1.13.11.2: catechol 2,3-dioxygenase
This is an abbreviated version!
For detailed information about catechol 2,3-dioxygenase, go to the full flat file.
Word Map on EC 1.13.11.2
-
1.13.11.2
-
heme
-
putida
-
carboxylase
-
hydroxylase
-
rubisco
-
ferredoxins
-
ribulose-1,5-bisphosphate
-
l-arginine
-
non-heme
-
rieske
-
tetrahydrobiopterin
-
dioxygenation
-
ribulose
-
toluene
-
2-oxoglutarate
-
naphthalene
-
biphenyls
-
rhodococcus
-
fmn
-
nnos
-
bioremediation
-
mixed-function
-
nitric-oxide
-
phenanthrene
-
photorespiration
-
photorespiratory
-
1,5-bisphosphate
-
biliverdin
-
bh4
-
l-citrulline
-
sphingomonas
-
ring-hydroxylating
-
comamonas
-
dihydroxylation
-
carbazole
-
xylene
-
l-arg
-
2-oxoglutarate-dependent
-
heme-heme
-
diiron
-
ironii
-
4-methylcatechol
-
monooxygenation
-
rubp
-
testosteroni
-
sphingobium
-
ethylbenzene
-
4.1.1.39
-
degradation
-
environmental protection
-
fluoranthene
-
rhodochrous
- 1.13.11.2
- heme
- putida
- carboxylase
- hydroxylase
- rubisco
- ferredoxins
- ribulose-1,5-bisphosphate
- l-arginine
-
non-heme
-
rieske
- tetrahydrobiopterin
-
dioxygenation
- ribulose
- toluene
- 2-oxoglutarate
- naphthalene
- biphenyls
- rhodococcus
- fmn
- nnos
-
bioremediation
-
mixed-function
-
nitric-oxide
- phenanthrene
-
photorespiration
-
photorespiratory
-
1,5-bisphosphate
- biliverdin
- bh4
- l-citrulline
- sphingomonas
-
ring-hydroxylating
- comamonas
-
dihydroxylation
- carbazole
- xylene
- l-arg
-
2-oxoglutarate-dependent
-
heme-heme
-
diiron
-
ironii
- 4-methylcatechol
-
monooxygenation
- rubp
- testosteroni
- sphingobium
- ethylbenzene
-
4.1.1.39
- degradation
- environmental protection
- fluoranthene
- rhodochrous
Reaction
Synonyms
2,3-dihydroxybenzenesulfonate 2,3-dioxygenase, 3-sulfocatechol-2,3-dioxygenase, 3SC23O, A23O, AtdB, BupB, C2,3O, C23D, C23o, C23O-2G, C23O1, C23O2, C23Os, CatE, catechol 2,3 dioxygenase, catechol 2,3-di-2,3-pyrocatechase, catechol 2,3-dioxygenase, catechol 2,3-oxygenase, catechol oxygenase, catechol-2,3-dioxygenase, CbzE, CD-2,3, EC 1.13.1.2, ECDO, extradiol dioxygenase MhpB, Extradiol-cleaving catecholic dioxygenase, meta-cleavage dioxygenase, metapyrocatechase, More, oxygenase, PheB, pyrocatechol 2,3-dioxygenase, Saci_2295, SSO1223, SsoC2,3O, ssol_2912, tbuE, TdnC, TodE, XylE
ECTree
1.13.11.2 catechol 2,3-dioxygenaseAdvanced search results
results (
results (Substrates Products
Substrates Products on EC 1.13.11.2 - catechol 2,3-dioxygenase
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SUBSTRATE 
PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate)
(Substrate)
LITERATURE
(Substrate)
(Substrate)
COMMENTARY
(Product)
(Product)
LITERATURE
(Product)
(Product)
Reversibility
r=reversible
ir=irreversible
?=not specified
r=reversible
ir=irreversible
?=not specified
2,3-dihydroxybiphenylcatechol + O2
?
Halalkalibacterium ligniniphilum
WP_017726464.1
% of the activity as compared to 3-ethylcatechol
-
-
?
