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https://doi.org/10.1002/adsc.200505439
Title: | Efficient NADPH recycling in enantioselective bioreduction of a ketone with permeabilized cells of a microorganism containing a ketoreductase and a glucose 6-phosphate dehydrogenase | Authors: | Zhang, J. Witholt, B. Li, Z. |
Keywords: | Cofactor recycling Enzyme catalysis Glucose 6-phosphate dehydrogenase Ketoreductase Permeabilized cells Reduction |
Issue Date: | Mar-2006 | Citation: | Zhang, J., Witholt, B., Li, Z. (2006-03). Efficient NADPH recycling in enantioselective bioreduction of a ketone with permeabilized cells of a microorganism containing a ketoreductase and a glucose 6-phosphate dehydrogenase. Advanced Synthesis and Catalysis 348 (4-5) : 429-433. ScholarBank@NUS Repository. https://doi.org/10.1002/adsc.200505439 | Abstract: | We have demonstrated, for the first time, the efficient recycling of NADPH in a bioreduction with permeabilized cells of a single microorganism. Permeabilized cells of Bacillus pumilus Phe-C3 containing an NADPH-dependent ketoreductase and a glucose 6-phosphate dehydrogenase (G-6-PDH) were successfully used for the reduction of ethyl 3-oxo-4,4,4-trifluorobutanoate (1) to give (R)-ethyl 3-hydroxy-4,4,4-trifluorobutanoate (2) in 95% ee with the recycling of NADPH for 4220 times from the externally added NADP+. The permeabilized cells were shown to be stable and active for a long period, allowing for high product concentration with high cofactor TTN by continuing the bioreduction with renewed addition of NADP+. This provides with not only a practical synthesis of (R)-2 but also a useful method applicable to many microbial oxidoreductions, since G-6-PDH is a very common enzyme existing in many microorganisms. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA. | Source Title: | Advanced Synthesis and Catalysis | URI: | http://scholarbank.nus.edu.sg/handle/10635/88821 | ISSN: | 16154150 | DOI: | 10.1002/adsc.200505439 |
Appears in Collections: | Staff Publications |
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