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