Genome Mining-Driven Isolation of New Gromomycins and Insights into Their Mode of Action

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Authors: Dmytro Bratiichuk, Franziska Fries, Marc Stierhof, Leon Morguet, Josef Zapp, Mathias Müsken, Yuriy Rebets, Maksym Myronovskyi, Rolf Müller, Jennifer Herrmann, Andriy Luzhetskyy
Cited by: 2
References: 48

Abstract

High Resolution Image Download MS PowerPoint Slide The growing threat of multidrug-resistant bacterial infections highlights the urgent need for antibiotics with novel mechanisms of action. Gromomycins, a newly identified class of triterpene antibiotics, exhibit potent activity against Gram-positive bacteria, including drug-resistant species, through a previously uncharacterized mode of action. Here, we report the discovery of a gromomycin-like biosynthetic gene cluster in the Actinoplanes genus through a genome mining approach, leading to the isolation and characterization of new bioactive derivatives that overcome resistance to clinically used drugs in vancomycin-resistant enterococci. Mechanistic studies revealed that gromomycins induce rapid potassium ion leakage and depolarization of the bacterial membrane, resulting in bactericidal activity against Staphylococcus aureus . Gromomycins disrupt the integrity of the cytoplasmic membrane, as evidenced by large pore formation, leakage of intracellular contents, and subsequent cell lysis. Supplementation with membrane lipids and fatty acids neutralized their antibacterial activity, suggesting a direct membrane-targeting mechanism, further supported by the inability to raise gromomycin resistance and their toxic effects on eukaryotic cells. Collectively, these findings deepen our understanding of gromomycin activity and demonstrate the utility of genome mining to uncover structurally novel and biologically active natural products.

Fields of Study & Subjects

Microbial Natural Products and Biosynthesis RNA and protein synthesis mechanisms Bacterial Genetics and Biotechnology

Publication details

Journal / source
ACS Chemical Biology
Publisher
American Chemical Society (ACS)
Volume
21
Issue
3
Pages
546–557
Publication date
5 March 2026
Language
EN