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Calcium induces binding and formation of a spin-coupled dimanganese(II,II) center in the apo-water oxidation complex of photosystem II as precursor to the functional tetra-Mn/Ca cluster.钙在光系统II的脱辅基水氧化复合物中诱导自旋耦合的二价锰(II,II)中心的结合与形成,作为功能性四锰/钙簇的前体。
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Structure and orientation of the oxygen-evolving manganese complex of green algae and higher plants investigated by X-ray absorption linear dichroism spectroscopy on oriented photosystem II membrane particles.通过对定向光系统II膜颗粒进行X射线吸收线性二色光谱研究绿藻和高等植物中析氧锰复合物的结构与取向
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本文引用的文献

1
Strontium EXAFS Reveals the Proximity of Calcium to the Manganese Cluster of Oxygen-Evolving Photosystem II.锶扩展X射线吸收精细结构谱揭示了钙与放氧光系统II的锰簇的接近程度。
J Phys Chem B. 1998 Oct 15;102(42):8248-8256. doi: 10.1021/jp981658q.
2
Structural Effects of Calcium Depletion on the Manganese Cluster of Photosystem II: Determination by X-ray Absorption Spectroscopy.钙缺失对光系统II锰簇的结构影响:通过X射线吸收光谱法测定
J Phys Chem B. 1998;102:8257-8265. doi: 10.1021/jp981668r.
3
The effect of chloride on the thermal inactivation of oxygen evolution.氯离子对氧释放的热失活的影响。
Photosynth Res. 1988 Jun;16(3):261-76. doi: 10.1007/BF00028844.
4
Photoproduction of hydrogen peroxide in Photosystem II membrane fragments: A comparison of four signals.光系统 II 膜片段中过氧化氢的光生产:四种信号的比较。
Photosynth Res. 1993 Jan;38(3):409-16. doi: 10.1007/BF00046768.
5
Global target analysis of picosecond chlorophyll fluorescence kinetics from pea chloroplasts: A new approach to the characterization of the primary processes in photosystem II alpha- and beta-units.全局分析皮秒叶绿素荧光动力学从豌豆叶绿体:一个新的方法来表征的主要过程在光系统 II 的阿尔法和贝塔单位。
Biophys J. 1992 May;61(5):1147-63. doi: 10.1016/s0006-3495(92)81924-0.
6
Site-directed mutagenesis in photosystem II of the cyanobacterium Synechocystis sp. PCC 6803: Donor D is a tyrosine residue in the D2 protein.在集胞藻 PCC 6803 的光系统 II 中进行定点突变:供体 D 是 D2 蛋白中的一个酪氨酸残基。
Proc Natl Acad Sci U S A. 1988 Nov;85(22):8477-81. doi: 10.1073/pnas.85.22.8477.
7
Stoichiometry, inhibitor sensitivity, and organization of manganese associated with photosynthetic oxygen evolution.与光合作用放氧相关的锰的化学计量、抑制剂敏感性和组织。
Proc Natl Acad Sci U S A. 1981 Dec;78(12):7507-11. doi: 10.1073/pnas.78.12.7507.
8
Chlorophyll fluorescence transients of Photosystem II membrane particles as a tool for studying photosynthetic oxygen evolution.光系统II膜颗粒的叶绿素荧光瞬变作为研究光合放氧的工具。
Photosynth Res. 2000;65(1):41-52. doi: 10.1023/A:1006469809812.
9
First steps towards time-resolved BioXAS at room temperature: state transitions of the manganese complex of oxygenic photosynthesis.室温下时间分辨生物X射线吸收光谱的初步进展:光合放氧锰配合物的状态转变
J Synchrotron Radiat. 2002 Sep 1;9(Pt 5):304-8. doi: 10.1107/s0909049502012955. Epub 2002 Aug 31.
10
An evaluation of structural models for the photosynthetic water-oxidizing complex derived from spectroscopic and X-ray diffraction signatures.基于光谱和X射线衍射特征对光合水氧化复合物结构模型的评估。
J Biol Inorg Chem. 2002 Jan;7(1-2):2-22. doi: 10.1007/s00775-001-0305-3. Epub 2001 Nov 8.

