Khan S, Spudich J L, McCray J A, Trentham D R
Department of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Proc Natl Acad Sci U S A. 1995 Oct 10;92(21):9757-61. doi: 10.1073/pnas.92.21.9757.
Chemotactic signaling in Escherichia coli involves transmission of both negative and positive signals. In order to examine mechanisms of signal processing, behavioral responses to dual inputs have been measured by using photoactivable "caged" compounds, computer video analysis, and chemoreceptor deletion mutants. Signaling from Tar and Tsr, two receptors that sense amino acids and pH, was studied. In a Tar deletion mutant the photoactivated release of protons, a Tsr repellent, and of serine, a Tsr attractant, in separate experiments at pH 7.0 resulted in tumbling (negative) or smooth-swimming (positive) responses in ca. 50 and 140 ms, respectively. Simultaneous photorelease of protons and serine resulted in a single tumbling or smooth-swimming response, depending on the relative amounts of the two effectors. In contrast, in wild-type E. coli, proton release at pH 7.0 resulted in a biphasic response that was attributed to Tsr-mediated tumbling followed by Tar-mediated smooth-swimming. In wild-type E. coli at more alkaline pH values the Tar-mediated signal was stronger than the Tsr signal, resulting in a strong smooth-swimming response preceded by a diminished tumbling response. These observations imply that (i) a single receptor time-averages the binding of different chemotactic ligands generating a single response; (ii) ligand binding to different receptors can result in a nonintegrated response with the tumbling response preceding the smooth-swimming response; (iii) however, chemotactic signals of different intensities derived from different receptors can also result in an apparently integrated response; and (iv) the different chemotactic responses to protons at neutral and alkaline pH may contribute to E. coli migration toward neutrality.
大肠杆菌中的趋化信号传导涉及负信号和正信号的传递。为了研究信号处理机制,已通过使用光可激活的“笼形”化合物、计算机视频分析和化学感受器缺失突变体来测量对双重输入的行为反应。研究了来自Tar和Tsr这两种感知氨基酸和pH值的受体的信号传导。在Tar缺失突变体中,在pH 7.0的单独实验中,光激活释放质子(一种Tsr排斥剂)和丝氨酸(一种Tsr吸引剂),分别在约50毫秒和140毫秒内导致翻滚(负向)或平滑游动(正向)反应。质子和丝氨酸的同时光释放导致单一的翻滚或平滑游动反应,这取决于两种效应物的相对量。相比之下,在野生型大肠杆菌中,pH 7.0时质子释放导致双相反应,这归因于Tsr介导的翻滚,随后是Tar介导的平滑游动。在更碱性的pH值下,野生型大肠杆菌中Tar介导的信号比Tsr信号更强,导致强烈的平滑游动反应之前有减弱的翻滚反应。这些观察结果表明:(i)单个受体对不同趋化配体的结合进行时间平均,产生单一反应;(ii)配体与不同受体的结合可导致非整合反应,翻滚反应先于平滑游动反应;(iii)然而,来自不同受体的不同强度的趋化信号也可导致明显的整合反应;(iv)在中性和碱性pH下对质子的不同趋化反应可能有助于大肠杆菌向中性迁移。