• 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

滞后链DNA复制起点是多拷贝质粒pMV158接合转移所必需的。

Lagging-strand DNA replication origins are required for conjugal transfer of the promiscuous plasmid pMV158.

作者信息

Lorenzo-Díaz Fabián, Espinosa Manuel

机构信息

Department of Protein Science, Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Ramiro de Maeztu 9, E-28040 Madrid, Spain.

出版信息

J Bacteriol. 2009 Feb;191(3):720-7. doi: 10.1128/JB.01257-08. Epub 2008 Nov 21.

DOI:10.1128/JB.01257-08
PMID:19028894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2632109/
Abstract

The promiscuous streptococcal plasmid pMV158 is mobilizable by auxiliary plasmids and replicates by the rolling-circle mechanism in a variety of bacterial hosts. The plasmid has two lagging-strand origins, ssoA and ssoU, involved in the conversion of single-stranded DNA intermediates into double-stranded plasmid DNA during vegetative replication. Transfer of the plasmid also would involve conversion of single-stranded DNA molecules into double-stranded plasmid forms in the recipient cells by conjugative replication. To test whether lagging-strand origins played a role in horizontal transfer, pMV158 derivatives defective in one or in both sso's were constructed and tested for their ability to colonize new hosts by means of intra- and interspecies mobilization. Whereas either sso supported transfer between strains of Streptococcus pneumoniae, only plasmids that had an intact ssoU could be efficiently mobilized from S. pneumoniae to Enterococcus faecalis. Thus, it appears that ssoU is a critical factor for pMV158 promiscuity and that the presence of a functional sso plays an essential role in plasmid transfer.

摘要

杂乱链球菌质粒pMV158可被辅助质粒动员,并通过滚环机制在多种细菌宿主中复制。该质粒有两个后随链起始位点,即ssoA和ssoU,在营养复制过程中参与单链DNA中间体转化为双链质粒DNA。质粒的转移也将涉及通过接合复制在受体细胞中将单链DNA分子转化为双链质粒形式。为了测试后随链起始位点是否在水平转移中起作用,构建了在一个或两个sso位点有缺陷的pMV158衍生物,并通过种内和种间动员测试它们定殖新宿主的能力。虽然任一sso都支持肺炎链球菌菌株间的转移,但只有具有完整ssoU的质粒才能从肺炎链球菌有效地转移至粪肠球菌。因此,似乎ssoU是pMV158杂乱性的关键因素,并且功能性sso的存在在质粒转移中起重要作用。

相似文献

1
Lagging-strand DNA replication origins are required for conjugal transfer of the promiscuous plasmid pMV158.滞后链DNA复制起点是多拷贝质粒pMV158接合转移所必需的。
J Bacteriol. 2009 Feb;191(3):720-7. doi: 10.1128/JB.01257-08. Epub 2008 Nov 21.
2
Lagging-strand replication from the ssoA origin of plasmid pMV158 in Streptococcus pneumoniae: in vivo and in vitro influences of mutations in two conserved ssoA regions.肺炎链球菌中质粒pMV158的ssoA起始位点的滞后链复制:两个保守ssoA区域突变的体内和体外影响
J Bacteriol. 1998 Jan;180(1):83-9. doi: 10.1128/JB.180.1.83-89.1998.
3
Lagging-strand origins of the promiscuous plasmid pMV158: physical and functional characterization.多拷贝质粒pMV158的滞后链复制起点:物理及功能特性分析
Microbiology (Reading). 1995 Mar;141 ( Pt 3):655-62. doi: 10.1099/13500872-141-3-655.
4
Bringing them together: plasmid pMV158 rolling circle replication and conjugation under an evolutionary perspective.从进化角度看质粒pMV158的滚环复制与接合:将它们联系起来
Plasmid. 2014 Jul;74:15-31. doi: 10.1016/j.plasmid.2014.05.004. Epub 2014 Jun 2.
5
A functional lagging strand origin does not stabilize plasmid pMV158 inheritance in Escherichia coli.一个功能性滞后链起点并不能稳定质粒pMV158在大肠杆菌中的遗传。
Plasmid. 2000 Jan;43(1):49-58. doi: 10.1006/plas.1999.1430.
6
Determination of specific DNA strand discontinuities with nucleotide resolution in exponentionally growing bacteria harboring rolling circle-replicating plasmids.在含有滚环复制质粒的指数生长细菌中以核苷酸分辨率测定特定DNA链的不连续性。
FEMS Microbiol Lett. 1997 Jul 15;152(2):363-9. doi: 10.1111/j.1574-6968.1997.tb10453.x.
7
Characterization of a single-strand origin, ssoU, required for broad host range replication of rolling-circle plasmids.滚环质粒广泛宿主范围复制所需的单链起源ssoU的特性分析。
Mol Microbiol. 1999 Aug;33(3):466-75. doi: 10.1046/j.1365-2958.1999.01471.x.
8
Identification of a Single Strand Origin of Replication in the Integrative and Conjugative Element ICEBs1 of Bacillus subtilis.枯草芽孢杆菌整合性接合元件ICEBs1中复制单链起始位点的鉴定。
PLoS Genet. 2015 Oct 6;11(10):e1005556. doi: 10.1371/journal.pgen.1005556. eCollection 2015 Oct.
9
Large-scale filter mating assay for intra- and inter-specific conjugal transfer of the promiscuous plasmid pMV158 in Gram-positive bacteria.用于革兰氏阳性菌中滥交质粒pMV158种内和种间接合转移的大规模滤膜杂交试验。
Plasmid. 2009 Jan;61(1):65-70. doi: 10.1016/j.plasmid.2008.09.005. Epub 2008 Oct 26.
10
Mobilizable Rolling-Circle Replicating Plasmids from Gram-Positive Bacteria: A Low-Cost Conjugative Transfer.革兰阳性菌可移动的滚环复制质粒:一种低成本的接合转移系统。
Microbiol Spectr. 2014 Oct;2(5). doi: 10.1128/microbiolspec.PLAS-0008-2013.

