EC Number | Activating Compound | Comment | Organism | Structure |
---|---|---|---|---|
1.1.1.184 | 2-propanol | increases conversion, giving the conversion of 90% compared to 9% in control at a substrate concentration of 70 mM in 1 h. Operational stability increases at higher temperatures with the addition of 2-propanol in the reaction mixture with good conversion (90%) and enantiomeric excess (more than 99%) at 45°C and 50°C. It may be used as a co-substrate for the bioreduction reaction, which may help in widening its applicability in terms of substrate tolerance, reduced time of conversion, increased conversion rate and thermostability | Candida viswanathii | |
1.1.1.184 | hexane | activity retention is highest in the presence of hexane, reaction shows maximum conversion and enantiomeric excess of 96 and more than 99%, respectively in 15%, v/v hexane with 2-propanol as the cosubstrate | Candida viswanathii | |
1.1.1.184 | additional information | for free cells, activity retention is low in ethanol, butanol and benzyl alcohol | Candida viswanathii |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
1.1.1.184 | Candida viswanathii | - |
- |
- |
1.1.1.184 | Candida viswanathii MTCC 5158 | - |
- |
- |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
1.1.1.184 | 1-acetonaphtone + NADPH + H+ | - |
Candida viswanathii | ? + NADP+ | - |
? | |
1.1.1.184 | 1-acetonaphtone + NADPH + H+ | - |
Candida viswanathii MTCC 5158 | ? + NADP+ | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
1.1.1.184 | carbonyl reductase | - |
Candida viswanathii |