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Literature summary 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

EC Number Organism UniProt Comment Textmining
1.11.2.1 Cyclocybe aegerita
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
1.11.2.1 fast protein liquid chromatography Cyclocybe aegerita

Specific Activity [micromol/min/mg]

EC Number Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
1.11.2.1 74.8
-
 purified enzyme, using veratryl alcohol as substrate, pH and temperature not specified in the publication Cyclocybe aegerita
1.11.2.1 217
-
 purified enzyme, using naphthalene as substrate, pH and temperature not specified in the publication Cyclocybe aegerita

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.11.2.1 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 ?
1.11.2.1 veratryl alcohol + H2O2 + H+
-
 Cyclocybe aegerita veratraldehyde + H2O
-
 ?

Synonyms

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