Chemistry and the hydrogenases

被引:577
作者
Evans, DJ [1 ]
Pickett, CJ [1 ]
机构
[1] John Innes Ctr Plant Sci Res, Dept Chim Biol, Norwich NR4 7UH, Norfolk, England
关键词
D O I
10.1039/b201317g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reversible reduction protons to dihydrogen -2H(+) + 2ereversible arrowH(2) is deceptively the simplest of reactions but one that requires multistep catalysis to proceed at practical rates. flow the metal-sulfur clusters of the hydrogenases, catalyse this, interconversion is currently the subject of extensive structural, spectroscopic and mechanistic studies of the enzymes, of synthetic assemblies and of in silico models. This is driven both by curiosity and by the view that an understanding of the underlying chemistry may inform the design of new electrocatalytic systems for hydrogen production or uptake, pertinent to energy transduction technology in an 'Hydrogen Economy'. Can chemists design materials that replace the expensive platinum metal catalysts of fuel cells with metal-sulfur cluster assemblies utilising abundant Ni, Fe and S as in the natural systems? Here we review the state of the art.
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页码:268 / 275
页数:8
相关论文
共 60 条
  • [1] THE STRUCTURE AND MECHANISM OF IRON-HYDROGENASES
    ADAMS, MWW
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1020 (02) : 115 - 145
  • [2] Modeling the active sites in metalloenzymes. 3. Density functional calculations on models for [Fe]-hydrogenase: Structures and vibrational frequencies of the observed redox forms and the reaction mechanism at the diiron active center
    Cao, ZX
    Hall, MB
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (16) : 3734 - 3742
  • [3] Primordial carbonylated iron-sulfur compounds and the synthesis of pyruvate
    Cody, GD
    Boctor, NZ
    Filley, TR
    Hazen, RM
    Scott, JH
    Sharma, A
    Yoder, HS
    [J]. SCIENCE, 2000, 289 (5483) : 1337 - 1340
  • [4] DIHYDROGEN COMPLEXES OF METALLOPORPHYRINS - CHARACTERIZATION AND HYDROGEN-TRANSFER REACTIVITY
    COLLMAN, JP
    WAGENKNECHT, PS
    HEMBRE, RT
    LEWIS, NS
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (03) : 1294 - 1295
  • [5] The bio-organometallic chemistry of active site iron in hydrogenases
    Darensbourg, MY
    Lyon, EJ
    Smee, JJ
    [J]. COORDINATION CHEMISTRY REVIEWS, 2000, 206 : 533 - 561
  • [6] Synthesis and structure of a thiolate-bridged nickel-iron complex: towards a mimic of the active site of NiFe-hydrogenase
    Davies, SC
    Evans, DJ
    Hughes, DL
    Longhurst, S
    Sanders, JR
    [J]. CHEMICAL COMMUNICATIONS, 1999, (19) : 1935 - 1936
  • [7] FTIR characterization of the active site of the Fe-hydrogenase from Desulfovibrio desulfuricans
    De Lacey, AL
    Stadler, C
    Cavazza, C
    Hatchikian, EC
    Fernandez, VM
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (45) : 11232 - 11233
  • [8] Crystal structure of a carbon monoxide dehydrogenase reveals a [Ni-4Fe-5S] cluster
    Dobbek, H
    Svetlitchnyi, V
    Gremer, L
    Huber, R
    Meyer, O
    [J]. SCIENCE, 2001, 293 (5533) : 1281 - 1285
  • [9] Life on carbon monoxide:: X-ray structure of Rhodospirillum rubrum Ni-Fe-S carbon monoxide dehydrogenase
    Drennan, CL
    Heo, JY
    Sintchak, MD
    Schreiter, E
    Ludden, PW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) : 11973 - 11978
  • [10] EVANS DJ, 2002, SCIENCE, V297, P1696