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Probing the functional role of Ca2+ in the oxygen-evolving complex of photosystem II by metal ion inhibition.

机译:金属离子抑制探测Ca2 +在光系统II的氧化复合物中的功能作用。

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Photosynthetic oxygen evolution in photosystem II (PSII) takes place in the oxygen-evolving complex (OEC) that is comprised of a tetranuclear manganese cluster (Mn4), a redox-active tyrosine residue (YZ), and Ca2+ and Cl- cofactors. The OEC is successively oxidized by the absorption of 4 quanta of light that results in the oxidation of water and the release of O2. Ca2+ is an essential cofactor in the water-oxidation reaction, as its depletion causes the loss of the oxygen-evolution activity in PSII. In recent X-ray crystal structures, Ca2+ has been revealed to be associated with the Mn4 cluster of PSII. Although several mechanisms have been proposed for the water-oxidation reaction of PSII, the role of Ca2+ in oxygen evolution remains unclear. In this study, we probe the role of Ca2+ in oxygen evolution by monitoring the S1 to S2 state transition in PSII membranes and PSII core complexes upon inhibition of oxygen evolution by Dy3+, Cu2+, and Cd2+ ions. By using a cation-exchange procedure in which Ca2+is not removed prior to addition of the studied cations, we achieve a high degree of reversible inhibition of PSII membranes and PSII core complexes by Dy3+, Cu2+, and Cd2+ ions. EPR spectroscopy is used to quantitate the number of bound Dy3+ and Cu2+ ions per PSII center and to determine the proximity of Dy3+ to other paramagnetic centers in PSII. We observe, for the first time, the S2 state multiline electron paramagnetic resonance (EPR) signal in Dy3+- and Cd2+-inhibited PSII and conclude that the Ca2+ cofactor is not specifically required for the S1 to S2 state transition of PSII. This observation provides direct support for the proposal that Ca2+ plays a structural role in the early S-state transitions, which can be fulfilled by other cations of similar ionic radius, and that the functional role of Ca2+ to activate water in the O-O bond-forming reaction that occurs in the final step of the S state cycle can only be fulfilled by Ca2+ and Sr2+, which have similar Lewis acidities.
机译:照相氧化物II(PSII)中的光合氧量进化发生在氧化复合物(OEC)中,该复合物(OEC)由四核锰簇(MN4),氧化还原活性酪氨酸残基(YZ)和CA2 +和CL-辅因子组成。通过吸收4光连续地氧化OEC,这导致水的氧化和O 2的释放。 CA2 +是水氧化反应中的必需辅助因子,因为其耗竭导致PSII中的氧化活性丧失。在最近的X射线晶体结构中,已揭示CA2 +与PSII的MN4簇相关。虽然已经提出了MSII的水氧化反应的几种机制,但是Ca2 +在氧进化中的作用仍然尚不清楚。在这项研究中,通过在抑制DY3 +,Cu2 +和CD2 +离子的氧气蒸煮后,通过监测S1至S2状态转变,探讨Ca2 +在氧气蒸发中的作用。通过使用在添加研究之前未除去CA2 +的阳离子交换程序,通过DY3 +,Cu2 +和CD2 +离子达到高度可逆抑制Psii膜和Psii核心复合物的可逆抑制。 EPR光谱法用于定量每PSII中心的结合DY3 +和Cu2 +离子的数量,并确定PSII中的DY3 +的邻近达到的副啮色中心。我们首次观察到Dy3 + - 和CD2 +----incibited PSII中的S2状态多线电子顺磁共振(EPR)信号并得出结论,S1至S2的PSII状态过渡没有特别需要CA2 + Cofactor。该观察结果为该提议提供了直接支持,即CA2 +在早期的S状态转变中发挥结构作用,其可以由类似离子半径的其他阳离子实现,并且Ca2 +在OO键合中激活水的功能作用在S状态循环的最终步骤中发生的反应只能通过Ca2 +和Sr2 +实现,所述+和SR2 +具有类似的路易斯酸性。

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