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Role of Protons in Photosynthetic Water Oxidation: pH Influence on the Rate Constants of the S-state Transitions and Hypotheses on the S2→S3 Transition

机译:质子在光合水氧化中的作用:pH对S状态转变速率常数和S2→S3转变假设的影响

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The mode of proton relocation from the wateroxidizing Mn complex of Photosystem Ⅱ (PSⅡ) toward the aqueous phase is of key importance in photosynthetic water oxidation. An adequate description of the interrelation of proton and electron removal from the Mn complex is still lacking. We reinvestigate the influence of the pH on the rate constants of the redox transitions of the Mn complex (S-state transitions). For high-activity PSⅡ membrane particles from spinach, near-UV absorption transients (at 360 nm) induced by trains of ns-Laser flashes were analyzed. To obtain the rate constants of the 'pure' S-state transitions, a stringent deconvolution of the raw transients was carried out. The transients of the S1→S2 and S2→S3 transitions exhibit mono-exponential behavior whereas the transients of the 'S3→S0 + O2' transition display a lag-phase behavior that is assignable to formation of a reaction intermediate by deprotonation. The rate constants of the electron transfer (ET) in the S1→S2 and S3→S0 transitions exhibit a negligible pHdependence only. The rate constant of the S2→S3 transition decreases below pH 6 significantly, but clearly less than those of the lag-phase in the S3 →S0 transition. Two models for the coupling of electron and proton transfer in the S2→S3 transition are discussed.
机译:质子从光系统Ⅱ(PSⅡ)的水氧化锰配合物向水相的重定位模式对光合水的氧化至关重要。仍然缺乏对质子和电子从Mn络合物中去除的相互关系的充分描述。我们重新研究了pH对Mn配合物的氧化还原转变速率常数(S态转变)的影响。对于菠菜中的高活性PSⅡ膜颗粒,分析了一系列ns-Laser闪光引起的近紫外吸收瞬变(在360 nm处)。为了获得“纯” S状态跃迁的速率常数,对原始瞬变进行了严格的反卷积。 S1→S2和S2→S3跃迁的瞬态表现出单指数行为,而“ S3→S0 + O2”跃迁的瞬态表现出滞后行为,该行为可归因于通过去质子化形成反应中间体。 S1→S2和S3→S0跃迁中电子转移(ET)的速率常数仅表现出可忽略的pH依赖性。在pH 6以下,S2→S3跃迁的速率常数显着降低,但明显小于S3→S0跃迁的滞后阶段的速率常数。讨论了在S2→S3跃迁中电子和质子传递耦合的两个模型。

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