3,5-dichlorocatechol + O2
2-hydroxy-3,5-dimethyl-6-oxohexa-2,4-dienoic acid
30.8% of the activity as compared to catechol
-
-
?
3-ethylcatechol + O2
?
Halalkalibacterium ligniniphilum
WP_017726464.1
best substrate. The enzyme can cleave the catechol ring when substitutions occur at C3 more efficiently than C4 substitutes. The enzyme can cleave aromatic compounds with two 6-carbon ring structures
-
-
?
3-methoxycatechol + O2
2-hydroxy-3-methoxy-6-oxohexa-2,4-dienoate
-
-
-
-
?
3-methylcatechol + O2
2-hydroxy-3-methoxymuconate semialdehyde
211.7% compared to the activity with catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-3-methylmuconate-6-semialdehyde
-
-
-
-
?
3-phenylcatechol + O2
2-hydroxy-3-phenylmuconate semialdehyde
-
-
-
?
3-sulfocatechol + O2 + H2O
(2E,4Z)-2-hydroxymuconate + bisulfite + H+
-
-
-
-
?
4-bromocatechol + O2
4-bromo-2-hydroxymuconate semialdehyde
-
-
-
?
4-hydroxymethylcatechol + O2
2-hydroxy-4-hydroxymethylmuconate semialdehyde
rapid inactivation of enzyme during turnover
-
-
?
4-n-butylcatechol + O2
?
activity is 1.85fold higher than with catechol
-
-
?
tetrachlorohydroquinone + O2
?
-
immobilized enzyme, no activity with the free enzyme
-
-
?
2,3-dihydroxybiphenyl + O2
?
1.3% of the activity with 2,3-dihydroxybiphenyl
-
-
?
2,3-dihydroxybiphenyl + O2
?
1.3% of the activity with 2,3-dihydroxybiphenyl
-
-
?
2,3-dihydroxybiphenyl + O2
?
9.47% compared to the activity with catechol
-
-
?
2,3-dihydroxybiphenyl + O2
?
Sphingobium scionense DSM 19371
9.47% compared to the activity with catechol
-
-
?
3,4-dimethylcatechol + O2
2-hydroxy-5-methyl-6-oxo-hepta-2,4-dienoate
-
-
-
-
?
3,4-dimethylcatechol + O2
2-hydroxy-5-methyl-6-oxo-hepta-2,4-dienoate
-
-
-
-
?
3,5-dichlorocatechol + O2
?
-
immobilized enzyme, no activity with the free enzyme
-
-
?
3,5-dichlorocatechol + O2
?
-
immobilized enzyme, no activity with the free enzyme
-
-
?
3,5-dimethylcatechol + O2
2-hydroxy-3,5-dimethyl-6-oxohexa-2,4-dienoic acid
-
-
-
-
?
3,5-dimethylcatechol + O2
2-hydroxy-3,5-dimethyl-6-oxohexa-2,4-dienoic acid
-
-
-
-
?
3-chlorocatechol + O2
2-chloro-2-hydroxy-6-oxohexa-2,4-dienoate
-
weak
-
-
?
3-chlorocatechol + O2
2-chloro-2-hydroxy-6-oxohexa-2,4-dienoate
-
weak
-
-
?
3-chlorocatechol + O2
2-chloro-2-hydroxy-6-oxohexa-2,4-dienoate
-
weak
-
-
?
3-chlorocatechol + O2
2-chloro-2-hydroxy-6-oxohexa-2,4-dienoate
-
-
-
-
?
3-chlorocatechol + O2
2-chloro-2-hydroxy-6-oxohexa-2,4-dienoate
-
weak
-
-
?
3-chlorocatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
82.3% of the activity as compared to catechol
-
-
?
3-chlorocatechol + O2
3-chloro-2-hydroxymuconate semialdehyde
rapid inactivation of enzyme during turnover
-
-
?
3-chlorocatechol + O2
3-chloro-2-hydroxymuconate semialdehyde
about 9% of the rate with catechol
-
-
?
3-chlorocatechol + O2
3-chloro-2-hydroxymuconate semialdehyde
about 95% of the rate with catechol
-
-
?
