Your browser doesn't support javascript.
loading
Resting Escherichia coli as Chassis for Microbial Electrosynthesis: Production of Chiral Alcohols.
Mayr, Jeannine C; Grosch, Jan-Hendrik; Hartmann, Lena; Rosa, Luis F M; Spiess, Antje C; Harnisch, Falk.
Afiliação
  • Mayr JC; Institute of Biochemical Engineering, Braunschweig Integrated Centre of Systems Biology (BRICS), Technische Universität Braunschweig, Rebenring 56, 38106, Braunschweig, Germany.
  • Grosch JH; Institute of Biochemical Engineering, Braunschweig Integrated Centre of Systems Biology (BRICS), Technische Universität Braunschweig, Rebenring 56, 38106, Braunschweig, Germany.
  • Hartmann L; Center of Pharmaceutical Engineering (PVZ), Technische Universität Braunschweig, Franz-Liszt-Straße 35a, 38106, Braunschweig, Germany.
  • Rosa LFM; Institute of Biochemical Engineering, Braunschweig Integrated Centre of Systems Biology (BRICS), Technische Universität Braunschweig, Rebenring 56, 38106, Braunschweig, Germany.
  • Spiess AC; Department of Environmental Microbiology, Helmholtz-Centre for Environmental Research, UFZ Permoserstraße 15, 04318, Leipzig, Germany.
  • Harnisch F; Institute of Biochemical Engineering, Braunschweig Integrated Centre of Systems Biology (BRICS), Technische Universität Braunschweig, Rebenring 56, 38106, Braunschweig, Germany.
ChemSusChem ; 12(8): 1631-1634, 2019 Apr 23.
Article em En | MEDLINE | ID: mdl-30762315
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.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article