EC Number | Application | Comment | Organism |
---|---|---|---|
1.4.1.28 | synthesis | reductive amination of cyclohexanone (up to 100 mM) into cyclohexylamine is performed with an AmDH and formate dehydrogenase system with more than 99% conversion using Escherichia coli whole cell as well as purified enzymes. Chiral amine are produced from the corresponding ketone using inexpensive ammonium formate as sole sacrificial agent and enzymes omega-transaminase, AmDH, and formate dehydrogenase | Laribacter hongkongensis |
1.4.1.28 | synthesis | reductive amination of cyclohexanone (up to 100 mM) into cyclohexylamine using transgenic Escherichia coli as whole-cell reactors as well as purified enzymes | Laribacter hongkongensis |
EC Number | Cloned (Comment) | Organism |
---|---|---|
1.4.1.28 | expression in Escherichia coli | Laribacter hongkongensis |
EC Number | Crystallization (Comment) | Organism |
---|---|---|
1.4.1.28 | homology modeling of structure. The coordination of the amine group to E108 holds the tetrahedral carbon of the substrate bearing the amine | Laribacter hongkongensis |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
1.4.1.28 | Laribacter hongkongensis | - |
- |
- |
EC Number | Specific Activity Minimum [µmol/min/mg] | Specific Activity Maximum [µmol/min/mg] | Comment | Organism |
---|---|---|---|---|
1.4.1.28 | 170 | - |
substrate cyclohexanone, pH not specified in the publication, temperature not specified in the publication | Laribacter hongkongensis |
1.4.1.28 | 364 | - |
substrate isovaleraldehyde, pH not specified in the publication, temperature not specified in the publication | Laribacter hongkongensis |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
1.4.1.28 | 3-methylbutanal + NH3 + NADH + H+ | 214% of the activity with cyclohexanone | Laribacter hongkongensis | 3-methylbutan-1-amine + H2O + NAD+ | - |
? | |
1.4.1.28 | acetophenone + NH3 + NADH + H+ | - |
Laribacter hongkongensis | (S)-alpha-methylbenzylamine + H2O + NAD+ | - |
? | |
1.4.1.28 | benzaldehyde + NH3 + NAD(P)H + H+ | - |
Laribacter hongkongensis | benzylamine + H2O + NAD(P)+ | - |
? | |
1.4.1.28 | benzaldehyde + NH3 + NADH + H+ | 10.4% of the activity with cyclohexanone | Laribacter hongkongensis | benzylamine + H2O + NAD+ | - |
? | |
1.4.1.28 | butan-2-one + NH3 + NADH + H+ | 5.5% of the activity with cyclohexanone | Laribacter hongkongensis | 2-butylamine + H2O + NAD+ | - |
? | |
1.4.1.28 | cyclohexanone + NH3 + NAD(P)H + H+ | - |
Laribacter hongkongensis | cyclohexylamine + H2O + NAD(P)+ | - |
? | |
1.4.1.28 | cyclohexanone + NH3 + NADH + H+ | - |
Laribacter hongkongensis | cyclohexylamine + H2O + NAD+ | - |
? | |
1.4.1.28 | cyclopentanone + NH3 + NADH + H+ | 3.4% of the activity with cyclohexanone | Laribacter hongkongensis | cyclopentylamine + H2O + NAD+ | - |
? | |
1.4.1.28 | isovaleraldehyde + NH3 + NAD(P)H + H+ | - |
Laribacter hongkongensis | 3-methylbutan-1-amine + H2O + NAD(P)+ | - |
? | |
1.4.1.28 | additional information | poor substrates: linear aliphatic carbonyl compounds such as 3-heptanone, 2-pentanone as well as cyclopentanone | Laribacter hongkongensis | ? | - |
- |
EC Number | Subunits | Comment | Organism |
---|---|---|---|
1.4.1.28 | ? | x * 36800, SDS-PAGE, recombinant protein | Laribacter hongkongensis |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
1.4.1.28 | AMDH | - |
Laribacter hongkongensis |
EC Number | pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|---|
1.4.1.28 | 9 | - |
- |
Laribacter hongkongensis |
EC Number | Cofactor | Comment | Organism | Structure |
---|---|---|---|---|
1.4.1.28 | NADH | - |
Laribacter hongkongensis |
EC Number | General Information | Comment | Organism |
---|---|---|---|
1.4.1.28 | metabolism | in the docking analysis, cyclohexanone is well-orientated with -5.4 kcal/mol of binding energy and 3.16 A distance from the side chain of E104, key residue for interacting ammonia and substrate | Laribacter hongkongensis |