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Recombinant Cyanobacteria for the Asymmetric Reduction of C=C Bonds Fueled by the Biocatalytic Oxidation of Water
Authors:Katharina Köninger  Dr Álvaro Gómez Baraibar  Dr Carolin Mügge  Dr Caroline E Paul  Dr Frank Hollmann  Dr Marc M Nowaczyk  Prof Dr Robert Kourist
Institution:1. Junior Research Group for Microbial Biotechnology, Ruhr-Universit?t Bochum, Bochum, Germany;2. Department of Biotechnology, Delft University of Technology, The Netherlands;3. Chair of Plant Biochemistry, Ruhr-Universit?t Bochum, Germany
Abstract:A recombinant enoate reductase was expressed in cyanobacteria and used for the light‐catalyzed, enantioselective reduction of C=C bonds. The coupling of oxidoreductases to natural photosynthesis allows asymmetric syntheses fueled by the oxidation of water. Bypassing the addition of sacrificial cosubstrates as electron donors significantly improves the atom efficiency and avoids the formation of undesired side products. Crucial factors for product formation are the availability of NADPH and the amount of active enzyme in the cells. The efficiency of the reaction is comparable to typical whole‐cell biotransformations in E. coli. Under optimized conditions, a solution of 100 mg prochiral 2‐methylmaleimide was reduced to optically pure 2‐methylsuccinimide (99 % ee, 80 % yield of isolated product). High product yields and excellent optical purities demonstrate the synthetic usefulness of light‐catalyzed whole‐cell biotransformations using recombinant cyanobacteria.
Keywords:biotechnology  enzyme catalysis  photocatalysis  photosynthesis  reduction
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