The E. coli escape wave in response to external Zn2+ is zinc reserve-dependent.

IF 3.6 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Asma Braham, Laurence Lemelle, Eleonore Gallay, Agnès Rodrigue, Vincent Calvez, Christophe Place
{"title":"The E. coli escape wave in response to external Zn<sup>2+</sup> is zinc reserve-dependent.","authors":"Asma Braham, Laurence Lemelle, Eleonore Gallay, Agnès Rodrigue, Vincent Calvez, Christophe Place","doi":"10.1007/s10534-025-00744-z","DOIUrl":null,"url":null,"abstract":"<p><p>The chemotaxis response of E. coli to metal cations is less understood than their response to organic molecules. Using dark-field videomicroscopy, E. coli behavior was analyzed in a 17 mm-long microfluidic channel exposed to a Zn(NO<sub>3</sub>)<sub>2</sub> chemorepellent gradient, generated by a 250 mM solution placed in a well at the channel extremity, with or without prior Zn<sup>2+</sup> pre-exposure of the cultures (10 µM). The bacteria exhibited an escape wave away from the zinc source. Compared to unexposed cultures, zinc pre-exposure resulted in a constant and shorter passage time at a given position of the wave peak, despite unchanged growth and swimming speed. The time lag decreased with growth duration. Given the one-dimensional gradient setup, this decrease is associated to a reduced diffusion duration from the Zn<sup>2</sup>⁺ source. The content of Zn<sup>2</sup>⁺ in the extracellular medium at the peak of the wave is therefore lower, but allows bacteria to escape more rapidly. These findings suggested an increase in bacterial Zn<sup>2</sup>⁺ sensitivity. By analogy to Ni<sup>2</sup>⁺ binding to the cytoplasmic HAMP domain of the Tar receptor, Zn<sup>2</sup>⁺ likely triggers a chemorepellent response through a cytoplasmic receptor. The activation of this receptor relies on the available zinc pool, which is specifically buffered by substantial other intracellular zinc reservoirs. In this model, saturating the reservoirs in pre-exposed cultures would enable the fastest response time, and a gradual filling of the reservoirs in unexposed cells would reduce a delay in chemotactic escape.</p>","PeriodicalId":491,"journal":{"name":"Biometals","volume":" ","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biometals","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s10534-025-00744-z","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The chemotaxis response of E. coli to metal cations is less understood than their response to organic molecules. Using dark-field videomicroscopy, E. coli behavior was analyzed in a 17 mm-long microfluidic channel exposed to a Zn(NO3)2 chemorepellent gradient, generated by a 250 mM solution placed in a well at the channel extremity, with or without prior Zn2+ pre-exposure of the cultures (10 µM). The bacteria exhibited an escape wave away from the zinc source. Compared to unexposed cultures, zinc pre-exposure resulted in a constant and shorter passage time at a given position of the wave peak, despite unchanged growth and swimming speed. The time lag decreased with growth duration. Given the one-dimensional gradient setup, this decrease is associated to a reduced diffusion duration from the Zn2⁺ source. The content of Zn2⁺ in the extracellular medium at the peak of the wave is therefore lower, but allows bacteria to escape more rapidly. These findings suggested an increase in bacterial Zn2⁺ sensitivity. By analogy to Ni2⁺ binding to the cytoplasmic HAMP domain of the Tar receptor, Zn2⁺ likely triggers a chemorepellent response through a cytoplasmic receptor. The activation of this receptor relies on the available zinc pool, which is specifically buffered by substantial other intracellular zinc reservoirs. In this model, saturating the reservoirs in pre-exposed cultures would enable the fastest response time, and a gradual filling of the reservoirs in unexposed cells would reduce a delay in chemotactic escape.

大肠杆菌对外源Zn2+反应的逃逸波依赖于锌的储量。
大肠杆菌对金属阳离子的趋化反应比它们对有机分子的反应更不为人所知。使用暗场视频显微镜,在一个17 mM长的微流体通道中分析大肠杆菌的行为,该微流体通道暴露于Zn(NO3)2化学驱避梯度中,该梯度是由放置在通道末端的井中250 mM溶液产生的,培养物事先暴露或不暴露Zn2+(10µM)。细菌表现出远离锌源的逃逸波。与未暴露的培养物相比,锌预暴露导致在波峰的给定位置上的持续时间不变且更短,尽管生长和游泳速度不变。滞后时间随生长时间的延长而减小。在一维梯度设置下,这种降低与Zn2 +源的扩散持续时间缩短有关。因此,在波峰处,细胞外介质中Zn2 +的含量较低,但可以让细菌更快地逃逸。这些发现表明细菌Zn2⁺的敏感性增加。类似于Ni2⁺结合到Tar受体的细胞质HAMP结构域,Zn2⁺很可能通过细胞质受体触发化学驱避反应。该受体的激活依赖于可用的锌池,锌池被大量其他细胞内锌库特异性缓冲。在这个模型中,使预先暴露的培养物中的贮液池饱和可以实现最快的响应时间,而在未暴露的细胞中逐渐填充贮液池可以减少趋化逃逸的延迟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Biometals
Biometals 生物-生化与分子生物学
CiteScore
5.90
自引率
8.60%
发文量
111
审稿时长
3 months
期刊介绍: BioMetals is the only established journal to feature the important role of metal ions in chemistry, biology, biochemistry, environmental science, and medicine. BioMetals is an international, multidisciplinary journal singularly devoted to the rapid publication of the fundamental advances of both basic and applied research in this field. BioMetals offers a forum for innovative research and clinical results on the structure and function of: - metal ions - metal chelates, - siderophores, - metal-containing proteins - biominerals in all biosystems. - BioMetals rapidly publishes original articles and reviews. BioMetals is a journal for metals researchers who practice in medicine, biochemistry, pharmacology, toxicology, microbiology, cell biology, chemistry, and plant physiology who are based academic, industrial and government laboratories.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信