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烷基鼠李糖苷,一类具有两亲性的物质,通过多种机制对致病菌发挥广谱抗生物膜活性。

Alkyl rhamnosides, a series of amphiphilic materials exerting broad-spectrum anti-biofilm activity against pathogenic bacteria via multiple mechanisms.

机构信息

a Beijing Key Laboratory of Molecular Pharmaceutics and New Drug System, School of Pharmaceutical Sciences , Peking University Health Science Center , Beijing , China.

b Institute of Medicinal Biotechnology, Chinese Academy of Medical Science & Peking Union Medical College , Beijing , China.

出版信息

Artif Cells Nanomed Biotechnol. 2018;46(sup3):S217-S232. doi: 10.1080/21691401.2018.1491474. Epub 2019 Jan 8.

Abstract

As novel amphiphilic materials, six uncharged alkyl rhamnosides incorporating various alkyl chain and one rhamnose amine quaternary ammonium salt were successfully synthesized in this study. Their amphiphilic properties (HLB and CMC), antimicrobial and anti-biofilm activity against S. aureus and P. aeruginosa were investigated. Differentially regulated proteins and pathways were identified by comparative proteomics research to first give a sight on how alkyl rhamnosides performed the anti-biofilm activity at protein and pathway levels. Among the uncharged alkyl rhamnosides, dodecyl rhamnoside and octyl rhamnoside showed the best antimicrobial and anti-biofilm ability against S. aureus and against P. aeruginosa, respectively. Interestingly, the relationships between amphiphilic properties or MIC with anti-biofilm activity were first established. Uncharged alkyl rhamnoside with an optimized HLB value of 5.0 had both the strongest antibacterial and anti-biofilm activity against S. aureus, and MIC was the maximum biofilm inhibitory concentration for all alkyl rhamnosides. Alkyl rhamnosides have a significant overall regulatory effect on the proteomics and pathways of bacterial biofilms, including energy production, substrates transportation, signal transduction, key molecules balance, and so on. These amphiphilic materials have a great potential to be used as additives in pharmaceutic, cosmetic, food industry, hospital and in other non-medical fields.

摘要

作为新型两亲性材料,本研究成功合成了六种不带电荷的烷基鼠李糖苷,其中包含各种烷基链和一个鼠李糖胺季铵盐。研究了它们的两亲性性质(HLB 和 CMC)、抗金黄色葡萄球菌和铜绿假单胞菌的抗菌和抗生物膜活性。通过比较蛋白质组学研究鉴定了差异调节的蛋白质和途径,首次从蛋白质和途径水平上了解了烷基鼠李糖苷如何发挥抗生物膜活性。在不带电荷的烷基鼠李糖苷中,十二烷基鼠李糖苷和辛基鼠李糖苷分别对金黄色葡萄球菌和铜绿假单胞菌表现出最佳的抗菌和抗生物膜能力。有趣的是,首先建立了两亲性性质或 MIC 与抗生物膜活性之间的关系。具有优化 HLB 值为 5.0 的不带电荷的烷基鼠李糖苷对金黄色葡萄球菌具有最强的抗菌和抗生物膜活性,而 MIC 是所有烷基鼠李糖苷的最大生物膜抑制浓度。烷基鼠李糖苷对细菌生物膜的蛋白质组学和途径具有显著的整体调节作用,包括能量产生、底物运输、信号转导、关键分子平衡等。这些两亲性材料有望在制药、化妆品、食品工业、医院和其他非医疗领域用作添加剂。

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