• 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

Lon 依赖的 CcdA 蛋白水解是无质粒分离菌中 CcdB 激活的关键控制因素。

Lon-dependent proteolysis of CcdA is the key control for activation of CcdB in plasmid-free segregant bacteria.

作者信息

Van Melderen L, Bernard P, Couturier M

机构信息

Département de Biologie Moléculaire, Université Libre de Bruxelles, Rhode Saint Genèse.

出版信息

Mol Microbiol. 1994 Mar;11(6):1151-7. doi: 10.1111/j.1365-2958.1994.tb00391.x.

DOI:10.1111/j.1365-2958.1994.tb00391.x
PMID:8022284
Abstract

The ccd locus contributes to the stability of plasmid F by post-segregational killing of plasmid-free bacteria. The ccdB gene product is a potent cell-killing protein and its activity is negatively regulated by the CcdA protein. In this paper, we show that the CcdA protein is unstable and that the degradation of CcdA is dependent on the Lon protease. Differences in the stability of the killer CcdB protein and its antidote CcdA are the key to post-segregational killing. Because the half-life of active CcdA protein is shorter than that of active CcdB protein, persistence of the CcdB protein leads to the death of plasmid-free bacterial segregants.

摘要

ccd位点通过对无质粒细菌的后分离杀伤作用来促进质粒F的稳定性。ccd B基因产物是一种强效的细胞杀伤蛋白,其活性受到Ccd A蛋白的负调控。在本文中,我们表明Ccd A蛋白不稳定,且Ccd A的降解依赖于Lon蛋白酶。杀伤性Ccd B蛋白与其解毒剂Ccd A稳定性的差异是后分离杀伤的关键。由于活性Ccd A蛋白的半衰期短于活性Ccd B蛋白,Ccd B蛋白的持续存在会导致无质粒细菌分离菌死亡。

相似文献

1
Lon-dependent proteolysis of CcdA is the key control for activation of CcdB in plasmid-free segregant bacteria.Lon 依赖的 CcdA 蛋白水解是无质粒分离菌中 CcdB 激活的关键控制因素。
Mol Microbiol. 1994 Mar;11(6):1151-7. doi: 10.1111/j.1365-2958.1994.tb00391.x.
2
ATP-dependent degradation of CcdA by Lon protease. Effects of secondary structure and heterologous subunit interactions.Lon蛋白酶对CcdA的ATP依赖性降解。二级结构和异源亚基相互作用的影响。
J Biol Chem. 1996 Nov 1;271(44):27730-8. doi: 10.1074/jbc.271.44.27730.
3
Efficiency of the pTF-FC2 pas poison-antidote stability system in Escherichia coli is affected by the host strain, and antidote degradation requires the lon protease.pTF-FC2 pas 毒素-抗毒素稳定性系统在大肠杆菌中的效率受宿主菌株影响,且抗毒素的降解需要lon蛋白酶。
J Bacteriol. 1998 Oct;180(20):5458-62. doi: 10.1128/JB.180.20.5458-5462.1998.
4
The ratio between CcdA and CcdB modulates the transcriptional repression of the ccd poison-antidote system.CcdA与CcdB之间的比例调节ccd毒素-抗毒素系统的转录抑制。
Mol Microbiol. 2001 Jul;41(1):73-82. doi: 10.1046/j.1365-2958.2001.02492.x.
5
The antidote and autoregulatory functions of the F plasmid CcdA protein: a genetic and biochemical survey.F质粒CcdA蛋白的解毒和自调控功能:一项遗传学与生物化学研究
Mol Gen Genet. 1994 Sep 1;244(5):530-8. doi: 10.1007/BF00583904.
6
The 41 carboxy-terminal residues of the miniF plasmid CcdA protein are sufficient to antagonize the killer activity of the CcdB protein.微小F质粒CcdA蛋白的41个羧基末端残基足以拮抗CcdB蛋白的杀伤活性。
Mol Gen Genet. 1991 Apr;226(1-2):297-304. doi: 10.1007/BF00273616.
7
Intricate interactions within the ccd plasmid addiction system.ccd质粒成瘾系统内的复杂相互作用。
J Biol Chem. 2002 Feb 1;277(5):3733-42. doi: 10.1074/jbc.M105505200. Epub 2001 Dec 7.
8
An increased content of protease La, the lon gene product, increases protein degradation and blocks growth in Escherichia coli.蛋白酶La(lon基因产物)含量的增加会增强蛋白质降解并阻碍大肠杆菌的生长。
J Biol Chem. 1987 Apr 5;262(10):4508-15.
9
F plasmid CcdB killer protein: ccdB gene mutants coding for non-cytotoxic proteins which retain their regulatory functions.F质粒CcdB杀伤蛋白:编码保留其调节功能的非细胞毒性蛋白的ccdB基因突变体。
Mol Microbiol. 1995 Mar;15(6):1031-7. doi: 10.1111/j.1365-2958.1995.tb02278.x.
10
Proteolysis and modulation of the activity of the cell division inhibitor SulA in Escherichia coli lon mutants.大肠杆菌lon突变体中细胞分裂抑制剂SulA的蛋白水解作用及活性调节
J Bacteriol. 1990 Dec;172(12):7297-300. doi: 10.1128/jb.172.12.7297-7300.1990.

