Enzymatic Oxidation of Methane

被引:261
作者
Sirajuddin, Sarah
Rosenzweig, Amy C. [1 ]
机构
[1] Northwestern Univ, Dept Mol Biosci, Evanston, IL 60208 USA
基金
美国国家卫生研究院;
关键词
METHYLOCOCCUS-CAPSULATUS-BATH; METHYLOSINUS-TRICHOSPORIUM OB3B; MONOOXYGENASE HYDROXYLASE COMPONENT; PROTEIN-PROTEIN INTERACTIONS; X-RAY-ABSORPTION; H BOND-CLEAVAGE; ACTIVE-SITE; ELECTRON-TRANSFER; CRYSTAL-STRUCTURE; DIOXYGEN ACTIVATION;
D O I
10.1021/acs.biochem.5b00198
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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, proteinprotein 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.
引用
收藏
页码:2283 / 2294
页数:12
相关论文
共 139 条
[1]  
ANDERSSON KK, 1991, NEW J CHEM, V15, P411
[2]   ACCESSIBILITY TO THE ACTIVE-SITE OF METHANE MONOOXYGENASE - THE 1ST DEMONSTRATION OF EXOGENOUS LIGAND-BINDING TO THE DIIRON CLUSTER [J].
ANDERSSON, KK ;
ELGREN, TE ;
QUE, L ;
LIPSCOMB, JD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (22) :8711-8713
[3]   KINETIC-STUDIES ON THE REACTIONS OF SEPARATED A-SUBUNIT, B-SUBUNIT AND C-SUBUNIT OF PANULIRUS-INTERRUPTUS DEOXY-HEMOCYANIN WITH HYDROGEN-PEROXIDE [J].
ANDREW, CR ;
MCKILLOP, KP ;
SYKES, AG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1163 (01) :17-25
[4]   The structure and mechanism of methanol dehydrogenase [J].
Anthony, C ;
Williams, P .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2003, 1647 (1-2) :18-23
[5]   THE C-TYPE CYTOCHROMES OF METHYLOTROPHIC BACTERIA [J].
ANTHONY, C .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1099 (01) :1-15
[6]   Alkane-oxidizing metalloenzymes in the carbon cycle [J].
Austin, Rachel Narehood ;
Groves, John T. .
METALLOMICS, 2011, 3 (08) :775-787
[7]   Two isozymes of particulate methane monooxygenase with different methane oxidation kinetics are found in Methylocystis sp strain SCZ [J].
Baani, Mohamed ;
Liesack, Werner .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (29) :10203-10208
[8]   Mechanistic studies on the hydroxylation of methane by methane monooxygenase [J].
Baik, MH ;
Newcomb, M ;
Friesner, RA ;
Lippard, SJ .
CHEMICAL REVIEWS, 2003, 103 (06) :2385-2419
[9]   Structural and mechanistic insights into methane oxidation by particulate methane monooxygenase [J].
Balasubramanian, Ramakrishnan ;
Rosenzweig, Amy C. .
ACCOUNTS OF CHEMICAL RESEARCH, 2007, 40 (07) :573-580
[10]   Oxidation of methane by a biological dicopper centre [J].
Balasubramanian, Ramakrishnan ;
Smith, Stephen M. ;
Rawat, Swati ;
Yatsunyk, Liliya A. ;
Stemmler, Timothy L. ;
Rosenzweig, Amy C. .
NATURE, 2010, 465 (7294) :115-U131