| Literature DB >> 29807982 |
Xue Chen1,2, Jillian M Hagel1,2, Limei Chang1,2, Joseph E Tucker2,3, Stacey A Shiigi4, Yuora Yelpaala4, Hsiang-Yun Chen4, Rodrigo Estrada4, Jeffrey Colbeck4, Maria Enquist-Newman4, Ana B Ibáñez4, Guillaume Cottarel4, Genevieve M Vidanes4, Peter J Facchini5,6.
Abstract
The ultimate step in the formation of thebaine, a pentacyclic opiate alkaloid readily converted to the narcotic analgesics codeine and morphine in the opium poppy, has long been presumed to be a spontaneous reaction. We have detected and purified a novel enzyme from opium poppy latex that is capable of the efficient formation of thebaine from (7S)-salutaridinol 7-O-acetate at the expense of labile hydroxylated byproducts, which are preferentially produced by spontaneous allylic elimination. Remarkably, thebaine synthase (THS), a member of the pathogenesis-related 10 protein (PR10) superfamily, is encoded within a novel gene cluster in the opium poppy genome that also includes genes encoding the four biosynthetic enzymes immediately upstream. THS is a missing component that is crucial to the development of fermentation-based opiate production and dramatically improves thebaine yield in engineered yeast.Entities:
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Year: 2018 PMID: 29807982 DOI: 10.1038/s41589-018-0059-7
Source DB: PubMed Journal: Nat Chem Biol ISSN: 1552-4450 Impact factor: 15.040