引用本文的文献

1
Dynamic evolution of ceftazidime-avibactam resistance due to interchanges between and during treatment of infection.治疗 感染期间, 和 之间的交换导致头孢他啶-阿维巴坦耐药性的动态演变。
Front Cell Infect Microbiol. 2023 Aug 21;13:1244511. doi: 10.3389/fcimb.2023.1244511. eCollection 2023.
2
NDM-5-Producing Co-Harboring Gene in Companion Animals in China.中国伴侣动物中携带产NDM-5基因的共携带情况。
Animals (Basel). 2022 May 20;12(10):1310. doi: 10.3390/ani12101310.
3
Recognition of Streptococcal Promoters by the Pneumococcal SigA Protein.肺炎球菌SigA蛋白对链球菌启动子的识别。
Front Mol Biosci. 2021 Jun 24;8:666504. doi: 10.3389/fmolb.2021.666504. eCollection 2021.
4
Development of Strong Anaerobic Fluorescent Reporters for Clostridium acetobutylicum and Clostridium ljungdahlii Using HaloTag and SNAP-tag Proteins.利用 HaloTag 和 SNAP-tag 蛋白开发用于梭菌属丙酮丁醇梭菌和梭菌属吕克氏菌的强厌氧荧光报告基因。
Appl Environ Microbiol. 2020 Oct 1;86(20). doi: 10.1128/AEM.01271-20.
5
Combining Modules for Versatile and Optimal Labeling of Lactic Acid Bacteria: Two pMV158-Family Promiscuous Replicons, a Pneumococcal System for Constitutive or Inducible Gene Expression, and Two Fluorescent Proteins.用于乳酸菌通用和优化标记的组合模块:两个pMV158家族的混杂复制子、一个用于组成型或诱导型基因表达的肺炎球菌系统以及两种荧光蛋白。
Front Microbiol. 2019 Jun 26;10:1431. doi: 10.3389/fmicb.2019.01431. eCollection 2019.
6
A Dual-Replicon Shuttle Vector System for Heterologous Gene Expression in a Broad Range of Gram-Positive and Gram-Negative Bacteria.一种用于在多种革兰氏阳性和革兰氏阴性细菌中进行异源基因表达的双复制子穿梭载体系统。
Curr Microbiol. 2018 Oct;75(10):1391-1400. doi: 10.1007/s00284-018-1535-8. Epub 2018 Jul 9.
7
Replication of Staphylococcal Resistance Plasmids.葡萄球菌耐药质粒的复制
Front Microbiol. 2017 Nov 23;8:2279. doi: 10.3389/fmicb.2017.02279. eCollection 2017.
8
Colocation of the Multiresistance Gene and the Fosfomycin Resistance Gene on a Novel Plasmid in Staphylococcus arlettae from a Chicken Farm.鸡场耐甲氧西林金黄色葡萄球菌中新质粒上多药耐药基因和磷霉素耐药基因的共存。
Antimicrob Agents Chemother. 2017 Nov 22;61(12). doi: 10.1128/AAC.01388-17. Print 2017 Dec.
9
Crosstalk between vertical and horizontal gene transfer: plasmid replication control by a conjugative relaxase.垂直基因转移与水平基因转移之间的相互作用:由接合松弛酶控制的质粒复制
Nucleic Acids Res. 2017 Jul 27;45(13):7774-7785. doi: 10.1093/nar/gkx450.
10
Discovery of a new family of relaxases in Firmicutes bacteria.在厚壁菌门细菌中发现一个新的松弛酶家族。
PLoS Genet. 2017 Feb 16;13(2):e1006586. doi: 10.1371/journal.pgen.1006586. eCollection 2017 Feb.

