• 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

质粒pCU1的N接合转移系统。

N conjugative transfer system of plasmid pCU1.

作者信息

Thatte V, Bradley D E, Iyer V N

出版信息

J Bacteriol. 1985 Sep;163(3):1229-36. doi: 10.1128/jb.163.3.1229-1236.1985.

DOI:10.1128/jb.163.3.1229-1236.1985
PMID:2863255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC219264/
Abstract

The mating and plasmid DNA transfer functions in Escherichia coli K-12 strains that are determined by the IncN group plasmid pCU1 are specified by a single 19.4-kilobase (kb) segment of the 39-kb plasmid. Analysis of this tra region by transposon Tn5 mutagenesis and by complementation tests indicated that a subset of tra comprising six complementation groups (presumably transcription units) determines sensitivity to the N pilus-specific bacteriophages IKe and PRD1. Deletion derivatives and molecular clones that contained only this part of tra conferred sensitivity to IKe and PRD1 and the ability to produce N pili without conferring the Tra phenotype. The entire tra region contained two other complementation groups. If the 19.4-kb tra region is interrupted by DNA that is irrelevant to the Tra phenotype, such DNA must be less than 2 kb long. There are two regions within tra where this is a possibility. These observations are compared with those obtained recently with a related plasmid.

摘要

由IncN组质粒pCU1决定的大肠杆菌K-12菌株中的交配和质粒DNA转移功能,由39kb质粒的一个19.4千碱基(kb)的单一区段所规定。通过转座子Tn5诱变和互补试验对这个tra区域进行分析表明,tra的一个子集包括六个互补组(推测为转录单位)决定了对N菌毛特异性噬菌体IKe和PRD1的敏感性。仅包含tra这一部分的缺失衍生物和分子克隆赋予了对IKe和PRD1的敏感性以及产生N菌毛的能力,但不赋予Tra表型。整个tra区域还包含另外两个互补组。如果19.4kb的tra区域被与Tra表型无关的DNA中断,那么这种DNA的长度必须小于2kb。在tra内有两个区域存在这种可能性。将这些观察结果与最近用一个相关质粒获得的结果进行了比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c926/219264/30a14c17fba9/jbacter00220-0428-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c926/219264/63162acdb709/jbacter00220-0426-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c926/219264/913f0de43401/jbacter00220-0426-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c926/219264/30a14c17fba9/jbacter00220-0428-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c926/219264/63162acdb709/jbacter00220-0426-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c926/219264/913f0de43401/jbacter00220-0426-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c926/219264/30a14c17fba9/jbacter00220-0428-a.jpg

