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Suertides A-C: selective antibacterial cyclic hexapeptides from Amycolatopsis sp. MST-135876v3.

Heather J LaceyRachel ChenDaniel VuongMark F FisherErnest LaceyPeter J RutledgeAndrew M Piggott
Published in: The Journal of antibiotics (2022)
Amycolatopsis sp. MST-135876 was isolated from soil collected from the riverbank of El Pont de Suert, Catalonia, Spain. Cultivation of MST-135876 on a range of media led to the discovery of a previously unreported dichlorinated cyclic hexapeptide, suertide A (D-Ser, 5-Cl-D-Trp, 6-Cl-D-Trp, L-Ile, D-Val, D-Glu), featuring an unprecedented pair of adjacent 5/6-chlorotryptophan residues. Supplementing the growth medium with KBr resulted in production of the mono- and dibrominated analogues suertides B and C, respectively. Suertides A-C displayed selective activity against Bacillus subtilis (MIC 1.6 µg ml<sup>-1</sup>) and Staphylococcus aureus (MIC 3.1, 6.3, and 12.5 µg ml<sup>-1</sup>, respectively), while suertides A and B showed appreciable activity against methicillin-resistant S. aureus (MIC 1.6 and 6.3 µg ml<sup>-1</sup>, respectively).
Keyphrases
  • staphylococcus aureus
  • bacillus subtilis
  • small molecule
  • methicillin resistant staphylococcus aureus
  • biofilm formation
  • high throughput
  • escherichia coli
  • molecular dynamics simulations
  • cystic fibrosis