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  • Elucidating the mechanism of chain termination switching in the picromycin (cas 19721-56-3)/methymycin polyketide synthase
  • Add time:08/31/2019         Source:sciencedirect.com

    BackgroundA single modular polyketide synthase (PKS) gene cluster is responsible for production of both the 14-membered macrolide antibiotic picromycin and the 12-membered macrolide antibiotic methymycin in Streptomyces Venezuelas. Building on the success of the heterologous expression system engineered using the erythromycin PKS, we have constructed an analogous system for the picromycin/methymycin PKS. Through heterologous expression and construction of a hybrid PKS, we have examined the contributions that the PKS, its internal thioesterase domain (pikTE) and the Pik TEII thioesterase domain make in termination and cyclization of the two polyketide intermediates.

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    Prev:Photopolymerized thiol-ene systems as shape memory polymers
    Next: Macrolactonization to 10-deoxymethynolide catalyzed by the recombinant thioesterase of the picromycin (cas 19721-56-3)/methymycin polyketide synthase)

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