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底物与固氮酶的相互作用:铁与钼

Substrate interactions with nitrogenase: Fe versus Mo.

作者信息

Seefeldt Lance C, Dance Ian G, Dean Dennis R

机构信息

Department of Chemistry and Biochemistry, Utah State University, Logan, Utah 84332, USA.

出版信息

Biochemistry. 2004 Feb 17;43(6):1401-9. doi: 10.1021/bi036038g.

Abstract

Biological nitrogen reduction is catalyzed by a complex two-component metalloenzyme called nitrogenase. For the Mo-dependent enzyme, the site of substrate reduction is provided by a [7Fe-9S-Mo-X-homocitrate] metallocluster, where X is proposed to be an N atom. Recent progress with organometallic model compounds, theoretical calculations, and biochemical, kinetic, and biophysical studies on nitrogenase has led to the formulation of two opposing models of where N(2) or alternative substrates might bind during catalysis. One model involves substrate binding to the Mo atom, whereas the other model involves the participation of one or more Fe atoms located in the central region of the metallocluster. Recently gathered evidence that has provided the basis for both models is summarized, and a perspective on future research in resolving this fundamental mechanistic question is presented.

摘要

生物固氮由一种名为固氮酶的复杂双组分金属酶催化。对于依赖钼的酶,底物还原位点由一个[7铁-9硫-钼-X-高柠檬酸]金属簇提供,其中X被认为是一个氮原子。有机金属模型化合物、理论计算以及对固氮酶的生化、动力学和生物物理研究方面的最新进展,导致了关于N₂或其他底物在催化过程中可能结合位置的两种相反模型的形成。一种模型涉及底物与钼原子结合,而另一种模型涉及位于金属簇中心区域的一个或多个铁原子的参与。本文总结了最近为这两种模型提供依据的证据,并对解决这一基本机制问题的未来研究提出了展望。

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