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Literature summary for 1.14.12.11 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
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Natural Substrates/ Products (Substrates)

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

Organism

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

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2-cresol + NADH + H+ + O2 activity in strain UV4 Pseudomonas putida ?
-
 ?
3-cresol + NADH + H+ + O2 activity in strain UV4formation of the corresponding cis-diol and catechol Pseudomonas putida ?
-
 ?
3-cresol + NADH + H+ + O2 activity in strain UV4, 3-cresol is a better substrate than 2-cresol Pseudomonas putida ?
-
 ?
4-xylene + NADH + H+ + O2 activity in strain 39/D Pseudomonas putida 4-xylenol + NAD+ + H2O
-
 ?
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

Synonyms Comment Organism
TDO
-
 Pseudomonas putida

Cofactor

Cofactor Comment Organism Structure
NADH
-
 Pseudomonas putida