| Literature DB >> 27573978 |
Aitao Li1,2, Adriana Ilie1,2, Zhoutong Sun1,2, Richard Lonsdale1,2, Jian-He Xu3, Manfred T Reetz4,5.
Abstract
Biocatalytic cascade reactions using isolated stereoselective enzymes or whole cells in one-pot processes lead to value-added chiral products in a single workup. The concept has been restricted mainly to starting materials and intermediate products that are accepted by the respective wild-type enzymes. In the present study, we exploited directed evolution as a means to create E. coli whole cells for regio- and stereoselective cascade sequences that are not possible using man-made catalysts. The approach is illustrated using P450-BM3 in combination with appropriate alcohol dehydrogenases as catalysts in either two-, three-, or four-step cascade reactions starting from cyclohexane, cyclohexanol, or cyclohexanone, respectively, leading to either (R,R)-, (S,S)-, or meso-cyclohexane-1,2-diol. The one-pot conversion of cyclohexane into (R)- or (S)-2-hydroxycyclohexanone in the absence of ADH is also described.Entities:
Keywords: C−H activation; P450 monooxygenase; cascade reactions; directed evolution; enantioselectivity
Year: 2016 PMID: 27573978 DOI: 10.1002/anie.201605990
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336