Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4756605 | Catalysis Communications | 2017 | 5 Pages |
â¢A carbonyl reductase was discovered to reduce NBPO to (R)-NBHP with high activity.â¢A GDH-catalyzed cofactor-recycling system was used to regenerate NADPH.â¢The process was optimized and applied to produce (R)-NBHP (> 99% ee).â¢The asymmetric reduction was conducted at high substrate loading (400 g/L).
The 3-hydroxypiperidine moiety is a privileged scaffold encountered in many bioactive compounds. An NADPH-dependent reductase (YGL039W) from Kluyveromyces marxianus ATCC 748 was isolated to show excellent catalytic activity in (R)-N-Boc-3-hydroxypiperidine [(R)-NBHP] production. Using a GDH-catalyzed cofactor-recycling system to ensure a sufficient supply of NADPH, the effects of temperature, pH, metal ions, substrate concentration, biocatalyst dosage, and cofactors on the YGL039W-catalyzed bioreduction were investigated and optimized. Finally, an extremely high concentration of N-Boc-piperidin-3-one (NBPO, 400Â g/L) could be completely reduced to (R)-NBHP (>Â 99% ee), with a total turnover number of 20,000. This process shows significant potential for the industrial production of (R)-NBHP.
Graphical abstractDownload high-res image (78KB)Download full-size image