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Mechanism of Ni,Fe-Containing Carbon Monoxide Dehydrogenases
被引:5
作者:
Dobbek, Holger
[1
]
机构:
[1] Humboldt Univ, Inst Biol Struct Biol Biochem, Dept Life Sci, Berlin, Germany
来源:
METALLOCOFACTORS THAT ACTIVATE SMALL MOLECULES: WITH FOCUS ON BIOINORGANIC CHEMISTRY
|
2019年
/
179卷
关键词:
Carbon dioxide;
Carbon monoxide;
Iron-sulfur cluster;
Nickel;
Small molecule activation;
WOOD-LJUNGDAHL PATHWAY;
N-BUTYL ISOCYANIDE;
CO DEHYDROGENASE;
ACETYL-COA;
CLOSTRIDIUM-THERMOACETICUM;
RHODOSPIRILLUM-RUBRUM;
ACTIVE-SITE;
ENZYME COMPLEX;
OXIDATION;
CLUSTER;
D O I:
10.1007/430_2018_27
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:
Carbon monoxide dehydrogenases catalyze the reversible oxidation of CO with water to CO2, two protons and two electrons. Phylogenetically diverse bacteria and archaea living under anaerobic conditions employ different classes of Ni,Fe-containing carbon monoxide dehydrogenases to use CO as an energy source or to contribute in converting CO2 to acetyl-CoA. The active site of carbon monoxide dehydrogenases contains a unique [NiFe4S4]-cluster, the only known example in nature where Ni is integrated into a heterocubane structure. The Ni ion serves as the catalytic nucleophilic center for activating CO and CO2, in which it is supported by an electrophilic Fe ion placed in exo to the heterocubane cluster. This review gives an overview on current ideas how Ni,Fe-containing carbon monoxide dehydrogenases reversibly oxidize CO to CO2, with a focus on recent structural studies of the enzymes.
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页码:153 / 166
页数:14
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