Characterization of a Nitrite Reductase Involved in Nitrifier Denitrification

被引:38
|
作者
Lawton, Thomas J. [1 ,2 ]
Bowen, Kimberly E. [1 ,2 ]
Sayavedra-Soto, Luis A. [3 ]
Arp, Daniel J. [3 ]
Rosenzweig, Amy C. [1 ,2 ]
机构
[1] Northwestern Univ, Dept Mol Biosci, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[3] Oregon State Univ, Dept Bot & Plant Pathol, Corvallis, OR 97331 USA
关键词
NITROUS-OXIDE PRODUCTION; NITROSOMONAS-EUROPAEA; ALCALIGENES-FAECALIS; CRYSTAL-STRUCTURE; ELECTRON-TRANSFER; MULTICOPPER OXIDASE; KINETIC-ANALYSIS; AMMONIA; PROTEIN; SITE;
D O I
10.1074/jbc.M113.484543
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:25575 / 25583
页数:9
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