3-chlorocatechol + O2
3-chloro-2-hydroxymuconate semialdehyde
Pseudomonas putida mt-2 / ATCC 33015 / DSM 3931 / NCIB 12182 / NCIMB 12182
rapid inactivation of enzyme during turnover
-
-
?
3-chlorocatechol + O2
3-chloro-2-hydroxymuconate semialdehyde
about 9% of the rate with catechol
-
-
?
3-formylcatechol + O2
3-formyl-2-hydroxymuconate semialdehyde
-
-
-
?
3-formylcatechol + O2
3-formyl-2-hydroxymuconate semialdehyde
Pseudomonas putida mt-2 / ATCC 33015 / DSM 3931 / NCIB 12182 / NCIMB 12182
-
-
-
?
3-isopropylcatechol + O2
?
Halalkalibacterium ligniniphilum
WP_017726464.1
50% of the activity as compared to 3-ethylcatechol
-
-
?
3-isopropylcatechol + O2
?
Halalkalibacterium ligniniphilum L1
WP_017726464.1
50% of the activity as compared to 3-ethylcatechol
-
-
?
3-methoxycatechol + O2
2-hydroxy-3-methoxymuconate semialdehyde
rapid inactivation of enzyme during turnover
-
-
?
3-methoxycatechol + O2
2-hydroxy-3-methoxymuconate semialdehyde
rapid inactivation of enzyme during turnover
-
-
?
3-methylcatechol + O2
2-hydroxy-3-methylmuconate semialdehyde
-
19% of the activity with catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-3-methylmuconate semialdehyde
-
19% of the activity with catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-3-methylmuconate semialdehyde
poor substrate
-
-
?
3-methylcatechol + O2
2-hydroxy-3-methylmuconate semialdehyde
-
most effective substrate
-
-
?
3-methylcatechol + O2
2-hydroxy-3-methylmuconate semialdehyde
-
most effective substrate
-
-
?
3-methylcatechol + O2
2-hydroxy-3-methylmuconate semialdehyde
about 30% of activity with catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
-
-
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
-
-
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
-
weak
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
-
weak
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
Halalkalibacterium ligniniphilum
WP_017726464.1
62.5% of the activity as compared to 3-ethylcatechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
Halalkalibacterium ligniniphilum L1
WP_017726464.1
62.5% of the activity as compared to 3-ethylcatechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
6.12% activity compared to catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
-
-
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
-
-
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
about 105% of the rate with catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
about 43% of the rate with catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
-
-
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
about 105% of the rate with catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
-
-
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
wild-type enzyme shows 6.1% of the activity as compared to catechol. The activities of the mutant enzyme T254A increases 3.7fold as compared to catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
about 30% of the rate with catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
about 30% of the rate with catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
90.8% of the activity as compared to catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoate
-
isoform C23O1 shows 49.5% activity compared to catechol, isoform C23O2 shows 239.2% activity compared to catechol
-
-
?
3-methylcatechol + O2
2-hydroxy-6-oxohepta-2,4-dienoic acid
-
-
-
-
?
3-methylcatechol + O2
?
33% of the activity with 4-chlorocatechol
-
-
?
3-methylcatechol + O2
?
33% of the activity with 4-chlorocatechol
-
-
?
3-methylcatechol + O2
cis,cis-2-hydroxy-6-oxohepta-2,4-dienoate
-
-
-
-
?
4,5-dichlorocatechol + O2
?
4.6% compared to the activity with catechol
-
-
?
4,5-dichlorocatechol + O2
?
Sphingobium scionense DSM 19371
4.6% compared to the activity with catechol
-
-
?
4,5-dichlorocatechol + O2
?
23.4% of the activity as compared to catechol
-
-
?
4-alkylcatechol + O2
?
initial step of long-chain alkylphenol cleavage pathway
-
-
?
4-alkylcatechol + O2
?
alkyl chain length C1-C5 is accepted as substrate
-
-
?
4-alkylcatechol + O2
?
initial step of long-chain alkylphenol cleavage pathway
-
-
?
4-alkylcatechol + O2
?
alkyl chain length C1-C5 is accepted as substrate
-
-
?
