The reliable design and prediction of enzyme promiscuity to access transformations not observed in nature remains a long-standing challenge. Herein, we present the first example of an intramolecular stereoselective Stetter reaction catalyzed by benzaldehyde lyase, guided by the rational structure screening of various ThDP-dependent enzymes using molecular dynamics (MD) simulations. After optimization, high productivity (up to 99 %) and stereoselectivity (up to 99:1 e.r.) for this novel enzyme function was achieved.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.202100534 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!