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Viability Enzymatic and Protein Profiles of Pseudomonas aeruginosa Biofilm and Planktonic Cells after Monomeric/Gemini Surfactant Treatment

机译:单体/双子表面活性剂处理后铜绿假单胞菌生物膜和浮游细胞的活力酶和蛋白质谱

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摘要

This study set out to investigate the biological activity of monomeric surfactants dodecyltrimethylammonium bromide (DTAB) and the next generation gemini surfactant hexamethylene-1,6-bis-(N,N-dimethyl-N-dodecylammonium bromide) (C6) against the environmental strain Pseudomonas aeruginosa PB_1. Minimal inhibitory concentrations (MIC) were determined using the dilution method. The viability of the planktonic cells and biofilm was assessed using the plate count method. Enzymatic profile was determined using the API-ZYM system. Proteins were extracted from the biofilm and planktonic cells and analysed using SDS-PAGE. The MIC of the gemini surfactants was 70 times lower than that of its monomeric analogue. After 4 h of treatment at MIC (0.0145 mM for C6 and 1.013 mM for DTAB), the number of viable planktonic cells was reduce by less than 3 logarithm units. At the concentration ≥MIC, a reduction in the number of viable cells was observed in mature biofilms (p < 0.05). Treatment for 4 h with gemini surfactant at 20 MIC caused complete biofilm eradication. At sub-MIC, the concentration of some enzymes reduced and their protein profiles changed. The results of this study show that due to its superior antibacterial activity, gemini compound >C6 can be applied as an effective microbiocide against P. aeruginosa in both planktonic and biofilm forms.
机译:这项研究着手研究单体表面活性剂十二烷基三甲基溴化铵(DTAB)和下一代双子表面活性剂六亚甲基-1,6-双-(N,N-二甲基-N-十二烷基溴化铵)(C6)对环境菌株的生物活性。铜绿假单胞菌PB_1。使用稀释法确定最小抑菌浓度(MIC)。使用板计数法评估浮游细胞和生物膜的活力。使用API​​-ZYM系统确定酶学特征。从生物膜和浮游细胞中提取蛋白质,并使用SDS-PAGE分析。双子表面活性剂的MIC比其单体类似物的MIC低70倍。在MIC处理4小时(C6为0.0145 mM,DTAB为1.013 mM)后,存活的浮游细胞减少了少于3个对数单位。在浓度≥MIC时,在成熟的生物膜中观察到活细胞数量减少(p <0.05)。在20 MIC下用双子座表面活性剂处理4小时导致完全清除生物膜。在亚MIC下,某些酶的浓度降低,其蛋白质谱发生变化。这项研究的结果表明,由于双生子化合物> C6 具有卓越的抗菌活性,因此可以以浮游生物和生物膜的形式作为有效的抗铜绿假单胞菌杀菌剂。

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