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Literature summary for 1.14.12.11 extracted from

  • Boyd, D.R.; Sharma, N.D.; Gunaratne, N.; Haughey, S.A.; Kennedy, M.A.; Malone, J.F.; Allen, C.C.; Dalton, H.
    Dioxygenase-catalysed oxidation of monosubstituted thiophenes: sulfoxidation versus dihydrodiol formation (2003), Org. Biomol. Chem., 1, 984-994.
    View publication on PubMed
Search for more literature for 1.14.12.11

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
toluene + NADH + O2 Pseudomonas putida
-
 (1S,2R)-3-methylcyclohexa-3,5-diene-1,2-diol + NAD+
-
 ?
toluene + NADH + O2 Pseudomonas putida UV4
-
 (1S,2R)-3-methylcyclohexa-3,5-diene-1,2-diol + NAD+
-
 ?

Organism

Organism UniProt Comment Textmining
Pseudomonas putida
-
-
-
Pseudomonas putida UV4
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2-chlorothiophene + NADH
-
 Pseudomonas putida ?
-
 ?
2-chlorothiophene + NADH
-
 Pseudomonas putida UV4 ?
-
 ?
2-ethylthiophene + NADH
-
 Pseudomonas putida ?
-
 ?
2-ethylthiophene + NADH
-
 Pseudomonas putida UV4 ?
-
 ?
2-methylthiophene + NADH
-
 Pseudomonas putida ?
-
 ?
2-methylthiophene + NADH
-
 Pseudomonas putida UV4 ?
-
 ?
additional information a high number of 2- or 3-substituted thiophenes were tested as substrates and were found to be metabolized Pseudomonas putida ?
-
 ?
additional information a high number of 2- or 3-substituted thiophenes were tested as substrates and were found to be metabolized Pseudomonas putida UV4 ?
-
 ?
thiophene + NADH
-
 Pseudomonas putida ?
-
 ?
toluene + NADH + O2
-
 Pseudomonas putida (1S,2R)-3-methylcyclohexa-3,5-diene-1,2-diol + NAD+
-
 ?
toluene + NADH + O2
-
 Pseudomonas putida UV4 (1S,2R)-3-methylcyclohexa-3,5-diene-1,2-diol + NAD+
-
 ?

Cofactor

Cofactor Comment Organism Structure
NADH
-
 Pseudomonas putida