CO DEHYDROGENASE

被引:115
作者
FERRY, JG
机构
[1] Department of Biochemistry, Pennsylvania State University, University Park
关键词
CARBON MONOXIDE; ACETATE; CARBON CYCLE; AEROBIC; ANAEROBIC;
D O I
10.1146/annurev.mi.49.100195.001513
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Structurally and functionally diverse CO dehydrogenases are key components of various energy-yielding pathways in aerobic and anaerobic microbes from the Bacteria and Archaea domains. Aerobic microbes utilize Mo-Fe-flavin CO dehydrogenases to oxidize CO in respiratory pathways. Phototrophic anaerobes grow by converting CO to H-2, a process initiating with a CO dehydrogenase that contains nickel and iron-sulfur centers. Acetate-producing anaerobes employ a nickel/iron-sulfur CO dehydrogenase to synthesize acetyl-CoA from a methyl group, CO, and CoA. A similar enzyme is responsible for the cleavage of acetyl-CoA by anaerobic Archaea that obtain energy by fermenting acetate to CH4 and CO2. Acetotrophic sulfate reducers from the Bacteria and Archaea also utilize CO dehydrogenase to cleave acetyl-CoA yielding methyl and carbonyl groups. These microbes obtain energy for growth via a respiratory pathway in which the methyl and carbonyl groups are oxidized to CO2, and sulfate is reduced to sulfide.
引用
收藏
页码:305 / 333
页数:29
相关论文
共 136 条
[31]  
Ferry James G., 1993, P304
[32]   BIOCHEMISTRY OF METHANOGENESIS [J].
FERRY, JG .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 27 (06) :473-503
[33]   CO2 IS THE 1ST SPECIES FORMED UPON CO OXIDATION BY CO DEHYDROGENASE FROM PSEUDOMONAS-CARBOXYDOVORANS [J].
FUTO, S ;
MEYER, O .
ARCHIVES OF MICROBIOLOGY, 1986, 145 (04) :358-360
[34]   NICOTINIC-ACID HYDROXYLASE FROM CLOSTRIDIUM-BARKERI - ELECTRON-PARAMAGNETIC-RESONANCE STUDIES SHOW THAT SELENIUM IS COORDINATED WITH MOLYBDENUM IN THE CATALYTICALLY ACTIVE SELENIUM-DEPENDENT ENZYME [J].
GLADYSHEV, VN ;
KHANGULOV, SV ;
STADTMAN, TC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (01) :232-236
[35]   COORDINATION OF SELENIUM TO MOLYBDENUM IN FORMATE DEHYDROGENASE-H FROM ESCHERICHIA-COLI [J].
GLADYSHEV, VN ;
KHANGULOV, SV ;
AXLEY, MJ ;
STADTMAN, TC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (16) :7708-7711
[36]  
GORST CM, 1991, J BIOL CHEM, V266, P20687
[37]  
GRAHAME DA, 1991, J BIOL CHEM, V266, P22227
[38]  
GRAHAME DA, 1987, J BIOL CHEM, V262, P3706
[39]   SUBSTRATE AND COFACTOR REACTIVITY OF A CARBON-MONOXIDE DEHYDROGENASE CORRINOID ENZYME COMPLEX - STEPWISE REDUCTION OF IRON-SULFUR AND CORRINOID CENTERS, THE CORRINOID CO2+/1+ REDOX MIDPOINT POTENTIAL, AND OVERALL SYNTHESIS OF ACETYL-COA [J].
GRAHAME, DA .
BIOCHEMISTRY, 1993, 32 (40) :10786-10793
[40]   EVIDENCE FOR A NICKEL-CONTAINING CARBON-MONOXIDE DEHYDROGENASE IN METHANOBREVIBACTER-ARBORIPHILICUS [J].
HAMMEL, KE ;
CORNWELL, KL ;
DIEKERT, GB ;
THAUER, RK .
JOURNAL OF BACTERIOLOGY, 1984, 157 (03) :975-978