Structural basis of enzymatic benzene ring reduction

被引:0
|
作者
Tobias Weinert
Simona G Huwiler
Johannes W Kung
Sina Weidenweber
Petra Hellwig
Hans-Joachim Stärk
Till Biskup
Stefan Weber
Julien J H Cotelesage
Graham N George
Ulrich Ermler
Matthias Boll
机构
[1] Max Planck Institute of Biophysics,Department of Analytical Chemistry
[2] Microbiology,Department of Geological Sciences
[3] Faculty of Biology,undefined
[4] University of Freiburg,undefined
[5] Laboratoire de Bioélectrochimie et Spectroscopie,undefined
[6] UMR 7140,undefined
[7] Chimie de la Matière Complexe,undefined
[8] Université de Strasbourg–CNRS,undefined
[9] Helmholtz Centre for Environmental Research UFZ,undefined
[10] Institute of Physical Chemistry,undefined
[11] University of Freiburg,undefined
[12] University of Saskatchewan,undefined
[13] Canadian Light Source,undefined
来源
Nature Chemical Biology | 2015年 / 11卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Structural, spectroscopic and kinetic analyses suggest that class II benzoyl-CoA reductases from anaerobic bacteria use an unusual tungsten cofactor and a conserved histidine to perform a reduction akin to the widely used Birch reduction in organic chemistry.[graphic not available: see fulltext]
引用
收藏
页码:586 / 591
页数:5
相关论文
共 50 条
  • [1] Structural basis of enzymatic benzene ring reduction
    Weinert, Tobias
    Huwiler, Simona G.
    Kung, Johannes W.
    Weidenweber, Sina
    Hellwig, Petra
    Staerk, Hans-Joachim
    Biskup, Till
    Weber, Stefan
    Cotelesage, Julien J. H.
    George, Graham N.
    Ermler, Ulrich
    Boll, Matthias
    NATURE CHEMICAL BIOLOGY, 2015, 11 (08) : 586 - 591
  • [2] Erratum: Structural basis of enzymatic benzene ring reduction
    Tobias Weinert
    Simona G Huwiler
    Johannes W Kung
    Sina Weidenweber
    Petra Hellwig
    Hans-Joachim Stärk
    Till Biskup
    Stefan Weber
    Julien J H Cotelesage
    Graham N George
    Ulrich Ermler
    Matthias Boll
    Nature Chemical Biology, 2015, 11 : 741 - 741
  • [3] Correction: Corrigendum: Structural basis of enzymatic benzene ring reduction
    Tobias Weinert
    Simona G Huwiler
    Johannes W Kung
    Sina Weidenweber
    Petra Hellwig
    Hans-Joachim Stärk
    Till Biskup
    Stefan Weber
    Julien J H Cotelesage
    Graham N George
    Ulrich Ermler
    Matthias Boll
    Nature Chemical Biology, 2015, 11 (10) : 815 - 815
  • [4] Structural basis of enzymatic benzene ring reduction (vol 11, pg 586, 2015)
    Weinert, Tobias
    Huwiler, Simona G.
    Kung, Johannes W.
    Weidenweber, Sina
    Hellwig, Petra
    Staerk, Hans-Joachim
    Biskup, Till
    Weber, Stefan
    Cotelesage, Julien J. H.
    George, Graham N.
    Ermler, Ulrich
    Boll, Matthias
    NATURE CHEMICAL BIOLOGY, 2015, 11 (10) : 815 - 815
  • [5] Structural basis of enzymatic benzene ring reduction (vol 11, pg 586, 2015)
    Weinert, Tobias
    Huwiler, Simona G.
    Kung, Johannes W.
    Weidenweber, Sina
    Hellwig, Petra
    Staerk, Hans-Joachim
    Biskup, Till
    Weber, Stefan
    Cotelesage, Julien J. H.
    George, Graham N.
    Ermler, Ulrich
    Boll, Matthias
    NATURE CHEMICAL BIOLOGY, 2015, 11 (09) : 741 - 741
  • [6] ELECTROCHEMICAL REDUCTION OF THE BENZENE RING
    STERNBERG, HW
    MARKBY, R
    WENDER, I
    JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1961, 108 (08) : C181 - C181
  • [7] ELECTROCHEMICAL REDUCTION OF THE BENZENE RING
    STERNBERG, HW
    MARKBY, R
    WENDER, I
    JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1963, 110 (05) : 425 - 429
  • [8] THE STRUCTURAL BASIS OF ENZYMATIC CATALYSIS
    RICHARDS, JH
    LABGOLD, M
    SLUTTER, C
    RICHMOND, T
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1991, 202 : 239 - BIOT
  • [9] Enantioselective Enzymatic Naphthoyl Ring Reduction
    Willistein, Max
    Haas, Julian
    Fuchs, Jonathan
    Estelmann, Sebastian
    Ferlaino, Sascha
    Mueller, Michael
    Luedeke, Steffen
    Boll, Matthias
    CHEMISTRY-A EUROPEAN JOURNAL, 2018, 24 (48) : 12505 - 12508
  • [10] ELECTROCHEMICAL REDUCTION OF BENZENE RING BY ELECTROGENERATIVE HYDROGENATION
    LANGER, SH
    YURCHAK, S
    JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1969, 116 (09) : 1228 - &