Probing the breadth of macrolide glycosyltransferases: in vitro remodeling of a polyketide antibiotic creates active bacterial uptake and enhances potency

Min Yang, Mark R. Proctor, David N. Bolam, James C. Errey, Robert A. Field, Harry J. Gilbert, Benjamin G. Davis

Research output: Contribution to journalArticlepeer-review

79 Citations (Scopus)

Abstract

The glycan portion of macrolide antibiotics modulates their efficacy. High-level expression of three macrolide GTs and kinetic analysis has revealed a highly selective synthetic "tool kit" with such plasticity that 12 glycan-modified macrolide antibiotics have been readily created. One of these (1-Gal) is enhanced over its parent oleandomycin (1) by "glycotargeting", allowing higher uptake through active internalization by virtue of the attachment of a glycan (Gal) not normally found on 1. Subsequent release of the targeting glycan by endogenous galactosidase activity releases 1.

Original languageEnglish
Pages (from-to)9336-9337
Number of pages2
JournalJournal of the American Chemical Society
Volume127
Issue number26
Early online date11 Jun 2005
DOIs
Publication statusPublished - 6 Jul 2005

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