• 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

Phage T4 expression vector: protection from proteolysis.

作者信息

Singer B S, Gold L

机构信息

Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder 80309.

出版信息

Gene. 1991 Sep 30;106(1):1-6. doi: 10.1016/0378-1119(91)90558-s.

DOI:10.1016/0378-1119(91)90558-s
PMID:1937029
Abstract

We have developed an efficient method for the expression of heterologous genes during infection by T4, a bacteriophage known to inhibit the proteolytic systems of Escherichia coli. This system enables us to clone genes in a plasmid expression vector and move them readily into T4. We have used lacZ as a reporter gene to show that both plasmid and phage exhibit low basal expression or high-level expression under the control of a T7 promoter. This system promises a possible solution to the problem of degradation and/or toxicity of overproduced proteins.

摘要

相似文献

1
Phage T4 expression vector: protection from proteolysis.
Gene. 1991 Sep 30;106(1):1-6. doi: 10.1016/0378-1119(91)90558-s.
2
A plasmid vector for cloning directly at the transcription initiation site of a bacteriophage T7 promoter.一种用于直接在噬菌体T7启动子转录起始位点进行克隆的质粒载体。
Nucleic Acids Res. 1988 Sep 12;16(17):8738. doi: 10.1093/nar/16.17.8738.
3
An efficient method for constructing a chimeric bacteriophage T4 to estimate the regulatory signals.
Biochem Biophys Res Commun. 1991 Aug 30;179(1):620-7. doi: 10.1016/0006-291x(91)91417-b.
4
[Determination of the direction of the transcription of bacteriophage T4 genes by heat induction of the transcription from recombinant plasmid Pl-promoter: 2 directions in the region of genes 25-29].[通过重组质粒Pl-启动子转录的热诱导来确定噬菌体T4基因的转录方向:基因25-29区域中的两个方向]
Genetika. 1988 Jan;24(1):42-52.
5
A plasmid expression vector that permits stabilization of both mRNAs and proteins encoded by the cloned genes.一种质粒表达载体,可使克隆基因编码的mRNA和蛋白质都得到稳定。
Gene. 1986;45(2):193-201. doi: 10.1016/0378-1119(86)90254-4.
6
[Cloning of the DNA BglII fragments of bacteriophage T4 in the vector plasmid pSCC31].[噬菌体T4的DNA BglII片段在载体质粒pSCC31中的克隆]
Genetika. 1988 Jan;24(1):34-41.
7
Bacteriophage T4, a new vector for the expression of cloned genes.噬菌体T4,一种用于克隆基因表达的新型载体。
Gene. 1985;37(1-3):31-6. doi: 10.1016/0378-1119(85)90254-9.
8
Fate of cloned bacteriophage T4 DNA after phage T4 infection of clone-bearing cells.携带克隆的细胞被噬菌体T4感染后克隆的噬菌体T4 DNA的命运。
J Mol Biol. 1983 Oct 25;170(2):343-55. doi: 10.1016/s0022-2836(83)80152-1.
9
Activation and quantitative estimation of bacteriophage T4 late regulatory signal in cis- and transconditions.
Mol Gen Genet. 1992 May;233(1-2):319-21. doi: 10.1007/BF00587595.
10
Regulation of transcription in the segment of the bacteriophage T4 genome containing three of the head protein genes: plasmid-specific and phage chromosome-specific effects.噬菌体T4基因组中包含三个头部蛋白基因的片段的转录调控:质粒特异性和噬菌体染色体特异性效应。
Virology. 1984 Dec;139(2):283-94. doi: 10.1016/0042-6822(84)90374-x.

引用本文的文献

1
Strategies for achieving high-level expression of genes in Escherichia coli.在大肠杆菌中实现基因高水平表达的策略。
Microbiol Rev. 1996 Sep;60(3):512-38. doi: 10.1128/mr.60.3.512-538.1996.
2
Bacteriophage T4 as a surface display vector.噬菌体T4作为一种表面展示载体。
Virus Genes. 1995;10(2):173-7. doi: 10.1007/BF01702598.
3
Artificial mobile DNA element constructed from the EcoRI endonuclease gene.由EcoRI核酸内切酶基因构建的人工移动DNA元件。
Proc Natl Acad Sci U S A. 1992 Mar 1;89(5):1544-7. doi: 10.1073/pnas.89.5.1544.