Application | Comment | Organism |
---|---|---|
synthesis | the enzyme from Rhodococcus aetherivorans JB1208 shows high regioselectivity and strong substrate tolerance for alicyclic dinitrile and affords a potentially industrial route to gabapentin (a precursor of gamma-aminobutyric acid, which has been approved for treatment of a variety of central nervous system disorders, partial seizures, and restless legs syndrome) | Rhodococcus aetherivorans |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Rhodococcus aetherivorans | A0A2Z6FCE3 AND A0A2Z6FCD3 | A0A2Z6FCE3: alpha-subunit, A0A2Z6FCD3: beta-subunit | - |
Rhodococcus aetherivorans JB1208 | A0A2Z6FCE3 AND A0A2Z6FCD3 | A0A2Z6FCE3: alpha-subunit, A0A2Z6FCD3: beta-subunit | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
1-cyanocyclohexaneacetonitrile + H2O | - |
Rhodococcus aetherivorans | 1-cyanocyclohexaneacetamide | - |
? | |
1-cyanocyclohexaneacetonitrile + H2O | - |
Rhodococcus aetherivorans JB1208 | 1-cyanocyclohexaneacetamide | - |
? |