.02.031 |