相似文献

1
N conjugative transfer system of plasmid pCU1.质粒pCU1的N接合转移系统。
J Bacteriol. 1985 Sep;163(3):1229-36. doi: 10.1128/jb.163.3.1229-1236.1985.
2
Cloning of a plasmid region specifying the N transfer system of bacterial conjugation in Escherichia coli.大肠杆菌中决定细菌接合作用N转移系统的质粒区域的克隆
Gene. 1983 Mar;21(3):227-36. doi: 10.1016/0378-1119(83)90006-9.
3
The oriT region of the conjugative transfer system of plasmid pCU1 and specificity between it and the mob region of other N tra plasmids.质粒pCU1接合转移系统的oriT区域及其与其他N型转移质粒mob区域之间的特异性。
J Bacteriol. 1992 Jan;174(2):499-507. doi: 10.1128/jb.174.2.499-507.1992.
4
Identification and cloning of the conjugative transfer region of Staphylococcus aureus plasmid pGO1.金黄色葡萄球菌质粒pGO1接合转移区域的鉴定与克隆
J Bacteriol. 1989 Feb;171(2):684-91. doi: 10.1128/jb.171.2.684-691.1989.
5
Cloning and genetic analysis of tra cistrons of the Tra 2/Tra 3 region of plasmid RP1.质粒RP1的Tra 2/Tra 3区域tra顺反子的克隆与遗传分析。
Plasmid. 1989 Jul;22(1):59-69. doi: 10.1016/0147-619x(89)90036-x.
6
Conjugal transfer system of the IncN plasmid pKM101.IncN 质粒 pKM101 的接合转移系统
J Bacteriol. 1985 Jan;161(1):402-10. doi: 10.1128/jb.161.1.402-410.1985.
7
Genetic analysis of the transfer region of the IncN plasmid N3.IncN 质粒 N3 转移区域的遗传分析
Res Microbiol. 1990 Jul-Aug;141(6):621-31. doi: 10.1016/0923-2508(90)90057-w.
8
TraC of IncN plasmid pKM101 associates with membranes and extracellular high-molecular-weight structures in Escherichia coli.IncN 质粒 pKM101 的 TraC 与大肠杆菌的细胞膜及细胞外高分子量结构相关联。
J Bacteriol. 1999 Sep;181(18):5563-71. doi: 10.1128/JB.181.18.5563-5571.1999.
9
Genetic analysis of the mobilization and leading regions of the IncN plasmids pKM101 and pCU1.IncN质粒pKM101和pCU1的转移与先导区域的遗传分析
J Bacteriol. 1999 Apr;181(8):2572-83. doi: 10.1128/JB.181.8.2572-2583.1999.
10
Characteristics and function of thick and thin conjugative pili determined by transfer-derepressed plasmids of incompatibility groups I1, I2, I5, B, K and Z.由不相容群I1、I2、I5、B、K和Z的转移去阻遏质粒所决定的粗细结合菌毛的特征与功能
J Gen Microbiol. 1984 Jun;130(6):1489-502. doi: 10.1099/00221287-130-6-1489.

引用本文的文献

1
Two pKM101-encoded proteins, the pilus-tip protein TraC and Pep, assemble on the Escherichia coli cell surface as adhesins required for efficient conjugative DNA transfer.两个 pKM101 编码蛋白,菌毛尖端蛋白 TraC 和 Pep,作为大肠杆菌细胞表面上用于有效接合性 DNA 转移的黏附素组装。
Mol Microbiol. 2019 Jan;111(1):96-117. doi: 10.1111/mmi.14141. Epub 2018 Oct 21.
2
Investigating the impact of bisphosphonates and structurally related compounds on bacteria containing conjugative plasmids.研究双膦酸盐及其结构相关化合物对含可转移质粒细菌的影响。
Biochem Biophys Res Commun. 2012 Aug 10;424(4):697-703. doi: 10.1016/j.bbrc.2012.07.012. Epub 2012 Jul 13.
3

