Sci Sin. 1976 Jul-Aug;19(4):460-74.
Based upon the known reactions of nitrogenase and the principles of coordination catalysis, a model of nitrogenase active-centre is proposed. An octa-atomic cluster, Fe2S2-Mo2O2, of pseudo-cubane-type structure is supposed to form a coupled twin of trinuclear (2Mo-1Fe) active-centre, which also catalyzes the reduction of H+ to H2. With this model, mechanisms of all the known nitrogenase-catalyzed reactions are explained, together with the non-inhibition of the hydrogen-evolution reaction by CO, and the mixed character of inhibition of other nitrogenase-catalyzed reactions. Electron transport by 2-stepped ATP-driving with some electron back-flow is shown to give a reasonable explanation for the observed ATP/2e- ratio and for the reductant-independent ATP hydrolysis catalyzed by nitrogenase. The close analogy between electron transport by 2-stepped ATP-driving in nitrogenase catalysis and electron transport by 2-stepped photo-driving in photosynthesis by green plants in illustrated.
基于固氮酶的已知反应和配位催化原理,提出了一种固氮酶活性中心模型。假定一个具有假立方烷型结构的八原子簇Fe₂S₂-Mo₂O₂形成一个三核(2Mo-1Fe)活性中心的耦合孪体,该孪体也催化H⁺还原为H₂。利用该模型,解释了所有已知的固氮酶催化反应的机制,以及CO对析氢反应的无抑制作用,和对其他固氮酶催化反应抑制的混合特性。通过两步ATP驱动并伴有一些电子回流的电子传递,对观察到的ATP/2e⁻比值以及固氮酶催化的与还原剂无关的ATP水解给出了合理的解释。文中阐述了固氮酶催化中两步ATP驱动的电子传递与绿色植物光合作用中两步光驱动的电子传递之间的密切相似性。