Department of Environmental Chemistry, Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Kraków, Poland.
Department of Physical Chemistry and Electrochemistry, Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Kraków, Poland.
Biochim Biophys Acta Biomembr. 2018 Dec;1860(12):2576-2587. doi: 10.1016/j.bbamem.2018.09.014. Epub 2018 Sep 21.
Water soluble perfluorinated compounds (PFCs) as perfluorooctanesulfonate (PFOS), perfluorooctanoate (PFOA) and their shorter chain homologues are persistent organic pollutants widely distributed in the environment. PFCs accumulate in soils and sediments and because of their toxicity endanger the decomposer organisms. PFCs are toxic to a wide spectrum of soil bacteria and their biocide activity was related with their membrane activity; however, the exact mechanism of PFCs - bacterial membrane interactions is unknown. Therefore, to shed light on these questions we applied phospholipid Langmuir monolayers as simplified models of bacterial membranes and studied their interactions with selected environmentally relevant PFCs. The mechanical properties of the monolayers were characterized by surface pressure-mean molecular area isotherms and the analysis of compression modulus. The effects of PFC on the texture of the model membranes were studied with Brewster angle microscopy, whereas their influence on molecular packing in the 2D crystal lattice was searched by the Grazing Incidence X-ray diffraction technique. The effects of PFCs on the phospholipid polar heargroup conformation were studied by PM-IRRAS spectroscopy, whereas the effectivenes of the incorporation of PFCs into the model membrane was monitored in penetration tests. It turned out that the membranes rich in phosphatidylethanolamine typical to Gram negative bacteria are much PFCs susceptible than the cardiolipin rich membranes imitating Gram positive species. Moreover, the studies indicated that the switch from eight‑carbon atom perfluorinated chains to shorter chain homologues is not necessarily environmentally benign as perfluorobutane sulfonate caused also significant structural changes in the model membranes.
水溶性全氟化合物(PFCs),如全氟辛烷磺酸(PFOS)、全氟辛酸(PFOA)及其短链同系物,是广泛分布于环境中的持久性有机污染物。PFCs 会在土壤和沉积物中积累,由于其毒性,会危及分解者生物。PFCs 对广泛的土壤细菌具有毒性,其杀菌活性与其膜活性有关;然而,PFCs 与细菌膜相互作用的确切机制尚不清楚。因此,为了阐明这些问题,我们应用磷脂 Langmuir 单层作为细菌膜的简化模型,并研究了它们与选定的环境相关 PFCs 的相互作用。通过表面压-平均分子面积等温线和压缩模量分析来表征单层的机械性能。利用偏光显微镜研究了 PFC 对模型膜结构的影响,而利用掠入射 X 射线衍射技术研究了其对 2D 晶格中分子堆积的影响。通过 PM-IRRAS 光谱研究了 PFCs 对磷脂极性头部基团构象的影响,而通过渗透试验监测了 PFCs 掺入模型膜的效果。结果表明,富含磷脂酰乙醇胺的膜(典型的革兰氏阴性菌)比富含心磷脂的膜(模仿革兰氏阳性菌)更容易受到 PFCs 的影响。此外,研究表明,从八碳全氟链向短链同系物的转变不一定对环境有利,因为全氟丁烷磺酸也会导致模型膜发生显著的结构变化。