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Literature summary for 1.11.1.10 extracted from

  • Longoria, A.; Tinoco, R.; Vazquez-Duhalt, R.
    Chloroperoxidase-mediated transformation of highly halogenated monoaromatic compounds (2008), Chemosphere, 72, 485-490.
    View publication on PubMed

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.006
-
2,3,5,6-Tetrachlorophenol
-
Leptoxyphium fumago
0.03
-
H2O2 cosubstrate: 2,3,5,6-tetrachlorophenol Leptoxyphium fumago
0.038
-
2,3,5,6-tetrachloroaniline
-
Leptoxyphium fumago
0.1
-
H2O2 cosubstrate: pentachlorophenol Leptoxyphium fumago
0.12
-
Pentachlorophenol
-
Leptoxyphium fumago
0.269
-
H2O2 cosubstrate: 2,3,5,6-tetrachloroaniline Leptoxyphium fumago

Organism

Organism UniProt Comment Textmining
Leptoxyphium fumago
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2,3,5,6-tetrachloroaniline + HCl + H2O2 the main product from peroxidase oxidation is a polymeric and insoluble material Leptoxyphium fumago pentachloroaniline + H2O
-
?
2,3,5,6-tetrachlorophenol + HCl + H2O2 the main product from peroxidase oxidation is a polymeric and insoluble material Leptoxyphium fumago pentachlorophenol + H2O
-
?
pentachlorophenol + HCl + H2O the main product from peroxidase oxidation is a polymeric and insoluble material Leptoxyphium fumago ?
-
?

Turnover Number [1/s]

Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
35.95
-
2,3,5,6-tetrachloroaniline
-
Leptoxyphium fumago
46.97
-
Pentachlorophenol
-
Leptoxyphium fumago
60.8
-
2,3,5,6-Tetrachlorophenol
-
Leptoxyphium fumago