| Literature DB >> 30762315 |
Jeannine C Mayr1, Jan-Hendrik Grosch1,2, Lena Hartmann1, Luis F M Rosa3, Antje C Spiess1,2, Falk Harnisch3.
Abstract
Chiral alcohols constitute important building blocks that can be produced enantioselectively by using nicotinamide adenine dinucleotide (phosphate) [NAD(P)H]-dependent oxidoreductases. For NAD(P)H regeneration, electricity delivers the cheapest reduction equivalents. Enzymatic electrosynthesis suffers from cofactor and enzyme instability, whereas microbial electrosynthesis (MES) exploits whole cells. Here, we demonstrate MES by using resting Escherichia coli as biocatalytic chassis for a production platform towards fine chemicals through electric power. This chassis was exemplified for the synthesis of chiral alcohols by using a NADPH-dependent alcohol dehydrogenase from Lactobacillus brevis for synthesis of (R)-1-phenylethanol from acetophenone. The E. coli strain and growth conditions affected the performance. Maximum yields of (39.4±5.7) % at a coulombic efficiency of (50.5±6.0) % with enantiomeric excess >99 % was demonstrated at a rate of (83.5±13.9) μm h-1 , confirming the potential of MES for synthesis of high-value compounds.Entities:
Keywords: biocatalysis; cofactor regeneration; electrobiotechnology; enantioselectivity; microbial electrosynthesis
Year: 2019 PMID: 30762315 DOI: 10.1002/cssc.201900413
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928