Dimerization and membrane anchors in extracellular targeting of vancomycin group antibiotics.

Antibiotics of the vancomycin group are shown to enhance their affinities for the bacterial cell wall by the devices of either dimerization (vancomycin and other glycopeptides which dimerize even more strongly) or use of a membrane anchor (teicoplanin); a chelate mechanism is suggested in both cases...

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Veröffentlicht in:	Antimicrob Agents Chemother
Hauptverfasser:	Beauregard, D A, Williams, D H, Gwynn, M N, Knowles, D J
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	American Society for Microbiology (ASM) 1995
Schlagworte:	Research Article
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC162627/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7793894/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/AAC.39.3.781
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