Genome-mining-guided discovery of coumarubrin: A novel aminocoumarin-substituted rubromycin antibiotic
Heiner G Weddeling, Sven T Sowa, Selina Bosshardt, Lukas Schwimbersky, Malik Rakhmanov, Robin Teufel

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.
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…
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Taxonomy
TopicsMicrobial Natural Products and Biosynthesis · Genomics and Phylogenetic Studies · RNA and protein synthesis mechanisms
