Berg H C, Purcell E M
Biophys J. 1977 Nov;20(2):193-219. doi: 10.1016/S0006-3495(77)85544-6.
Statistical fluctuations limit the precision with which a microorganism can, in a given time T, determine the concentration of a chemoattractant in the surrounding medium. The best a cell can do is to monitor continually the state of occupation of receptors distributed over its surface. For nearly optimum performance only a small fraction of the surface need be specifically adsorbing. The probability that a molecule that has collided with the cell will find a receptor is Ns/(Ns + pi a), if N receptors, each with a binding site of radius s, are evenly distributed over a cell of radius a. There is ample room for many indenpendent systems of specific receptors. The adsorption rate for molecules of moderate size cannot be significantly enhanced by motion of the cell or by stirring of the medium by the cell. The least fractional error attainable in the determination of a concentration c is approximately (TcaD) - 1/2, where D is diffusion constant of the attractant. The number of specific receptors needed to attain such precision is about a/s. Data on bacteriophage absorption, bacterial chemotaxis, and chemotaxis in a cellular slime mold are evaluated. The chemotactic sensitivity of Escherichia coli approaches that of the cell of optimum design.
统计涨落限制了微生物在给定时间T内测定周围介质中趋化剂浓度的精度。细胞所能做的最好的事情就是持续监测分布在其表面的受体的占据状态。为了达到近乎最佳的性能,只需要一小部分表面进行特异性吸附。如果N个受体,每个受体都有一个半径为s的结合位点,均匀分布在半径为a的细胞上,那么与细胞碰撞的分子找到受体的概率是Ns/(Ns + πa)。有足够的空间容纳许多独立的特异性受体系统。对于中等大小的分子,细胞的运动或细胞对介质的搅拌并不能显著提高吸附速率。测定浓度c时可达到的最小分数误差约为(TcaD)-1/2,其中D是趋化剂的扩散常数。达到这种精度所需的特异性受体数量约为a/s。对噬菌体吸附、细菌趋化性和细胞黏菌中的趋化性数据进行了评估。大肠杆菌的趋化敏感性接近最佳设计细胞的趋化敏感性。