• 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

Construction of a stable expression vector carrying sop genes [ZJ1].

作者信息

Du X, Ding J, Wu X, Yu Z, Men D

机构信息

Institute of Microbiology, Chinese Academy of Science, Beijing, China.

出版信息

Chin J Biotechnol. 1996;12(2):99-109.

PMID:8988356
Abstract

Mini-F, the fifth fragment of F plasmid from EcoRI digestion, is known to carry an efficient partitioning function. Two pBR322 plasmid derivatives, pDMC32 and pDMC311, have been constructed from this fragment. The plasmid pDMC32 carries all the relative genes for plasmid stability, ccd, repD, and sop genes (sopA, sopB, and sopC), along with oriS and oriV, while pDMC311 carries only sop genes (sopA, sopB, and sopC). The plasmid maintenance proportions for pDMC32 and pDMC311 in E. coli were 93% and 100%, respectively, after 100 generations continuous cultivation of cells harboring the derivatives, MI32 (pDMC32) and MI311 (pDMC311), in a phosphate-limited basal medium. As a control, the maintenance proportion of plasmid pBR322 dropped down to a low of 10% at generation 55 of continuous cultivation of E. coli MIR322 (pBR322) in the same medium. In order to make a stable expression vector that carries only sop genes, plasmid pDMC40 was constructed by adding a trp promoter from pDR720 to pBR322. The stable expression vector pDMC48 was then derived from pDMC40 by inserting sop genes into it from pDMC311. The maintenance proportion of plasmid pDMC48 in E. coli was still 100% after 100 generations of continuous cultivation of cells harboring the plasmid in phosphate-limited basal medium.

摘要

相似文献

1
Construction of a stable expression vector carrying sop genes [ZJ1].
Chin J Biotechnol. 1996;12(2):99-109.
2
Partition functions of mini-F affect plasmid DNA topology in Escherichia coli.微小F的分配函数影响大肠杆菌中的质粒DNA拓扑结构。
J Mol Biol. 1995 Feb 24;246(3):388-400. doi: 10.1006/jmbi.1994.0094.
3
[Structural organization and control of expression of the sop-operon of linear plasmid prophage N15].[线性质粒原噬菌体N15的sop操纵子的结构组织与表达调控]
Mol Biol (Mosk). 2004 Mar-Apr;38(2):297-302.
4
Partition of the linear plasmid N15: interactions of N15 partition functions with the sop locus of the F plasmid.线性质粒N15的分配:N15分配功能与F质粒sop位点的相互作用
J Bacteriol. 1999 Nov;181(22):6898-906. doi: 10.1128/JB.181.22.6898-6906.1999.
5
[Sop proteins can cause transcriptional silencing of genes located close to the centromere sites of linear plasmid N15].[Sop蛋白可导致位于线性质粒N15着丝粒位点附近的基因发生转录沉默]
Mol Biol (Mosk). 2010 Mar-Apr;44(2):294-300.
6
Construction of highly efficient E. coli expression systems containing low oxygen induced promoter and partition region.构建含低氧诱导启动子和分区区域的高效大肠杆菌表达系统。
Appl Microbiol Biotechnol. 2005 Aug;68(3):346-54. doi: 10.1007/s00253-005-1913-6. Epub 2005 Feb 12.
7
The F plasmid centromere, sopC, is required for full repression of the sopAB operon.F质粒着丝粒sopC是sopAB操纵子完全抑制所必需的。
J Mol Biol. 1999 Jul 16;290(3):627-38. doi: 10.1006/jmbi.1999.2909.
8
Role of the ATP-binding site of SopA protein in partition of the F plasmid.SopA蛋白的ATP结合位点在F质粒分配中的作用。
J Mol Biol. 2001 Nov 30;314(3):387-99. doi: 10.1006/jmbi.2001.5158.
9
Bacterial DNA segregation by dynamic SopA polymers.通过动态SopA聚合物进行细菌DNA分离
Proc Natl Acad Sci U S A. 2005 Dec 6;102(49):17658-63. doi: 10.1073/pnas.0507222102. Epub 2005 Nov 23.
10
Subcellular positioning of F plasmid mediated by dynamic localization of SopA and SopB.由SopA和SopB的动态定位介导的F质粒的亚细胞定位。
J Mol Biol. 2006 Mar 3;356(4):850-63. doi: 10.1016/j.jmb.2005.11.088. Epub 2005 Dec 20.