Yang Sijie, Abdel-Razek Osama A, Cheng Fei, Bandyopadhyay Debjyoti, Shetye Gauri S, Wang Guirong, Luk Yan-Yeung
Department of Chemistry, Syracuse University, Syracuse, NY 13244, United States.
Department of Surgery, Upstate Medical University, State University of New York, Syracuse, NY 13210, United States.
Bioorg Med Chem. 2014 Feb 15;22(4):1313-7. doi: 10.1016/j.bmc.2014.01.004. Epub 2014 Jan 10.
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.
已知天然和合成的溴代呋喃酮均能抑制细菌生物膜的形成,但它们对哺乳动物细胞的毒性往往未被报道。在此,我们设计并合成了一类新型的溴代呋喃酮(BBFs),其含有一个具有明确区域化学结构的单溴基团的双环结构。这类分子对哺乳动物细胞(人神经母细胞瘤SK-N-SH)的毒性降低,且不抑制细菌(铜绿假单胞菌和大肠杆菌)生长,但保留了对细菌生物膜形成的抑制活性。此外,所有的BBFs均抑制铜绿假单胞菌中致病因子弹性蛋白酶B的产生。为探究BBFs对群体感应的影响,我们使用报告基因检测法,发现6-BBF和7-BBF对lasI群体感应回路中的LasR蛋白表现出拮抗活性,而5-BBF对rhlI群体感应回路表现出激动活性。本研究表明,可通过设计溴代呋喃酮的结构变异来实现控制生物膜形成的靶向功能。