Six strains of acetic acid bacteria were evaluated with respect to their capability to catalyze the stereoselective reduction of ketones. The cells were permeabilized before the bioconversions. The best strains were Gluconobacter oxydans DSM 50049 and Acetobacter aceti DSM 2002. Using either of these two strains it was possible to reduce all 12 ketones to (S)-alcohols with an enantiomeric excess of ≥94 %. The highest level of enzymatic activity was found in Acetobacter aceti DSM 2002
<div><p>A novel carbonyl reductase (<i>Ac</i>CR) catalyzing the asymmetric reduction of ketones to e...
The reduction of methyl acetoacetate was carried out in continuously operated biotransformation proc...
Gröger H, Borchert S, Kraußer M, Hummel W. Enzyme-Catalyzed Asymmetric Reduction of Ketones. In: Fli...
Gluconobacter oxydans (ATCC 621) were permeabilized with toluene and then lyophilized. This crude en...
The biocatalytic asymmetric reduction of prochiral ketones for the production of enantiopure alcohol...
Chiral secondary alcohols are valuable intermediates for many important enantiopure pharmaceuticals ...
Acetic acid bacteria (five strains of Acetobacter and five strains of Gluconobacter) were used for t...
Gröger H, Hummel W, Metzner R. Asymmetric Biocatalytic Reduction of Ketones. In: Carreira EM, Yamamo...
Two genes encoding recombinant cytosolic oxidoreductases from Gluconobacter oxydans, gox0313 and gox...
Alcohol dehydrogenases or carbonyl reductases have been extensively developed for the asymmetric red...
Background: The bacterium Acetobacter sp. CCTCC M209061 is a promising whole-cell biocatalyst with...
A novel strain, Microbacterium sp., which can be used as a catalyst in the asymmetric reduction of s...
Whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to optically acti...
Whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to optically acti...
Abstract Background Chiral alcohols are widely used in the synthesis of chiral pharmaceuticals, flav...
<div><p>A novel carbonyl reductase (<i>Ac</i>CR) catalyzing the asymmetric reduction of ketones to e...
The reduction of methyl acetoacetate was carried out in continuously operated biotransformation proc...
Gröger H, Borchert S, Kraußer M, Hummel W. Enzyme-Catalyzed Asymmetric Reduction of Ketones. In: Fli...
Gluconobacter oxydans (ATCC 621) were permeabilized with toluene and then lyophilized. This crude en...
The biocatalytic asymmetric reduction of prochiral ketones for the production of enantiopure alcohol...
Chiral secondary alcohols are valuable intermediates for many important enantiopure pharmaceuticals ...
Acetic acid bacteria (five strains of Acetobacter and five strains of Gluconobacter) were used for t...
Gröger H, Hummel W, Metzner R. Asymmetric Biocatalytic Reduction of Ketones. In: Carreira EM, Yamamo...
Two genes encoding recombinant cytosolic oxidoreductases from Gluconobacter oxydans, gox0313 and gox...
Alcohol dehydrogenases or carbonyl reductases have been extensively developed for the asymmetric red...
Background: The bacterium Acetobacter sp. CCTCC M209061 is a promising whole-cell biocatalyst with...
A novel strain, Microbacterium sp., which can be used as a catalyst in the asymmetric reduction of s...
Whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to optically acti...
Whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to optically acti...
Abstract Background Chiral alcohols are widely used in the synthesis of chiral pharmaceuticals, flav...
<div><p>A novel carbonyl reductase (<i>Ac</i>CR) catalyzing the asymmetric reduction of ketones to e...
The reduction of methyl acetoacetate was carried out in continuously operated biotransformation proc...
Gröger H, Borchert S, Kraußer M, Hummel W. Enzyme-Catalyzed Asymmetric Reduction of Ketones. In: Fli...