• 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

[弗氏柠檬酸杆菌4111菌株中质粒定位及限制修饰基因的克隆]

[Plasmid localization and cloning of restriction modification genes from Citrobacter freundii 4111 strain].

作者信息

Kravets A N, Solonin A S, Zakharova M V, Tarutina Z E

出版信息

Mol Gen Mikrobiol Virusol. 1992 Jul-Aug(7-8):4-7.

PMID:1338550
Abstract

Over 60 producing strains of restriction endonucleases type II have been found among 500 different strains, mostly Enterobacteriaceae. The strain Citrobacter freundii 4111 produces restriction endonuclease CfrBI, a new isoschisomer of StyI. The genes of the restriction-modification system CfrBI were located on the multicopy plasmid pZE8 containing the Co1E1-type replicon and cloned to E. coli K802. The deletion variant of 3.2-kb pZE8 which contains intact restriction-modification and a DNA fragment responsible for autonomous plasmid replication was selected among the recombinant plasmids. The strain with higher R. CfrBI production (at least 10,000,000 U/g cells, which is 500-fold higher than the wild strain) was constructed.

摘要

在500种不同菌株中发现了60多种II型限制性内切酶产生菌株,其中大部分是肠杆菌科细菌。弗氏柠檬酸杆菌4111菌株产生限制性内切酶CfrBI,它是StyI的一种新的同裂酶。限制性修饰系统CfrBI的基因位于含有ColE1型复制子的多拷贝质粒pZE8上,并克隆到大肠杆菌K802中。在重组质粒中筛选出了3.2-kb pZE8的缺失变体,它含有完整的限制性修饰和负责质粒自主复制的DNA片段。构建了具有更高CfrBI产量的菌株(至少10000000 U/g细胞,比野生菌株高500倍)。

相似文献

1
[Plasmid localization and cloning of restriction modification genes from Citrobacter freundii 4111 strain].[弗氏柠檬酸杆菌4111菌株中质粒定位及限制修饰基因的克隆]
Mol Gen Mikrobiol Virusol. 1992 Jul-Aug(7-8):4-7.
2
[Cloning of the restriction-modification genes of Bacillus centrosporus in Escherichia coli].[嗜中芽孢杆菌限制修饰基因在大肠杆菌中的克隆]
Genetika. 1988 Feb;24(2):210-5.
3
Cloning and sequences of the genes encoding the CfrBI restriction-modification system from Citrobacter freundii.弗氏柠檬酸杆菌中编码CfrBI限制修饰系统的基因的克隆与序列分析
Gene. 1993 Jul 15;129(1):77-81. doi: 10.1016/0378-1119(93)90698-3.
4
[Characteristics of RecA-independent recombination of plasmids in E. coli cells producing restriction endonuclease EcoRI].[在产生限制性内切酶EcoRI的大肠杆菌细胞中质粒的RecA非依赖性重组的特征]
Mol Gen Mikrobiol Virusol. 1985 May(5):13-9.
5
Cloning and sequencing of the gene for the lactose carrier of Citrobacter freundii.弗氏柠檬酸杆菌乳糖载体基因的克隆与测序
Biochem Biophys Res Commun. 1994 Sep 30;203(3):1882-8. doi: 10.1006/bbrc.1994.2407.
6
[Plasmid recombination stimulated by restriction endonuclease EcoRI in vivo: formation of recombinant plasmids in recA+-cells of E. coli].[体内限制性内切酶EcoRI刺激的质粒重组:大肠杆菌recA⁺细胞中重组质粒的形成]
Mol Gen Mikrobiol Virusol. 1985 Apr(4):15-21.
7
[Reduced restriction of EcoK in the presence of the plasmid pKM ard+. II. Cloning of the gene ard].[在质粒pKM ard+存在时EcoK的限制作用降低。II. ard基因的克隆]
Mol Biol (Mosk). 1987 May-Jun;21(3):847-52.
8
A rapid and efficient method for cloning genes of type II restriction-modification systems by use of a killer plasmid.一种利用杀伤性质粒快速高效克隆II型限制修饰系统基因的方法。
Appl Environ Microbiol. 2007 Jul;73(13):4286-93. doi: 10.1128/AEM.00119-07. Epub 2007 Apr 27.
9
[Properties of the replicator region of the natural plasmid pLG13 containing genes of the EcoRV restriction-modification system].[含有EcoRV限制修饰系统基因的天然质粒pLG13复制区的特性]
Mol Biol (Mosk). 1991 Nov-Dec;25(6):1615-25.
10
[Localization of the genes coding for the specific modification-restriction system in the E. coli tF strain].[大肠杆菌tF菌株中编码特异性修饰-限制系统的基因定位]
Vet Med Nauki. 1987;24(8):9-12.

引用本文的文献

1
An alternative approach to study the enzymatic specificities of the CfrBI restriction-modification system.一种研究CfrBI限制修饰系统酶特异性的替代方法。
Heliyon. 2019 Jun 8;5(6):e01846. doi: 10.1016/j.heliyon.2019.e01846. eCollection 2019 Jun.