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Information on EC 1.14.13.51 - 6-oxocineole dehydrogenase Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
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The expected taxonomic range for this enzyme is: Bacteria, Eukaryota
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6-oxocineole dehydrogenase
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6-oxocineole + NADPH + H+ + O2 = 1,6,6-trimethyl-2,7-dioxabicyclo[3.2.2]nonan-3-one + NADP+ + H2O
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Monoterpenoid biosynthesis
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Biosynthesis of secondary metabolites
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1,8-cineole degradation
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6-oxocineole,NADPH:oxygen oxidoreductase
The product undergoes non-enzymic cleavage and subsequent ring closure to form the lactone 4,5-dihydro-5,5-dimethyl-4-(3-oxobutyl)furan-2(3H)-one.
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6-oxocineole oxygenase
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strain C1
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brenda
Rhodococcus C1
strain C1
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brenda
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6-oxocineole + NADPH + O2
1,6,6-trimethyl-2,7-dioxabicyclo-[3.2.2]nonan-3-one + NADP+ + H2O
additional information
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6-oxocineole + NADPH + O2
1,6,6-trimethyl-2,7-dioxabicyclo-[3.2.2]nonan-3-one + NADP+ + H2O
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this product reacts spontaneously to 3-(1-hydroxy-1-methylethyl)-6-oxoheptanoic acid and subsequently lactonizes to 4,5-dihydro-5,5-dimethyl-4-(3'-oxobutyl)-furan-2(3H)-one
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6-oxocineole + NADPH + O2
1,6,6-trimethyl-2,7-dioxabicyclo-[3.2.2]nonan-3-one + NADP+ + H2O
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grown on 1,8-cineole or succinate as carbon source
this product reacts spontaneously to 3-(1-hydroxy-1-methylethyl)-6-oxoheptanoic acid and subsequently lactonizes to 4,5-dihydro-5,5-dimethyl-4-(3'-oxobutyl)-furan-2(3H)-one
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6-oxocineole + NADPH + O2
1,6,6-trimethyl-2,7-dioxabicyclo-[3.2.2]nonan-3-one + NADP+ + H2O
Rhodococcus C1
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this product reacts spontaneously to 3-(1-hydroxy-1-methylethyl)-6-oxoheptanoic acid and subsequently lactonizes to 4,5-dihydro-5,5-dimethyl-4-(3'-oxobutyl)-furan-2(3H)-one
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6-oxocineole + NADPH + O2
1,6,6-trimethyl-2,7-dioxabicyclo-[3.2.2]nonan-3-one + NADP+ + H2O
Rhodococcus C1
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grown on 1,8-cineole or succinate as carbon source
this product reacts spontaneously to 3-(1-hydroxy-1-methylethyl)-6-oxoheptanoic acid and subsequently lactonizes to 4,5-dihydro-5,5-dimethyl-4-(3'-oxobutyl)-furan-2(3H)-one
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additional information
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no substrates: substrate analogues, i.e. (+)-camphor, (S)-(+)-carvone, cyclohexanene, 1,3-cyclohexanedione, dihydrocarvone, 2-, 3-, and 4-methylcyclohexanone, fenchone, menthone, pinan-3-one, pulegone, verbenone
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additional information
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Rhodococcus C1
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no substrates: substrate analogues, i.e. (+)-camphor, (S)-(+)-carvone, cyclohexanene, 1,3-cyclohexanedione, dihydrocarvone, 2-, 3-, and 4-methylcyclohexanone, fenchone, menthone, pinan-3-one, pulegone, verbenone
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6-oxocineole + NADPH + O2
1,6,6-trimethyl-2,7-dioxabicyclo-[3.2.2]nonan-3-one + NADP+ + H2O
6-oxocineole + NADPH + O2
1,6,6-trimethyl-2,7-dioxabicyclo-[3.2.2]nonan-3-one + NADP+ + H2O
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grown on 1,8-cineole or succinate as carbon source
this product reacts spontaneously to 3-(1-hydroxy-1-methylethyl)-6-oxoheptanoic acid and subsequently lactonizes to 4,5-dihydro-5,5-dimethyl-4-(3'-oxobutyl)-furan-2(3H)-one
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6-oxocineole + NADPH + O2
1,6,6-trimethyl-2,7-dioxabicyclo-[3.2.2]nonan-3-one + NADP+ + H2O
Rhodococcus C1
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grown on 1,8-cineole or succinate as carbon source
this product reacts spontaneously to 3-(1-hydroxy-1-methylethyl)-6-oxoheptanoic acid and subsequently lactonizes to 4,5-dihydro-5,5-dimethyl-4-(3'-oxobutyl)-furan-2(3H)-one
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0.001
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succinate grown cells
0.3 - 0.4
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1,8-cineole-grown cells
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5-10 vol% ethanol stabilizes the crude cell extract
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Williams, D.R.; Trudgill, P.W.; Taylor, D.G.
Metabolism of 1,8-cineole by a Rhodococcus species: Ring cleavage reactions
J. Gen. Microbiol.
135
1957-1967
1989
Rhodococcus, Rhodococcus C1
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brenda
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