Antimicrobial peptides are a rich source of potential antibiotic candidates. The tridecaptins, a family of linear lipo-tridecapeptides, are easily synthesized and show strong activity against Gram-negative bacteria. However, their composition includes several expensive amino acids, such as D/L diaminobutyric acid and Dallo-isoleucine, significantly increasing their cost of synthesis. Herein, we report a series of new tridecaptin derivatives that are much cheaper to synthesize and retain strong activity against multidrug-resistant Gram-negative bacteria.
Structural and mechanistic studies on antimicrobial peptides that target multi-drug resistant bacteriaAuthor: Ballantine, R., Jul 2021
Student thesis: Doctoral Thesis › Doctor of Philosophy