UCIBIO, REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica, Portugal.
UCIBIO, REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica, Portugal.
J Inorg Biochem. 2017 Dec;177:423-434. doi: 10.1016/j.jinorgbio.2017.09.007. Epub 2017 Sep 11.
The reduction of the potent greenhouse gas nitrous oxide requires a catalyst to overcome the large activation energy barrier of this reaction. Its biological decomposition to the inert dinitrogen can be accomplished by denitrifiers through nitrous oxide reductase, the enzyme that catalyzes the last step of the denitrification, a pathway of the biogeochemical nitrogen cycle. Nitrous oxide reductase is a multicopper enzyme containing a mixed valence CuA center that can accept electrons from small electron shuttle proteins, triggering electron flow to the catalytic sulfide-bridged tetranuclear copper "CuZ center". This enzyme has been isolated with its catalytic center in two forms, CuZ*(4Cu1S) and CuZ(4Cu2S), proven to be spectroscopic and structurally different. In the last decades, it has been a challenge to characterize the properties of this complex enzyme, due to the different oxidation states observed for each of its centers and the heterogeneity of its preparations. The substrate binding site in those two "CuZ center" forms and which is the active form of the enzyme is still a matter of debate. However, in the last years the application of different spectroscopies, together with theoretical calculations have been useful in answering these questions and in identifying intermediate species of the catalytic cycle. An overview of the spectroscopic, kinetics and structural properties of the two forms of the catalytic "CuZ center" is given here, together with the current knowledge on nitrous oxide reduction mechanism by nitrous oxide reductase and its intermediate species.
减少强效温室气体一氧化二氮需要一种催化剂来克服该反应的巨大活化能障碍。通过反硝化细菌,通过一氧化二氮还原酶,将其生物分解为惰性的氮气,可以完成其生物分解,一氧化二氮还原酶是一种多铜酶,含有混合价 CuA 中心,可以从小型电子穿梭蛋白接受电子,触发电子流向催化的硫桥合四铜“CuZ 中心”。该酶已与其催化中心的两种形式(CuZ*(4Cu1S)和 CuZ(4Cu2S)一起分离,证明在光谱和结构上有所不同。在过去的几十年中,由于其每个中心的氧化态不同以及其制剂的异质性,因此对这种复杂酶的特性进行表征一直是一个挑战。在这两种“CuZ 中心”形式的底物结合位点以及哪种是酶的活性形式仍然存在争议。但是,近年来,不同光谱技术的应用以及理论计算对于回答这些问题以及鉴定催化循环的中间物种非常有用。本文概述了两种催化“CuZ 中心”形式的光谱,动力学和结构特性,以及关于一氧化二氮还原酶及其中间物种的一氧化二氮还原机制的最新知识。