# Genome-mining-guided discovery of coumarubrin: A novel aminocoumarin-substituted rubromycin antibiotic

**Authors:** Heiner G Weddeling, Sven T Sowa, Selina Bosshardt, Lukas Schwimbersky, Malik Rakhmanov, Robin Teufel

PMC · DOI: 10.1093/jimb/kuaf018 · 2025-07-04

## TL;DR

Scientists discovered a new antibiotic, coumarubrin, by studying bacterial genes, which shows strong activity against Gram-positive bacteria.

## Contribution

The discovery of a novel aminocoumarin-substituted rubromycin antibiotic through genome-mining and experimental validation.

## Key findings

- Lentzea tibetensis produces a new aminocoumarin-substituted rubromycin called coumarubrin.
- HRMS and NMR confirmed the structure of coumarubrin.
- Coumarubrin shows potent inhibitory activity against Gram-positive bacteria.

## Abstract

Rubromycins are bacterial aromatic polyketides containing a hallmark spiroketal pharmacophore produced by type II polyketide synthases and accessory enzymes. They generally display cytotoxic and antimicrobial properties, frequently disrupting cellular processes and proteins associated with nucleic acids, such as DNA helicase or telomerase. Among the known rubromycin congeners, hyaluromycin stands out due to a 2-amino-3-hydroxycyclopent-2-enone (C5N) substitution that is presumably installed by an amide bond synthetase (ABS). Here, we used bioinformatic analysis to identify uncharacterized biosynthetic gene clusters and potential rubromycin producer strains encoding putative ABSs but lacking the enzymes responsible for C5N formation, suggesting potentially novel substituents. One of these strains, Lentzea tibetensis, was successfully cultivated and confirmed to produce a previously undescribed aminocoumarin-substituted rubromycin polyketide, named coumarubrin, as verified by high-resolution mass spectrometry (HRMS) and comprehensive nuclear magnetic resonance (NMR) spectroscopy. Electronic circular dichroism spectroscopy indicates an absolute configuration identical to that of previously characterized rubromycins, while the first bioactivity assays demonstrated potent inhibitory activity against Gram-positive bacteria.

One-Sentence Summary: This study reports the discovery of a novel member of the rubromycins, antibiotic and cytotoxic aromatic polyketides produced by Actinobacteria, which is fused to a distinct aminocoumarin moiety.

Graphical Abstract

## Linked entities

- **Proteins:** DDX41 (DEAD-box helicase 41), dna-helicase (DNA-Helicase), tert.L (telomerase reverse transcriptase L homeolog)
- **Chemicals:** hyaluromycin (PubChem CID 162983858), aminocoumarin (PubChem CID 74217)
- **Species:** Lentzea tibetensis (taxon 2591470)

## Full-text entities

- **Diseases:** cytotoxic (MESH:D064420)
- **Chemicals:** 2-amino-3-hydroxycyclopent-2-enone (MESH:C000628799), hyaluromycin (MESH:C000590755), aminocoumarin (MESH:D049933), Rubromycins (-)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12284476/full.md

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Source: https://tomesphere.com/paper/PMC12284476