Abstract
Alcohol dehydrogenases (ADHs) catalyze the reversible reduction of a carbonyl group to its corresponding alcohol. ADHs are widely employed for organic synthesis due to their lack of harm to the environment, broad substrate acceptance, and high enantioselectivity. This review focuses on the impact and relevance of ADH enantioselectivities on their biotechnological application. Stereoselective ADHs are beneficial to reduce challenging ketones such as ketones owning two bulky substituents or similar-sized substituents to the carbonyl carbon. Meanwhile, in cascade reactions, non-stereoselective ADHs can be utilized for the quantitative oxidation of racemic alcohol to ketone and dynamic kinetic resolution.
Original language | English |
---|---|
Pages (from-to) | 2897-2909 |
Number of pages | 13 |
Journal | Applied Microbiology and Biotechnology |
Volume | 104 |
Issue number | 7 |
DOIs | |
Publication status | Published - Apr 1 2020 |
Externally published | Yes |
Keywords
- Alcohol dehydrogenase
- Asymmetric reduction
- Cascade
- Enantioselectivity
- Enzyme engineering
- Pharmaceutical intermediate
ASJC Scopus subject areas
- Biotechnology
- Applied Microbiology and Biotechnology