期刊论文详细信息
FEBS Letters
The reactivity of hydrazine with photosystem II strongly depends on the redox state of the water oxidizing system
Renger, G.1  Messinger, J.1 
[1] Max Volmer Institut für Biophysikalische und Physikalische Chemie der Technischen Universität, Straße des 17. Juni 135, D 1000 Berlin, Germany
关键词: Photosystem II;    Water oxidation;    Si-state lifetimes;    Hydrazine;    Hydroxylamine;   
DOI  :  10.1016/0014-5793(90)80829-8
学科分类:生物化学/生物物理
来源: John Wiley & Sons Ltd.
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【 摘 要 】

The decay kinetics of the redox states S2 and S3 of the water-oxidizing enzyme have been analyzed in isolated spinach thylakoids in the absence and presence of the exogenous reductant hydrazine. In control samples without NH2NH2 a biphasic decay is observed. The rapid decline of S2 and S3 with yD as reductant exhibits practically the same kinetics with t 1/2 = 6-7 s at pH = 7.2 and 7°C. The slow reduction (order of 5-10 min at 7°C) of S2 and S3 with endogenous electron donors other than yD is about twice as fast for S2 as for S3 under these conditions. In contrast, the hydrazine-induced reductive shifts of the formal redox states Si (i = 0⋯3) are characterized by a totally different kinetic pattern: (a) at 1 mMNH2NH2 and incubation on ice the decay of S2 is estimated to be at least 25 times faster (t 1/2⩽0.4 min) than the corresponding reaction of S3 (t 1/2≈13 min); (b) the NH2NH2-induced decay of S2 is even slower (about twice) than the transformation of S1 into the formal redox state ‘S−1’ (t 1/2≈6 min), which gives rise to the two-digit phase shift of the oxygen-yield pattern induced by a flash train in dark adapted thylakoids. (c) the NH2NH2-induced transformation S0→‘S−2’ [Renger, Messinger and Hanssum (1990) in: Curr. Res. Photosynth. (Baltscheffsky, M., ed). Vol. 1, pp. 845-848, Kluwer, Dordrecht] is about three times faster (t 1/2≈ min) than the reaction. Based on these results, the following dependence on the redox state Si of the reactivity towards NH2NH2 is obtained: S3 < S1 < S0 ⪡ S2. The implications of this surprising order of reactivity are discussed.

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