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巴氏芽孢梭菌铁氧化还原蛋白中[4Fe-4S]2+、[4Fe-4Se]2+及混合(S,Se)簇的表征:一项共振拉曼研究

Characterization of [4Fe-4S]2+, [4Fe-4Se]2+ and hybrid (S, Se) clusters in Clostridium pasteurianum ferredoxin. A resonance Raman study.

作者信息

Moulis J M, Meyer J, Lutz M

出版信息

Biochem J. 1984 May 1;219(3):829-32. doi: 10.1042/bj2190829.

Abstract

Resonance Raman spectra of native 2[4Fe-4S] ferredoxin from Clostridium pasteurianum and of its selenium-substituted analogue 2[4Fe-4Se] are compared. The experimental conditions used in this study included low temperature (approx. 25K) and the absence of a glass sample cell, thus ensuring high signal-to-noise ratios. The spectra of the 2[4Fe-4S] and 2[4Fe-4Se] ferredoxins display similar numbers of bands, but the resonance Raman patterns differ largely, except for two bands observed at 353 cm-1 and 365 cm-1 in spectra of the native ferredoxin, which are only moderately shifted upon S----Se substitution and are attributed to Fe-S(cysteine) stretching modes. The activities of the latter modes, enhanced by 457.9 nm excitation, are nearly equal in both ferredoxins. These data were used to demonstrate the presence of hybrid clusters [4Fe-(4-n)S-nSe] (n = 1, 2, 3) in a ferredoxin the active sites of which had been reconstituted in the presence of both S and Se.

摘要

对来自巴氏芽孢杆菌的天然2[4Fe-4S]铁氧化还原蛋白及其硒取代类似物2[4Fe-4Se]的共振拉曼光谱进行了比较。本研究中使用的实验条件包括低温(约25K)且不存在玻璃样品池,从而确保了高信噪比。2[4Fe-4S]和2[4Fe-4Se]铁氧化还原蛋白的光谱显示出相似数量的谱带,但共振拉曼模式差异很大,除了在天然铁氧化还原蛋白光谱中在353 cm-1和365 cm-1处观察到的两条谱带,它们在S----Se取代时仅发生适度位移,且归因于Fe-S(半胱氨酸)伸缩模式。后一种模式的活性在457.9 nm激发下增强,在两种铁氧化还原蛋白中几乎相等。这些数据被用于证明在一种铁氧化还原蛋白中存在杂化簇[4Fe-(4-n)S-nSe](n = 1, 2, 3),该铁氧化还原蛋白的活性位点是在S和Se同时存在的情况下重构的。

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