• 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

棒状链霉菌线性质粒pSCL2复制起点的预测与功能分析

Prediction and functional analysis of the replication origin of the linear plasmid pSCL2 in Streptomyces clavuligerus.

作者信息

Wu Wei, Leblanc Shannon K D, Piktel James, Jensen Susan E, Roy Kenneth L

机构信息

Department of Biological Sciences, CW 405 Biological Sciences Bldg., University of Alberta, Edmonton, Canada.

出版信息

Can J Microbiol. 2006 Apr;52(4):293-300. doi: 10.1139/w05-126.

DOI:10.1139/w05-126
PMID:16699579
Abstract

pSCL2 (120 kb), one of the linear plasmids found in Streptomyces clavuligerus NRRL3585, was isolated and partially sequenced. Computational analysis of the central region of pSCL2 revealed the presence of two open reading frames that appear to encode proteins highly homologous to RepL1 and RepL2, replication proteins from pSLA2-L, the large linear plasmid in Streptomyces rochei. The S. clavuligerus open reading frames were designated repC1 and repC2, encoding the proteins RepC1 (150 amino acids) and RepC2 (102 amino acids), respectively. The RepC and RepL proteins have identical translation features and very similar predicted secondary and tertiary structures. Functional analysis confirmed that RepC1 is essential for replication initiation of pSCL2, whereas RepC2 is dispensable but may play a role in copy number control. The RepC and RepL proteins do not show similarity to any other bacterial plasmid replication proteins. Three regions of DNA sequence, Box 1 (1050-850 bp), Box 2 (723-606 bp), and Box 3 (224-168 bp), located upstream of repC1, were also shown to be essential or very important for replication of pSCL2.

摘要

pSCL2(120 kb)是在棒状链霉菌NRRL3585中发现的线性质粒之一,已被分离并进行了部分测序。对pSCL2中心区域的计算分析表明,存在两个开放阅读框,它们似乎编码与RepL1和RepL2高度同源的蛋白质,RepL1和RepL2是来自罗氏链霉菌中大线性质粒pSLA2-L的复制蛋白。棒状链霉菌的开放阅读框被命名为repC1和repC2,分别编码蛋白质RepC1(150个氨基酸)和RepC2(102个氨基酸)。RepC和RepL蛋白具有相同的翻译特征以及非常相似的预测二级和三级结构。功能分析证实,RepC1对于pSCL2的复制起始至关重要,而RepC2是可有可无的,但可能在拷贝数控制中发挥作用。RepC和RepL蛋白与任何其他细菌质粒复制蛋白均无相似性。位于repC1上游的三个DNA序列区域,即Box 1(1050 - 850 bp)、Box 2(723 - 606 bp)和Box 3(224 - 168 bp),也被证明对pSCL2的复制至关重要或非常重要。

