| Literature DB >> 24485124 |
Sijie Yang1, Osama A Abdel-Razek2, Fei Cheng1, Debjyoti Bandyopadhyay1, Gauri S Shetye1, Guirong Wang2, Yan-Yeung Luk3.
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.Entities:
Keywords: Biofilm inhibition; Cell signaling; Furanones; Toxicity; Virulence factor
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Year: 2014 PMID: 24485124 PMCID: PMC6454546 DOI: 10.1016/j.bmc.2014.01.004
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641