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Literature summary extracted from

  • Pust, S.; Vervoort, J.; Decker, K.; Bacher, A.; Muller, F.
    13C, 15N, and 31P NMR studies on 6-hydroxy-L-nicotine oxidase from Arthrobacter oxidans (1989), Biochemistry, 28, 516-521.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
1.5.3.5 6-hydroxy-D-nicotine competitive inhibitor Paenarthrobacter nicotinovorans

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.5.3.5 (S)-6-hydroxynicotine + H2O + O2 Paenarthrobacter nicotinovorans
-
 1-(6-hydroxypyrid-3-yl)-4-(methylamino)-butan-1-one + H2O2 transitional product is 6-hydroxy-N-methylmyosmine that hydrolyses spontaneously ?
1.5.3.5 additional information Paenarthrobacter nicotinovorans enzyme production is induced by growing cells in D,L-nicotine as only source of carbon and nitrogen ?
-
 ?

Organism

EC Number Organism UniProt Comment Textmining
1.5.3.5 Paenarthrobacter nicotinovorans
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 formerly Arthrobacter oxidans
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.5.3.5 (S)-6-hydroxynicotine + H2O + O2
-
 Paenarthrobacter nicotinovorans 1-(6-hydroxypyrid-3-yl)-4-(methylamino)-butan-1-one + H2O2 transitional product is 6-hydroxy-N-methylmyosmine that hydrolyses spontaneously ?
1.5.3.5 additional information enzyme production is induced by growing cells in D,L-nicotine as only source of carbon and nitrogen Paenarthrobacter nicotinovorans ?
-
 ?

Cofactor

EC Number Cofactor Comment Organism Structure
1.5.3.5 FAD 1 FAD per subunit, non-covalently bound Paenarthrobacter nicotinovorans