• 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

相似文献

1
Isolation of specialized transducing bacteriophages carrying deletions of the regulatory region of the Escherichia coli K-12 tryptophan operon.携带大肠杆菌K-12色氨酸操纵子调控区缺失的特异性转导噬菌体的分离。
J Bacteriol. 1976 Oct;128(1):283-9. doi: 10.1128/jb.128.1.283-289.1976.
2
Isolation of specialized lambda transducing bacteriophages for flagellar genes (fla) of Escherichia coli K-12.用于大肠杆菌K-12鞭毛基因（fla）的特异性λ转导噬菌体的分离
J Virol. 1977 Jun;22(3):654-61. doi: 10.1128/JVI.22.3.654-661.1977.
3
In vitro synthesis of enzymes of the tryptophan operon of Escherichia coli.大肠杆菌色氨酸操纵子酶的体外合成
Mol Gen Genet. 1975;136(3):185-97. doi: 10.1007/BF00334014.
4
Isolation and characterization of specialized phi80 transducing phages carrying regions of the Salmonella typhimurium trp operon.携带鼠伤寒沙门氏菌色氨酸操纵子区域的特异性φ80转导噬菌体的分离与鉴定。
J Bacteriol. 1974 May;118(2):505-13. doi: 10.1128/jb.118.2.505-513.1974.
5
Isolation of specialized transducing bacteriophages carrying the structural genes of the hexuronate system in Escherichia coli K-12: exu region.在大肠杆菌K-12中携带己糖醛酸系统结构基因的特异性转导噬菌体的分离：exu区域
J Bacteriol. 1978 Feb;133(2):549-57. doi: 10.1128/jb.133.2.549-557.1978.
6
Isolation of specialized transducing bacteriophages for gluconate 6-phosphate dehydrogenase (gnd) of Escherichia coli.用于分离大肠杆菌6-磷酸葡萄糖酸脱氢酶（gnd）的特异性转导噬菌体。
J Bacteriol. 1974 Feb;117(2):468-76. doi: 10.1128/jb.117.2.468-476.1974.
7
Insertion of bacteriophage lambda into the deo operon of Escherichia coli K-12 and isolation of plaque-forming lambdadeo+ transducing bacteriophages.将噬菌体λ插入大肠杆菌K-12的deo操纵子并分离形成噬菌斑的λdeo⁺转导噬菌体。
J Bacteriol. 1978 Nov;136(2):668-81. doi: 10.1128/jb.136.2.668-681.1978.
8
Isolation and characterization of mutations creating high-efficiency transcription initiation signals within the trp operon of Escherichia coli.大肠杆菌色氨酸操纵子内产生高效转录起始信号的突变的分离与鉴定。
J Bacteriol. 1976 Nov;128(2):557-72. doi: 10.1128/jb.128.2.557-572.1976.
9
Naturally occurring sites within the Shigella dysenteriae tryptophan operon severely limit tryptophan biosynthesis.痢疾志贺氏菌色氨酸操纵子内的天然存在位点严重限制色氨酸的生物合成。
J Bacteriol. 1976 May;126(2):668-78. doi: 10.1128/jb.126.2.668-678.1976.
10
Isolation of specialized transducing bacteriophage lambda carrying genes of the L-arabinose operon of Escherichia coli B/r.携带大肠杆菌B/r L-阿拉伯糖操纵子基因的特异性转导噬菌体λ的分离
J Bacteriol. 1975 Sep;123(3):1043-54. doi: 10.1128/jb.123.3.1043-1054.1975.

