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Surface Physicochemistry and Ionic Strength Affects eDNA’s Role in Bacterial Adhesion to Abiotic Surfaces

机译:表面物理化学和离子强度影响eDNA在细菌与非生物表面粘附中的作用

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摘要

Extracellular DNA (eDNA) is an important structural component of biofilms formed by many bacteria, but few reports have focused on its role in initial cell adhesion. The aim of this study was to investigate the role of eDNA in bacterial adhesion to abiotic surfaces, and determine to which extent eDNA-mediated adhesion depends on the physicochemical properties of the surface and surrounding liquid. We investigated eDNA alteration of cell surface hydrophobicity and zeta potential, and subsequently quantified the effect of eDNA on the adhesion of Staphylococcus xylosus to glass surfaces functionalised with different chemistries resulting in variable hydrophobicity and charge. Cell adhesion experiments were carried out at three different ionic strengths. Removal of eDNA from S. xylosus cells by DNase treatment did not alter the zeta potential, but rendered the cells more hydrophilic. DNase treatment impaired adhesion of cells to glass surfaces, but the adhesive properties of S. xylosus were regained within 30 minutes if DNase was not continuously present, implying a continuous release of eDNA in the culture. Removal of eDNA lowered the adhesion of S. xylosus to all surfaces chemistries tested, but not at all ionic strengths. No effect was seen on glass surfaces and carboxyl-functionalised surfaces at high ionic strength, and a reverse effect occurred on amine-functionalised surfaces at low ionic strength. However, eDNA promoted adhesion of cells to hydrophobic surfaces irrespective of the ionic strength. The adhesive properties of eDNA in mediating initial adhesion of S. xylosus is thus highly versatile, but also dependent on the physicochemical properties of the surface and ionic strength of the surrounding medium.
机译:细胞外DNA(eDNA)是由许多细菌形成的生物膜的重要结构成分,但很少有报道关注其在初始细胞黏附中的作用。这项研究的目的是研究eDNA在细菌与非生物表面粘附中的作用,并确定eDNA介导的粘附程度取决于表面和周围液体的物理化学性质。我们研究了细胞表面疏水性和zeta电位的eDNA改变,随后定量了eDNA对木糖葡萄球菌对玻璃表面粘附的影响,该表面具有不同的化学功能,从而导致可变的疏水性和电荷。细胞粘附实验是在三种不同的离子强度下进行的。通过DNase处理从木糖链球菌中去除eDNA不会改变Zeta电位,但使细胞更具亲水性。 DNase处理会损害细胞与玻璃表面的粘附力,但是如果DNase不能连续存在,则在30分钟内即可恢复木糖链霉菌的粘附特性,这意味着eDNA在培养物中会持续释放。去除eDNA降低了木糖链球菌对测试的所有表面化学物质的粘附力,但并非在所有离子强度下均如此。在高离子强度下对玻璃表面和羧基官能化表面均未见效果,而在低离子强度下对胺官能化表面未产生反作用。但是,无论离子强度如何,eDNA都能促进细胞粘附至疏水表面。因此,在介导木糖链霉菌的初始粘附中,eDNA的粘附特性具有很高的通用性,但也取决于表面的物理化学特性和周围介质的离子强度。

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