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Literature summary extracted from

  • Boominathan, K.; Mahadevan, A.
    Dissimilation of aromatic substances by fungi (1989), Zentralbl. Mikrobiol., 144, 37-45.
No PubMed abstract available

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.13.11.37 benzene-1,2,4-triol + O2 Fusarium oxysporum
-
 3-hydroxy-cis-cis-muconate
-
 ?
1.13.11.37 benzene-1,2,4-triol + O2 Arcopilus cupreus
-
 3-hydroxy-cis-cis-muconate
-
 ?
1.13.11.37 benzene-1,2,4-triol + O2 Bipolaris oryzae
-
 3-hydroxy-cis-cis-muconate
-
 ?

Organism

EC Number Organism UniProt Comment Textmining
1.13.11.37 Arcopilus cupreus
-
-
-
1.13.11.37 Bipolaris oryzae
-
-
-
1.13.11.37 Fusarium oxysporum
-
 f. sp. vasinfectum
-

Source Tissue

EC Number Source Tissue Comment Organism Textmining
1.13.11.37 mycelium
-
 Fusarium oxysporum
-
1.13.11.37 mycelium
-
 Arcopilus cupreus
-
1.13.11.37 mycelium
-
 Bipolaris oryzae
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.13.11.37 benzene-1,2,4-triol + O2
-
 Fusarium oxysporum maleylacetate maleylacetate, i.e. cis-hexenedioate, is the isomer of 3-hydroxy-cis-cis-muconate ?
1.13.11.37 benzene-1,2,4-triol + O2
-
 Arcopilus cupreus maleylacetate maleylacetate, i.e. cis-hexenedioate, is the isomer of 3-hydroxy-cis-cis-muconate ?
1.13.11.37 benzene-1,2,4-triol + O2
-
 Bipolaris oryzae maleylacetate maleylacetate, i.e. cis-hexenedioate, is the isomer of 3-hydroxy-cis-cis-muconate ?
1.13.11.37 benzene-1,2,4-triol + O2
-
 Fusarium oxysporum 3-hydroxy-cis-cis-muconate
-
 ?
1.13.11.37 benzene-1,2,4-triol + O2
-
 Arcopilus cupreus 3-hydroxy-cis-cis-muconate
-
 ?
1.13.11.37 benzene-1,2,4-triol + O2
-
 Bipolaris oryzae 3-hydroxy-cis-cis-muconate
-
 ?