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Bicyclic brominated furanones: a new class of quorum sensing modulators that inhibit bacterial biofilm formation.


ABSTRACT: Both natural and synthetic brominated furanones are known to inhibit biofilm formation by bacteria, but their toxicity to mammalian cells is often not reported. Here, we designed and synthesized a new class of brominated furanones (BBFs) that contained a bicyclic structure having one bromide group with well-defined regiochemistry. This class of molecules exhibited reduction in the toxicity to mammalian cells (human neuroblastoma SK-N-SH) and did not inhibit bacteria (Pseudomonas aeruginosa and Escherichia coli) growth, but retained the inhibitory activity towards biofilm formation of bacteria. In addition, all the BBFs inhibited the production of virulence factor elastase B in P. aeruginosa. To explore the effect of BBFs on quorum sensing, we used a reporter gene assay and found that 6-BBF and 7-BBF exhibited antagonistic activities for LasR protein in the lasI quorum sensing circuit, while 5-BBF showed agonistic activity for the rhlI quorum sensing circuit. This study suggests that structural variation of brominated furanones can be designed for targeted functions to control biofilm formation.

SUBMITTER: Yang S 

PROVIDER: S-EPMC6454546 | biostudies-literature | 2014 Feb

REPOSITORIES: biostudies-literature

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Bicyclic brominated furanones: a new class of quorum sensing modulators that inhibit bacterial biofilm formation.

Yang Sijie S   Abdel-Razek Osama A OA   Cheng Fei F   Bandyopadhyay Debjyoti D   Shetye Gauri S GS   Wang Guirong G   Luk Yan-Yeung YY  

Bioorganic & medicinal chemistry 20140110 4


Both natural and synthetic brominated furanones are known to inhibit biofilm formation by bacteria, but their toxicity to mammalian cells is often not reported. Here, we designed and synthesized a new class of brominated furanones (BBFs) that contained a bicyclic structure having one bromide group with well-defined regiochemistry. This class of molecules exhibited reduction in the toxicity to mammalian cells (human neuroblastoma SK-N-SH) and did not inhibit bacteria (Pseudomonas aeruginosa and E  ...[more]

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