| Literature DB >> 36252029 |
Markus Günther1, Christin Reimer2,3, Rosa Herbst1, Johann E Kufs4,5, Julia Rautschek4, Nico Ueberschaar6, Shuaibing Zhang1, Gundela Peschel5, Lisa Reimer1, Lars Regestein5, Vito Valiante4, Falk Hillmann2, Pierre Stallforth1,7.
Abstract
Low-molecular-weight natural products from microbes are indispensable in the development of potent drugs. However, their biological roles within an ecological context often remain elusive. Here, we shed light on natural products from eukaryotic microorganisms that have the ability to transition from single cells to multicellular organisms: the social amoebae. These eukaryotes harbor a large number of polyketide biosynthetic genes in their genomes, yet virtually none of the corresponding products can be isolated or characterized. Using complementary molecular biology approaches, including CRISPR-Cas9, we generated polyketide synthase (pks5) inactivation and overproduction strains of the social amoeba Dictyostelium discoideum. Differential, untargeted metabolomics of wild-type versus mutant fruiting bodies allowed us to pinpoint candidate metabolites derived from the amoebal PKS5. Extrachromosomal expression of the respective gene led to the identification of a yellow polyunsaturated fatty acid. Analysis of the temporospatial production pattern of this compound in conjunction with detailed bioactivity studies revealed the polyketide to be a spore germination suppressor.Entities:
Keywords: amoeba; natural products; polyketide
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Year: 2022 PMID: 36252029 DOI: 10.1073/pnas.2116122119
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 12.779