The Enzyme Database

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Accepted name: (S)-1-hydroxy-N-methylcanadine 13-hydroxylase
Reaction: (S)-1-hydroxy-cis-N-methylcanadine + [reduced NADPH—hemoprotein reductase] + O2 = (13S,14R)-1,13-dihydroxy-cis-N-methylcanadine + [oxidized NADPH—hemoprotein reductase] + H2O
For diagram of noscapine biosynthesis, click here
Other name(s): CYP82X2 (gene name)
Systematic name: (S)-1-hydroxy-cis-N-methylcanadine,[reduced NADPH—hemoprotein reductase]:oxygen oxidoreductase (13-hydroxylating)
Comments: The enzyme, characterized from the plant Papaver somniferum (opium poppy), participates in the biosynthesis of the isoquinoline alkaloid noscapine.
Links to other databases: BRENDA, EXPASY, KEGG, MetaCyc
1.  Dang, T.T., Chen, X. and Facchini, P.J. Acetylation serves as a protective group in noscapine biosynthesis in opium poppy. Nat. Chem. Biol. 11 (2015) 104–106. [DOI] [PMID: 25485687]
2.  Li, Y. and Smolke, C.D. Engineering biosynthesis of the anticancer alkaloid noscapine in yeast. Nat. Commun. 7:12137 (2016). [DOI] [PMID: 27378283]
3.  Li, Y., Li, S., Thodey, K., Trenchard, I., Cravens, A. and Smolke, C.D. Complete biosynthesis of noscapine and halogenated alkaloids in yeast. Proc. Natl. Acad. Sci. USA 115 (2018) E3922–E3931. [DOI] [PMID: 29610307]
[EC created 2018]

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