Yellow polyketide pigment suppresses premature hatching in social amoeba

Author:

Günther Markus1ORCID,Reimer Christin23ORCID,Herbst Rosa1ORCID,Kufs Johann E.45ORCID,Rautschek Julia4,Ueberschaar Nico6ORCID,Zhang Shuaibing1,Peschel Gundela5ORCID,Reimer Lisa1,Regestein Lars5ORCID,Valiante Vito4ORCID,Hillmann Falk2ORCID,Stallforth Pierre17ORCID

Affiliation:

1. Department of Paleobiotechnology, Leibniz Institute for Natural Product Research and Infection Biology–Hans Knöll Institute, D-07745 Jena, Germany

2. Evolution of Microbial Interactions, Leibniz Institute for Natural Product Research and Infection Biology–Hans Knöll Institute, D-07745 Jena, Germany

3. Faculty of Biological Sciences, Friedrich Schiller University Jena, Jena, D-07743 Germany

4. Biobricks of Microbial Natural Product Syntheses, Leibniz Institute for Natural Product Research and Infection Biology–Hans Knöll Institute, D-07745 Jena, Germany

5. Bio Pilot Plant, Leibniz Institute for Natural Product Research and Infection Biology–Hans Knöll Institute, D-07745 Jena, Germany

6. Mass Spectrometry Platform, Friedrich Schiller University Jena, D-07743 Jena, Germany

7. Institute for Organic Chemistry and Macromolecular Chemistry, Friedrich Schiller University Jena, D-07743 Jena, Germany

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.

Funder

Deutsche Forschungsgemeinschaft

Werner Siemens-Stiftung

IPF | Leibniz-Gemeinschaft

European Social Fund ESF and the European Regional Development Fund EFRE

Bundesministerium für Bildung und Forschung

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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