Characterization of the Antibacterial Activity of Quinone-Based Compounds Originating from the Alnumycin Biosynthetic Gene Cluster of a Streptomyces Isolate

Author:

Sagurna Leonie1ORCID,Heinrich Sascha1ORCID,Kaufmann Lara-Sophie1,Rückert-Reed Christian2ORCID,Busche Tobias2,Wolf Alexander3,Eickhoff Jan3ORCID,Klebl Bert3,Kalinowski Jörn2ORCID,Bandow Julia E.1

Affiliation:

1. Applied Microbiology, Faculty of Biology and Biotechnology, Ruhr University Bochum, 44780 Bochum, Germany

2. Technology Platform Genomics, Center for Biotechnology, Bielefeld University, 33594 Bielefeld, Germany

3. Lead Discovery Center GmbH, 44227 Dortmund, Germany

Abstract

Bacteria of the genus Streptomyces produce various specialized metabolites. Single biosynthetic gene clusters (BGCs) can give rise to different products that can vary in terms of their biological activities. For example, for alnumycin and the shunt product K115, antimicrobial activity was described, while no antimicrobial activity was detected for the shunt product 1,6-dihydro 8-propylanthraquinone. To investigate the antibacterial activity of 1,6-dihydro 8-propylanthraquinone, we produced alnumycin and 1,6-dihydro 8-propylanthraquinone from a Streptomyces isolate containing the alnumycin BGC. The strain was cultivated in liquid glycerol–nitrate–casein medium (GN), and both compounds were isolated using an activity and mass spectrometry-guided purification. The structures were validated via nuclear magnetic resonance (NMR) spectroscopy. A minimal inhibitory concentration (MIC) test revealed that 1,6-dihydro 8-propylanthraquinone exhibits antimicrobial activity against E. coli ΔtolC, B. subtilis, an S. aureus type strain, and a vancomycin intermediate-resistance S. aureus strain (VISA). Activity of 1,6-dihydro 8-propylanthraquinone against E. coli ΔtolC was approximately 10-fold higher than that of alnumycin. We were unable to confirm gyrase inhibition for either compound and believe that the modes of action of both compounds are worth reinvestigating.

Funder

German Federal State of North Rhine–Westphalia and the European Union

European Regional Development Fund, Investing in Your Future (Research Infrastructure ‘Center for System-based Antibiotic Research (CESAR)’

German Research Foundation

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Microbiology (medical),General Pharmacology, Toxicology and Pharmaceutics,Biochemistry,Microbiology

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