Any feedback?
Please rate this page
(search_result.php)
(0/150)

BRENDA support

Refine search

Search Substrates and Products (Substrate)

show results
Don't show organism specific information (fast!)
Search organism in taxonomic tree (slow, choose "exact" as search mode, e.g. "mammalia" for rat,human,monkey,...)
(Not possible to combine with the first option)
Refine your search

Search term:

Results 1 - 10 of 18 > >>
download as CSV
download all results as CSV
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B11,2,3-trinitroglycerol + 2 NADPH + 2 H+ - Pseudomonas putida ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B12,4,6-trinitrophenol + 2 NADPH + 2 H+ - Pseudomonas putida ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B12,4,6-trinitrotoluene + 2 NADPH + 2 H+ - Pseudomonas putida N-hydroxy-2-methyl-3,5-dinitroaniline + 2 NADP+ + H2O - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B12,4,6-trinitrotoluene + 2 NADPH + 2 H+ - Pseudomonas putida N-hydroxy-2-methyl-3,5-dinitroaniline + 2 NADP+ + H2O i.e. 2-hydroxylamino-2,6-dinitrotoluene. The amount of N-hydroxy-2-methyl-3,5-dinitroaniline is larger than the amount of N-hydroxy-4-methyl-3,5-dinitroaniline formed. In a further nonenzymatic reaction nitrite is released and N-(2-methyl-3,5-dinitrophenyl)-N-4-methyl-3,5-dinitrophenyl-hydroxylamine and eventually N-(2-methyl-3,5-dinitrophenyl)-N-4-methyl-3,5-dinitroaniline are produced. In addition the aromatic ring of 2,4,6-trinitrotoluene is susceptibe to nucleophilic attack by hydride ions to form Meisenheimer complex intermediates (monohydride and dihydride complexes) which also form secondary diaryl hydroxylamines and secondary diarylamine with release of nitrite ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B12,4,6-trinitrotoluene + 2 NADPH + 2 H+ - Pseudomonas putida N-hydroxy-4-methyl-3,5-dinitroaniline + 2 NADP+ + H2O i.e. 4-hydroxylamino-2,6-dinitrotoluene. The amount of N-hydroxy-4-methyl-3,5-dinitroaniline is larger than the amount of N-hydroxy-2-methyl-3,5-dinitroaniline formed. In a further nonenzymatic reaction nitrite is released and N,N-bis-(3,5-dinitrotolyl)-hydroxylamine and eventually N,N-bis-(3,5-dinitrotolyl)-amine are produced. In addition the aromatic ring of 2,4,6-trinitrotoluene is susceptible to nucleophilic attack by hydride ions to form Meisenheimer complex intermediates (monohydride and dihydride complexes) which also form the secondary diaryl hydroxylamines and the secondary diarylamine with release of nitrite ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1CB1954 + NADPH + H+ - Pseudomonas putida ? + hydroxylamine + NADP+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1cyclohexenone + NADPH + H+ - Pseudomonas putida ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1glycerol trinitrate + NADPH + H+ - Pseudomonas putida ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1more 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 ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.7.1.B1more the enzyme shows no reactivity with CB1954 Pseudomonas putida ? - -
Results 1 - 10 of 18 > >>
download as CSV
download all results as CSV