4-chlorocatechol + O2
4-chloro-2-hydroxymuconate semialdehyde
-
-
-
?
4-chlorocatechol + O2
4-chloro-2-hydroxymuconate semialdehyde
44.88% activity compared to catechol
-
-
?
4-chlorocatechol + O2
4-chloro-2-hydroxymuconate semialdehyde
-
-
-
?
4-chlorocatechol + O2
4-chloro-2-hydroxymuconate semialdehyde
about 16% of the rate with catechol
-
-
?
4-chlorocatechol + O2
4-chloro-2-hydroxymuconate semialdehyde
about 75% of the rate with catechol
-
-
?
4-chlorocatechol + O2
4-chloro-2-hydroxymuconate semialdehyde
about 16% of the rate with catechol
-
-
?
4-chlorocatechol + O2
4-chloro-2-hydroxymuconate semialdehyde
at the same rate as catechol
-
-
?
4-chlorocatechol + O2
4-chloro-2-hydroxymuconate semialdehyde
17.4% compared to the activity with catechol
-
-
?
4-chlorocatechol + O2
4-chloro-2-hydroxymuconate semialdehyde
Sphingobium scionense DSM 19371
17.4% compared to the activity with catechol
-
-
?
4-chlorocatechol + O2
4-chloro-2-hydroxymuconate semialdehyde
-
isoform C23O1 shows 50.8% activity compared to catechol, isoform C23O2 shows 226.4% activity compared to catechol
-
-
?
4-chlorocatechol + O2
5-chloro-2-hydroxy-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-chlorocatechol + O2
5-chloro-2-hydroxy-6-oxohexa-2,4-dienoate
19.2% of the activity as compared to catechol
-
-
?
4-chlorocatechol + O2
5-chloro-2-hydroxy-6-oxohexa-2,4-dienoate
71.1% of the activity as compared to catechol
-
-
?
4-chlorocatechol + O2
5-chloro-2-hydroxymuconic semialdehyde
-
-
-
?
4-chlorocatechol + O2
?
39% of the activity with 4-chlorocatechol
-
-
?
4-chlorocatechol + O2
?
39% of the activity with 4-chlorocatechol
-
-
?
4-chlorocatechol + O2
?
the enzyme shows the highest activity against catechol and 4-chlorocatechol
-
-
?
4-chlorocatechol + O2
?
the enzyme shows the highest activity against catechol and 4-chlorocatechol
-
-
?
4-ethylcatechol + O2
4-ethyl-2-hydroxymuconate semialdehyde
effective substrate
-
-
?
4-ethylcatechol + O2
4-ethyl-2-hydroxymuconate semialdehyde
rapid inactivation of enzyme during turnover
-
-
?
4-ethylcatechol + O2
4-ethyl-2-hydroxymuconate semialdehyde
rapid inactivation of enzyme during turnover
-
-
?
4-formylcatechol + O2
4-formyl-2-hydroxymuconate semialdehyde
-
-
-
?
4-formylcatechol + O2
4-formyl-2-hydroxymuconate semialdehyde
rapid inactivation of enzyme during turnover
-
-
?
4-formylcatechol + O2
4-formyl-2-hydroxymuconate semialdehyde
rapid inactivation of enzyme during turnover
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
hypoxic strains with significantly higher affinities
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
hypoxic strains with significantly higher affinities
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
weak
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
weak
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
101.91% activity compared to catechol
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
hypoxic strains with significantly higher affinities
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
hypoxic strains with significantly higher affinities
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
highly specific for
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
hypoxic strains with significantly higher affinities
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
hypoxic strains with significantly higher affinities
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
hypoxic strains with significantly higher affinities
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
hypoxic strains with significantly higher affinities
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
hypoxic strains with significantly higher affinities
-
-
?
4-methylcatechol + O2
2-hydroxy-3-methyl-6-oxohexa-2,4-dienoate
-
best substrate for isoform C23O2 (280.7% activity compared to catechol), while isoform C23O1 shows 87.4% activity compared to catechol
-
-
?
