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[镍铁]氢化酶通过电子、氢气和一氧化碳激活的机制。

The mechanism of activation of a [NiFe]-hydrogenase by electrons, hydrogen, and carbon monoxide.

作者信息

Lamle Sophie E, Albracht Simon P J, Armstrong Fraser A

机构信息

Department of Chemistry, Inorganic Chemistry Laboratory, Oxford University, South Parks Road, Oxford OX1 3QR, England.

出版信息

J Am Chem Soc. 2005 May 11;127(18):6595-604. doi: 10.1021/ja0424934.

Abstract

Activation of the oxidized inactive state (termed Unready or Ni(u)) of the [NiFe]-hydrogenase from Allochromatium vinosum requires removal of an unidentified oxidizing entity [O], produced by partial reduction of O(2). Dynamic electrochemical kinetic studies, subjecting enzyme molecules on an electrode to sequences of potential steps and gas injections, establish the order of events in an otherwise complex sequence of reactions that involves more than one intermediate retaining [O] or its redox equivalent; fast and reversible electron transfer precedes the rate-determining step which is followed by a reaction with H(2), or the inhibitor CO, that renders the reductive activation process irreversible.

摘要

来自嗜酒色杆菌的[NiFe]-氢化酶的氧化非活性状态(称为未就绪或Ni(u))的激活需要去除一个由O₂部分还原产生的未知氧化实体[O]。动态电化学动力学研究通过对电极上的酶分子施加电位阶跃和气体注入序列,确定了一个原本复杂的反应序列中的事件顺序,该反应序列涉及不止一种保留[O]或其氧化还原等价物的中间体;快速且可逆的电子转移先于速率决定步骤,随后是与H₂或抑制剂CO的反应,这使得还原激活过程不可逆。

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