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对光系统II锰簇氮配位的多频电子自旋回波包络调制研究。

Multifrequency electron spin-echo envelope modulation studies of nitrogen ligation to the manganese cluster of photosystem II.

作者信息

Yeagle Gregory J, Gilchrist M Lane, Walker Lee M, Debus Richard J, Britt R David

机构信息

Department of Chemistry, University of California, Davis, 1 Shields Avenue, Davis, CA 95616, USA.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2008 Mar 27;363(1494):1157-66; discussion 1166. doi: 10.1098/rstb.2007.2211.

DOI:10.1098/rstb.2007.2211
PMID:17954435
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2614105/
Abstract

The CalEPR Center at UC-Davis (http://brittepr.ucdavis.edu) is equipped with five research grade electron paramagnetic resonance (EPR) instruments operating at various excitation frequencies between 8 and 130GHz. Of particular note for this RSC meeting are two pulsed EPR spectrometers working at the intermediate microwave frequencies of 31 and 35GHz. Previous lower frequency electron spin-echo envelope modulation (ESEEM) studies indicated that histidine nitrogen is electronically coupled to the Mn cluster in the S2 state of photosystem II (PSII). However, the amplitude and resolution of the spectra were relatively poor at these low frequencies, precluding any in-depth analysis of the electronic structure properties of this closely associated nitrogen nucleus. With the intermediate frequency instruments, we are much closer to the 'exact cancellation' limit, which optimizes ESEEM spectra for hyperfine-coupled nuclei such as 14N and 15N. Herein, we report the results from ESEEM studies of both 14N- and 15N-labelled PSII at these two frequencies. Spectral simulations were constrained by both isotope datasets at both frequencies, with a focus on high-resolution spectral examination of the histidine ligation to the Mn cluster in the S2 state.

摘要

加州大学戴维斯分校的CalEPR中心(http://brittepr.ucdavis.edu)配备了五台研究级电子顺磁共振(EPR)仪器,它们在8至130GHz的不同激发频率下运行。在本次皇家化学学会会议上特别值得一提的是两台工作在31和35GHz中间微波频率的脉冲EPR光谱仪。先前较低频率的电子自旋回波包络调制(ESEEM)研究表明,在光系统II(PSII)的S2状态下,组氨酸氮与锰簇存在电子耦合。然而,在这些低频下,光谱的幅度和分辨率相对较差,无法对这个紧密相关的氮原子核的电子结构性质进行任何深入分析。使用中频仪器,我们更接近“精确抵消”极限,这为诸如14N和15N等超精细耦合原子核优化了ESEEM光谱。在此,我们报告了在这两个频率下对14N和15N标记的PSII进行ESEEM研究的结果。光谱模拟受到两个频率下的同位素数据集的约束,重点是对S2状态下组氨酸与锰簇连接的高分辨率光谱检查。

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