4.6 Article

Biochemistry and occurrence of O-demethylation in plant metabolism

Journal

FRONTIERS IN PHYSIOLOGY
Volume 1, Issue -, Pages -

Publisher

FRONTIERS RESEARCH FOUNDATION
DOI: 10.3389/fphys.2010.00014

Keywords

O-demethylation; N-demethylation; 2-oxoglutarate/Fe(II)-dependent dioxygenase; benzylisoquinoline alkaloid biosynthesis

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Funding

  1. Natural Sciences and Engineering Research Council of Canada Discovery Grant

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Demethylases play a pivitol role in numerous biological processes from covalent histone modification and DNA repair to specialized metabolism in plants and microorganisms. Enzymes that catalyze O- and N-demethylation include 2-oxoglutarate (2OG)/Fe(II)-dependent dioxygenases, cytochromes P450, Rieske-domain proteins and flavin adenine dinucleotide (FAD)-dependent oxidases. Proposed mechanisms for demethylation by 2OG/Fe(II)-dependent enzymes involve hydroxylation at the O- or N-linked methyl group followed by formaldehyde elimination. Members of this enzyme family catalyze a wide variety of reactions in diverse plant metabolic pathways. Recently, we showed that 2OG/Fe(II)-dependent dioxygenases catalyze the unique O-demethylation steps of morphine biosynthesis in opium poppy, which provides a rational basis for the widespread occurrence of demethylases in benzylisoquinoline alkaloid metabolism.

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