Issue 49, 2023

Engineering ketoreductases for the enantioselective synthesis of chiral alcohols

Abstract

The use of engineered ketoreductases (KREDS), both as whole microbial cells and isolated enzymes, in the highly enantiospecific reduction of prochiral ketones is reviewed. The homochiral alcohol products are key intermediates in, for example, pharmaceuticals synthesis. The application of sophisticated protein engineering and enzyme immobilisation techniques to increase industrial viability are discussed.

Graphical abstract: Engineering ketoreductases for the enantioselective synthesis of chiral alcohols

Supplementary files

Article information

Article type
Feature Article
Submitted
26 Mar 2023
Accepted
04 May 2023
First published
05 May 2023
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2023,59, 7518-7533

Engineering ketoreductases for the enantioselective synthesis of chiral alcohols

L. Qiao, Z. Luo, H. Chen, P. Zhang, A. Wang and R. A. Sheldon, Chem. Commun., 2023, 59, 7518 DOI: 10.1039/D3CC01474F

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements