...
首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >pH and monovalent cations regulate cytosolic free Ca(2+) in E. coli.
【24h】

pH and monovalent cations regulate cytosolic free Ca(2+) in E. coli.

机译:pH和一价阳离子调节大肠杆菌中的游离胞质Ca(2+)。

获取原文
获取原文并翻译 | 示例

摘要

The results here show for the first time that pH and monovalent cations can regulate cytosolic free Ca(2+) in E. coli through Ca(2+) influx and efflux, monitored using aequorin. At pH 7.5 the resting cytosolic free Ca(2+) was 0.2-0.5 microM. In the presence of external Ca(2+) (1 mM) at alkaline pH this rose to 4 microM, being reduced to 0.9 microM at acid pH. Removal of external Ca(2+) caused an immediate decrease in cytosolic free Ca(2+) at 50-100 nM s(-1). Efflux rates were the same at pH 5.5, 7.5 and 9.5. Thus, ChaA, a putative Ca(2+)/H(+)exchanger, appeared not to be a major Ca(2+)-efflux pathway. In the absence of added Na(+), but with 1 mM external Ca(2+), cytosolic free Ca(2+) rose to approximately 10 microM. The addition of Na(+)(half maximum 60 mM) largely blocked this increase and immediately stimulated Ca(2+) efflux. However, this effect was not specific, since K(+) also stimulated efflux. In contrast, an increase in osmotic pressure by addition of sucrose did not significantly stimulate Ca(2+) efflux. The results were consistent with H(+) and monovalent cations competing with Ca(2+) for a non-selective ion influx channel. Ca(2+) entry and efflux in chaA and yrbG knockouts were not significantly different from wild type, confirming that neither ChaA nor YrbG appear to play a major role in regulating cytosolic Ca(2+) in Escherichia coli. The number of Ca(2+) ions calculated to move per cell per second ranged from <1 to 100, depending on conditions. Yet a single eukaryote Ca(2+) channel, conductance 100 pS, should conduct >6 million ions per second. This raises fundamental questions about the nature and regulation of Ca(2+) transport in bacteria, and other small living systems such as mitochondria, requiring a new mathematical approach to describe such ion movements. The results have important significance in the adaptation of E. coli to different ionic environments such as the gut, fresh water and in sea water near sewage effluents.
机译:这里的结果首次显示,pH和单价阳离子可以通过Ca(2+)的流入和流出调节大肠杆菌中的胞质游离Ca(2+),使用水母发光蛋白进行监测。在pH 7.5时,静止的游离胞质Ca(2+)为0.2-0.5 microM。在碱性pH下存在外部Ca(2+)(1 mM)的情况下,该浓度上升至4 microM,在酸性pH下降低至0.9 microM。外部Ca(2+)的去除导致50-100 nM s(-1)的胞质游离Ca(2+)立即下降。在pH 5.5、7.5和9.5时外排率相同。因此,ChaA,推定的Ca(2 +)/ H(+)交换器,似乎不是主要的Ca(2+)外排途径。在没有添加Na(+),但有1 mM外部Ca(2+)的情况下,无胞质Ca(2+)上升到大约10 microM。 Na(+)(一半最大60 mM)的添加很大程度上阻止了这种增加,并立即刺激Ca(2+)外排。但是,此作用不是特异性的,因为K(+)也刺激外排。相比之下,通过添加蔗糖的渗透压的增加不会显着刺激Ca(2+)外排。结果与H(+)和与Ca(2+)竞争非选择性离子流入通道的单价阳离子相一致。 Ca(2+)进入和外排的chaA和yrbG基因敲除与野生型没有显着差异,证实ChaA和YrbG似乎都不在调节大肠杆菌中的胞质Ca(2+)中起主要作用。计算得出每个单元每秒移动的Ca(2+)离子的数量在1到100之间,具体取决于条件。然而,单个真核Ca(2+)通道电导为100 pS,应每秒传导> 600万个离子。这就提出了有关细菌和其他小型生物系统(例如线粒体)中Ca(2+)传输的性质和调控的基本问题,需要一种新的数学方法来描述这种离子运动。该结果对于大肠杆菌适应肠道,淡水和污水流出物附近的海水等不同离子环境具有重要意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号