AnatomyOrganismsDiseasesChemicals and DrugsAnalytical, Diagnostic and Therapeutic Techniques and EquipmentPhenomena and ProcessesInformation ScienceHealth Care
CatecholsCatechol 1,2-DioxygenaseProtocatechuate-3,4-DioxygenaseDioxygenasesOxygenasesCatechol 2,3-DioxygenaseEstrogens, CatecholAdipatesCatechol O-Methyltransferase4-Hydroxyphenylpyruvate DioxygenaseCysteine DioxygenaseTryptophan OxygenasePseudomonasBiodegradation, EnvironmentalHomogentisate 1,2-Dioxygenase3-Hydroxyanthranilate 3,4-DioxygenaseCatechol OxidasePhenolHydroxybenzoatesPseudomonas putidaKynurenineSorbic AcidMolecular Sequence DataRhodococcusBenzoatesChlorobenzenesSubstrate SpecificityTolueneChlorobenzoatesEquileninAmino Acid SequenceMixed Function OxygenasesBenzeneBenzoic AcidSphingomonasTryptophanShellfish PoisoningBurkholderiaPhenolsAlcaligenesGentisatesBase SequenceKineticsOxidation-ReductionAcinetobacterHydroquinonesGenes, BacterialCresolsPlanococcus BacteriaDNA CleavageCloning, MolecularEscherichia coliHydroxylationRalstoniaHydrocarbons, AromaticParabensBrevibacteriumHydroxyestronesIronGram-Negative Aerobic Rods and CocciSalicylatesToluidinesXylenesChromatography, High Pressure LiquidComamonasBinding SitesIntramolecular LyasesPlasmidsHomogentisic AcidBacterial ProteinsRecombinant ProteinsSequence Homology, Amino AcidBiotransformationCatalysisCleavage Stage, Ovumortho-AminobenzoatesFerrous CompoundsMutationEnzyme InductionQuinonesSiderophoresPseudomonas stutzeriAcinetobacter calcoaceticusVanillic AcidMonophenol MonooxygenaseFerredoxinsModels, MolecularArthrobacterBiphenyl Compounds
EnzymesNADHDegradationToxicWaterCommonMicroorganismsApplication
Enzymes2
  • The isofunctional enzymes of catechol 1,2-dioxygenase from species of Acinetobacter, Pseudomonas, Nocardia, Alcaligenes and Corynebacterium oxidize 3-methylcatechol according to both the intradiol and extradiol cleavage patterns. (wikipedia.org)
  • Oxygenases belong to the oxidoreductive group of enzymes (E.C. Class 1), which oxidize the substrates by transferring oxygen from molecular oxygen (O 2 ) and utilize FAD/NADH/NADPH as the co-substrate. (biomedcentral.com)
NADH1
  • The enzyme 1,2-dihydroxy-6-methylcyclohexa-3,5-dienecarboxylate dehydrogenase uses 1,2-dihydroxy-6-methylcyclohexa-3,5-dienecarboxylate and NAD+ to produce 3-methylcatechol, NADH and CO2. (wikipedia.org)
Degradation1
  • A number of bacteria that can degrade a variety of aromatic compounds have been identified and the pathways involved in the degradation have been extensively characterized [ 3 , 4 ]. (biomedcentral.com)
Toxic1
  • Many of these compounds have been reported to be toxic to the living organisms [ 3 ]. (biomedcentral.com)
Water1
  • They play a key role in the metabolism of organic compounds by increasing their reactivity or water solubility or bringing about cleavage of the aromatic ring. (biomedcentral.com)
Common1
  • The 2,3-dihydrobenzofuran derivative, 7-acetyl-4,6-dimethoxy-2-isopropenyl-2,3-dihydrobenzofuran, had an ED 50 value of 1.3 μg (5.4×10 -9 mol)/cm 2 against the common cutworm. (go.jp)
Microorganisms1
Application1