A strategy for biocatalyst immobilization in flow directly from the crude cell extract is described. The efficiency and the stability of the immobilized enzyme were demonstrated during the asymmetric reduction of a range of ketones. The cascade two-step chemo-enzymatic preparation of chiral epoxides was possible through the initial ketone bioreduction to an intermediate halohydrin followed by its intramolecular cyclization.

Rapid, selective and stable HaloTag-Lb ADH immobilization directly from crude cell extract for the continuous biocatalytic production of chiral alcohols and epoxides / Dobber, J.; Pohl, M.; Ley, S. V.; Musio, B.. - In: REACTION CHEMISTRY & ENGINEERING. - ISSN 2058-9883. - 3:1(2018), pp. 8-12. [10.1039/c7re00173h]

Rapid, selective and stable HaloTag-Lb ADH immobilization directly from crude cell extract for the continuous biocatalytic production of chiral alcohols and epoxides

Musio B.
2018-01-01

Abstract

A strategy for biocatalyst immobilization in flow directly from the crude cell extract is described. The efficiency and the stability of the immobilized enzyme were demonstrated during the asymmetric reduction of a range of ketones. The cascade two-step chemo-enzymatic preparation of chiral epoxides was possible through the initial ketone bioreduction to an intermediate halohydrin followed by its intramolecular cyclization.
2018
Rapid, selective and stable HaloTag-Lb ADH immobilization directly from crude cell extract for the continuous biocatalytic production of chiral alcohols and epoxides / Dobber, J.; Pohl, M.; Ley, S. V.; Musio, B.. - In: REACTION CHEMISTRY & ENGINEERING. - ISSN 2058-9883. - 3:1(2018), pp. 8-12. [10.1039/c7re00173h]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11589/223784
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