Literature DB >> 23857587

Characterization of a nitrite reductase involved in nitrifier denitrification.

Thomas J Lawton1, Kimberly E Bowen, Luis A Sayavedra-Soto, Daniel J Arp, Amy C Rosenzweig.   

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.

Entities:  

Keywords:  Copper; Crystal Structure; Denitrification; Electron Transfer; Nitrifier; Nitrite Reductase; Nitrogen Metabolism; Nitrosomonas europaea; Oxygen Binding

Mesh:

Substances:

Year:  2013        PMID: 23857587      PMCID: PMC3757218          DOI: 10.1074/jbc.M113.484543

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  54 in total

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4.  Atomic resolution structures of native copper nitrite reductase from Alcaligenes xylosoxidans and the active site mutant Asp92Glu.

Authors:  Mark J Ellis; Fraser E Dodd; Gary Sawers; Robert R Eady; S Samar Hasnain
Journal:  J Mol Biol       Date:  2003-04-25       Impact factor: 5.469

5.  Crystal structure of the soluble domain of the major anaerobically induced outer membrane protein (AniA) from pathogenic Neisseria: a new class of copper-containing nitrite reductases.

Authors:  Martin J Boulanger; Michael E P Murphy
Journal:  J Mol Biol       Date:  2002-02-01       Impact factor: 5.469

6.  Functional analysis of conserved aspartate and histidine residues located around the type 2 copper site of copper-containing nitrite reductase.

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Journal:  J Biochem       Date:  2000-02       Impact factor: 3.387

7.  Complete genome sequence of the ammonia-oxidizing bacterium and obligate chemolithoautotroph Nitrosomonas europaea.

Authors:  Patrick Chain; Jane Lamerdin; Frank Larimer; Warren Regala; Victoria Lao; Miriam Land; Loren Hauser; Alan Hooper; Martin Klotz; Jeanette Norton; Luis Sayavedra-Soto; Dave Arciero; Norman Hommes; Mark Whittaker; Daniel Arp
Journal:  J Bacteriol       Date:  2003-05       Impact factor: 3.490

8.  Nitrite reductase of Nitrosomonas europaea is not essential for production of gaseous nitrogen oxides and confers tolerance to nitrite.

Authors:  Hubertus J E Beaumont; Norman G Hommes; Luis A Sayavedra-Soto; Daniel J Arp; David M Arciero; Alan B Hooper; Hans V Westerhoff; Rob J M van Spanning
Journal:  J Bacteriol       Date:  2002-05       Impact factor: 3.490

9.  Crystal structure of a novel red copper protein from Nitrosomonas europaea.

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Authors:  Daniel J Arp; Lisa Y Stein
Journal:  Crit Rev Biochem Mol Biol       Date:  2003       Impact factor: 8.250

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Review 4.  Improving Nitrogen Use Efficiency in Aerobic Rice Based on Insights Into the Ecophysiology of Archaeal and Bacterial Ammonia Oxidizers.

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5.  Copper nitrite reductase from Sinorhizobium meliloti 2011: Crystal structure and interaction with the physiological versus a nonmetabolically related cupredoxin-like mediator.

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7.  An unprecedented dioxygen species revealed by serial femtosecond rotation crystallography in copper nitrite reductase.

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8.  Redox-coupled structural changes in nitrite reductase revealed by serial femtosecond and microfocus crystallography.

Authors:  Yohta Fukuda; Ka Man Tse; Mamoru Suzuki; Kay Diederichs; Kunio Hirata; Takanori Nakane; Michihiro Sugahara; Eriko Nango; Kensuke Tono; Yasumasa Joti; Takashi Kameshima; Changyong Song; Takaki Hatsui; Makina Yabashi; Osamu Nureki; Hiroyoshi Matsumura; Tsuyoshi Inoue; So Iwata; Eiichi Mizohata
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9.  Design and evaluation of primers targeting genes encoding NO-forming nitrite reductases: implications for ecological inference of denitrifying communities.

Authors:  Germán Bonilla-Rosso; Lea Wittorf; Christopher M Jones; Sara Hallin
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10.  Identification of a tyrosine switch in copper-haem nitrite reductases.

Authors:  Jianshu Dong; Daisuke Sasaki; Robert R Eady; Svetlana V Antonyuk; S Samar Hasnain
Journal:  IUCrJ       Date:  2018-06-25       Impact factor: 4.769

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