bioRxiv · 10.1101/581074
Aromatic polyketide biosynthesis: fidelity, evolution and engineering
Abstract
We report the formicapyridines which are structurally and biosynthetically related to the pentacyclic fasamycin and formicamycin aromatic polyketides but comprise a rare pyridine moiety. These new compounds are trace level metabolites formed by derailment of the major biosynthetic pathway. Inspired by evolutionary logic we show that rational mutation of a single gene in the biosynthetic gene cluster leads to a significant increase both in total formicapyridine production and their enrichment relative to the fasamycins/formicamycins. Our observations broaden the polyketide biosynthetic landscape and identify a non-catalytic role for ABM superfamily proteins in type II polyketide synthase assemblages for maintaining biosynthetic pathway fidelity.
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Qin, Z., Devine, R., Hutchings, M. I., Wilkinson, B.. 2019-03-18. Aromatic polyketide biosynthesis: fidelity, evolution and engineering. https://doi.org/10.1101/581074
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