Author/Authors :
Gao، نويسنده , , Chao and Zhang، نويسنده , , Lijie and Xie، نويسنده , , Yingjian and Hu، نويسنده , , Chunhui and Zhang، نويسنده , , Yue and Li، نويسنده , , Lixiang and Wang، نويسنده , , Yu and Ma، نويسنده , , Cuiqing and Xu، نويسنده , , Ping، نويسنده ,
Abstract :
Production of (3S)-acetoin ((3S)-AC), an important platform chemical, is desirable but difficult to perform. An NADPH-dependent carbonyl reductase (Gox0644) from Gluconobacter oxydans DSM 2003 was confirmed to have a good ability to reduce diacetyl (DA) to produce (3S)-AC. In this work, the NADPH-dependent carbonyl reductase was expressed and purified. Glucose dehydrogenase from Bacillus subtilis 168 was coupled with the NADPH-dependent carbonyl reductase to produce (3S)-AC from DA. Under the optimal conditions, 12.2 g l−1 (3S)-AC was produced from 14.3 g l−1 DA in 75 min. Because DA can be biotechnological produced, the two-enzymes coupling system might be a promising alternative for the (3S)-AC production.
Keywords :
cofactor regeneration , (3S)-Acetoin , diacetyl , Carbonyl reductase , Glucose dehydrogenase