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Literature summary extracted from

  • MacLeod, A.J.; Rossiter, J.T.
    Degradation of 2-hydroxybut-3-enylglucosinolate (progoitrin) (1987), Phytochemistry, 26, 669-673.
No PubMed abstract available

Activating Compound

EC Number Activating Compound Comment Organism Structure
3.2.1.147 ascorbic acid maximal activation at 1.57 mM Brassica napus

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.2.1.147 Cu2+ strong Brassica napus
3.2.1.147 Fe2+ slightly suppresses reaction but causes a significant effect by directing degradation of 2-hydroxybut-3-enylglucosinolate to 1-cyano-2-hydroxy-3-ene rather than to 5-vinyloxazolidine-2-thione Brassica napus

Organism

EC Number Organism UniProt Comment Textmining
3.2.1.147 Brassica napus
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.2.1.147 2-hydroxybut-3-enylglucosinolate + H2O
-
Brassica napus additional information in absence of ascorbate 5-vinyloxazolidine-2-thione is the only product, whereas in the presence of added ascorbate 1-cyano-2-hydroxybut-3-ene is also formed ?
3.2.1.147 sinigrin + H2O
-
Brassica napus D-glucose + 3-isothiocyanatoprop-1-ene + SO42-
-
?