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Results 1 - 10 of 10
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the reaction diagram Show all sequences 1.17.5.1more no substrate: phenylacetate, inactive electron acceptors: NAD+, NADP+, FAD, FMN, triphenyltetrazoliumchloride Thauera aromatica ? - ?
Display the reaction diagram Show all sequences 1.17.5.1more no substrates: phenylacetate, acetyl-CoA, benzoyl-CoA, propionyl-CoA, crotonyl-CoA, succinyl-CoA, 3-hydroxybenzoyl-CoA Thauera aromatica ? - ?
Display the reaction diagram Show all sequences 1.17.5.1more anaerobic metabolism of phenylacetate, catalyzes the first step in the conversion of phenylacetyl-CoA to phenylglyoxylate, the second step being carried out by EC 3.1.2.25, cytochrome c probably does not act as physiological electron acceptor Thauera aromatica ? - ?
Display the reaction diagram Show all sequences 1.17.5.1phenylacetyl-CoA + H2O + 2,6-dichlorophenolindophenol four-electron oxidation, uses dichlorophenolindophenol as artificial electron acceptor, 2 mol dichlorophenolindophenol is reduced per mol phenylacetyl-CoA, catalyzes the anaerobic oxidation of the methylene group in the alpha-position to the CoA-activated carboxyl group, molecular oxygen is not required for the oxidation Thauera aromatica phenylglyoxylyl-CoA + reduced 2,6-dichlorophenolindophenol - ?
Display the reaction diagram Show all sequences 1.17.5.1phenylacetyl-CoA + H2O + 2,6-dichlorophenolindophenol uses 2,6-dichlorophenolindophenol as artificial electron acceptor Thauera aromatica phenylglyoxylyl-CoA + reduced 2,6-dichlorophenolindophenol - ?
Display the reaction diagram Show all sequences 1.17.5.1phenylacetyl-CoA + H2O + duroquinone at 0.3 mM duroquinone, 150% of the activity with 0.25 mM 2,6-dichlorophenolindophenol Thauera aromatica phenylglyoxylyl-CoA + duroquinol - ?
Display the reaction diagram Show all sequences 1.17.5.1phenylacetyl-CoA + H2O + menadione at 0.3 mM menadione, 60% of the activity with 0.25 mM 2,6-dichlorophenolindophenol Thauera aromatica phenylglyoxylyl-CoA + menadiol - ?
Display the reaction diagram Show all sequences 1.17.5.1phenylacetyl-CoA + H2O + quinone - Thauera aromatica phenylglyoxylyl-CoA + quinol - ?
Display the reaction diagram Show all sequences 1.17.5.1phenylacetyl-CoA + H2O + quinone four-electron oxidation, catalyzes an alpha-oxidation without utilizing molecular oxygen, ubiquinone is most likely the natural electron acceptor, specific for phenylacetyl-CoA, enzyme preparation catalyzes the reaction phenylacetyl-CoA + 2 H2O + 2 quinone = phenylglyoxylate + 2 quinone H2 + CoASH with phenylglyoxylyl-CoA as free intermediate, which is subsequently hydrolyzed Thauera aromatica phenylglyoxylyl-CoA + quinol - ?
Display the reaction diagram Show all sequences 1.17.5.1phenylacetyl-CoA + H2O + ubiquinone ubiquinone is most likely the natural electron acceptor, involved in anaerobic metabolism of phenylalanine, catalyzes the first step in the conversion of phenylacetyl-CoA to phenylglyoxylate, the second step being carried out by EC 3.1.2.25 Thauera aromatica phenylglyoxylyl-CoA + ubiquinol - ?
Results 1 - 10 of 10