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Peptidoglycan-Directed Chemical Ligation for Selective Inhibition on Gram-Positive Bacteria

Overview
Journal ACS Omega
Specialty Chemistry
Date 2023 Jan 23
PMID 36687063
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Abstract

Microbicides with distinct antibacterial mechanisms show potential to combat multi-drug resistance bacteria. We herein report peptidoglycan-directed chemical ligation (PGCL) between alkyne-bearing vancomycin and an azide-tagged cationic polymer. The former binds peptidoglycan and inhibits peptidoglycan crosslinking, while the latter interferes the integrity of the bacterial membrane. PGCL results in enhanced bactericidal activity against Gram-positive () over Gram-negative (). These data indicate the potential of PGCL to selectively and synergistically inhibit Gram-positive pathogens via dual modality antibacterial mechanisms of peptidoglycan-inhibiting antibiotics and bacterial membrane-disrupting polycations.

References
1.
Jones J, Liu L, Rank L, Wetzel D, Woods E, Biok N . Cationic Homopolymers Inhibit Spore and Vegetative Cell Growth of . ACS Infect Dis. 2021; 7(5):1236-1247. PMC: 8130196. DOI: 10.1021/acsinfecdis.0c00843. View

2.
Semsarilar M, Perrier S . 'Green' reversible addition-fragmentation chain-transfer (RAFT) polymerization. Nat Chem. 2010; 2(10):811-20. DOI: 10.1038/nchem.853. View

3.
Bessa L, Fazii P, Di Giulio M, Cellini L . Bacterial isolates from infected wounds and their antibiotic susceptibility pattern: some remarks about wound infection. Int Wound J. 2013; 12(1):47-52. PMC: 7950398. DOI: 10.1111/iwj.12049. View

4.
Timofeeva L, Kleshcheva N . Antimicrobial polymers: mechanism of action, factors of activity, and applications. Appl Microbiol Biotechnol. 2010; 89(3):475-92. DOI: 10.1007/s00253-010-2920-9. View

5.
Choi S, Myc A, Silpe J, Sumit M, Wong P, McCarthy K . Dendrimer-based multivalent vancomycin nanoplatform for targeting the drug-resistant bacterial surface. ACS Nano. 2012; 7(1):214-28. DOI: 10.1021/nn3038995. View