Carbon dioxide activation at the Ni,Fe-cluster of anaerobic carbon monoxide dehydrogenase

被引:464
作者
Jeoung, Jae-Hun
Dobbek, Holger
机构
[1] Univ Bayreuth, Lab Prot Kristallog, D-95440 Bayreuth, Germany
[2] Univ Bayreuth, Forsch Zent Biomakromol, D-95440 Bayreuth, Germany
关键词
D O I
10.1126/science.1148481
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Anaerobic CO dehydrogenases catalyze the reversible oxidation of CO to CO2 at a complex Ni-, Fe-, and S-containing metal center called cluster C. We report crystal structures of CO dehydrogenase II from Carboxydothermus hydrogenoformans in three different states. In a reduced state, exogenous CO2 supplied in solution is bound and reductively activated by cluster C. In the intermediate structure, CO2 acts as a bridging ligand between Ni and the asymmetrically coordinated Fe, where it completes the square-planar coordination of the Ni ion. It replaces a water/hydroxo ligand bound to the Fe ion in the other two states. The structures define the mechanism of CO oxidation and CO2 reduction at the Ni-Fe site of cluster C.
引用
收藏
页码:1461 / 1464
页数:4
相关论文
共 22 条
[1]   Ni-Zn-[Fe4-S4] and Ni-Ni-[Fe4-S4] clusters in closed and open subunits of acetyl-CoA synthase/carbon monoxide dehydrogenase [J].
Darnault, C ;
Volbeda, A ;
Kim, EJ ;
Legrand, P ;
Vernéde, X ;
Lindahl, PA ;
Fontecilla-Camps, JC .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (04) :271-279
[2]   A multinuclear ENDOR study of the C-cluster in CO dehydrogenase from Clostridium thermoaceticum:: Evidence for HxO and histidine coordination to the [Fe4S4] center [J].
DeRose, VJ ;
Telser, J ;
Anderson, ME ;
Lindahl, PA ;
Hoffman, BM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (34) :8767-8776
[3]   Crystal structure of a carbon monoxide dehydrogenase reveals a [Ni-4Fe-5S] cluster [J].
Dobbek, H ;
Svetlitchnyi, V ;
Gremer, L ;
Huber, R ;
Meyer, O .
SCIENCE, 2001, 293 (5533) :1281-1285
[4]   Carbon monoxide induced decomposition of the active site [Ni-4Fe-5S] cluster of CO dehydrogenase [J].
Dobbek, H ;
Svetlitchnyi, V ;
Liss, J ;
Meyer, O .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (17) :5382-5387
[5]   A Ni-Fe-Cu center in a bifunctional carbon monoxide dehydrogenase/acetyl-CoA synthase [J].
Doukov, TI ;
Iverson, TM ;
Seravalli, J ;
Ragsdale, SW ;
Drennan, CL .
SCIENCE, 2002, 298 (5593) :567-572
[6]   Life on carbon monoxide:: X-ray structure of Rhodospirillum rubrum Ni-Fe-S carbon monoxide dehydrogenase [J].
Drennan, CL ;
Heo, JY ;
Sintchak, MD ;
Schreiter, E ;
Ludden, PW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) :11973-11978
[7]   REACTIVITY OF CARBON-MONOXIDE DEHYDROGENASE FROM RHODOSPIRILLUM-RUBRUM WITH CARBON-DIOXIDE, CARBONYL SULFIDE, AND CARBON-DISULFIDE [J].
ENSIGN, SA .
BIOCHEMISTRY, 1995, 34 (16) :5372-5381
[8]   Effect of sodium sulfide on Ni-containing carbon monoxide dehydrogenases [J].
Feng, J ;
Lindahl, PA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (29) :9094-9100
[9]   Carbon monoxide dehydrogenase from Rhodospirillum rubrum:: Effect of redox potential on catalysis [J].
Feng, J ;
Lindahl, PA .
BIOCHEMISTRY, 2004, 43 (06) :1552-1559
[10]   Evidence for a proposed intermediate redox state in the CO/CO2 active site of acetyl-CoA synthase (carbon monoxide dehydrogenase) from Clostridium thermoaceticum [J].
Fraser, DM ;
Lindahl, PA .
BIOCHEMISTRY, 1999, 38 (48) :15706-15711