Počet záznamů: 1

Biotransformation of nitriles to hydroxamic acids via a nitrile hydratase–amidase cascade reaction

  1. 1.
    0360786 - MBU-M 2012 RIV NL eng J - Článek v odborném periodiku
    Vejvoda, Vojtěch - Martínková, Ludmila - Veselá, Alicja Barbara - Kaplan, Ondřej - Lutz-Wahl, S. - Fischer, L. - Uhnáková, Bronislava
    Biotransformation of nitriles to hydroxamic acids via a nitrile hydratase–amidase cascade reaction.
    Journal of Molecular Catalysis B-Enzymatic. Roč. 71, 1-2 (2011), s. 51-55 ISSN 1381-1177
    Grant CEP: GA MŠk(CZ) LC06010; GA MŠk OC09046
    Výzkumný záměr: CEZ:AV0Z50200510
    Klíčová slova: Nitrile hydratase * Rhodococcus erythropolis * Amidase
    Kód oboru RIV: EE - Mikrobiologie, virologie
    Impakt faktor: 2.735, rok: 2011

    The transformation of benzonitrile into benzohydroxamic acid was performed by a cascade bienzymatic reaction involving nitrile hydration and acyl transfer of the intermediate benzamide onto hydroxylamine. The first step was catalyzed by either a cell-free extract from Rhodococcus erythropolis A4 (nitrile hydratase) or cell-free extracts from recombinant Escherichia coli strains expressing nitrile hydratases from Raoultella terrigena 77.1 and Klebsiella oxytoca 38.1.2; the biocatalyst in the second step was a cellfree extract from R. erythropolis A4 (amidase). When using the cell-free extract from R. erythropolis A4 in the first step, the hydrolytic amidase activity was suppressed by ammonium ions, which, however, did not inhibit the acyl transfer reaction catalyzed by the same enzyme. Aromatic and aliphatic nitriles were examined as substrates of the recombinant nitrile hydratases by using a colorimetric assay of hydroxamic acids produced in a coupled acyl transfer reaction
    Trvalý link: http://hdl.handle.net/11104/0198253