H. Miya et al., STEREOSELECTIVE REDUCTION OF ETHYL 2-METHYL-3-OXOBUTANOATE BY BACTERIA, Bioscience, biotechnology, and biochemistry, 60(1), 1996, pp. 95-98
More than 450 bacterial strains were examined for their ability to red
uce ethyl 2-methyl-3-oxobutanoate (1) to ethyl 3-hydroxy-2-methylbutan
oate. Nine strains of enteric bacteria were found to predominantly yie
ld the product with a syn configuration. Of these strains, five gave e
thyl (2R,3S) 3-hydroxy-2-methylbutanoate (2a) with more than 98% diast
ereoisomeric excess (d,e,) and over 99% enantiomeric excess (e,e,) Kle
bsiella pneumoniae IFO 3319 was found to give the highest d.e., f.e.,
and chemical yield at a high concentration of 1. Reduction of 1 was th
en done with the bacterium in a 200-liter fermentor. Two kilograms of
1 was converted to 2a with 99% d.e., >99% e.e., and 99% chemical yield
.