4-methylcatechol + O2
2-hydroxy-4-methyl-6-oxohexa-2,4-dienoate
about 47% of the rate with catechol
-
-
?
4-methylcatechol + O2
2-hydroxy-4-methyl-6-oxohexa-2,4-dienoate
about 89% of the rate with catechol
-
-
?
4-methylcatechol + O2
2-hydroxy-4-methyl-6-oxohexa-2,4-dienoate
about 47% of the rate with catechol
-
-
?
4-methylcatechol + O2
2-hydroxy-4-methyl-6-oxohexa-2,4-dienoate
about 65% of the rate with catechol
-
-
?
4-methylcatechol + O2
2-hydroxy-4-methyl-6-oxohexa-2,4-dienoate
about 65% of the rate with catechol
-
-
?
4-methylcatechol + O2
2-hydroxy-4-methylmuconate semialdehyde
very effective substrate
-
-
?
4-methylcatechol + O2
2-hydroxy-4-methylmuconate semialdehyde
rapid inactivation of enzyme during turnover
-
-
?
4-methylcatechol + O2
2-hydroxy-4-methylmuconate semialdehyde
111.4% compared to the activity with catechol
-
-
?
4-methylcatechol + O2
2-hydroxy-4-methylmuconate semialdehyde
Sphingobium scionense DSM 19371
111.4% compared to the activity with catechol
-
-
?
4-methylcatechol + O2
2-hydroxy-5-methyl-6-oxohexa-2,4-dienoate
Halalkalibacterium ligniniphilum
WP_017726464.1
2.7% of the activity as compared to 3-ethylcatechol
-
-
?
4-methylcatechol + O2
2-hydroxy-5-methyl-6-oxohexa-2,4-dienoate
Halalkalibacterium ligniniphilum L1
WP_017726464.1
2.7% of the activity as compared to 3-ethylcatechol
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-
?
4-methylcatechol + O2
2-hydroxy-5-methyl-6-oxohexa-2,4-dienoate
-
-
-
-
?
4-methylcatechol + O2
2-hydroxy-5-methyl-6-oxohexa-2,4-dienoate
Oceanimonas marisflavi 102-Na3
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-
-
-
?
4-methylcatechol + O2
2-hydroxy-5-methyl-6-oxohexa-2,4-dienoate
wild-type enzyme shows 92.1% of the activity as compared to catechol. The activities of the mutant enzyme T254A increases 2.5fold as compared to catechol
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?
4-methylcatechol + O2
2-hydroxy-5-methyl-6-oxohexa-2,4-dienoate
67.7% of the activity as compared to catechol
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-
?
4-methylcatechol + O2
?
activity is 5.72fold higher than with catechol
-
-
?
4-methylcatechol + O2
?
about 65% of activity with catechol
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?
4-nitrocatechol + O2
2-hydroxy-4-nitromuconate semialdehyde
-
-
-
?
4-nitrocatechol + O2
2-hydroxy-4-nitromuconate semialdehyde
rapid inactivation of enzyme during turnover
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
hypoxic strains have enzymes with significantly higher affinities for catechol than for nonhypoxic strains
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
hypoxic strains have enzymes with significantly higher affinities for catechol than for nonhypoxic strains
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
highly specific for
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
highly specific for
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
-
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
extradiol dioxygenase reaction
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
highly specific for
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
metacleavage enzyme of catechol metabolism
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
enzyme is a important component in the degradation pathways of toluene and xylene and catalyses the dioxygenolytic cleavage of the aromatic ring
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
metapyrocatechase 1 takes part in oxidation of aromatic compounds, producing catechol as an intermediate, metapyrocatechase 2 is involved in oxidation of methyl-substituted aromatic substrates
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
enzyme is induced by benzenesulfonate, catechol or toluene p-sulfonate
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
hypoxic strains have enzymes with significantly higher affinities for catechol than for nonhypoxic strains
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
enzyme is a important component in the degradation pathways of toluene and xylene and catalyses the dioxygenolytic cleavage of the aromatic ring
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
hypoxic strains have enzymes with significantly higher affinities for catechol than for nonhypoxic strains
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
enzyme is a important component in the degradation pathways of toluene and xylene and catalyses the dioxygenolytic cleavage of the aromatic ring
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
-
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
highly specific for
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
hypoxic strains have enzymes with significantly higher affinities for catechol than for nonhypoxic strains
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
best substrates
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
enzyme is a important component in the degradation pathways of toluene and xylene and catalyses the dioxygenolytic cleavage of the aromatic ring
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
degradation of aromatic compounds
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
benzoate degadation pathway
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
key role in the degradation of aromatic molecules
-
?
