1.11.1.10: chloride peroxidase
This is an abbreviated version!
For detailed information about chloride peroxidase, go to the full flat file.
Word Map on EC 1.11.1.10
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1.11.1.10
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fumago
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caldariomyces
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horseradish
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chlorination
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peroxidases
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halogen
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halide
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haloperoxidase
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bromination
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lactoperoxidase
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inaequalis
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ferryl
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curvularia
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soret
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bromoperoxidase
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monochlorodimedone
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low-spin
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p450cam
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vanadium-dependent
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thioanisole
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peroxidase-catalyzed
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thiolate-ligated
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pyrrocinia
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oxoferryl
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n,n-dimethylaniline
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peroxygenases
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agrocybe
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vanadium-containing
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hypohalous
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aegerita
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degradation
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synthesis
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environmental protection
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biotechnology
- 1.11.1.10
- fumago
-
caldariomyces
- horseradish
-
chlorination
- peroxidases
-
halogen
- halide
- haloperoxidase
-
bromination
- lactoperoxidase
- inaequalis
-
ferryl
-
curvularia
-
soret
-
bromoperoxidase
- monochlorodimedone
-
low-spin
-
p450cam
-
vanadium-dependent
- thioanisole
-
peroxidase-catalyzed
-
thiolate-ligated
- pyrrocinia
-
oxoferryl
- n,n-dimethylaniline
-
peroxygenases
-
agrocybe
-
vanadium-containing
-
hypohalous
- aegerita
- degradation
- synthesis
- environmental protection
- biotechnology
Reaction
Synonyms
CCPO, Chloride peroxidase, chloroperoxidase, chloroproxidase, CPO, CPO-I, CPO2, haeme-thiolate peroxidase, heme-containing CPO, heme-thiolate chloroperoxidase, More, peroxidase, chloride, Vanadium chloride peroxidase, vCPO
ECTree
1.11.1.10 chloride peroxidaseAdvanced search results
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results (Natural Substrates Products
Natural Substrates Products on EC 1.11.1.10 - chloride peroxidase
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NATURAL SUBSTRATE 
NATURAL 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-chlorodimedone + chloride + H2O2
1,1-dimethyl-4,4-dichloro-3,5-cyclohexanedione + 2 H2O
model substrate monochlorodimedone
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?
monochlorodimedon + chloride + H2O2
dichlorodimedon + 2 H2O
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?
RH + chloride + H2O2
RCl + 2 H2O
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?
additional information
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transformation of aromatic pollutants into chlorinated derivatives by microbial enzymes may occur in polluted sites. This biocatalytic process should be considered because the toxicity and environmental impact of aromatic compounds may be increased
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additional information
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production of polyhalogenated carbazoles (PHCs) from halogenation of carbazole in the presence of bromide and/or chloride under the catalysis of chloroperoxidase (CPO) isolated from the marine fungus Caldariomyces fumago, see also EC 1.11.1.18. A total of 25 congeners including mono-to tetra-substituted chlorinated, brominated, and mixed halogenated carbazoles (with substitution patterns of -BrCl, -BrCl2, -BrCl3, -Br2Cl, -Br2Cl2, and -Br3Cl) are produced from the reactions under various conditions. The PHC product profiles are apparently dependent on the halide concentrations. In the CPO-mediated chlorination of carbazole, 3-mono- and 3,6-dichlorocarbazoles predominated in the formation products. In addition to the less abundant mixed halogenated carbazoles (-Br2Cl), 1,3,6-tri- and 1,3,6,8-tetrabromocarbazoles are the dominant products in reactions containing both Br- and Cl-
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additional information
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the immobilized enzyme CPO catalyzes degradation of mesotrione (2-[(4-methylsulfonyl)-2-nitrobenzoyl]cyclohexan-1,3-dione) in wastewater
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