Packer H L, Armitage J P
Department of Biochemistry, University of Oxford, England.
J Bacteriol. 1994 Jan;176(1):206-12. doi: 10.1128/jb.176.1.206-212.1994.
Rhodobacter sphaeroides exhibits two behavioral responses when exposed to some compounds: (i) a chemotactic response that results in accumulation and (ii) a sustained increase in swimming speed. This latter chemokinetic response occurs without any apparent long-term change in the size of the electrochemical proton gradient. The results presented here show that the chemokinetic response is separate from the chemotactic response, although some compounds can induce both responses. Compounds that caused only chemokinesis induced a sustained increase in the rate of flagellar rotation, but chemoeffectors which were also chemotactic caused an additional short-term change in both the stopping frequency and the duration of stops and runs. The response to a change in chemoattractant concentration was a transient increase in the stopping frequency when the concentration was reduced, with adaptation taking between 10 and 60 s. There was also a decrease in the stopping frequency when the concentration was increased, but adaptation took up to 60 min. The nature and duration of both the chemotactic and chemokinetic responses were concentration dependent. Weak organic acids elicited the strongest chemokinetic responses, and although many also caused chemotaxis, there were conditions under which chemokinesis occurred in the absence of chemotaxis. The transportable succinate analog malonate caused chemokinesis but not chemotaxis, as did acetate when added to a mutant able to transport but not grow on acetate. Chemokinesis also occurred after incubation with arsenate, conditions under which chemotaxis was lost, indicating that phosphorylation at some level may have a role in chemotaxis. Aspartate was the only chemoattractant amino acid to cause chemokinesis. Glutamate caused chemotaxis but not chemokinesis. These data suggest that (i) chemotaxis and chemokinesis are separate responses, (ii) metabolism is required for chemotaxis but not chemokinesis, (iii) a reduction in chemoattractant concentration may cause the major chemotactic signal, and (iv) a specific transport pathway(s) may be involved in chemokinetic signalling in R. sphaeroides.
(i)趋化反应,导致细菌聚集;(ii)游泳速度持续增加。后一种化学动力学反应发生时,电化学质子梯度的大小没有任何明显的长期变化。此处呈现的结果表明,尽管某些化合物可同时诱导这两种反应,但化学动力学反应与趋化反应是分开的。仅引起化学动力学反应的化合物会使鞭毛旋转速率持续增加,但也是趋化剂的化学效应物会导致停止频率以及停止和游动持续时间出现额外的短期变化。当化学引诱剂浓度降低时,对其浓度变化的反应是停止频率短暂增加,适应时间在10至60秒之间。当浓度增加时,停止频率也会降低,但适应时间长达60分钟。趋化反应和化学动力学反应的性质及持续时间均取决于浓度。弱有机酸引发最强的化学动力学反应,尽管许多弱有机酸也会引起趋化反应,但在某些条件下,化学动力学反应可在无趋化反应的情况下发生。可转运的琥珀酸类似物丙二酸会引起化学动力学反应但不会引起趋化反应,当将乙酸盐添加到能够转运但不能利用乙酸盐生长的突变体中时,乙酸盐也是如此。与砷酸盐孵育后也会发生化学动力学反应,此时趋化反应丧失,这表明在某种程度上磷酸化可能在趋化反应中起作用。天冬氨酸是唯一能引起化学动力学反应的化学引诱剂氨基酸。谷氨酸会引起趋化反应但不会引起化学动力学反应。这些数据表明:(i)趋化反应和化学动力学反应是分开的反应;(ii)趋化反应需要新陈代谢,但化学动力学反应不需要;(iii)化学引诱剂浓度降低可能会引发主要的趋化信号;(iv)特定的转运途径可能参与球形红细菌的化学动力学信号传导。