4.5 Article

pH-dependent redox potential: how to use it correctly in the activation energy analysis

期刊

BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
卷 1604, 期 1, 页码 13-21

出版社

ELSEVIER
DOI: 10.1016/S0005-2728(03)00020-3

关键词

configurational free energy; activation energy; electron transfer; proton transfer; cytochrome bc(1) complex; Rieske protein

向作者/读者索取更多资源

The activation barrier (the activation free energy) for the reaction's elementary act proper does not depend on the presence of reactants outside the reaction complex. The barrier is determined directly by the concentration-independent configurational free energy. In the case of redox reactants with pH-dependent redox potential, only the pH-independent quantity, the configurational redox potential enters immediately into expression for activation energy. Some typical cases of such reactions have been discussed (e.g., simultaneous proton and electron detachment, acid dissociation followed by oxidation, dissociation after oxidation, and others). For these mechanisms, the algorithms for calculation of the configurational redox potential from the experimentally determined redox potentials have been described both for the data related to a dissolved reactant or to a prosthetic group of an enzyme. Some examples of pH-dependent enzymatic redox reactions, in particular for the Rieske iron-sulfur protein, have been discussed. (C) 2003 Elsevier Science B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据