| Literature DB >> 32808246 |
Can Cui1,2, Hui Lin3, Wei Pu1,2, Chao Guo1, Yan Liu1, Xiao-Qiong Pei1, Zhong-Liu Wu4.
Abstract
Asymmetric epoxidation catalyzed with styrene monooxygenase (SMO) is a powerful enzymatic process producing enantiopure styrene epoxide derivatives. To establish a more diversified reservoir of SMOs, a new SMO from Bradyrhizobium sp. ORS 375, named BrSMO, was mined from the database and characterized. BrSMO was constituted of an epoxygenase component of 415 amino acid residues and an NADH-dependent flavin reductase component of 175 residues. BrSMO catalyzed the epoxidation of styrene and 7 more styrene derivatives, yielding the corresponding (S)-epoxides with excellent enantiomeric excesses (95- > 99% ee), with the highest activity achieved for styrene. BrSMO also catalyzed the asymmetric sulfoxidation of 7 sulfides, producing the corresponding (R)-sulfoxides (20-90% ee) with good yields.Entities:
Keywords: Asymmetric epoxidation; Asymmetric sulfoxidation; Bradyrhizobium; Styrene monooxygenase; Whole-cell biotransformation
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Year: 2020 PMID: 32808246 DOI: 10.1007/s12010-020-03413-8
Source DB: PubMed Journal: Appl Biochem Biotechnol ISSN: 0273-2289 Impact factor: 2.926