• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

高渗透压通过减少大肠杆菌起始体积来调节细菌细胞大小。

High Osmolarity Modulates Bacterial Cell Size through Reducing Initiation Volume in Escherichia coli.

机构信息

School of Life Sciences, Central China Normal University, Wuhan, China

出版信息

mSphere. 2018 Oct 24;3(5):e00430-18. doi: 10.1128/mSphere.00430-18.

DOI:10.1128/mSphere.00430-18
PMID:30355666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6200984/
Abstract

Bacterial cell size is closely associated with biomass growth and cell cycle progression, including chromosome replication and cell division. It is generally proposed that cells tightly control the timing of chromosome replication through maintaining a constant cell volume per origin upon initiating chromosome replication (constant initiation volume) under various growth conditions. Here, we quantitatively characterize the cell size and cell cycle of cells growing exponentially under hyperosmotic stress, which is a common environmental stressor that profoundly affects the bacterial water content. The bacterial cell size is reduced by hyperosmotic stress, even though the C and D periods are remarkably prolonged, indicating a significantly reduced initiation volume. The reduced initiation volume originates from the higher concentration of DnaA initiator protein caused by water loss at high osmolarity. Our study shows suggests a fundamental role of water content in regulating bacterial cell size and has also revealed a new role of the DnaA protein in regulating the chromosome replication elongation beyond regulating the replication initiation process. Bacterial cell size depends on growth rate, cell cycle progression, and the cell volume per origin upon initiating chromosome replication (initiation volume). Here, we perform the first systematic and quantitative study of the effect of hyperosmotic stress on the cell size and cell cycle. We find that hyperosmotic stress significantly reduces the initiation volume. The reduced initiation volume is attributed to the increased DnaA concentration caused by water loss at high osmolarity, indicating a fundamental role of water content in cell size and cell cycle regulation.

摘要

细菌细胞大小与生物量生长和细胞周期进程密切相关,包括染色体复制和细胞分裂。通常认为,细胞通过在各种生长条件下起始染色体复制时保持每个起始点的恒定细胞体积(恒定起始体积),来紧密控制染色体复制的时间。在这里,我们定量表征了在高渗胁迫下指数生长的 细胞的细胞大小和细胞周期,高渗胁迫是一种常见的环境胁迫因子,会深刻影响细菌的含水量。尽管 C 和 D 期显著延长,细菌细胞大小仍因高渗胁迫而减小,表明起始体积显著减小。起始体积的减小源于高渗透压下水分流失导致的 DnaA 起始蛋白浓度升高。我们的研究表明,含水量在调节细菌细胞大小方面起着基础性作用,同时也揭示了 DnaA 蛋白在调节染色体复制延伸过程中的一个新作用,超越了其在调节复制起始过程中的作用。细菌细胞大小取决于生长速率、细胞周期进程以及起始染色体复制时的每个起始点的细胞体积(起始体积)。在这里,我们首次对高渗胁迫对 细胞大小和细胞周期的影响进行了系统和定量的研究。我们发现高渗胁迫显著降低了起始体积。起始体积的减小归因于高渗透压下水分流失导致的 DnaA 浓度升高,表明含水量在细胞大小和细胞周期调控中起着基础性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/8dd0fd7e11cf/sph0051826650007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/4e41906c671a/sph0051826650001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/b2a616a59db0/sph0051826650002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/e13a50b8bb99/sph0051826650003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/eb26d1b6abd3/sph0051826650004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/73db9076632d/sph0051826650005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/a4fca925627d/sph0051826650006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/8dd0fd7e11cf/sph0051826650007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/4e41906c671a/sph0051826650001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/b2a616a59db0/sph0051826650002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/e13a50b8bb99/sph0051826650003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/eb26d1b6abd3/sph0051826650004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/73db9076632d/sph0051826650005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/a4fca925627d/sph0051826650006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23cd/6200984/8dd0fd7e11cf/sph0051826650007.jpg

