Literature DB >> 25806595

Enzymatic oxidation of methane.

Sarah Sirajuddin1, Amy C Rosenzweig1.   

Abstract

Methane monooxygenases (MMOs) are enzymes that catalyze the oxidation of methane to methanol in methanotrophic bacteria. As potential targets for new gas-to-liquid methane bioconversion processes, MMOs have attracted intense attention in recent years. There are two distinct types of MMO, a soluble, cytoplasmic MMO (sMMO) and a membrane-bound, particulate MMO (pMMO). Both oxidize methane at metal centers within a complex, multisubunit scaffold, but the structures, active sites, and chemical mechanisms are completely different. This Current Topic review article focuses on the overall architectures, active site structures, substrate reactivities, protein-protein interactions, and chemical mechanisms of both MMOs, with an emphasis on fundamental aspects. In addition, recent advances, including new details of interactions between the sMMO components, characterization of sMMO intermediates, and progress toward understanding the pMMO metal centers are highlighted. The work summarized here provides a guide for those interested in exploiting MMOs for biotechnological applications.

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Year:  2015        PMID: 25806595      PMCID: PMC5257249          DOI: 10.1021/acs.biochem.5b00198

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  118 in total

1.  Component interactions in the soluble methane monooxygenase system from Methylococcus capsulatus (Bath).

Authors:  G T Gassner; S J Lippard
Journal:  Biochemistry       Date:  1999-09-28       Impact factor: 3.162

2.  Steady-state kinetic analysis of soluble methane mono-oxygenase from Methylococcus capsulatus (Bath).

Authors:  J Green; H Dalton
Journal:  Biochem J       Date:  1986-05-15       Impact factor: 3.857

3.  Crystal structures of the methane monooxygenase hydroxylase from Methylococcus capsulatus (Bath): implications for substrate gating and component interactions.

Authors:  A C Rosenzweig; H Brandstetter; D A Whittington; P Nordlund; S J Lippard; C A Frederick
Journal:  Proteins       Date:  1997-10

4.  Resolution of the methane mono-oxygenase of Methylococcus capsulatus (Bath) into three components. Purification and properties of component C, a flavoprotein.

Authors:  J Colby; H Dalton
Journal:  Biochem J       Date:  1978-05-01       Impact factor: 3.857

5.  Dioxygen Activation and Methane Hydroxylation by Soluble Methane Monooxygenase: A Tale of Two Irons and Three Proteins A list of abbreviations can be found in Section 7.

Authors:  Maarten Merkx; Daniel A. Kopp; Matthew H. Sazinsky; Jessica L. Blazyk; Jens Müller; Stephen J. Lippard
Journal:  Angew Chem Int Ed Engl       Date:  2001-08-03       Impact factor: 15.336

Review 6.  Methane monooxygenase: functionalizing methane at iron and copper.

Authors:  Matthew H Sazinsky; Stephen J Lippard
Journal:  Met Ions Life Sci       Date:  2015

Review 7.  Dioxygen activation in soluble methane monooxygenase.

Authors:  Christine E Tinberg; Stephen J Lippard
Journal:  Acc Chem Res       Date:  2011-03-10       Impact factor: 22.384

8.  Revisiting the mechanism of dioxygen activation in soluble methane monooxygenase from M. capsulatus (Bath): evidence for a multi-step, proton-dependent reaction pathway.

Authors:  Christine E Tinberg; Stephen J Lippard
Journal:  Biochemistry       Date:  2009-12-29       Impact factor: 3.162

9.  Isolation and characterization of a novel coenzyme Q from some methane-oxidizing bacteria.

Authors:  M D Collins; P N Green
Journal:  Biochem Biophys Res Commun       Date:  1985-12-31       Impact factor: 3.575

10.  Expression and characterization of ferredoxin and flavin adenine dinucleotide binding domains of the reductase component of soluble methane monooxygenase from Methylococcus capsulatus (Bath).

Authors:  Jessica L Blazyk; Stephen J Lippard
Journal:  Biochemistry       Date:  2002-12-31       Impact factor: 3.162

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  62 in total

1.  Metalloproteins: Simple structure, complex function.

Authors:  Angela Lombardi
Journal:  Nat Chem Biol       Date:  2015-10       Impact factor: 15.040

2.  Perturbing the Copper(III)-Hydroxide Unit through Ligand Structural Variation.

Authors:  Debanjan Dhar; Gereon M Yee; Andrew D Spaeth; David W Boyce; Hongtu Zhang; Büsra Dereli; Christopher J Cramer; William B Tolman
Journal:  J Am Chem Soc       Date:  2015-12-22       Impact factor: 15.419

3.  Communal metabolism of methane and the rare Earth element switch.

Authors:  Zheng Yu; Ludmila Chistoserdova
Journal:  J Bacteriol       Date:  2017-06-19       Impact factor: 3.490

4.  High-Resolution Extended X-ray Absorption Fine Structure Analysis Provides Evidence for a Longer Fe···Fe Distance in the Q Intermediate of Methane Monooxygenase.

Authors:  George E Cutsail; Rahul Banerjee; Ang Zhou; Lawrence Que; John D Lipscomb; Serena DeBeer
Journal:  J Am Chem Soc       Date:  2018-11-16       Impact factor: 15.419

5.  Formation and Electronic Structure of an Atypical CuA Site.

Authors:  Matthew O Ross; Oriana S Fisher; Marcos N Morgada; Matthew D Krzyaniak; Michael R Wasielewski; Alejandro J Vila; Brian M Hoffman; Amy C Rosenzweig
Journal:  J Am Chem Soc       Date:  2019-03-07       Impact factor: 15.419

6.  Metal Catalysts for Heterogeneous Catalysis: From Single Atoms to Nanoclusters and Nanoparticles.

Authors:  Lichen Liu; Avelino Corma
Journal:  Chem Rev       Date:  2018-04-16       Impact factor: 60.622

Review 7.  Dioxygen Activation by Nonheme Diiron Enzymes: Diverse Dioxygen Adducts, High-Valent Intermediates, and Related Model Complexes.

Authors:  Andrew J Jasniewski; Lawrence Que
Journal:  Chem Rev       Date:  2018-02-05       Impact factor: 60.622

8.  How a cofactor-free protein environment lowers the barrier to O2 reactivity.

Authors:  Melodie M Machovina; Emerald S Ellis; Thomas J Carney; Fikile R Brushett; Jennifer L DuBois
Journal:  J Biol Chem       Date:  2019-01-02       Impact factor: 5.157

9.  Characterization of Methanobactin from Methylosinus sp. LW4.

Authors:  Grace E Kenney; Anthony W Goering; Matthew O Ross; Caroline J DeHart; Paul M Thomas; Brian M Hoffman; Neil L Kelleher; Amy C Rosenzweig
Journal:  J Am Chem Soc       Date:  2016-08-26       Impact factor: 15.419

10.  Rapid protein immobilization for thin film continuous flow biocatalysis.

Authors:  Joshua Britton; Colin L Raston; Gregory A Weiss
Journal:  Chem Commun (Camb)       Date:  2016-08-09       Impact factor: 6.222

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