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参与硝化反硝化的亚硝酸盐还原酶的特性。

Characterization of a nitrite reductase involved in nitrifier denitrification.

机构信息

From the Departments of Molecular Biosciences and of Chemistry, Northwestern University, Evanston, Illinois 60208 and.

Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon 97331.

出版信息

J Biol Chem. 2013 Aug 30;288(35):25575-25583. doi: 10.1074/jbc.M113.484543. Epub 2013 Jul 15.

Abstract

Nitrifier denitrification is the conversion of nitrite to nitrous oxide by ammonia-oxidizing organisms. This process, which is distinct from denitrification, is active under aerobic conditions in the model nitrifier Nitrosomonas europaea. The central enzyme of the nitrifier dentrification pathway is a copper nitrite reductase (CuNIR). To understand how a CuNIR, typically inactivated by oxygen, functions in this pathway, the enzyme isolated directly from N. europaea (NeNIR) was biochemically and structurally characterized. NeNIR reduces nitrite at a similar rate to other CuNIRs but appears to be oxygen tolerant. Crystal structures of oxidized and reduced NeNIR reveal a substrate channel to the active site that is much more restricted than channels in typical CuNIRs. In addition, there is a second fully hydrated channel leading to the active site that likely acts a water exit pathway. The structure is minimally affected by changes in pH. Taken together, these findings provide insight into the molecular basis for NeNIR oxygen tolerance.

摘要

亚硝化-硝化反硝化是氨氧化菌将亚硝酸盐转化为一氧化二氮的过程。与反硝化不同,该过程在模式硝化菌硝化单胞菌属(Nitrosomonas europaea)中是在有氧条件下进行的。硝化反硝化途径的中心酶是铜亚硝酸盐还原酶(CuNIR)。为了了解通常被氧气失活的 CuNIR 如何在该途径中发挥作用,直接从硝化单胞菌属(N. europaea)中分离出的酶(NeNIR)进行了生化和结构表征。NeNIR 还原亚硝酸盐的速度与其他 CuNIR 相当,但似乎对氧气具有耐受性。氧化和还原态 NeNIR 的晶体结构揭示了一个通往活性位点的底物通道,该通道比典型的 CuNIR 中的通道受到更严格的限制。此外,还有一个通向活性位点的第二个完全水合通道,可能充当水出口途径。该结构受 pH 值变化的影响很小。总的来说,这些发现为 NeNIR 对氧气的耐受性的分子基础提供了深入的了解。

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