相似文献

1
High Osmolarity Modulates Bacterial Cell Size through Reducing Initiation Volume in Escherichia coli.高渗透压通过减少大肠杆菌起始体积来调节细菌细胞大小。
mSphere. 2018 Oct 24;3(5):e00430-18. doi: 10.1128/mSphere.00430-18.
2
DnaA and the timing of chromosome replication in Escherichia coli as a function of growth rate.大肠杆菌中DnaA与染色体复制时间作为生长速率的函数关系
BMC Syst Biol. 2011 Dec 21;5:201. doi: 10.1186/1752-0509-5-201.
3
Hda, a novel DnaA-related protein, regulates the replication cycle in Escherichia coli.Hda是一种与DnaA相关的新型蛋白质,它调控大肠杆菌的复制周期。
EMBO J. 2001 Aug 1;20(15):4253-62. doi: 10.1093/emboj/20.15.4253.
4
Robust control of initiation of prokaryotic chromosome replication: essential considerations for a minimal cell.原核生物染色体复制起始的稳健控制:最小细胞的基本考量
Biotechnol Bioeng. 2004 Dec 5;88(5):575-84. doi: 10.1002/bit.20223.
5
Coupling chromosomal replication to cell growth by the initiator protein DnaA in Escherichia coli.在大肠杆菌中,起始蛋白 DnaA 将染色体复制与细胞生长偶联。
J Theor Biol. 2012 Dec 7;314:164-72. doi: 10.1016/j.jtbi.2012.08.045. Epub 2012 Sep 11.
6
Cell Size Is Coordinated with Cell Cycle by Regulating Initiator Protein DnaA in E. coli.通过调控大肠杆菌中的起始蛋白DnaA,细胞大小与细胞周期相互协调。
Biophys J. 2020 Dec 15;119(12):2537-2557. doi: 10.1016/j.bpj.2020.10.034. Epub 2020 Nov 13.
7
Initiator (DnaA) protein concentration as a function of growth rate in Escherichia coli and Salmonella typhimurium.大肠杆菌和鼠伤寒沙门氏菌中引发蛋白(DnaA)浓度与生长速率的函数关系。
J Bacteriol. 1991 Aug;173(16):5194-9. doi: 10.1128/jb.173.16.5194-5199.1991.
8
Regulation of replication initiation: lessons from Caulobacter crescentus.复制起始的调控:来自新月柄杆菌的经验教训。
Genes Genet Syst. 2019 Dec 10;94(5):183-196. doi: 10.1266/ggs.19-00011. Epub 2019 Sep 6.
9
Loss of Hda activity stimulates replication initiation from I-box, but not R4 mutant origins in Escherichia coli.Hda活性的丧失会刺激大肠杆菌中I-box区域的复制起始,但不会刺激R4突变体起源区域的复制起始。
Mol Microbiol. 2009 Jan;71(1):107-22. doi: 10.1111/j.1365-2958.2008.06516.x. Epub 2008 Nov 6.
10
Overview of controls in the Escherichia coli cell cycle.大肠杆菌细胞周期中的调控概述。
Bioessays. 1995 Jun;17(6):527-36. doi: 10.1002/bies.950170609.

引用本文的文献

1
Uropathogenic in a Diabetic Dog with Recurrent UTIs: Genomic Insights and the Impact of Glucose and Antibiotics on Biofilm Formation.一只患有复发性尿路感染的糖尿病犬的尿路致病性:基因组学见解以及葡萄糖和抗生素对生物膜形成的影响
Microorganisms. 2025 Aug 20;13(8):1946. doi: 10.3390/microorganisms13081946.
2
The design of unit cells by combining the self-reproduction systems and metabolic cushioning loads.通过结合自我复制系统和代谢缓冲负荷来设计晶胞。
Commun Biol. 2025 Feb 15;8(1):241. doi: 10.1038/s42003-025-07655-2.
3
Quantifying the fractal complexity of nutrient transport channels in biofilms under varying cell shape and growth environment.

