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Interactions of a bacterial trehalose lipid with phosphatidylglycerol membranes at low ionic strength

机译:低离子强度下细菌海藻糖脂质与磷脂酰甘油膜的相互作用

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Trehalose lipids are bacterial biosurfactants which present interesting physicochemical and biological properties. These glycolipids have a number of different commercial applications and there is an increasing interest in their use as therapeutic agents. The amphiphilic nature of trehalose lipids points to the membrane as their hypothetical site of action and therefore the study of the interaction between these biosurfactants and biological membranes is critical. In this study, we examine the interactions between a trehalose lipid (TL) from Rhodococcus sp. and dimyristoylphosphatidylglycerol (DMPG) membranes at low ionic strength, by means of differential scanning calorimetry, light scattering, fluorescence polarization and infrared spectroscopy. We describe that there are extensive interactions between TL and DMPG involving the perturbation of the thermotropic intermediate phase of the phospholipid, the desta-bilization and shifting of the DMPG gel to liquid crystalline phase transition to lower temperatures, the perturbation of the sample transparency, and the modification of the order of the phospholipid palisade in the gel phase. We also report an increase of fluidity of the phosphatidylglycerol acyl chains and dehydration of the interfacial region of the bilayer. These changes would increase the monolayer negative spontaneous curvature of the phospholipid explaining the destabilizing effect on the intermediate state exerted by this biosurfactant. The observations contribute to get insight into the biological mechanism of action of the biosurfactant and help to understand the properties of the intermediate phase display by DMPG at low ionic strength.
机译:海藻糖脂质是细菌生物表面活性剂,具有令人感兴趣的理化和生物学特性。这些糖脂具有许多不同的商业应用,并且越来越多地将它们用作治疗剂。海藻糖脂质的两亲性质指向膜作为其假定的作用部位,因此研究这些生物表面活性剂与生物膜之间的相互作用至关重要。在这项研究中,我们检查了红球藻属的海藻糖脂质(TL)之间的相互作用。并通过差示扫描量热法,光散射,荧光偏振和红外光谱法研究了低离子强度的二豆蔻酰磷脂酰甘油(DMPG)膜。我们描述了TL和DMPG之间存在广泛的相互作用,包括磷脂的热致中间相的扰动,DMPG凝胶的去稳定化和转移到液晶相转变到较低的温度,样品透明度的扰动以及凝胶相中磷脂栅栏顺序的修饰。我们还报告了磷脂酰甘油酰基链的流动性的增加和双层界面区域的脱水。这些变化将增加磷脂的单层负自发曲率,解释了这种生物表面活性剂对中间状态产生的去稳定作用。这些观察结果有助于深入了解生物表面活性剂的生物学作用机理,并有助于了解低离子强度下DMPG中间相显示的性质。

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