Artificial metalloenzymes for enantioselective catalysis

被引:117
作者
Bos, Jeffrey [1 ]
Roelfes, Gerard [1 ]
机构
[1] Univ Groningen, Stratingh Inst Chem, NL-9747 AG Groningen, Netherlands
关键词
BIOTIN-STREPTAVIDIN TECHNOLOGY; DIELS-ALDER REACTIONS; ASYMMETRIC CATALYSIS; TRANSFER HYDROGENATION; H ACTIVATION; DNA; COMPLEXES; PROTEIN; ENZYME; SITE;
D O I
10.1016/j.cbpa.2014.02.002
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
Artificial metalloenzymes have emerged over the last decades as an attractive approach towards combining homogeneous catalysis and biocatalysis. A wide variety of catalytic transformations have been established by artificial metalloenzymes, thus establishing proof of concept. The field is now slowly transforming to take on new challenges. These include novel designs, novel catalytic reactions, some of which have no equivalent in both homogenous catalysis and biocatalysis and the incorporation of artificial metalloenzymes in chemoenzymatic cascades. Some of these developments represent promising steps towards integrating artificial metalloenzymes in biological systems. This review will focus on advances in this field and perspectives discussed.
引用
收藏
页码:135 / 143
页数:9
相关论文
共 49 条
  • [1] Incorporation of Manganese Complexes into Xylanase: New Artificial Metalloenzymes for Enantioselective Epoxidation
    Allard, Mathieu
    Dupont, Claude
    Munoz Robles, Victor
    Doucet, Nicolas
    Lledos, Agusti
    Marechal, Jean-Didier
    Urvoas, Agathe
    Mahy, Jean-Pierre
    Ricoux, Remy
    [J]. CHEMBIOCHEM, 2012, 13 (02) : 240 - 251
  • [2] Designing Enzyme-like Catalysts: A Rhodium(II) Metallopeptide Case Study
    Ball, Zachary T.
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2013, 46 (02) : 560 - 570
  • [3] Ligand denticity controls enantiomeric preference in DNA-based asymmetric catalysis
    Boersma, Arnold J.
    de Bruin, Bas
    Feringa, Ben L.
    Roelfes, Gerard
    [J]. CHEMICAL COMMUNICATIONS, 2012, 48 (18) : 2394 - 2396
  • [4] An enantioselective artificial metallo-hydratase
    Bos, Jeffrey
    Garcia-Herraiz, Ana
    Roelfes, Gerard
    [J]. CHEMICAL SCIENCE, 2013, 4 (09) : 3578 - 3582
  • [5] Enantioselective Artificial Metalloenzymes by Creation of a Novel Active Site at the Protein Dimer Interface
    Bos, Jeffrey
    Fusetti, Fabrizia
    Driessen, Arnold J. M.
    Roelfes, Gerard
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (30) : 7472 - 7475
  • [6] Structural Basis for Enantioselectivity in the Transfer Hydrogenation of a Ketone Catalyzed by an Artificial Metalloenzyme
    Cherrier, Mickal V.
    Engilberge, Sylvain
    Amara, Patricia
    Chevalley, Alice
    Salmain, Michele
    Fontecilla-Camps, Juan C.
    [J]. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2013, 2013 (21) : 3596 - 3600
  • [7] Enantioselective transfer hydrogenation of ketone catalysed by artificial metalloenzymes derived from bovine β-lactoglobulin
    Chevalley, Alice
    Salmain, Michele
    [J]. CHEMICAL COMMUNICATIONS, 2012, 48 (98) : 11984 - 11986
  • [8] A serine-substituted P450 catalyzes highly efficient carbene transfer to olefins in vivo
    Coelho, Pedro S.
    Wang, Z. Jane
    Ener, Maraia E.
    Baril, Stefanie A.
    Kannan, Arvind
    Arnold, Frances H.
    Brustad, Eric M.
    [J]. NATURE CHEMICAL BIOLOGY, 2013, 9 (08) : 485 - U33
  • [9] X-ray structure and designed evolution of an artificial transfer hydrogenase
    Creus, Marc
    Pordea, Anca
    Rossel, Thibaud
    Sardo, Alessia
    Letondor, Christophe
    Ivanova, Anita
    Le Trong, Isolde
    Stenkamp, Ronald E.
    Ward, Thomas R.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (08) : 1400 - 1404
  • [10] Artificial Copper Enzymes for Asymmetric Diels-Alder Reactions
    Deuss, Peter J.
    Popa, Gina
    Slawin, Alexandra M. Z.
    Laan, Wouter
    Kamer, Paul C. J.
    [J]. CHEMCATCHEM, 2013, 5 (05) : 1184 - 1191