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Merck
  • Discovery of a Novel DNA Gyrase-Targeting Antibiotic through the Chemical Perturbation of Streptomyces venezuelae Sporulation.

Discovery of a Novel DNA Gyrase-Targeting Antibiotic through the Chemical Perturbation of Streptomyces venezuelae Sporulation.

Cell chemical biology (2019-07-08)
Scott McAuley, Alan Huynh, Alison Howells, Chris Walpole, Anthony Maxwell, Justin R Nodwell
摘要

Common approaches to antibiotic discovery include small-molecule screens for growth inhibition in target pathogens and screens for inhibitors of purified enzymes. These approaches have a shared intent of seeking to directly target a vital Achilles heel in a pathogen of interest. Here, we report the first screen against a sporulation pathway in a non-pathogenic bacterium as a means of discovering novel antibiotics-this effort has resulted in two important discoveries. First, we show that the sporulation program of Streptomyces venezuelae is exquisitely sensitive to numerous forms of DNA damage. Second, we have identified a DNA gyrase inhibitor. This molecule, EN-7, is active against pathogenic species that are resistant to ciprofloxacin and other clinically important antibiotics. We suggest that this strategy could be applied to other morphogenetic pathways in prokaryotes or eukaryotes as a means of identifying novel chemical matter having scientific and clinical utility.

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Sigma-Aldrich
氯霉素,大包装, ≥98% (HPLC)
Sigma-Aldrich
万古霉素 盐酸盐 来源于东方链霉菌, ≥900 μg per mg (as vancomycin base)
Sigma-Aldrich
利福平, ≥95% (HPLC), powder or crystals
Sigma-Aldrich
丝裂霉素 C 来源于头状链霉菌, powder, BioReagent, suitable for cell culture
Sigma-Aldrich
氰化羰基-3-氯苯腙, ≥97% (TLC), powder
Sigma-Aldrich
环丙沙星, ≥98% (HPLC)
Sigma-Aldrich
Kanamycin B sulfate salt, aminoglycoside antibiotic
硫酸博来霉素, European Pharmacopoeia (EP) Reference Standard