Academic Journal

Semi-rational engineering an aldo–keto reductase for stereocomplementary reduction of α-keto amide compounds

التفاصيل البيبلوغرافية
العنوان: Semi-rational engineering an aldo–keto reductase for stereocomplementary reduction of α-keto amide compounds
المؤلفون: Ruixuan Bai, Baoling Chen, Liangyu Zheng
المصدر: Microbial Cell Factories, Vol 22, Iss 1, Pp 1-14 (2023)
بيانات النشر: BMC, 2023.
سنة النشر: 2023
المجموعة: LCC:Microbiology
مصطلحات موضوعية: α-keto amides, α-hydroxyl amides, Aldo–keto reductase, Stereocomplementary, Semi-rational engineering, Switch, Microbiology, QR1-502
الوصف: Abstract Enantio-pure α-hydroxy amides are valuable intermediates for the synthesis of chiral pharmaceuticals. The asymmetric reduction of α-keto amides to generate chiral α-hydroxy amides is a difficult and challenging task in biocatalysis. In this study, iolS, an aldo–keto reductase from Bacillus subtilis 168 was exhibited as a potential biocatalyst, which could catalyze the reduction of diaryl α-keto amide such as 2-oxo-N, 2-diphenyl-acetamide (ONDPA) with moderate S-selectivity (76.1%, ee) and 60.5% conversion. Through semi-rational engineering, two stereocomplementary variants (I57F/F126L and N21A/F126A) were obtained with ee value of 97.6% (S) and 99.9% (R) toward ONDPA (1a), respectively, delivering chiral α-hydroxy amide with > 98% conversions. Moreover, the excellent S- and R-preference variants displayed improved stereoselectivities toward the other α-keto amide compounds. Molecular dynamic and docking analysis revealed that the two key residues at 21 and 126 were identified as the “switch”, which specifically controlled the stereopreference of iolS by regulating the shape of substrate binding pocket as well as the substrate orientation. Our results offer an effective strategy to obtain α-hydroxy amides with high optical purity and provide structural insights into altering the stereoselectivity of AKRs. Graphical Abstract
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1475-2859
Relation: https://doaj.org/toc/1475-2859
DOI: 10.1186/s12934-023-02225-9
URL الوصول: https://doaj.org/article/5a9d1e5bf76d475eab62430ee452e4f8
رقم الانضمام: edsdoj.5a9d1e5bf76d475eab62430ee452e4f8
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14752859
DOI:10.1186/s12934-023-02225-9