Literature DB >> 35020279

Modular Halogenation, α-Hydroxylation, and Acylation by a Remarkably Versatile Polyketide Synthase.

Franziska Hemmerling1, Roy A Meoded1, Amy E Fraley1, Hannah A Minas1, Cora L Dieterich1, Michael Rust1, Reiko Ueoka1,2, Katja Jensen1, Eric J N Helfrich1,3,4, Cedric Bergande1, Maurice Biedermann1, Nancy Magnus5, Birgit Piechulla5, Jörn Piel1.   

Abstract

Bacterial multimodular polyketide synthases (PKSs) are large enzymatic assembly lines that synthesize many bioactive natural products of therapeutic relevance. While PKS catalysis is mostly based on fatty acid biosynthetic principles, polyketides can be further diversified by post-PKS enzymes. Here, we characterized a remarkably versatile trans-acyltransferase (trans-AT) PKS from Serratia that builds structurally complex macrolides via more than ten functionally distinct PKS modules. In the oocydin PKS, we identified a new oxygenation module that α-hydroxylates polyketide intermediates, a halogenating module catalyzing backbone γ-chlorination, and modular O-acetylation by a thioesterase-like domain. These results from a single biosynthetic assembly line highlight the expansive biochemical repertoire of trans-AT PKSs and provide diverse modular tools for engineered biosynthesis from a close relative of E. coli.
© 2022 Wiley-VCH GmbH.

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Keywords:  Bacterial Natural Products; Biosynthesis; Chlorination; Enzymes; Polyketides

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Year:  2022        PMID: 35020279     DOI: 10.1002/anie.202116614

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

1.  Cleavage Off-Loading and Post-assembly-Line Conversions Yield Products with Unusual Termini during Biosynthesis.

Authors:  Yi-Ming Shi; Merle Hirschmann; Yan-Ni Shi; Helge B Bode
Journal:  ACS Chem Biol       Date:  2022-07-21       Impact factor: 4.634

  1 in total

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