首页> 外文期刊>Biochemistry >X-ray absorption spectroscopy on layered photosystem II membrane particles suggests manganese-centered oxidation of the oxygen-evolving complex for the S-0-S-1, S-1-S-2, and S-2-S-3 transitions of the water oxidation cycle
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X-ray absorption spectroscopy on layered photosystem II membrane particles suggests manganese-centered oxidation of the oxygen-evolving complex for the S-0-S-1, S-1-S-2, and S-2-S-3 transitions of the water oxidation cycle

机译:层状光系统II膜颗粒上的X射线吸收光谱表明,对于S-0-S-1,S-1-S-2和S-2-S-3跃迁,以锰为中心的氧释放复合物氧化水的氧化循环

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By application of microsecond light flashes the oxygen-evolving complex (OEC) was driven through its functional cycle, the S-state cycle. The S-state population distribution obtained by the application of n flashes (n = 0 ... 6) was determined by analysis of EPR spectra; Mn K-edge X-ray absorption spectra were collected. Taking into consideration the likely statistical error in the data and the variability stemming from the use of three different approaches for the determination of edge positions, we obtained an upshift of the edge position by 0.8-1.5, 0.5-0.9, and 0.6-1.3 eV for the S-0-S-1, S-1-S-2, and S-2-S-3 transitions, respectively, and a downshift by 2.3-3.1 eV for the S-3-S-0 transition. These results are highly suggestive of Mn oxidation state changes for all four S-state transitions. In the So-state spectrum, a clearly resolved shoulder in the X-ray spectrum around 6555 eV points toward the presence of Mn(II). We propose that photosynthetic oxygen evolution involves cycling of the photosystem II manganese complex through four distinct oxidation states of this tetranuclear complex: Mn(II)-Mn(III) -Mn(IV)(2) in the So-state, Mn(III)(2)-Mn(IV)(2) in the S-1-state, Mn(III)(1)-Mn(IV)(3) in the S-2-state, and Mn(IV)(4) in the S-3-state. [References: 35]
机译:通过施加微秒的闪光,氧气释放复合物(OEC)被驱动通过其功能循环,即S状态循环。通过EPR光谱分析确定通过应用n次闪光(n = 0 ... 6)获得的S态总体分布;收集Mn K边缘X射线吸收光谱。考虑到数据中可能存在的统计误差以及由于使用三种不同方法确定边缘位置而产生的可变性,我们将边缘位置上移了0.8-1.5、0.5-0.9和0.6-1.3 eV分别针对S-0-S-1,S-1-S-2和S-2-S-3过渡,而对于S-3-S-0过渡则降档2.3-3.1 eV。这些结果高度暗示了所有四个S-态转变的Mn氧化态变化。在So-state光谱中,在6555 eV附近的X射线光谱中清晰分辨的谱线指向Mn(II)的存在。我们提出光合作用的氧逸出涉及光系统II锰配合物通过该四核配合物的四个不同氧化态的循环:Mn(II)-Mn(III)-Mn(IV)(2)处于So状态,Mn(III) S-1状态的)(2)-Mn(IV)(2),S-2-状态的Mn(III)(1)-Mn(IV)(3)和Mn(IV)(4 )处于S-3-状态。 [参考:35]

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