Literature DB >> 21855349

Substituted lactam and cyclic azahemiacetals modulate Pseudomonas aeruginosa quorum sensing.

Venkata L A Malladi1, Adam J Sobczak, Natalie Maricic, Senthil Kumar Murugapiran, Lisa Schneper, John Makemson, Kalai Mathee, Stanislaw F Wnuk.   

Abstract

Quorum sensing (QS) is a population-dependent signaling process bacteria use to control multiple processes including virulence that is critical for establishing infection. The most common QS signaling molecule used by Gram-negative bacteria are acylhomoserine lactones. The development of non-native acylhomoserine lactone (AHL) ligands has emerged as a promising new strategy to inhibit QS in Gram-negative bacteria. In this work, we have synthesized a set of optically pure γ-lactams and their reduced cyclic azahemiacetal analogues, bearing the additional alkylthiomethyl substituent, and evaluated their effect on the AHL-dependent Pseudomonas aeruginosa las and rhl QS pathways. The concentration of these ligands and the simple structural modification such as the length of the alkylthio substituent has notable effect on activity. The γ-lactam derivatives with nonylthio or dodecylthio chains acted as inhibitors of las signaling with moderate potency. The cyclic azahemiacetal with shorter propylthio or hexylthio substituent was found to strongly inhibit both las and rhl signaling at higher concentrations while the propylthio analogue strongly stimulated the las QS system at lower concentrations.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21855349      PMCID: PMC3171587          DOI: 10.1016/j.bmc.2011.07.044

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  31 in total

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Journal:  J Bacteriol       Date:  1997-09       Impact factor: 3.490

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5.  Identification of a positive regulator of the Mu middle operon.

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9.  Functional analysis of the Pseudomonas aeruginosa autoinducer PAI.

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10.  An enantioselective, modular, and general route to the cytochalasins: synthesis of L-696,474 and cytochalasin B.

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