引用本文的文献

1
Ciprofloxacin-driven purifying selection on viral genomes accelerates soil NO production.环丙沙星对病毒基因组的净化选择加速土壤一氧化氮的产生。
Proc Natl Acad Sci U S A. 2025 Jul 22;122(29):e2503199122. doi: 10.1073/pnas.2503199122. Epub 2025 Jul 16.
2
The Escherichia coli RelB antitoxin C terminus is essential for RelE toxin suppression and transcriptional repression.大肠杆菌RelB抗毒素的C末端对于RelE毒素抑制和转录抑制至关重要。
J Biol Chem. 2025 Jun 18;301(8):110389. doi: 10.1016/j.jbc.2025.110389.
3
A noncanonical intrinsic terminator in the HicAB toxin-antitoxin operon promotes the transmission of conjugative antibiotic resistance plasmids.
HicAB毒素-抗毒素操纵子中的一种非典型内在终止子促进接合性抗生素耐药质粒的传播。
Nucleic Acids Res. 2025 Feb 27;53(5). doi: 10.1093/nar/gkaf125.
4
Analysis of co-occurrence of type II toxin-antitoxin systems and antibiotic resistance determinants in .II型毒素-抗毒素系统与抗生素耐药决定因素的共现分析 于……中 (原文此处不完整)
mSystems. 2025 Mar 18;10(3):e0095724. doi: 10.1128/msystems.00957-24. Epub 2025 Feb 27.
5
Structural duality enables a single protein to act as a toxin-antidote pair for meiotic drive.结构双重性使单个蛋白质能够充当减数分裂驱动的毒素-解毒剂对。
Proc Natl Acad Sci U S A. 2024 Nov 5;121(45):e2408618121. doi: 10.1073/pnas.2408618121. Epub 2024 Nov 1.
6
Structural Variations and Rearrangements in Bacterial Type II Toxin-Antitoxin Systems.细菌 II 型毒素-抗毒素系统中的结构变异和重排。
Subcell Biochem. 2024;104:245-267. doi: 10.1007/978-3-031-58843-3_11.
7
Encoding Genetic Circuits with DNA Barcodes Paves the Way for High-Throughput Profiling of Dose-Response Curves of Metabolite Biosensors.用 DNA 条码对遗传电路进行编码,为高通量分析代谢物生物传感器的剂量反应曲线铺平了道路。
Methods Mol Biol. 2024;2760:309-318. doi: 10.1007/978-1-0716-3658-9_18.
8
Single-cell evidence for plasmid addiction mediated by toxin-antitoxin systems.单细胞证据表明毒素-抗毒素系统介导的质粒成瘾。
Nucleic Acids Res. 2024 Feb 28;52(4):1847-1859. doi: 10.1093/nar/gkae018.
9
A ParDE toxin-antitoxin system is responsible for the maintenance of the virulence plasmid but not for type III secretion-associated growth inhibition.一个 ParDE 毒素-抗毒素系统负责维持毒性质粒,但与 III 型分泌系统相关的生长抑制无关。
Front Cell Infect Microbiol. 2023 May 9;13:1166077. doi: 10.3389/fcimb.2023.1166077. eCollection 2023.
10
Dynamics-Based Regulatory Switches of Type II Antitoxins: Insights into New Antimicrobial Discovery.基于动力学的II型抗毒素调控开关:对抗菌新发现的见解
Antibiotics (Basel). 2023 Mar 23;12(4):637. doi: 10.3390/antibiotics12040637.