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通过取向光系统II膜的电子顺磁共振光谱探测光合放氧复合体的锰位点:g = 4和g = 2多线信号

The manganese site of the photosynthetic oxygen-evolving complex probed by EPR spectroscopy of oriented photosystem II membranes: the g = 4 and g = 2 multiline signals.

作者信息

Kim D H, Britt R D, Klein M P, Sauer K

机构信息

Chemical Biodynamics Division, Lawrence Berkeley Laboratory, University of California, Berkeley 94720.

出版信息

Biochemistry. 1992 Jan 21;31(2):541-7. doi: 10.1021/bi00117a034.

DOI:10.1021/bi00117a034
PMID:1310041
Abstract

The g = 4 and g = 2 multiline EPR signals arising from the Mn cluster of the photosynthetic oxygen-evolving complex (OEC) in the S2 state were studied in preparations of oriented photosystem II (PSII) membranes. The ammonia-modified forms of these two signals were also examined. The g = 4 signal obtained in oriented PSII membranes treated with NH4Cl at pH 7.5 displays at least 16 partially resolved Mn hyperfine transitions with a regular spacing of 36 G [Kim, D.H., Britt, R.D., Klein, M.P., & Sauer, K. (1990) J. Am. Chem. Soc. 112, 9389-9391]. The observation of this g = 4 "multiline signal" provides strong spectral evidence for a tetranuclear Mn origin for the g = 4 signal and is strongly suggestive of a model in which different spin state configurations of a single exchange-coupled Mn cluster give rise to the g = 4 and g = 2 multiline signals. A simulation shows the observed spectrum to be consistent with an S = 3/2 or S = 5/2 state of a tetranuclear Mn complex. The resolution of hyperfine structure on the NH3-modified g = 4 signal is strongly dependent on sample orientation, with no resolved hyperfine structure when the membrane normal is oriented perpendicular to the applied magnetic field. The dramatic NH3-induced changes in the g = 4 signal resolved in the spectra of oriented samples are suggestive that NH3 binding at the Cl- site of the OEC may represent direct coordination of NH3 to the Mn cluster.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在定向光合系统II(PSII)膜制剂中,研究了处于S2状态的光合放氧复合体(OEC)的Mn簇产生的g = 4和g = 2多线EPR信号。还研究了这两种信号的氨修饰形式。在pH 7.5用NH4Cl处理的定向PSII膜中获得的g = 4信号显示至少16个部分分辨的Mn超精细跃迁,规则间距为36 G [Kim, D.H., Britt, R.D., Klein, M.P., & Sauer, K. (1990) J. Am. Chem. Soc. 112, 9389-9391]。对这种g = 4“多线信号”的观察为g = 4信号的四核Mn起源提供了强有力的光谱证据,并强烈暗示了一种模型,即单个交换耦合Mn簇的不同自旋态构型产生了g = 4和g = 2多线信号。模拟表明观察到的光谱与四核Mn配合物的S = 3/2或S = 5/2状态一致。NH3修饰的g = 4信号上超精细结构的分辨率强烈依赖于样品取向,当膜法线垂直于外加磁场取向时,没有分辨出超精细结构。在定向样品光谱中分辨出的g = 4信号中NH3诱导的显著变化表明,OEC的Cl-位点处的NH3结合可能代表NH3与Mn簇的直接配位。(摘要截短于250字)

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