M. Chartrain et al., ASYMMETRIC BIOREDUCTION OF CYCLOHEXYLPHENYL KETONE TO ITS CORRESPONDING ALCOHOL (-MAGNOLIAE MY-1785()CYCLOHEXYLPHENYL ALCOHOL BY THE YEAST CANDIDA), Journal of fermentation and bioengineering, 83(4), 1997, pp. 395-396
The screening of 129 fungal and yeasts strains yielded Candida magnoli
ae MY 1785 as a suitable biocatalyst for the asymmetric bioreduction o
f cyclohexylphenyl ketone to its corresponding alcohol. Preparative am
ounts of pure alcohol were prepared and purified. Polarimetry and chir
al HPLC analyses indicated that C. magnoliae produced the (+) cyclohex
ylphenyl alcohol with an enantiomeric excess of 75%. A 55% bioconversi
on yield was achieved at the preparative scale.