本文引用的文献

1
Large-scale filter mating assay for intra- and inter-specific conjugal transfer of the promiscuous plasmid pMV158 in Gram-positive bacteria.用于革兰氏阳性菌中滥交质粒pMV158种内和种间接合转移的大规模滤膜杂交试验。
Plasmid. 2009 Jan;61(1):65-70. doi: 10.1016/j.plasmid.2008.09.005. Epub 2008 Oct 26.
2
Bacteriophage N4 virion RNA polymerase interaction with its promoter DNA hairpin.噬菌体N4病毒粒子RNA聚合酶与其启动子DNA发夹的相互作用。
Proc Natl Acad Sci U S A. 2007 Apr 24;104(17):7033-8. doi: 10.1073/pnas.0610627104. Epub 2007 Apr 16.
3
Plasmid rolling-circle replication: highlights of two decades of research.质粒滚环复制:二十年研究亮点
Plasmid. 2005 Mar;53(2):126-36. doi: 10.1016/j.plasmid.2004.12.008. Epub 2005 Jan 22.
4
The activity of a single-stranded promoter of plasmid ColIb-P9 depends on its secondary structure.质粒ColIb-P9单链启动子的活性取决于其二级结构。
Mol Microbiol. 2004 Jul;53(2):405-17. doi: 10.1111/j.1365-2958.2004.04114.x.
5
Reconstitution of a staphylococcal plasmid-protein relaxation complex in vitro.体外重建葡萄球菌质粒 - 蛋白质松弛复合物
J Bacteriol. 2004 Jun;186(11):3374-83. doi: 10.1128/JB.186.11.3374-3383.2004.
6
An accessory protein is required for relaxosome formation by small staphylococcal plasmids.小葡萄球菌质粒形成松弛体需要一种辅助蛋白。
J Bacteriol. 2004 Jun;186(11):3363-73. doi: 10.1128/JB.186.11.3363-3373.2004.
7
A classification scheme for mobilization regions of bacterial plasmids.细菌质粒动员区域的分类方案。
FEMS Microbiol Rev. 2004 Feb;28(1):79-100. doi: 10.1016/j.femsre.2003.09.001.
8
Features of the plasmid pMV158-encoded MobM, a protein involved in its mobilization.质粒pMV158编码的MobM的特征,MobM是一种参与其转移的蛋白质。
J Mol Biol. 2004 Jan 16;335(3):733-43. doi: 10.1016/j.jmb.2003.11.017.
9
Conjugal transfer of plasmid pMV158: uncoupling of the pMV158 origin of transfer from the mobilization gene mobM, and modulation of pMV158 transfer in Escherichia coli mediated by IncP plasmids.质粒pMV158的接合转移:转移起始点与动员基因mobM的解偶联,以及IncP质粒介导的大肠杆菌中pMV158转移的调控
Microbiology (Reading). 2000 Sep;146 ( Pt 9):2259-2265. doi: 10.1099/00221287-146-9-2259.
10
Plasmid rolling-circle replication: recent developments.质粒滚环复制:最新进展
Mol Microbiol. 2000 Aug;37(3):477-84. doi: 10.1046/j.1365-2958.2000.02001.x.