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Literature summary for 1.14.14.108 extracted from

  • Williams, D.R.; Trudgill, P.W.; Taylor, D.G.
    Metabolism of 1,8-cineole by a Rhodococcus species: Ring cleavage reactions (1989), J. Gen. Microbiol., 135, 1957-1967.
No PubMed abstract available

Organism

Organism UniProt Comment Textmining
Pseudomonas putida
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-
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Pseudomonas putida C1 / ATCC 17453
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-
-

Purification (Commentary)

Purification (Comment) Organism
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Pseudomonas putida

Reaction

Reaction Comment Organism Reaction ID
(+)-bornane-2,5-dione + FMNH2 + O2 = (+)-5-oxo-1,2-campholide + FMN + H2O mechanism Pseudomonas putida

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(+)-bornane-2,5-dione + FMNH2 + O2 i.e. 2,5-diketocamphane Pseudomonas putida 3,4,4-trimethyl-5-carboxy-methyl-DELTA2-cyclopentenone + FMN + H2O i.e. cyclopentenoic acid ?
(+)-bornane-2,5-dione + FMNH2 + O2 i.e. 2,5-diketocamphane Pseudomonas putida C1 / ATCC 17453 3,4,4-trimethyl-5-carboxy-methyl-DELTA2-cyclopentenone + FMN + H2O i.e. cyclopentenoic acid ?
(+)-bornanone + FMNH2 + O2 (+)-camphor Pseudomonas putida 1,2-campholide + FMN + H2O
-
?
(+)-bornanone + FMNH2 + O2 (+)-camphor Pseudomonas putida C1 / ATCC 17453 1,2-campholide + FMN + H2O
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?
1,3,3-trimethyl-2-oxabicyclo-(2,2,2)octane + NADH + O2 6-oxocineole Pseudomonas putida 1,6,6-trimethyl-2,7-dioxa(3,2,2)bicyclononan-3-one + NAD+ + H2O
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?
1,3,3-trimethyl-2-oxabicyclo-(2,2,2)octane + NADH + O2 6-oxocineole Pseudomonas putida C1 / ATCC 17453 1,6,6-trimethyl-2,7-dioxa(3,2,2)bicyclononan-3-one + NAD+ + H2O
-
?
6-oxocineole + FMNH2 + O2
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Pseudomonas putida 3-(1-hydroxy-1-methylethyl)-6-oxoheptanoic acid + FMN + H2O
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?
6-oxocineole + FMNH2 + O2
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Pseudomonas putida C1 / ATCC 17453 3-(1-hydroxy-1-methylethyl)-6-oxoheptanoic acid + FMN + H2O
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?
additional information rubredoxin not mentioned Pseudomonas putida ?
-
?
additional information rubredoxin not mentioned Pseudomonas putida C1 / ATCC 17453 ?
-
?

Cofactor

Cofactor Comment Organism Structure
FMN
-
Pseudomonas putida