Huang Chenming, Liu Junling, Fang Jiali, Jia Xian, Zheng Zhendong, You Song, Qin Bin
Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, China.
Department of Oncology, General Hospital of Northern Theater Command, Shenyang, China.
Front Bioeng Biotechnol. 2022 Jun 30;10:929784. doi: 10.3389/fbioe.2022.929784. eCollection 2022.
Biocatalyzed asymmetric reduction of ketones is an environmentally friendly approach and one of the most cost-effective routes for producing chiral alcohols. In comparison with the well-studied reduction of prochiral ketones to generate chiral alcohols with one chiral center, resolution of racemates by ketoreductases (KREDs) to produce chiral compounds with at least two chiral centers is also an important strategy in asymmetric synthesis. The development of protein engineering and the combination with chemo-catalysts further enhanced the application of KREDs in the efficient production of chiral alcohols with high stereoselectivity. This review discusses the advances in the research area of KRED catalyzed asymmetric synthesis for biomanufacturing of chiral chemicals with at least two chiral centers through the kinetic resolution (KR) approach and the dynamic kinetic resolution (DKR) approach.
生物催化的酮不对称还原是一种环境友好的方法,也是生产手性醇最具成本效益的途径之一。与已得到充分研究的将前手性酮还原以生成具有一个手性中心的手性醇相比,通过酮还原酶(KREDs)拆分外消旋体以生产具有至少两个手性中心的手性化合物也是不对称合成中的一项重要策略。蛋白质工程的发展以及与化学催化剂的结合进一步增强了KREDs在高效生产具有高立体选择性的手性醇方面的应用。本文综述了通过动力学拆分(KR)方法和动态动力学拆分(DKR)方法,KRED催化不对称合成用于生物制造具有至少两个手性中心的手性化学品这一研究领域的进展。