4.6 Article

Characterization of a Nitrite Reductase Involved in Nitrifier Denitrification

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JOURNAL OF BIOLOGICAL CHEMISTRY
卷 288, 期 35, 页码 25575-25583

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DOI: 10.1074/jbc.M113.484543

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  1. Agriculture and Food Research Initiative Competitive Grant from the U. S. Department of Agriculture [2010-65115-20380]
  2. Oregon Agricultural Experimental Station
  3. NIFA [581274, 2010-65115-20380] Funding Source: Federal RePORTER

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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.

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