Stiefel E I
Proc Natl Acad Sci U S A. 1973 Apr;70(4):988-92. doi: 10.1073/pnas.70.4.988.
The reactions catalyzed by Mo enzymes each find the product differing from the substrate by two electrons and two protons (or some multiple thereof). The coordination chemistry of Mo suggests that there is a distinct relationship between acid-base and redox properties of Mo complexes, and that a coupled electron-proton transfer (to or from substrate) may be mediated by Mo in enzymes. Each of the Mo enzymes (nitrogenase, nitrate reductase, xanthine oxidase, aldehyde oxidase, and sulfite oxidase) is discussed; it is shown that a simple molecular mechanism embodying coupled proton-electron transfer can explain many key experimental observations. In view of this mechanism, the reasons for the use of Mo (from an evolutionary and chemical point of view) are discussed and other metals that may replace Mo are considered.
钼酶催化的反应中,每个反应的产物与底物相比,在电子和质子数量上都有两个单位的差异(或其倍数)。钼的配位化学表明,钼配合物的酸碱性质和氧化还原性质之间存在明显的关系,并且在酶中,钼可能介导了电子-质子的耦合转移(向底物或从底物转移)。本文讨论了每种钼酶(固氮酶、硝酸还原酶、黄嘌呤氧化酶、醛氧化酶和亚硫酸盐氧化酶);结果表明,一个体现质子-电子耦合转移的简单分子机制可以解释许多关键的实验观察结果。基于这一机制,从进化和化学的角度讨论了使用钼的原因,并考虑了可能替代钼的其他金属。