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Influence of extracellular polymeric substances on deposition and redeposition of Pseudomonas aeruginosa to surfaces

机译:细胞外聚合物物质对铜绿假单胞菌沉积和重新沉积对表面的影响

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In this study, the role of extracellular polymeric substances (EPS) in the initial adhesion of EPS-producing Pseudomonas aeruginosa SG81 and SG81R1, a non-EPS-producing strain, to substrata with different hydrophobicity was investigated. The release of EPS by SG81 was concurrent with a decrease in surface tension of a bacterial suspension from 70 to 45 mJ m?2 that was absent for SG81R1. Both strains adhered faster and in higher numbers to a hydrophilic than to a hydrophobic substratum, but the initial deposition rates and numbers of adhering bacteria in a stationary-end point were highest for the non-EPS-producing strain SG81R1, regardless of substratum hydrophobicity. Both strains adhered less to substrata pre-coated with isolated EPS of strain SG81. Furthermore, it was investigated whether bacteria, detached by passing air-bubbles, had left behind ‘footprints’ with an influence on adhesion of newly redepositing bacteria. Redeposition on glass was highest for non-EPS-producing SG81R1 and decreased linearly with the number of times these cycles of detachment and deposition were repeated to become similar to the redeposition of SG81 after six cycles. This indicates that P. aeruginosa SG81 leaves the substratum surface nearly completely covered with EPS after detachment, while SG81R1 releases only minor amounts of surface active EPS, completely covering the substratum after repeated cycles of detachment and adhesion. Atomic force microscopy showed a thick and irregular EPS layer (up to 32 nm) after the first detachment cycle of EPS-producing strain SG81, whereas the putatively non-EPS-producing strain SG81R1 left a 9?nm thin layer after one cycle. X-ray photoelectron spectroscopy indicated that the bacterial footprints consisted of uronic acids, the prevalence of which increased with the number of detachment and deposition cycles.
机译:在本研究中,研究了细胞外聚合物物质(EPS)在EPS-Msudomonas铜绿假单胞菌SG81和SG81R1的初始粘附中的作用,对具有不同疏水性的非eps-产生菌株的非eps-产生菌株。通过SG81释放EPS的释放同时,细菌悬浮液的表面张力降低,从70至45MJm≥2,其不存在SG81R1。两种菌株粘附得更快,更高的数量与疏水性外部的亲水性,但是对于非EPS的菌株SG81R1,静止终点中的初始沉积速率和粘附细菌的数量最高,而不管疏水性。两种菌株粘附到预涂覆菌株SG81的孤立的EPS的亚类。此外,研究了细菌是否通过通过气泡分离,留下了“足迹”,对新重新停养的细菌的粘附影响。对于非EPS的SG81R1,玻璃上的重新沉积最高,并且随着脱离循环循环的次数的次数而导入线性减少,重复六个循环后SG81的重新沉积。这表明P.铜绿假单胞菌SG81脱落后叶片表面几乎完全覆盖在脱落后用EPS覆盖,而SG81R1仅释放少量的表面活性EPS,在重复的脱离和粘附循环后完全覆盖下皮。原子力显微镜显微镜显示在EPS的菌株SG81的第一次分离循环之后呈厚和不规则的EPS层(最多32nm),而在一个循环之后,将借助于非EPS的菌株SG81R1留下了9μm薄层。 X射线光电子能谱表明,细菌足迹由核酸酸组成,其患病率随着脱离和沉积循环的数量而增加。

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