本文引用的文献

1
Killing of Klebsiella pneumoniae mediated by conjugation with bacteria carrying antibiotic-resistance plasmids of the group N.通过与携带N组抗生素抗性质粒的细菌接合介导的肺炎克雷伯菌杀灭作用
Plasmid. 1981 Jul;6(1):141-7. doi: 10.1016/0147-619x(81)90060-3.
2
Inverted repeats in the DNA of plasmid pCU1.质粒pCU1 DNA中的反向重复序列。
J Bacteriol. 1983 Mar;153(3):1502-12. doi: 10.1128/jb.153.3.1502-1512.1983.
3
Suicide plasmid vehicles for insertion mutagenesis in Rhizobium meliloti and related bacteria.用于苜蓿根瘤菌及相关细菌插入诱变的自杀质粒载体。
Identification of tail genes in the temperate phage 16-3 of Sinorhizobium meliloti 41.
鉴定苜蓿中华根瘤菌 16-3 型温和噬菌体中的尾部基因。
J Bacteriol. 2010 Mar;192(6):1617-23. doi: 10.1128/JB.01335-09. Epub 2010 Jan 15.
4
Repressor of phage 16-3 with altered binding specificity indicates spatial differences in repressor-operator complexes.具有改变的结合特异性的噬菌体16-3阻遏物表明阻遏物-操纵基因复合物存在空间差异。
J Bacteriol. 2006 Feb;188(4):1663-6. doi: 10.1128/JB.188.4.1663-1666.2006.
5
Host Ranges of the IncN Group Plasmid pCU1 and Its Minireplicon in Gram-Negative Purple Bacteria.革兰氏阴性紫色细菌中 IncN 组质粒 pCU1 及其复制子的宿主范围。
Appl Environ Microbiol. 1988 Sep;54(9):2273-6. doi: 10.1128/aem.54.9.2273-2276.1988.
6
Identification of cohesive ends and genes encoding the terminase of phage 16-3.噬菌体16-3粘性末端及编码末端酶的基因的鉴定
J Bacteriol. 2005 Apr;187(7):2526-31. doi: 10.1128/JB.187.7.2526-2531.2005.
7
Site-specific integrative elements of rhizobiophage 16-3 can integrate into proline tRNA (CGG) genes in different bacterial genera.根瘤菌噬菌体16-3的位点特异性整合元件可整合到不同细菌属的脯氨酸tRNA(CGG)基因中。
J Bacteriol. 2002 Jan;184(1):177-82. doi: 10.1128/JB.184.1.177-182.2002.
8
Genetic analysis of the mobilization and leading regions of the IncN plasmids pKM101 and pCU1.IncN质粒pKM101和pCU1的转移与先导区域的遗传分析
J Bacteriol. 1999 Apr;181(8):2572-83. doi: 10.1128/JB.181.8.2572-2583.1999.
9
Adaptation of a conjugal transfer system for the export of pathogenic macromolecules.一种用于致病性大分子输出的接合转移系统的改造
Trends Microbiol. 1996 Feb;4(2):64-8. doi: 10.1016/0966-842X(96)81513-7.
10
Structure, function, and regulation of the kilB locus of promiscuous plasmid RK2.多功能质粒RK2的kilB基因座的结构、功能及调控
J Bacteriol. 1993 Apr;175(8):2423-35. doi: 10.1128/jb.175.8.2423-2435.1993.
J Bacteriol. 1983 Dec;156(3):1292-300. doi: 10.1128/jb.156.3.1292-1300.1983.
4
Cloning of a plasmid region specifying the N transfer system of bacterial conjugation in Escherichia coli.大肠杆菌中决定细菌接合作用N转移系统的质粒区域的克隆
Gene. 1983 Mar;21(3):227-36. doi: 10.1016/0378-1119(83)90006-9.
5
Genetic map of the crown gall suppressive IncW plasmid pSa.冠瘿抑制性IncW质粒pSa的遗传图谱
Mol Gen Genet. 1982;186(1):10-5. doi: 10.1007/BF00422905.
6
Physical and genetic analysis of the Inc-W group plasmids R388, Sa, and R7K.Inc-W 族质粒 R388、Sa 和 R7K 的物理与遗传学分析。
Plasmid. 1982 May;7(3):239-50. doi: 10.1016/0147-619x(82)90005-1.
7
Restriction endonuclease cleavage map of pKM101: relationship to parental plasmid R46.pKM101的限制性内切核酸酶切割图谱:与亲本质粒R46的关系。
Mol Gen Genet. 1981;182(2):268-72. doi: 10.1007/BF00269669.
8
A rapid boiling method for the preparation of bacterial plasmids.一种制备细菌质粒的快速煮沸法。
Anal Biochem. 1981 Jun;114(1):193-7. doi: 10.1016/0003-2697(81)90473-5.
9
A physical and genetic map of the IncN plasmid R46.IncN 质粒 R46 的物理图谱和遗传图谱。
Plasmid. 1981 Mar;5(2):188-201. doi: 10.1016/0147-619x(81)90020-2.
10
Genetic localization and characterization of a pKM101-coded endonuclease.pKM101编码的核酸内切酶的基因定位与特性分析
J Bacteriol. 1983 Jun;154(3):1117-25. doi: 10.1128/jb.154.3.1117-1125.1983.