The synthesis and biological evaluation of a library of autoinducer-antibiotic conjugates
type: CreativeWork
description: Microbial resistance to antibiotics is a serious global health threat, and the discovery of new, safe and effective antibiotics is required urgently. A new class of antibiotics, namely sideophore-antibiotic conjugates, has shown promise in initial studies. Siderophores are used by bacteria for iron uptake, and so attaching antibiotics to them allows the antibiotic to be carried across cell membranes. This study investigated conjugates designed using a similar approach, but using bacterial autoinducers instead of siderophores. Autoinducers are required for coordination of bacterial behaviours and are involved in the control of swarming, virulence factor production and biofilm formation. The quorum sensing molecules produced by \textit{Pseudomonas aeruginosa} were chosen for investigation as \textit{P. aeruginosa} is a significant human pathogen which displays high resistance to many antibiotics and uses quorum sensing to coordinate its group behaviours. Ciprofloxacin and trimethoprim were chosen as the antibiotic partners. Ciprofloxacin is commonly used against \textit{P. aeruginosa} but resistance to it is developing, whereas \textit{P. aeruginosa} is inherently resistant to trimethoprim. It was hypothesised that the autoinducers would aid retention of the antibiotics in cells, hence increasing or restoring activity. An initial library was synthesised in two halves which were coupled together using a copper(I)-catalysed azide-alkyne cycloaddition. The autoinducers were functionalised with azide groups and the antibiotics (specifically ciprofloxacin and trimethoprim) were functionalised with alkynes. Two cleavable alkynyl ciprofloxacin derivatives were also included. A second set of compounds, namely homoserine lactone analogue-ciprofloxacin conjugates were then synthesised, building on the one known report of a conjugate of a quorum sensing modulator and an antibiotic. The most active conjugate found was a cleavable conjugate of homocysteine thiolactone (a homoserin…
abstract: Microbial resistance to antibiotics is a serious global health threat, and the discovery of new, safe and effective antibiotics is required urgently. A new class of antibiotics, namely sideophore-antibiotic conjugates, has shown promise in initial studies. Siderophores are used by bacteria for iron uptake, and so attaching antibiotics to them allows the antibiotic to be carried across cell membranes. This study investigated conjugates designed using a similar approach, but using bacterial autoinducers instead of siderophores. Autoinducers are required for coordination of bacterial behaviours and are involved in the control of swarming, virulence factor production and biofilm formation. The quorum sensing molecules produced by \textit{Pseudomonas aeruginosa} were chosen for investigation as \textit{P. aeruginosa} is a significant human pathogen which displays high resistance to many antibiotics and uses quorum sensing to coordinate its group behaviours. Ciprofloxacin and trimethoprim were chosen as the antibiotic partners. Ciprofloxacin is commonly used against \textit{P. aeruginosa} but resistance to it is developing, whereas \textit{P. aeruginosa} is inherently resistant to trimethoprim. It was hypothesised that the autoinducers would aid retention of the antibiotics in cells, hence increasing or restoring activity. An initial library was synthesised in two halves which were coupled together using a copper(I)-catalysed azide-alkyne cycloaddition. The autoinducers were functionalised with azide groups and the antibiotics (specifically ciprofloxacin and trimethoprim) were functionalised with alkynes. Two cleavable alkynyl ciprofloxacin derivatives were also included. A second set of compounds, namely homoserine lactone analogue-ciprofloxacin conjugates were then synthesised, building on the one known report of a conjugate of a quorum sensing modulator and an antibiotic. The most active conjugate found was a cleavable conjugate of homocysteine thiolactone (a homoserin…
author: Overvoorde, Lois May
language: en
keywords: antibiotics, autoinducers, biofilms, Pseudomonas aeruginosa, ciprofloxacin, conjugates, homoserine lactones, PQS, HHQ, trimethoprim, antibiotic resistance, siderophores, sideromycins
license: https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/cbe4ee66-bd7c-4587-8b40-b90c27d5cde1/download
license: https://creativecommons.org/licenses/by-nc-sa/4.0/
date published: 2018-09-07
date modified: 2026-07-22T22:24:30Z
provider: Cambridge University
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: University of Cambridge

PropertyValue
property ID: DOI
value: 10.17863/CAM.38239