catechol + O2
2-hydroxymuconate semialdehyde
Pseudomonas putida mt-2 / ATCC 33015 / DSM 3931 / NCIB 12182 / NCIMB 12182
-
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
Pseudomonas putida mt-2 / ATCC 33015 / DSM 3931 / NCIB 12182 / NCIMB 12182
degradation of aromatic compounds
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
highly specific for
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
highly specific for
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
hypoxic strains have enzymes with significantly higher affinities for catechol than for nonhypoxic strains
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
enzyme is a important component in the degradation pathways of toluene and xylene and catalyses the dioxygenolytic cleavage of the aromatic ring
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
catechol 2,3-dioxygenase is a key enzyme in the catabolism of monocyclic aromatic compounds including aniline and catalyzes the extradiol cleavage of catechol
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
cleavage of aromatic compounds, involved in alpha-ketoadiapate pathway
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
degradation of aromatic compounds
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
involved in metabolism of aromatic compounds
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
key enzyme for the degradation of aromatic compounds
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
catechol 2,3-dioxygenase is involved in the meta phenol degradation pathway
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
catechol 2,3-dioxygenase is a critical enzyme in the multistep biodegradation of 3,4-dichloroaniline by Pseudomonas sp. KB35B
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
catechol 2,3-dioxygenase is a critical enzyme in the multistep biodegradation of 3,4-dichloroaniline by Pseudomonas sp. KB35B
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?
catechol + O2
2-hydroxymuconate semialdehyde
poor substrate
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
involved in metabolism of aromatic compounds
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
cleavage of aromatic compounds, involved in alpha-ketoadiapate pathway
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
highly specific for
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
catechol 2,3-dioxygenase is involved in the meta phenol degradation pathway
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
highly specific for
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
hypoxic strains have enzymes with significantly higher affinities for catechol than for nonhypoxic strains
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
enzyme is a important component in the degradation pathways of toluene and xylene and catalyses the dioxygenolytic cleavage of the aromatic ring
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
most effective substrate
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
most effective substrate
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
hypoxic strains have enzymes with significantly higher affinities for catechol than for nonhypoxic strains
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
enzyme is a important component in the degradation pathways of toluene and xylene and catalyses the dioxygenolytic cleavage of the aromatic ring
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
hypoxic strains have enzymes with significantly higher affinities for catechol than for nonhypoxic strains
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
enzyme is a important component in the degradation pathways of toluene and xylene and catalyses the dioxygenolytic cleavage of the aromatic ring
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
involved in biodegradation of benzothiazoles
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
involved in biodegradation of benzothiazoles
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?
catechol + O2
2-hydroxymuconate semialdehyde
-
degradation of aromatic compounds, involved in toluene and ortho-xylene metabolism
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
degradation of aromatic compounds, involved in toluene and ortho-xylene metabolism
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?
catechol + O2
2-hydroxymuconate semialdehyde
and 4-chlorocatechol, best substrates
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?
catechol + O2
2-hydroxymuconate semialdehyde
both the ortho- and the meta-degradation pathways are functional in presence of phenol. However, the activation of the catechol 2,3-dioxygenase, only when phenol is present, and the accumulation of only intermediary compounds related to this pathway lead us to the conclusion that the aromatic ring is preferentially opened through the meta-pathway
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?
catechol + O2
2-hydroxymuconate semialdehyde
the enzyme shows the highest activity against catechol and 4-chlorocatechol
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?
catechol + O2
2-hydroxymuconate semialdehyde
both the ortho- and the meta-degradation pathways are functional in presence of phenol. However, the activation of the catechol 2,3-dioxygenase, only when phenol is present, and the accumulation of only intermediary compounds related to this pathway lead us to the conclusion that the aromatic ring is preferentially opened through the meta-pathway
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?