引用本文的文献

1
Plaque assay for lambda transducing phage carrying the E. coli metB gene.携带大肠杆菌metB基因的λ转导噬菌体的噬菌斑测定。
Mol Gen Genet. 1983;190(3):527-30. doi: 10.1007/BF00331087.
2
Temperate and virulent forms of phage theta attacking Bacillus licheniformis.攻击地衣芽孢杆菌的θ噬菌体的温和型和烈性形式。
Mol Gen Genet. 1978 Apr 17;160(3):311-7. doi: 10.1007/BF00332974.
3
HindII and HindIII restriction maps of the attphi80-tonB-trp region of the Escherichia coli genome, and location of the tonB gene.大肠杆菌基因组attphi80-tonB-trp区域的HindII和HindIII限制性图谱以及tonB基因的位置。
J Bacteriol. 1978 Dec;136(3):1165-73. doi: 10.1128/jb.136.3.1165-1173.1978.
4
Tryptophan-transducing bacteriophages: in vitro studies with restriction endonucleases HindII + III and Escherichia coli ribonucleic acid polymerase.色氨酸转导噬菌体：用限制性内切核酸酶HindII + III和大肠杆菌核糖核酸聚合酶进行的体外研究
J Bacteriol. 1977 Oct;132(1):270-81. doi: 10.1128/jb.132.1.270-281.1977.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Polarity and enzyme functions in mutants of the first three genes of the tryptophan operon of Escherichia coli.大肠杆菌色氨酸操纵子前三个基因的突变体中的极性和酶功能。
Genetics. 1971 Dec;69(4):409-33. doi: 10.1093/genetics/69.4.409.
3
Operator mutants of the tryptophan operon in Escherichia coli.大肠杆菌中色氨酸操纵子的操纵基因突变体。
J Mol Biol. 1969 Jan 14;39(1):159-79. doi: 10.1016/0022-2836(69)90340-4.
4
Evidence for the order promoter-operator-first structural gene in the tryptophan operon of Salmonella.沙门氏菌色氨酸操纵子中启动子-操纵基因-首个结构基因顺序的证据。
J Mol Biol. 1970 Aug;51(3):709-15. doi: 10.1016/0022-2836(70)90019-7.
5
Genetic evidence that the operator locus is distinct from the the z gene in the lac operon of Escherichia coli.关于大肠杆菌乳糖操纵子中操纵基因位点与z基因不同的遗传学证据。
J Mol Biol. 1969 Jul 14;43(1):215-8. doi: 10.1016/0022-2836(69)90090-4.
6
The promoter-operator region of the lac operon of Escherichia coli.大肠杆菌乳糖操纵子的启动子-操纵基因区域。
J Mol Biol. 1968 Dec;38(3):413-20. doi: 10.1016/0022-2836(68)90395-1.
7
Anthranilate synthetase, an enzyme specified by the tryptophan operon of Escherichia coli: purification and characterization of component I.邻氨基苯甲酸合成酶，一种由大肠杆菌色氨酸操纵子所编码的酶：组分I的纯化及特性分析
J Bacteriol. 1969 Feb;97(2):725-33. doi: 10.1128/jb.97.2.725-733.1969.
8
New controlling element in the Lac operon of E. coli.大肠杆菌乳糖操纵子中的新调控元件。
Nature. 1968 Mar 2;217(5131):825-7. doi: 10.1038/217825a0.
9
Operator and promoter are separate in the tryptophan operon in Salmonella typhimurium.在鼠伤寒沙门氏菌的色氨酸操纵子中，操纵基因和启动子是分开的。
Nature. 1974 Sep 13;251(5471):119-23. doi: 10.1038/251119a0.
10
The location of the repressor binding sites in the lac operon.阻遏蛋白结合位点在乳糖操纵子中的位置。
Proc Natl Acad Sci U S A. 1974 Jun;71(6):2314-8. doi: 10.1073/pnas.71.6.2314.

携带大肠杆菌K-12色氨酸操纵子调控区缺失的特异性转导噬菌体的分离。

Isolation of specialized transducing bacteriophages carrying deletions of the regulatory region of the Escherichia coli K-12 tryptophan operon.

作者信息

Jones B B, Reznikoff W S

出版信息

J Bacteriol. 1976 Oct;128(1):283-9. doi: 10.1128/jb.128.1.283-289.1976.

DOI:10.1128/jb.128.1.283-289.1976
PMID:789335
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC232854/
Abstract

A lysogen of a wild-type strain of Escherichia coli K-12 carrying a heat-inducible lambda-phi80 hybrid prophage was induced to yield transducing phages carrying all of the structural genes of the tryptophan operon. The presence or absence of elements of the trp regulatory region was determined by examining the effects of lambda genes N and cI on trp gene expression. The phages were further characterized by transduction studies and by examining anthranilate synthetase (EC 4.1.3.27) (TRYPE+D) synthesis in the presence of the lambda cI product. A number of phages deleted for the trp promoter were found. Recombination studies between trpOc bacteria and the transducing phages have yielded information that can be used to order the trp end points of some phages and to provide an estimate of the size of the trp promoter region.

摘要

携带热诱导型λ-φ80杂交原噬菌体的大肠杆菌K-12野生型菌株的溶原菌被诱导产生携带色氨酸操纵子所有结构基因的转导噬菌体。通过检测λ基因N和cI对trp基因表达的影响来确定trp调控区元件的存在与否。通过转导研究以及在λ cI产物存在的情况下检测邻氨基苯甲酸合成酶（EC 4.1.3.27）（TRYPE+D）的合成，对这些噬菌体进行了进一步表征。发现了一些缺失trp启动子的噬菌体。trpOc细菌与转导噬菌体之间的重组研究提供了可用于确定某些噬菌体trp端点顺序并估计trp启动子区域大小的信息。