本文引用的文献

1
High Salt Cross-Protects from Antibiotic Treatment through Increasing Efflux Pump Expression.高盐通过增加外排泵表达交叉保护免受抗生素治疗。
mSphere. 2018 Apr 11;3(2). doi: 10.1128/mSphere.00095-18. Print 2018 Apr 25.
2
The DnaA Tale.DnaA的故事
Front Microbiol. 2018 Feb 28;9:319. doi: 10.3389/fmicb.2018.00319. eCollection 2018.
3
Slowdown of Translational Elongation in under Hyperosmotic Stress.在高渗胁迫下翻译延伸的减缓。
量化不同细胞形状和生长环境下生物膜中营养传输通道的分形复杂性。
Microbiology (Reading). 2024 Nov;170(11). doi: 10.1099/mic.0.001511.
4
Delaying production with prokaryotic inducible expression systems.使用原核诱导表达系统延迟生产。
Microb Cell Fact. 2024 Sep 13;23(1):249. doi: 10.1186/s12934-024-02523-w.
5
: a near-minimal model organism for systems and synthetic biology.:一种用于系统生物学和合成生物学的近乎最小的模式生物。
Front Genet. 2024 Feb 9;15:1346707. doi: 10.3389/fgene.2024.1346707. eCollection 2024.
6
Water Stress-Driven Changes in Bacterial Cell Surface Properties.水胁迫导致细菌细胞表面特性发生变化。
Appl Environ Microbiol. 2022 Nov 8;88(21):e0073222. doi: 10.1128/aem.00732-22. Epub 2022 Oct 13.
7
Guidelines for a Morphometric Analysis of Prokaryotic and Eukaryotic Cells by Scanning Electron Microscopy.扫描电子显微镜分析原核和真核细胞形态的指南。
Cells. 2021 Nov 25;10(12):3304. doi: 10.3390/cells10123304.
8
Transgenesis of mammalian PABP reveals mRNA polyadenylation as a general stress response mechanism in bacteria.哺乳动物聚腺苷酸结合蛋白的转基因研究揭示了mRNA多聚腺苷酸化是细菌中的一种普遍应激反应机制。
iScience. 2021 Sep 11;24(10):103119. doi: 10.1016/j.isci.2021.103119. eCollection 2021 Oct 22.
9
Integrative characterization of the near-minimal bacterium Mesoplasma florum.近最小细菌花束支原体的综合特征描述。
Mol Syst Biol. 2020 Dec;16(12):e9844. doi: 10.15252/msb.20209844.
10
Trehalose as an osmolyte in Candidatus Accumulibacter phosphatis.海藻糖作为聚磷菌中的一种渗透调节物质。
Appl Microbiol Biotechnol. 2021 Jan;105(1):379-388. doi: 10.1007/s00253-020-10947-8. Epub 2020 Oct 19.
mBio. 2018 Feb 13;9(1):e02375-17. doi: 10.1128/mBio.02375-17.
4
Fundamental principles in bacterial physiology-history, recent progress, and the future with focus on cell size control: a review.细菌生理学基础——历史、最新进展及未来展望,重点关注细胞大小控制:综述。
Rep Prog Phys. 2018 May;81(5):056601. doi: 10.1088/1361-6633/aaa628. Epub 2018 Jan 9.
5
Salt-responsive gut commensal modulates T17 axis and disease.盐反应性肠道共生菌调节T17轴与疾病。
Nature. 2017 Nov 30;551(7682):585-589. doi: 10.1038/nature24628. Epub 2017 Nov 15.
6
Manipulating the Bacterial Cell Cycle and Cell Size by Titrating the Expression of Ribonucleotide Reductase.通过滴定核糖核苷酸还原酶的表达来操纵细菌细胞周期和细胞大小。
mBio. 2017 Nov 14;8(6):e01741-17. doi: 10.1128/mBio.01741-17.
7
Bacterial Cell Size: Multifactorial and Multifaceted.细菌细胞大小:多因素和多方面的。
Annu Rev Microbiol. 2017 Sep 8;71:499-517. doi: 10.1146/annurev-micro-090816-093803.
8
Fatty Acid Availability Sets Cell Envelope Capacity and Dictates Microbial Cell Size.脂肪酸可用性决定了细胞包膜的容量,并决定了微生物细胞的大小。
Curr Biol. 2017 Jun 19;27(12):1757-1767.e5. doi: 10.1016/j.cub.2017.05.076. Epub 2017 Jun 8.
9
Invariance of Initiation Mass and Predictability of Cell Size in Escherichia coli.大肠杆菌中起始质量的不变性和细胞大小的可预测性。
Curr Biol. 2017 May 8;27(9):1278-1287. doi: 10.1016/j.cub.2017.03.022. Epub 2017 Apr 13.
10
tCRISPRi: tunable and reversible, one-step control of gene expression.tCRISPRi:可调控和可逆的,一步式基因表达控制。
Sci Rep. 2016 Dec 20;6:39076. doi: 10.1038/srep39076.