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Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics

Gram-negative bacteria’s resistance such as Pseudomonas aeruginosa and the Burkholderia group to conventional antibiotics leads to therapeutic failure. Use of siderophores as Trojan horses to internalize antibacterial agents or toxic metals within bacteria is a promising strategy to overcome resista...

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Autores principales: Loupias, Pauline, Dechamps-Olivier, Isabelle, Dupont, Laurent, Vanlemmens, Pierre, Mullié, Catherine, Taudon, Nicolas, Bouchut, Anne, Dassonville-Klimpt, Alexandra, Sonnet, Pascal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958365/
https://www.ncbi.nlm.nih.gov/pubmed/31652873
http://dx.doi.org/10.3390/ph12040160
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author Loupias, Pauline
Dechamps-Olivier, Isabelle
Dupont, Laurent
Vanlemmens, Pierre
Mullié, Catherine
Taudon, Nicolas
Bouchut, Anne
Dassonville-Klimpt, Alexandra
Sonnet, Pascal
author_facet Loupias, Pauline
Dechamps-Olivier, Isabelle
Dupont, Laurent
Vanlemmens, Pierre
Mullié, Catherine
Taudon, Nicolas
Bouchut, Anne
Dassonville-Klimpt, Alexandra
Sonnet, Pascal
author_sort Loupias, Pauline
collection PubMed
description Gram-negative bacteria’s resistance such as Pseudomonas aeruginosa and the Burkholderia group to conventional antibiotics leads to therapeutic failure. Use of siderophores as Trojan horses to internalize antibacterial agents or toxic metals within bacteria is a promising strategy to overcome resistance phenomenon. To combat the Pseudomonas sp, we have synthesized and studied two piperazine-based siderophore mimetics carrying either catecholate moieties (1) or hydroxypyridinone groups (2) as iron chelators. These siderophore-like molecules were prepared in no more than four steps with good global yields. The physicochemical study has highlighted a strong iron affinity since their pFe values were higher than 20. 1 possesses even a pFe value superior than those of pyoverdine, the P. aeruginosa endogenous siderophore, suggesting its potential ability to compete with it. At physiological pH, 1 forms mainly a 2:3 complex with iron, whereas two species are observed for 2. Unfortunately, the corresponding Ga(III)-1 and 2 complexes showed no antibacterial activity against P. aeruginosa DSM 1117 strain. The evaluation of their siderophore-like activity showed that 1 and 2 could be internalized by the bacteria.
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spelling pubmed-69583652020-01-23 Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics Loupias, Pauline Dechamps-Olivier, Isabelle Dupont, Laurent Vanlemmens, Pierre Mullié, Catherine Taudon, Nicolas Bouchut, Anne Dassonville-Klimpt, Alexandra Sonnet, Pascal Pharmaceuticals (Basel) Article Gram-negative bacteria’s resistance such as Pseudomonas aeruginosa and the Burkholderia group to conventional antibiotics leads to therapeutic failure. Use of siderophores as Trojan horses to internalize antibacterial agents or toxic metals within bacteria is a promising strategy to overcome resistance phenomenon. To combat the Pseudomonas sp, we have synthesized and studied two piperazine-based siderophore mimetics carrying either catecholate moieties (1) or hydroxypyridinone groups (2) as iron chelators. These siderophore-like molecules were prepared in no more than four steps with good global yields. The physicochemical study has highlighted a strong iron affinity since their pFe values were higher than 20. 1 possesses even a pFe value superior than those of pyoverdine, the P. aeruginosa endogenous siderophore, suggesting its potential ability to compete with it. At physiological pH, 1 forms mainly a 2:3 complex with iron, whereas two species are observed for 2. Unfortunately, the corresponding Ga(III)-1 and 2 complexes showed no antibacterial activity against P. aeruginosa DSM 1117 strain. The evaluation of their siderophore-like activity showed that 1 and 2 could be internalized by the bacteria. MDPI 2019-10-23 /pmc/articles/PMC6958365/ /pubmed/31652873 http://dx.doi.org/10.3390/ph12040160 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Loupias, Pauline
Dechamps-Olivier, Isabelle
Dupont, Laurent
Vanlemmens, Pierre
Mullié, Catherine
Taudon, Nicolas
Bouchut, Anne
Dassonville-Klimpt, Alexandra
Sonnet, Pascal
Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics
title Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics
title_full Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics
title_fullStr Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics
title_full_unstemmed Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics
title_short Study of Iron Piperazine-Based Chelators as Potential Siderophore Mimetics
title_sort study of iron piperazine-based chelators as potential siderophore mimetics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958365/
https://www.ncbi.nlm.nih.gov/pubmed/31652873
http://dx.doi.org/10.3390/ph12040160
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