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Literature summary extracted from

  • Boyd, D.R.; Sharma, N.D.; Malone, J.F.; Allen, C.C.
    New families of enantiopure cyclohexenone cis-diol, o-quinol dimer and hydrate metabolites from dioxygenase-catalysed dihydroxylation of phenols (2009), Chem. Commun. (Camb. ), 2009, 3633-3635.
    View publication on PubMed

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.14.12.11 2-cresol + NADH + H+ + O2 Pseudomonas putida activity in strain UV4 ?
-
 ?
1.14.12.11 3-cresol + NADH + H+ + O2 Pseudomonas putida activity in strain UV4formation of the corresponding cis-diol and catechol ?
-
 ?
1.14.12.11 4-xylene + NADH + H+ + O2 Pseudomonas putida activity in strain 39/D 4-xylenol + NAD+ + H2O
-
 ?

Organism

EC Number Organism UniProt Comment Textmining
1.14.12.11 Pseudomonas putida
-
 strains 39/D and UV4
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.14.12.11 2-cresol + NADH + H+ + O2 activity in strain UV4 Pseudomonas putida ?
-
 ?
1.14.12.11 3-cresol + NADH + H+ + O2 activity in strain UV4formation of the corresponding cis-diol and catechol Pseudomonas putida ?
-
 ?
1.14.12.11 3-cresol + NADH + H+ + O2 activity in strain UV4, 3-cresol is a better substrate than 2-cresol Pseudomonas putida ?
-
 ?
1.14.12.11 4-xylene + NADH + H+ + O2 activity in strain 39/D Pseudomonas putida 4-xylenol + NAD+ + H2O
-
 ?
1.14.12.11 additional information the dioxygenase catalyzes the formation of cyclohexenone cis-diols, and o-quinol dimers from phenols via cis-dihydrodiol intermediate, substrate specificity and formed products, stereospecificity, overview Pseudomonas putida ?
-
 ?

Synonyms

EC Number Synonyms Comment Organism
1.14.12.11 TDO
-
 Pseudomonas putida

Cofactor

EC Number Cofactor Comment Organism Structure
1.14.12.11 NADH
-
 Pseudomonas putida