Basit öğe kaydını göster

dc.contributor.authorŞahin, Engin
dc.contributor.authorSerencam, Hüseyin
dc.contributor.authorDertli, Enes
dc.date.accessioned2020-11-25T19:24:35Z
dc.date.available2020-11-25T19:24:35Z
dc.date.issued2019en_US
dc.identifier.citationŞahin, E., Serencam, H., & Dertli, E. (2019). Whole cell application of Lactobacillus paracasei BD101 to produce enantiomerically pure (S)‐cyclohexyl (phenyl) methanol. Chirality, 31(3), 211-218.en_US
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1002/chir.23048?casa_token=jKxdVUNBEBMAAAAA%3A--EcySvGlulNuDMDYbiLKgKN0-HsNHOu9PmjjeyPat7iLMlNFXo0werFPJ2Uf32WEjV3nzwaLbGXM-xy
dc.identifier.urihttps://hdl.handle.net/20.500.12403/2220
dc.description.abstractIn 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.en_US
dc.language.isoengen_US
dc.publisherChiralityen_US
dc.relation.isversionof10.1002/chir.23048en_US
dc.subjectChiralityen_US
dc.subjectBiotransformationen_US
dc.titleWhole cell application of Lactobacillus paracasei BD101 to produce enantiomerically pure (S)‐cyclohexyl(phenyl)methanolen_US
dc.typearticleen_US
dc.relation.journalChiralityen_US
dc.contributor.departmentBayburt Üniversitesi, Sağlık Bilimleri Fakültesi, Beslenme ve Diyetetik Bölümüen_US
dc.contributor.authorID0000-0002-3723-1705en_US
dc.identifier.volume31en_US
dc.identifier.issue3en_US
dc.identifier.startpage211en_US
dc.identifier.endpage218en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster