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Literature summary extracted from
- Kinetic study of lipase catalyzed asymmetric transesterification of mandelonitrile in solvent-free system (2008), Chem. Eng. J., 138, 258-263.
No PubMed abstract available
Inhibitors
| EC Number | Inhibitors | Comment | Organism | Structure |
|---|---|---|---|---|
| 3.1.1.3 | benzaldehyde | greatly inhibits the enzyme activity | Alcaligenes sp. |  |
| 3.1.1.3 | benzoic acid | greatly inhibits the enzyme activity | Alcaligenes sp. | |
Organism
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 3.1.1.3 | Alcaligenes sp. | - |
- |
- |
Substrates and Products (Substrate)
| EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 3.1.1.3 | (R,S)-mandelonitrile + vinyl acetate | transesterification | Alcaligenes sp. | (S)-cyano(phenyl)methyl acetate + (R)-mandelonitrite | - |
? | |
Synonyms
| EC Number | Synonyms | Comment | Organism |
|---|---|---|---|
| 3.1.1.3 | lipase | - |
Alcaligenes sp. |
Temperature Optimum [°C]
| EC Number | Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
|---|---|---|---|---|
| 3.1.1.3 | 40 | - |
- |
Alcaligenes sp. |
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Release 2023.1 (January 2023)
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