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Molecular and Functional Aspects of Bacterial Chemotaxis

机译:细菌趋化性的分子和功能方面

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We consider the dynamics of chemotaxis in the model bacterium Escherichia coli. We analyze both its molecular mechanisms and the functional causes governing the evolution of the observed behaviors. We review molecular models of the transduction network controlling the bacterial chemotaxis in response to chemoattractant binding to the receptors. In particular, recent progress stimulated by FRET experiments is presented for statistical physics allosteric models. The response function to a pulse of chemoattractant is expressed in terms of microscopic parameters of the allosteric models. The functional causes for the shape of the response function, as measured in experimental tethering assay, are then investigated. A hydrodynamic equation, valid for space-time scales larger than the microscopic running length and time, is derived for the position of a swimming bacterium. It is then shown how optimization over the microscopic parameters of the response function yields the curve observed experimentally. In particular, the observed property of adaptation to the background level of aspartate emerges as being produced by fluctuations in the space-time chemoattractant profiles sensed by bacteria along their trajectories. This functional cause is distinct from arguments based on the extension of the dynamical range. Future directions and experiments to probe the adaptation of E. coli chemotaxis to the environmental conditions and its response to realistic space-time chemoattractant stimuli are finally discussed.
机译:我们考虑了模型细菌大肠杆菌中趋化性的动态。我们分析了其分子机制和控制观察到的行为演变的功能原因。我们审查了控制趋化因子结合受体的细菌趋化性的转导网络的分子模型。特别是,FRET实验激发了最新的进展,用于统计物理变构模型。对化学趋化剂脉冲的响应功能用变构模型的微观参数表示。然后研究了在实验性系链分析中测得的响应函数形状的功能原因。对于游泳细菌的位置,得出了一个对时空尺度大于微观运行长度和时间有效的流体动力学方程。然后显示响应函数的微观参数的优化如何产生实验观察到的曲线。特别地,观察到的对天冬氨酸背景水平的适应性表现为由细菌沿着其轨迹感知的时空趋化性分布的波动而产生。此功能性原因不同于基于动态范围扩展的参数。最后讨论了探索大肠杆菌趋化性对环境条件的适应性及其对现实时空趋化性刺激的响应的未来方向和实验。

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