Literature DB >> 16234916

The quest for the particulate methane monooxygenase active site.

Raquel L Lieberman1, Amy C Rosenzweig.   

Abstract

Particulate methane monooxygenase is a copper-containing, membrane-bound metalloenzyme that converts methane to methanol in Nature. How pMMO accomplishes this difficult reaction under ambient conditions is one of the major unsolved problems in bioinorganic chemistry. Despite considerable research efforts in the past 20 years, the active site of the enzyme remains unknown. We recently solved the first crystal structure of pMMO to 2.8 è resolution, revealing the overall structure, oligomerization state, subunit ratio, and composition and location of the metal centers. Almost none of the key structural features were predicted. In this Perspective, we review the state of knowledge before and after the structure determination, emphasizing elucidation of the pMMO active site.

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Year:  2005        PMID: 16234916     DOI: 10.1039/b506651d

Source DB:  PubMed          Journal:  Dalton Trans        ISSN: 1477-9226            Impact factor:   4.390


  17 in total

Review 1.  Chemistry and biology of the copper chelator methanobactin.

Authors:  Grace E Kenney; Amy C Rosenzweig
Journal:  ACS Chem Biol       Date:  2011-12-12       Impact factor: 5.100

Review 2.  Architecture and active site of particulate methane monooxygenase.

Authors:  Megen A Culpepper; Amy C Rosenzweig
Journal:  Crit Rev Biochem Mol Biol       Date:  2012-06-23       Impact factor: 8.250

Review 3.  Using synthetic chemistry to understand copper protein active sites: a personal perspective.

Authors:  William B Tolman
Journal:  J Biol Inorg Chem       Date:  2006-01-27       Impact factor: 3.358

Review 4.  Copper-dioxygen complex mediated C-H bond oxygenation: relevance for particulate methane monooxygenase (pMMO).

Authors:  Richard A Himes; Kenneth D Karlin
Journal:  Curr Opin Chem Biol       Date:  2009-03-13       Impact factor: 8.822

5.  Crystal structure and characterization of particulate methane monooxygenase from Methylocystis species strain M.

Authors:  Stephen M Smith; Swati Rawat; Joshua Telser; Brian M Hoffman; Timothy L Stemmler; Amy C Rosenzweig
Journal:  Biochemistry       Date:  2011-11-03       Impact factor: 3.162

Review 6.  A tale of two methane monooxygenases.

Authors:  Matthew O Ross; Amy C Rosenzweig
Journal:  J Biol Inorg Chem       Date:  2016-11-22       Impact factor: 3.358

7.  The copper chelator methanobactin from Methylosinus trichosporium OB3b binds copper(I).

Authors:  Amanda S Hakemian; Christine E Tinberg; Kalyan C Kondapalli; Joshua Telser; Brian M Hoffman; Timothy L Stemmler; Amy C Rosenzweig
Journal:  J Am Chem Soc       Date:  2005-12-14       Impact factor: 15.419

Review 8.  Methane-Oxidizing Enzymes: An Upstream Problem in Biological Gas-to-Liquids Conversion.

Authors:  Thomas J Lawton; Amy C Rosenzweig
Journal:  J Am Chem Soc       Date:  2016-07-19       Impact factor: 15.419

9.  The metal centers of particulate methane monooxygenase from Methylosinus trichosporium OB3b.

Authors:  Amanda S Hakemian; Kalyan C Kondapalli; Joshua Telser; Brian M Hoffman; Timothy L Stemmler; Amy C Rosenzweig
Journal:  Biochemistry       Date:  2008-06-10       Impact factor: 3.162

10.  Community analysis of betaproteobacterial ammonia-oxidizing bacteria using the amoCAB operon.

Authors:  Pilar Junier; Ok-Sun Kim; Thomas Junier; Tae-Seok Ahn; Johannes F Imhoff; Karl-Paul Witzel
Journal:  Appl Microbiol Biotechnol       Date:  2009-03-10       Impact factor: 4.813

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