光系统II的四锰配合物响应温度跃升逐步转变为双核Mn2(μ -O)2配合物:采用X射线吸收光谱的时间分辨结构研究。

Stepwise transition of the tetra-manganese complex of photosystem II to a binuclear Mn2(micro -O)2 complex in response to a temperature jump: a time-resolved structural investigation employing x-ray absorption spectroscopy.

作者信息

Pospísil Pavel, Michael Haumann, Dittmer Jens, Solé V Armando, Dau Holger

机构信息

Freie Universität Berlin, FB Physik, D-14195 Berlin, Germany.

出版信息

Biophys J. 2003 Feb;84(2 Pt 1):1370-86. doi: 10.1016/s0006-3495(03)74952-2.

DOI:10.1016/s0006-3495(03)74952-2
PMID:12547817
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1302713/
Abstract

In oxygenic photosynthesis, water is oxidized at a protein-cofactor complex comprising four Mn atoms and, presumably, one calcium. Using multilayers of Photosystem II membrane particles, we investigated the time course of the disassembly of the Mn complex initiated by a temperature jump from 25 degrees C to 47 degrees C and terminated by rapid cooling after distinct heating periods. We monitored polarographically the oxygen-evolution activity, the amount of the Y(D)(ox) radical and of released Mn(2+) by EPR spectroscopy, and the structure of the Mn complex by x-ray absorption spectroscopy (XAS, EXAFS). Using a novel approach to analyze time-resolved EXAFS data, we identify three distinct phases of the disassembly process: (1) Loss of the oxygen-evolution activity and reduction of Y(D)(ox) occur simultaneously (k(1) = 1.0 min(-1)). EXAFS spectra reveal the concomitant loss of an absorber-backscatterer interaction between heavy atoms separated by approximately 3.3 A, possibly related to Ca release. (2) Subsequently, two Mn(III) or Mn(IV) ions seemingly separated by approximately 2.7 A in the native complex are reduced to Mn(II) and released (k(2) = 0.18 min(-1)). The x-ray absorption spectroscopy data is highly suggestive that the two unreleased Mn ions form a di- micro -oxo bridged Mn(III)(2) complex. (3) Finally, the tightly-bound Mn(2)( micro -O)(2) unit is slowly reduced and released (k(3) = 0.014 min(-1)).

摘要

在有氧光合作用中,水在一种包含四个锰原子以及大概一个钙原子的蛋白质 - 辅因子复合物上被氧化。我们使用多层光系统II膜颗粒,研究了从25摄氏度温度跃升至47摄氏度引发的锰复合物分解的时间进程,并在不同加热时间段后通过快速冷却终止该进程。我们通过极谱法监测氧气释放活性,通过电子顺磁共振光谱法监测Y(D)(ox)自由基和释放的Mn(2+)的量,并通过X射线吸收光谱法(XAS、EXAFS)监测锰复合物的结构。使用一种新颖的方法分析时间分辨EXAFS数据,我们确定了分解过程的三个不同阶段:(1) 氧气释放活性的丧失和Y(D)(ox)的还原同时发生(k(1) = 1.0 min(-1))。EXAFS光谱揭示了由大约3.3 Å分开的重原子之间吸收体 - 背散射体相互作用的同时丧失,这可能与钙的释放有关。(2) 随后,天然复合物中似乎由大约2.7 Å分开的两个Mn(III)或Mn(IV)离子被还原为Mn(II)并释放(k(2) = 0.18 min(-1))。X射线吸收光谱数据强烈表明,两个未释放的锰离子形成了一个双 - μ - 氧桥连的Mn(III)₂复合物。(3) 最后,紧密结合的Mn₂(μ - O)₂单元被缓慢还原并释放(k(3) = 0.014 min(-1))。