Electronic Journal of Biotechnology ISSN: 0717-3458
  © 2000 by Universidad Católica de Valparaíso -- Chile
Vol. 3 No. 3, Issue of December 15, 2000


Figure 9.

Enantiomeric excess of the R-enantiomer of flurbiprofen as a function of the total substrate converted to product by the Candida rugosa lipase-catalyzed reaction in isooctane at 0.65 water activity.

Supported by UNESCO / MIRCEN network