Wei X, Bauer WD
Department of Plant Biology, Ohio State University, Columbus, Ohio 43210.
Appl Environ Microbiol. 1998 May 1;64(5):1708-14. doi: 10.1128/AEM.64.5.1708-1714.1998.
The changes in motility, chemotactic responsiveness, and flagellation of Rhizobium meliloti RMB7201, L5-30, and JJ1c10 were analyzed after transfer of the bacteria to buffer with no available C, N, or phosphate. Cells of these three strains remained viable for weeks after transfer to starvation buffer (SB) but lost all motility within just 8 to 72 h after transfer to SB. The rates of motility loss differed by severalfold among the strains. Each strain showed a transient, two- to sixfold increase in chemotactic responsiveness toward glutamine within a few hours after transfer to SB, even though motility dropped substantially during the same period. Strains L5-30 and JJ1c10 also showed increased responsiveness to the nonmetabolizable chemoattractant cycloleucine. Cycloleucine partially restored the motility of starving cells when added after transfer and prevented the loss of motility when included in the SB used for initial suspension of the cells. Thus, interactions between chemoattractants and their receptors appear to affect the regulation of motility in response to starvation independently of nutrient or energy source availability. Electron microscopic observations revealed that R. meliloti cells lost flagella and flagellar integrity during starvation, but not as fast, nor to such a great extent, as the cells lost motility. Even after prolonged starvation, when none of the cells were actively motile, about one-third to one-half of the initially flagellated cells retained some flagella. Inactivation of flagellar motors therefore appears to be a rapid and important response of R. meliloti to starvation conditions. Flagellar-motor inactivation was at least partially reversible by addition of either cycloleucine or glucose. During starvation, some cells appeared to retain normal flagellation, normal motor activity, or both for relatively long periods while other cells rapidly lost flagella, motor activity, or both, indicating that starvation-induced regulation of motility may proceed differently in various cell subpopulations.
将苜蓿中华根瘤菌RMB7201、L5 - 30和JJ1c10转移至无可用碳、氮或磷的缓冲液后,分析了它们在运动性、趋化反应性和鞭毛形成方面的变化。这三种菌株的细胞在转移至饥饿缓冲液(SB)后可存活数周,但在转移至SB后仅8至72小时内就失去了所有运动性。不同菌株的运动性丧失速率相差数倍。转移至SB后数小时内,每种菌株对谷氨酰胺的趋化反应性都出现了短暂的、两到六倍的增加,尽管在此期间运动性大幅下降。L5 - 30和JJ1c10菌株对不可代谢的趋化剂环亮氨酸的反应性也有所增加。转移后添加环亮氨酸可部分恢复饥饿细胞的运动性,并在用于细胞初始悬浮的SB中加入环亮氨酸时可防止运动性丧失。因此,趋化剂与其受体之间的相互作用似乎独立于营养或能量源的可用性,影响着饥饿状态下运动性的调节。电子显微镜观察显示,苜蓿中华根瘤菌细胞在饥饿期间失去鞭毛和鞭毛完整性,但失去的速度和程度不如细胞失去运动性那么快和大。即使在长时间饥饿后,当所有细胞都不再活跃运动时,约三分之一到一半最初有鞭毛的细胞仍保留一些鞭毛。因此,鞭毛马达的失活似乎是苜蓿中华根瘤菌对饥饿条件的快速且重要的反应。添加环亮氨酸或葡萄糖至少可部分逆转鞭毛马达的失活。在饥饿期间,一些细胞似乎在相对较长的时间内保持正常的鞭毛形成、正常的马达活性或两者皆有,而其他细胞则迅速失去鞭毛、马达活性或两者皆失,这表明饥饿诱导的运动性调节在不同细胞亚群中可能以不同方式进行。