首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Characterization of a Nitrite Reductase Involved in Nitrifier Denitrification
Authors:Thomas J Lawton  Kimberly E Bowen  Luis A Sayavedra-Soto  Daniel J Arp  Amy C Rosenzweig
Institution: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
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.
Keywords:Copper  Crystal Structure  Electron Transfer  Nitrogen Metabolism  Oxygen Binding  Nitrosomonas europaea  Denitrification  Nitrifier  Nitrite Reductase
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号