화학공학소재연구정보센터
Biotechnology Letters, Vol.18, No.9, 1073-1076, 1996
Enantioselectivity of the Nitrile Hydratase from Rhodococcus-Equi A4 Towards Substituted (R,S)-2-Arylpropionitriles
Rhodococcus equi A4 cells containing a nitrile hydratase and an amidase converted (R, S)-2-(4-methoxyphenyl)-propionitrile into the corresponding (S)-acid (e.e. 87%) and (R)-nitrile (e.e. > 95%) in 49% yield. The same reaction using (R, S)-2-(4- chlorophenyl)-propionitrile gave the (S)-acid (e.e. > 95%) and (R)-nitrile (e.e. 52%) in 20 and 34% yield, respectively.