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Literature summary for 1.11.2.1 extracted from

  • Kluge, M.; Ullrich, R.; Dolge, C.; Scheibner, K.; Hofrichter, M.
    Hydroxylation of naphthalene by aromatic peroxygenase from Agrocybe aegerita proceeds via oxygen transfer from H2O2 and intermediary epoxidation (2009), Appl. Microbiol. Biotechnol., 81, 1071-1076.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Cyclocybe aegerita
-
-
-

Purification (Commentary)

Purification (Comment) Organism
fast protein liquid chromatography Cyclocybe aegerita

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
74.8
-
purified enzyme, using veratryl alcohol as substrate, pH and temperature not specified in the publication Cyclocybe aegerita
217
-
purified enzyme, using naphthalene as substrate, pH and temperature not specified in the publication Cyclocybe aegerita

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
naphthalene + H2O2 the enzyme selectively hydroxylates the aromatic ring of naphthalene Cyclocybe aegerita naphthalene 1,2-oxide + H2O naphthalene 1,2-oxide is the primary product of Agrocybe aegerita peroxidase/peroxygenase-catalyzed oxygenation of naphthalene ?
veratryl alcohol + H2O2 + H+
-
Cyclocybe aegerita veratraldehyde + H2O
-
?

Synonyms

Synonyms Comment Organism
Agrocybe aegerita peroxidase/peroxygenase P II, main isoform Cyclocybe aegerita
aromatic peroxygenase
-
Cyclocybe aegerita