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The damage of outer membrane of Escherichia coli in the presence of TiO2 combined with UV light

机译:TiO2结合紫外线对大肠杆菌外膜的损伤

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摘要

The biological consequences of exposure to TiO2, UV light, and their combined effect were studied on the Escherichia coli (E. coli) cells. The damage of outer membrane was observed for the cells after treatment of TiO2 or UV light. TiO2 alone can break down lipopolysacchride (LPS), the outermost layer of the E. coli cells, but was not able to destroy peptidoglycan underneath. The same phenomenon was observed for E. coil under 500 W UV light treatment alone. However, the outer membrane of E. coil could be removed completely in the presence of both TiO2 and UV light, and the cells became elliptical or round without a mechanically strong network. From the analysis of the concentrations for Ca2+ and Mg2+, a large amount of Ca2+ and Mg2+ were detected in the solution of the treated cells by photo-catalysis, and this was attributed to the damage of LPS dispatches. After TiO2 or UV light treatment, a significant decrease in membrane fluidity of E. coil was found from an increase in fluorescence polarization by a fluorescence probe. The permeability of the treated cells increased to some degree that can be confirmed by quantum dots labeling technique.
机译:研究了暴露于TiO2,紫外线和它们的联合作用对大肠杆菌(E. coli)细胞的生物学影响。 TiO2或紫外线处理后,观察到细胞外膜的损伤。单独的TiO2可以分解大肠杆菌细胞最外层的脂多糖(LPS),但不能破坏其下面的肽聚糖。仅在500 W UV光处理下,对于大肠杆菌,观察到相同的现象。但是,在TiO2和UV光的共同作用下,线圈的外膜可以完全去除,并且细胞变成椭圆形或圆形,而没有机械性强的网络。通过分析Ca 2+和Mg 2+的浓度,通过光催化在处理过的细胞溶液中检测到大量的Ca 2+和Mg 2+,这归因于LPS释放的破坏。经过TiO2或UV光处理后,发现荧光探针在荧光偏振作用下的增加,大大降低了大肠杆菌的膜流动性。经处理的细胞的通透性增加到一定程度,这可以通过量子点标记技术确认。

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