Discovery of Six Ramoplanin Family Gene Clusters and the Lipoglycodepsipeptide Chersinamycin*.
Kelsey T MorganJeffrey ZhengDewey G McCaffertyPublished in: Chembiochem : a European journal of chemical biology (2020)
Ramoplanins and enduracidins are peptidoglycan lipid intermediate II-binding lipodepsipeptides with broad-spectrum activity against methicillin- and vancomycin-resistant Gram-positive pathogens. Targeted genome mining using probes from conserved sequences within the ramoplanin/enduracidin biosynthetic gene clusters (BGCs) was used to identify six microorganisms with BGCs predicted to produce unique lipodepsipeptide congeners of ramoplanin and enduracidin. Fermentation of Micromonospora chersina yielded a novel lipoglycodepsipeptide, called chersinamycin, which exhibited good antibiotic activity against Gram-positive bacteria (1-2 μg/mL) similar to the ramoplanins and enduracidins. The covalent structure of chersinamycin was determined by NMR spectroscopy and tandem mass spectrometry in conjunction with chemical degradation studies. These six new BGCs and isolation of a new antimicrobial peptide provide much-needed tools to investigate the fundamental aspects of lipodepsipeptide biosynthesis and to facilitate efforts to produce novel antibiotics capable of combating antibiotic-resistant infections.
Keyphrases
- tandem mass spectrometry
- gram negative
- genome wide
- ultra high performance liquid chromatography
- high performance liquid chromatography
- small molecule
- liquid chromatography
- multidrug resistant
- simultaneous determination
- copy number
- gas chromatography
- methicillin resistant staphylococcus aureus
- staphylococcus aureus
- genome wide identification
- cell wall
- solid phase extraction
- high resolution
- high throughput
- cancer therapy
- dna methylation
- antimicrobial resistance
- mass spectrometry
- fatty acid
- single molecule
- living cells
- single cell
- dna binding
- genome wide analysis
- photodynamic therapy
- nucleic acid
- genetic diversity