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A Polyketide Synthase Component for Oxygen Insertion into Polyketide Backbones
Authors:Roy A Meoded  Dr Reiko Ueoka  Dr Eric J N Helfrich  Dr Katja Jensen  Nancy Magnus  Prof?Dr Birgit Piechulla  Prof?Dr Jörn Piel
Affiliation:1. Institute of Microbiology, Eigen?ssische Technische Hochschule (ETH) Zurich, Zurich, Switzerland;2. Institute for Biological Sciences, University of Rostock, Rostock, Germany
Abstract:Enzymatic core components from trans‐acyltransferase polyketide synthases (trans‐AT PKSs) catalyze exceptionally diverse biosynthetic transformations to generate structurally complex bioactive compounds. Here we focus on a group of oxygenases identified in various trans‐AT PKS pathways, including those for pederin, oocydins, and toblerols. Using the oocydin pathway homologue (OocK) from Serratia plymuthica 4Rx13 and N‐acetylcysteamine (SNAC) thioesters as test surrogates for acyl carrier protein (ACP)‐tethered intermediates, we show that the enzyme inserts oxygen into β‐ketoacyl moieties to yield malonyl ester SNAC products. Based on these data and the identification of a non‐hydrolyzed oocydin congener with retained ester moiety, we propose a unified biosynthetic pathway of oocydins, haterumalides, and biselides. By providing access to internal ester, carboxylate pseudostarter, and terminal hydroxyl functions, oxygen insertion into polyketide backbones greatly expands the biosynthetic scope of PKSs.
Keywords:Baeyer–  Villiger oxidation  biosynthesis  natural products  polyketides  polyketide synthases
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