Synergistic CRISPR–Cas9 Host Engineering and Enzyme Evolution for Enantioselective Synthesis of a Vibegron Pyrrolidine Intermediate

View at publisher Summarise with VIRAT
Authors: Jinping Bao, Xiaozhi Ju, Han Zhang, Dongyu Tang, Juzhang Yan, Chengsen Cui, Shu‐Shan Gao
Cited by: 0
References: 39

Summary

No summary yet. VIRAT can read this paper and write a plain-language summary of its aim, methods, key findings and limitations.

Summarise with VIRAT Free to try with your Science Catalogs account.

Abstract

The stereoselective synthesis of chiral pyrrolidine motifs is essential to vibegron production but remains challenging using conventional chemical routes. Here we report an imine reductase (IRED) catalyzed asymmetric imine reduction to access a key vibegron intermediate. Directed evolution afforded a highly efficient variant delivering 94% conversion and >99% d.e. Combined enzyme and host engineering enabled clean whole cell catalysis, establishing a robust and scalable biocatalytic platform.

Fields of Study & Subjects

Enzyme Catalysis and Immobilization Asymmetric Hydrogenation and Catalysis Asymmetric Synthesis and Catalysis

Publication details

Journal / source
Organic Letters
Volume
28
Issue
12
Pages
3695–3700
Publication date
16 March 2026
Language
EN