catechol + O2
2-hydroxymuconate semialdehyde
the enzyme shows the highest activity against catechol and 4-chlorocatechol
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
and 4-chlorocatechol, best substrates
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-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
key enzyme for the degradation of aromatic compounds
-
-
?
catechol + O2
2-hydroxymuconate semialdehyde
-
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-
?
catechol + O2
2-hydroxymuconate-6-semialdehyde
Halalkalibacterium ligniniphilum
WP_017726464.1
1.5% of the activity as compared to 3-ethylcatechol
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-
?
catechol + O2
2-hydroxymuconate-6-semialdehyde
Halalkalibacterium ligniniphilum L1
WP_017726464.1
1.5% of the activity as compared to 3-ethylcatechol
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?
catechol + O2
2-hydroxymuconate-6-semialdehyde
-
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?
catechol + O2
2-hydroxymuconate-6-semialdehyde
100% activity
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?
catechol + O2
2-hydroxymuconate-6-semialdehyde
the enzyme is constitutively transcribed
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?
catechol + O2
2-hydroxymuconate-6-semialdehyde
the enzyme is constitutively transcribed
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?
catechol + O2
2-hydroxymuconate-6-semialdehyde
-
compared to the enzyme from Sphingobium yanoikuyae XLDN2-5, the recombinant Escherichia coli BL21 overexpressed C23O exhibits higher catalytic activity towards catechol. The whole cells provided a better environment for C23O to maintain its catalytic activity and stability compared with crude enzyme
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?
catechol + O2
2-hydroxymuconate-6-semialdehyde
-
compared to the enzyme from Sphingobium yanoikuyae XLDN2-5, the recombinant Escherichia coli BL21 overexpressed C23O exhibits higher catalytic activity towards catechol. The whole cells provided a better environment for C23O to maintain its catalytic activity and stability compared with crude enzyme
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?
catechol + O2
2-hydroxymuconate-6-semialdehyde
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?
catechol + O2
2-hydroxymuconate-6-semialdehyde
-
best substrate for isoform C23O1 (100% activity)
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?
hydroquinone + O2
?
-
immobilized enzyme, no activity with the free enzyme
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-
?
hydroquinone + O2
?
-
immobilized enzyme, no activity with the free enzyme
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?
phenol + O2
2-hydroxymuconic semialdehyde
utilize phenol as sole carbon and energy source, concentration of phenol diversify from 25 mg/l to 1000 mg/l, assay at 28°C, pH 6.8-7.0
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?
phenol + O2
2-hydroxymuconic semialdehyde
utilize phenol as sole carbon and energy source, concentration of phenol diversify from 25 mg/l to 1000 mg/l, assay at 28°C, pH 6.8-7.0
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?
additional information
?
-
Halalkalibacterium ligniniphilum
WP_017726464.1
no activities observed for pyrogallol and 3-fluorocatechol
-
-
-
additional information
?
-
Halalkalibacterium ligniniphilum L1
WP_017726464.1
no activities observed for pyrogallol and 3-fluorocatechol
-
-
-
additional information
?
-
no cleavage of 4-carboxycatechol, 4-carboxymethylcatechol and 4-tert-butylcatechol
-
-
?
additional information
?
-
no activity with 4-tert-butylcatechol
-
-
?
additional information
?
-
Pseudomonas putida mt-2 / ATCC 33015 / DSM 3931 / NCIB 12182 / NCIMB 12182
no cleavage of 4-carboxycatechol, 4-carboxymethylcatechol and 4-tert-butylcatechol
-
-
?
additional information
?
-
no activity with 4-tert-butylcatechol
-
-
?
additional information
?
-
-
preferred substrates are catechol and 2,3-dihydroxybiphenyl, reaction of EC 1.13.11.39
-
-
-
additional information
?
-
no activity with 2,3-dihydroxybiphenyl and 3,4-dihydrophenylacetate
-
-
-
additional information
?
-
-
the two isoforms cannot oxidize 1, 2-dihydroxynaphthalene
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-
?