相似文献

1
Prediction and functional analysis of the replication origin of the linear plasmid pSCL2 in Streptomyces clavuligerus.棒状链霉菌线性质粒pSCL2复制起点的预测与功能分析
Can J Microbiol. 2006 Apr;52(4):293-300. doi: 10.1139/w05-126.
2
Cloning and analysis of the replication origin and the telomeres of the large linear plasmid pSLA2-L in Streptomyces rochei.罗氏链霉菌中大线性质粒pSLA2-L的复制起点和端粒的克隆与分析
Mol Gen Genet. 2000 Jul;263(6):1015-21. doi: 10.1007/pl00008689.
3
Relationship between the replication functions of Streptomyces plasmids pJV1 and pIJ101.链霉菌质粒pJV1和pIJ101的复制功能之间的关系
Plasmid. 1993 Sep;30(2):131-40. doi: 10.1006/plas.1993.1040.
4
Characterization of a theta plasmid replicon with homology to all four large plasmids of Bacillus megaterium QM B1551.一种与巨大芽孢杆菌QM B1551的所有四个大质粒具有同源性的θ质粒复制子的特性分析。
Plasmid. 1998 Nov;40(3):175-89. doi: 10.1006/plas.1998.1359.
5
Genetic analysis of the minimal replicon of plasmid pIP417 and comparison with the other encoding 5-nitroimidazole resistance plasmids from Bacteroides spp.质粒pIP417最小复制子的遗传分析及其与拟杆菌属其他编码5-硝基咪唑抗性质粒的比较
Plasmid. 1995 Sep;34(2):132-43. doi: 10.1006/plas.1995.9994.
6
pSLA2-M of Streptomyces rochei is a composite linear plasmid characterized by self-defense genes and homology with pSLA2-L.罗氏链霉菌的pSLA2-M是一种复合线性质粒,其特征在于具有自我防御基因且与pSLA2-L具有同源性。
Biosci Biotechnol Biochem. 2011;75(6):1147-53. doi: 10.1271/bbb.110054. Epub 2011 Jun 13.
7
Characterization of pEC156, a ColE1-type plasmid from Escherichia coli E1585-68 that carries genes of the EcoVIII restriction-modification system.pEC156的特性分析,pEC156是来自大肠杆菌E1585-68的一种携带EcoVIII限制修饰系统基因的ColE1型质粒。
Plasmid. 2001 Sep;46(2):128-39. doi: 10.1006/plas.2001.1534.
8
Identification of a gene encoding the replication initiator protein of the Streptomyces integrating element, pSAM2.
Plasmid. 1994 Mar;31(2):166-83. doi: 10.1006/plas.1994.1018.
9
Complete nucleotide sequence and characterization of pUA140, a cryptic plasmid from Streptococcus mutans.变形链球菌隐蔽质粒pUA140的全核苷酸序列及特征分析
Plasmid. 2001 Sep;46(2):77-85. doi: 10.1006/plas.2001.1539.
10
Screening for plasmids among human bifidobacteria species: sequencing and analysis of pBC1 from Bifidobacterium catenulatum L48.在人类双歧杆菌物种中筛选质粒:来自链状双歧杆菌L48的pBC1的测序与分析
Plasmid. 2007 Mar;57(2):165-74. doi: 10.1016/j.plasmid.2006.07.004. Epub 2006 Aug 22.

引用本文的文献

1
Genome editing reveals that pSCL4 is required for chromosome linearity in .基因组编辑揭示了 pSCL4 在. 中维持染色体线性所必需的。
Microb Genom. 2021 Nov;7(11). doi: 10.1099/mgen.0.000669.
2
Streptomyces clavuligerus: The Omics Era.解旋酶: 组学时代。
J Ind Microbiol Biotechnol. 2021 Dec 23;48(9-10). doi: 10.1093/jimb/kuab072.
3
The sequence of a 1.8-mb bacterial linear plasmid reveals a rich evolutionary reservoir of secondary metabolic pathways.1.8 兆碱基的细菌线性质粒序列揭示了次级代谢途径的丰富进化资源库。
Genome Biol Evol. 2010 Jul 12;2:212-24. doi: 10.1093/gbe/evq013.
4
Two internal origins of replication in Streptomyces linear plasmid pFRL1.线性链霉菌质粒 pFRL1 中的两个内部复制原点。
Appl Environ Microbiol. 2010 Sep;76(17):5676-83. doi: 10.1128/AEM.02905-09. Epub 2010 Jul 2.
5
Characterization of replication and conjugation of Streptomyces circular plasmids pFP1 and pFP11 and their ability to propagate in linear mode with artificially attached telomeres.链霉菌环状质粒pFP1和pFP11的复制与接合特性及其在人工连接端粒后以线性模式传播的能力。
Appl Environ Microbiol. 2008 Jun;74(11):3368-76. doi: 10.1128/AEM.00402-08. Epub 2008 Apr 4.
6
Complete nucleotide sequence of the 113-kilobase linear catabolic plasmid pAL1 of Arthrobacter nitroguajacolicus Rü61a and transcriptional analysis of genes involved in quinaldine degradation.节杆菌Rü61a的113千碱基线性分解代谢质粒pAL1的完整核苷酸序列及喹哪啶降解相关基因的转录分析
J Bacteriol. 2007 May;189(10):3855-67. doi: 10.1128/JB.00089-07. Epub 2007 Mar 2.