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Chemo-bio catalysis using carbon supports: application in H2-driven cofactor recycling.
Zhao, Xu; Cleary, Sarah E; Zor, Ceren; Grobert, Nicole; Reeve, Holly A; Vincent, Kylie A.
Afiliação
  • Zhao X; Department of Chemistry, University of Oxford, Inorganic Chemistry Laboratory South Parks Road Oxford OX1 3QR UK holly.reeve@chem.ox.ac.uk kylie.vincent@chem.ox.ac.uk.
  • Cleary SE; Department of Chemistry, University of Oxford, Inorganic Chemistry Laboratory South Parks Road Oxford OX1 3QR UK holly.reeve@chem.ox.ac.uk kylie.vincent@chem.ox.ac.uk.
  • Zor C; Department of Materials, University of Oxford Parks Road Oxford OX1 3PH UK nicole.grobert@materials.ox.ac.uk.
  • Grobert N; Department of Materials, University of Oxford Parks Road Oxford OX1 3PH UK nicole.grobert@materials.ox.ac.uk.
  • Reeve HA; Department of Chemistry, University of Oxford, Inorganic Chemistry Laboratory South Parks Road Oxford OX1 3QR UK holly.reeve@chem.ox.ac.uk kylie.vincent@chem.ox.ac.uk.
  • Vincent KA; Department of Chemistry, University of Oxford, Inorganic Chemistry Laboratory South Parks Road Oxford OX1 3QR UK holly.reeve@chem.ox.ac.uk kylie.vincent@chem.ox.ac.uk.
Chem Sci ; 12(23): 8105-8114, 2021 May 07.
Article em En | MEDLINE | ID: mdl-34194700
ABSTRACT
Heterogeneous biocatalytic hydrogenation is an attractive strategy for clean, enantioselective C[double bond, length as m-dash]X reduction. This approach relies on enzymes powered by H2-driven NADH recycling. Commercially available carbon-supported metal (metal/C) catalysts are investigated here for direct H2-driven NAD+ reduction. Selected metal/C catalysts are then used for H2 oxidation with electrons transferred via the conductive carbon support material to an adsorbed enzyme for NAD+ reduction. These chemo-bio catalysts show improved activity and selectivity for generating bioactive NADH under ambient reaction conditions compared to metal/C catalysts. The metal/C catalysts and carbon support materials (all activated carbon or carbon black) are characterised to probe which properties potentially influence catalyst activity. The optimised chemo-bio catalysts are then used to supply NADH to an alcohol dehydrogenase for enantioselective (>99% ee) ketone reductions, leading to high cofactor turnover numbers and Pd and NAD+ reductase activities of 441 h-1 and 2347 h-1, respectively. This method demonstrates a new way of combining chemo- and biocatalysis on carbon supports, highlighted here for selective hydrogenation reactions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Sci Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Sci Ano de publicação: 2021 Tipo de documento: Article