EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
1.7.1.B1 | 1,2,3-trinitroglycerol + 2 NADPH + 2 H+ |
- |
Pseudomonas putida |
? |
- |
? |
1.7.1.B1 | 2,4,6-trinitrophenol + 2 NADPH + 2 H+ |
- |
Pseudomonas putida |
? |
- |
? |
1.7.1.B1 | 2,4,6-trinitrotoluene + 2 NADPH + 2 H+ |
- |
Pseudomonas sp. |
N-hydroxy-2-methyl-3,5-dinitroaniline + 2 NADP+ + H2O |
- |
? |
1.7.1.B1 | 2,4,6-trinitrotoluene + 2 NADPH + 2 H+ |
- |
Pseudomonas putida |
N-hydroxy-2-methyl-3,5-dinitroaniline + 2 NADP+ + H2O |
- |
? |
1.7.1.B1 | CB1954 + NADPH + H+ |
- |
Pseudomonas putida |
? + hydroxylamine + NADP+ |
- |
? |
1.7.1.B1 | cyclohexenone + NADPH + H+ |
- |
Pseudomonas putida |
? |
- |
? |
1.7.1.B1 | cyclohexenone + NADPH + H+ |
- |
Pseudomonas putida KT 2240 |
? |
- |
? |
1.7.1.B1 | glycerol trinitrate + NADPH + H+ |
- |
Pseudomonas putida |
? |
- |
? |
1.7.1.B1 | glycerol trinitrate + NADPH + H+ |
- |
Pseudomonas putida KT 2240 |
? |
- |
? |
1.7.1.B1 | more |
ability to reduce nitroaromatic compounds, enzyme demonstrates type I and type II hydride transferase activity and reduced the nitro groups of 2,4,6-trinitrotoluene to hydroxylaminodinitrotoluene derivatives. The condensations of the primary products of type I and type II hydride transferases react with each other to yield diarylamines and nitrite, the latter can be further reduced to ammonium and serves as a nitrogen source for microorganisms in vivo |
Pseudomonas putida |
? |
- |
? |