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Whole cell application of Lactobacillus paracasei BD101 to produce enantiomerically pure ( S )‐cyclohexyl(phenyl)methanol
Author(s) -
Şahin Engin,
Serencam Hüseyin,
Dertli Enes
Publication year - 2019
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/chir.23048
Subject(s) - lactobacillus paracasei , chemistry , biocatalysis , methanol , enantiomeric excess , alcohol , yield (engineering) , enantiomer , enantioselective synthesis , organic chemistry , catalysis , lactobacillus , fermentation , reaction mechanism , materials science , metallurgy
Abstract In this study, a total of 10 bacterial strains were screened for their ability to reduce cyclohexyl(phenyl)methanone 1 to its corresponding alcohol. Among these strains, Lactobacillus paracasei BD101 was found to be the most successful biocatalyst to reduce the ketones to the corresponding alcohols. The reaction conditions were systematically optimized for the reducing agent L paracasei BD101, which showed high enantioselectivity and conversion for the bioreduction. The preparative scale asymmetric reduction of cyclohexyl(phenyl)methanone ( 1 ) by L paracasei BD101 gave ( S )‐cyclohexyl(phenyl)methanol ( 2 ) with 92% yield and >99% enantiomeric excess. The preparative scale study was carried out, and a total of 5.602 g of ( S )‐cyclohexyl(phenyl)methanol in high enantiomerically pure form (>99% enantiomeric excess) was produced. L paracasei BD101 has been shown to be an important biocatalyst in asymmetric reduction of bulky substrates. This study demonstrates the first example of the effective synthesis of ( S )‐cyclohexyl(phenyl)methanol by the L paracasei BD101 as a biocatalyst in preparative scale.