| Literature DB >> 35020279 |
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.Entities:
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