Classification and functional origins of stereocomplementary alcohol dehydrogenases for asymmetric synthesis of chiral secondary alcohols: A review

L Zhang, Z Sun, G Xu, Y Ni - International Journal of Biological …, 2024 - Elsevier
Alcohol dehydrogenases (ADHs) mediated biocatalytic asymmetric reduction of ketones
have been widely applied in the synthesis of optically active secondary alcohols with highly …

[HTML][HTML] Biocatalytic approaches for the synthesis of optically pure vic-halohydrins

F Xue, C Li, Q Xu - Applied Microbiology and Biotechnology, 2021 - Springer
Enantiopure vicinal halohydrins (vic-halohydrins) are highly valuable building blocks for the
synthesis of many different natural products and pharmaceuticals, and biocatalytic methods …

Directed reconstruction of a novel ancestral alcohol dehydrogenase featuring shifted pH-profile, enhanced thermostability and expanded substrate spectrum

X Chen, Z Dou, T Luo, Z Sun, H Ma, G Xu, Y Ni - Bioresource Technology, 2022 - Elsevier
Ancestral enzymes are promising for industrial biotechnology due to high stability and
catalytic promiscuity. An effective protocol was developed for the directed resurrection of …

Novel Alcohol Dehydrogenase CgADH from Candida glabrata for Stereocomplementary Reduction of Bulky–Bulky Ketones Featuring Self-Sufficient NADPH …

Z Sun, J Zhang, D Yin, G Xu, Y Ni - ACS Sustainable Chemistry & …, 2022 - ACS Publications
Bioreduction of ketones with self-sufficient cofactor regeneration is green and sustainable for
the synthesis of chiral secondary alcohols. In this study, a novel alcohol dehydrogenase Cg …

Biocatalytic asymmetric synthesis of (R)‐1‐tetralol using Lactobacillus paracasei BD101

E Kalay, E Şahin - Chirality, 2021 - Wiley Online Library
Asymmetric bioreduction of ketones is a fundamental process in the production of organic
molecules. Compounds containing tetralone rings are found in the structure of many …

Multi‐faceted set‐up of a diverse ketoreductase library enables the synthesis of pharmaceutically‐relevant secondary alcohols

M Voss, R Küng, T Hayashi, M Jonczyk… - …, 2021 - Wiley Online Library
Enzymes are valuable tools to introduce chirality into small molecules. Especially,
ketoreductase (KRED)‐catalyzed transformations of ketones to yield chiral secondary …

Sequence and structure-guided discovery of a novel NADH-dependent 7β-hydroxysteroid dehydrogenase for efficient biosynthesis of ursodeoxycholic acid

B Huang, K Yang, C Amanze, Z Yan, H Zhou, X Liu… - Bioorganic …, 2023 - Elsevier
Abstract 7β-Hydroxysteroid dehydrogenases (7β-HSDHs) have attracted increasing
attention due to their crucial roles in the biosynthesis of ursodeoxycholic acid (UDCA) …

Chemo-enzymatic synthesis of furfuralcohol from chestnut shell hydrolysate by a sequential acid-catalyzed dehydration under microwave and Escherichia coli CCZU …

J Di, C Ma, J Qian, X Liao, B Peng, Y He - Bioresource technology, 2018 - Elsevier
In this study, chemo-enzymatic synthesis of furfuralcohol from biomass-derived xylose was
successfully demonstrated by a sequential acid-catalyzed dehydration under microwave …

Improvement of carbonyl reductase activity for the bioproduction of tert-butyl (3R, 5S)-6-chloro-3, 5-dihydroxyhexanoate

ZQ Liu, HH Yin, XJ Zhang, R Zhou, YM Wang… - Bioorganic …, 2018 - Elsevier
Abstract tert-Butyl (3R, 5S)-6-chloro-3, 5-dihydroxyhexanoate ((3R, 5S)-CDHH) is a key
chiral intermediate for the side chain synthesis of rosuvastatin. In this study, random …

Discovery of a new NADPH-dependent aldo-keto reductase from Candida orthopsilosis catalyzing the stereospecific synthesis of (R)-pantolactone by genome mining

J Wang, P Cheng, Y Wu, A Wang, F Liu, X Pei - Journal of biotechnology, 2019 - Elsevier
Abstract (R)-Pantolactone (PL) is a key chiral intermediate for the synthesis of calcium (R)-
pantothenate and (R)-panthenol used as food additives. The commercial production of (R) …