Thermodynamic and kinetic evidence for a two-step reaction between methane monooxygenase compound Q and substrates

被引:3
作者
Brazeau, BJ
Lipscomb, JD
机构
[1] Univ Minnesota, Dept Biochem Mol Biol & Biophys, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Ctr Met Biocatalysis, Minneapolis, MN 55455 USA
来源
OXYGEN AND LIFE: OXYGENASES, OXIDASE AND LIPID MEDIATORS | 2002年 / 1233卷
关键词
diiron; methane monooxygenase; compound Q; thermodynamics;
D O I
10.1016/S0531-5131(02)00145-0
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 monooxygenase (MMO) contains a binuclear iron cluster that forms a bis-mu-oxo FC(IV)(2) intermediate termed compound Q (Q) which has previously been shown to be the species that oxidizes methane to form methanol. This report summarizes the results from transient kinetic studies that were used to study the temperature dependence of the rate of Q decay as a function of substrate type, concentration, and deuteration. The Arrhenius plots for the rate of Q decay in the presence of methane were found to be nonlinear with both the temperature and rate at which the break is observed dependent upon methane concentration. In contrast, the Arrhenius plots for the reaction of Q with alternate substrates such as ethane and propane are linear. An analysis of the thermodynamic activation parameters in combination with the deuterium kinetic isotope effects (KIE) suggests that the reaction between Q and the substrate occurs in two steps, one being substrate binding and the other C-H bond cleavage. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:229 / 233
页数:5
相关论文
共 8 条
[1]   Kinetics and activation thermodynamics of methane monooxygenase compound Q formation and reaction with substrates [J].
Brazeau, BJ ;
Lipscomb, JD .
BIOCHEMISTRY, 2000, 39 (44) :13503-13515
[2]  
BRAZEAU BJ, 2000, BIOCHEM, V35, P233
[3]  
de Montellano P.R. Ortiz., 1995, CYTOCHROME P450 STRU
[4]   Methanotrophic bacteria [J].
Hanson, RS ;
Hanson, TE .
MICROBIOLOGICAL REVIEWS, 1996, 60 (02) :439-+
[5]   A TRANSIENT INTERMEDIATE OF THE METHANE MONOOXYGENASE CATALYTIC CYCLE CONTAINING AN FE(IV)FE(IV) CLUSTER [J].
LEE, SK ;
FOX, BG ;
FROLAND, WA ;
LIPSCOMB, JD ;
MUNCK, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (14) :6450-6451
[6]  
LIPSCOMB JD, 2001, 3 INT C OXYG LIF
[7]   Large kinetic isotope effects in methane oxidation catalyzed by methane monooxygenase: Evidence for C-H bond cleavage in a reaction cycle intermediate [J].
Nesheim, JC ;
Lipscomb, JD .
BIOCHEMISTRY, 1996, 35 (31) :10240-10247
[8]   An (Fe2O2)-O-IV diamond core structure for the key intermediate Q of methane monooxygenase [J].
Shu, LJ ;
Nesheim, JC ;
Kauffmann, K ;
Munck, E ;
Lipscomb, JD ;
Que, L .
SCIENCE, 1997, 275 (5299) :515-518