Vancomycin Derivatives That Inhibit Peptidoglycan Biosynthesis Without Binding d -Ala- d -Ala

Author:

Ge Min1,Chen Zhong1,Russell H.,Onishi 2,Kohler Joyce2,Silver Lynn L.2,Kerns Robert1,Fukuzawa Seketsu1,Thompson Christopher1,Kahne Daniel1

Affiliation:

1. department of Chemistry, Princeton University Princeton, NJ 08544, USA.

2. Infectious diseases, Merck Research Laboratories, Rahway, NJ 07065, USA.

Abstract

Vancomycin is an important drug for the treatment of Gram-positive bacterial infections. Resistance to vancomycin has begun to appear, posing a serious public health threat. Vancomycin analogs containing modified carbohydrates are very active against resistant microorganisms. Results presented here show that these carbohydrate derivatives operate by a different mechanism than vancomycin; moreover, peptide binding is not required for activity. It is proposed that carbohydrate-modified vancomycin compounds are effective against resistant bacteria because they interact directly with bacterial proteins involved in the transglycosylation step of cell wall biosynthesis. These results suggest new strategies for designing glycopeptide antibiotics that overcome bacterial resistance.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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