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Visco-Elastic Membrane Tethers Extracted from Escherichia coli by Optical Tweezers

机译:用光镊从大肠杆菌中提取粘弹性膜束缚

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摘要

Tethers were created between a living Escherichia coli bacterium and a bead by unspecifically attaching the bead to the outer membrane and pulling it away using optical tweezers. Upon release, the bead returned to the bacterium, thus showing the existence of an elastic tether between the bead and the bacterium. These tethers can be tens of microns long, several times the bacterial length. Using mutants expressing different parts of the outer membrane structure, we have shown that an intact core lipopolysaccharide is a necessary condition for tether formation, regardless of whether the beads were uncoated polystyrene or beads coated with lectin. A physical characterization of the tethers has been performed yielding visco-elastic tether force-extension relationships: for first pull tethers, a spring constant of 10–12 pN/μm describes the tether visco-elasticity, for subsequent pulls the spring constant decreases to 6–7 pN/μm, and typical relaxation timescales of hundreds of seconds are observed. Studies of tether stability in the presence of proteases, lipases, and amylases lead us to propose that the extracted tether is primarily composed of the asymmetric lipopolysaccharide containing bilayer of the outer membrane. This unspecific tethered attachment mechanism could be important in the initiation of bacterial adhesion.
机译:通过将珠子非特异性地附着在外膜上并使用光学镊子将其拉出,从而在活的大肠杆菌细菌和珠子之间产生了系链。释放后,珠子返回细菌,从而表明珠子和细菌之间存在弹性系链。这些系链的长度可能是数十微米,是细菌长度的数倍。使用表达外膜结构不同部分的突变体,我们已经证明完整的核心脂多糖是系链形成的必要条件,而不管珠子是未包被的聚苯乙烯还是被凝集素包被的珠子。已对绳索进行了物理表征,从而产生了粘弹性的绳索力-伸长关系:对于第一个拉动绳索,弹簧常数为10–12 pN /μm,描述了绳索的粘弹性,对于随后的拉动,弹簧常数减小至6观察到–7 pN /μm,典型的弛豫时间尺度为数百秒。在蛋白酶,脂肪酶和淀粉酶存在下对系链稳定性的研究使我们提出,提取的系链主要由外膜双层含不对称脂多糖组成。这种非特异性的束缚附着机制在细菌粘附的启动中可能很重要。

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