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Literature summary for 3.2.1.105 extracted from

  • Murata, J.; De Luca, V.
    localization of tabersonine 16-hydroxylase and 16-OH tabersonine-16-O-methyltransferase to leaf epidermal cells defines them as a major site of precursor biosynthesis in the vindoline pathway in Catharanthus roseus (2005), Plant J., 44, 581-594.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Catharanthus roseus
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Source Tissue

Source Tissue Comment Organism Textmining
leaf epidermis abaxial and adaxial Catharanthus roseus
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
strictosidine + H2O The structural diversity of monoterpenoid indole alkaloids comes first from the deglucosylation of strictosidine by strictosidine beta-glucosidase. The unstable and versatile aglycone is biochemically converted by mostly uncharacterized enzyme reactions to the Corynanthe, Iboga and Aspidosperma classes of alkaloids such as ajmalicine, catharanthine and tabersonine, respectively Catharanthus roseus D-glucose + strictosidine aglycone
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Synonyms

Synonyms Comment Organism
SGD
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Catharanthus roseus