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

In a recent "Angewandte Chemie International Edition" paper, the Piel group (IMB) in collaboration with the Piechulla group (University of Rostock) report a bacterial polyketide synthase that catalyzes a highly expanded set of biochemical reactions to generate complex bioactive molecules.

Figure Piel paper
The oocydin polyketide synthase is versatile like a Swiss army knife. During polyketide assembly, it catalyzes halogenation, α-hydroxylation, O-acylation and further reactions. This installs a great variety of functional groups in the polyketide.  

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.

Link to the paper in external page Angewandte Chemie International Edition
 

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