• 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

携带pUB110与噬菌体phi 105 DNA的EcoRI片段F的质粒嵌合体的枯草芽孢杆菌细胞对噬菌体phi 105的超感染免疫表达。

Expression of superinfection immunity to bacteriophage phi 105 by Bacillus subtilis cells carrying a plasmic chimera of pUB110 and EcoRI fragment F of phi 105 DNA.

作者信息

Cully D F, Garro A J

出版信息

J Virol. 1980 Jun;34(3):789-91. doi: 10.1128/JVI.34.3.789-791.1980.

DOI:10.1128/JVI.34.3.789-791.1980
PMID:6770103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC288768/
Abstract

A 2.1-megadalton, EcoRI-generated fragment of Bacillus subtilis phage phi 105 DNA was cloned into plasmid pUB110. The hybrid plasmid produces a biologically active product which renders B. subtilis immune to infection by phi 105.

摘要

将枯草芽孢杆菌噬菌体φ105 DNA经EcoRI酶切产生的一个2.1兆道尔顿的片段克隆到质粒pUB110中。该杂种质粒产生一种具有生物活性的产物，可使枯草芽孢杆菌对φ105的感染具有免疫性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2321/288768/2bdc472d6e6d/jvirol00174-0214-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2321/288768/2bdc472d6e6d/jvirol00174-0214-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2321/288768/2bdc472d6e6d/jvirol00174-0214-a.jpg

相似文献

1
Expression of superinfection immunity to bacteriophage phi 105 by Bacillus subtilis cells carrying a plasmic chimera of pUB110 and EcoRI fragment F of phi 105 DNA.携带pUB110与噬菌体phi 105 DNA的EcoRI片段F的质粒嵌合体的枯草芽孢杆菌细胞对噬菌体phi 105的超感染免疫表达。
J Virol. 1980 Jun;34(3):789-91. doi: 10.1128/JVI.34.3.789-791.1980.
2
Transductional selection of cloned bacteriophage phi 105 and SP02 deoxyribonucleic acids in Bacillus subtilis.枯草芽孢杆菌中克隆噬菌体φ105和SP02脱氧核糖核酸的转导选择
J Bacteriol. 1980 Aug;143(2):879-86. doi: 10.1128/jb.143.2.879-886.1980.
3
The temperate B. subtilis phage phi 105 genome contains at least two distinct regions encoding superinfection immunity.温和型枯草芽孢杆菌噬菌体phi 105基因组包含至少两个编码超感染免疫的不同区域。
Mol Gen Genet. 1985;200(3):490-2. doi: 10.1007/BF00425736.
4
Cloning of sporulation gene spoIVC in Bacillus subtilis.枯草芽孢杆菌中孢子形成基因spoIVC的克隆
Mol Gen Genet. 1985;199(3):471-5. doi: 10.1007/BF00330760.
5
Cloning of sporulation gene spoIIG in Bacillus subtilis.枯草芽孢杆菌中芽孢形成基因spoIIG的克隆
J Bacteriol. 1984 May;158(2):507-12. doi: 10.1128/jb.158.2.507-512.1984.
6
Cloning and expression in Escherichia coli of the gene coding for the protein linked to the ends of Bacillus subtilis phage phi 29 DNA.枯草芽孢杆菌噬菌体 phi 29 DNA 末端连接蛋白编码基因在大肠杆菌中的克隆与表达。
Gene. 1983 Jan-Feb;21(1-2):65-76. doi: 10.1016/0378-1119(83)90148-8.
7
Thermo-inducible gene expression in Bacillus subtilis using transcriptional regulatory elements from temperate phage phi 105.利用温和噬菌体phi 105的转录调控元件在枯草芽孢杆菌中进行热诱导基因表达。
Gene. 1984 Dec;32(1-2):181-94. doi: 10.1016/0378-1119(84)90046-5.
8
Characterization, overproduction and purification of the product of gene 1 of Bacillus subtilis phage phi 29.枯草芽孢杆菌噬菌体φ29基因1产物的特性鉴定、过量表达及纯化
Gene. 1989 Apr 30;77(2):195-204. doi: 10.1016/0378-1119(89)90067-x.
9
Overproduction and purification of the connector protein of Bacillus subtilis phage phi 29.枯草芽孢杆菌噬菌体phi 29连接蛋白的过量生产与纯化
Nucleic Acids Res. 1984 Mar 12;12(5):2351-65. doi: 10.1093/nar/12.5.2351.
10
Construction and characterization of recombinant phage phi 105 d(Cmrmet) for cloning in Bacillus subtilis.用于在枯草芽孢杆菌中克隆的重组噬菌体 phi 105 d（Cmrmet）的构建与特性分析
J Gen Microbiol. 1984 Aug;130(8):2155-64. doi: 10.1099/00221287-130-8-2155.

引用本文的文献

1
Anti-SOS effects induced in Bacillus subtilis by a phi 105 mutant prophage.由phi 105突变前噬菌体在枯草芽孢杆菌中诱导产生的抗SOS效应。
Arch Microbiol. 1993;160(6):486-91. doi: 10.1007/BF00245310.
2
Cloning restriction fragments that promote expression of a gene in Bacillus subtilis.克隆促进基因在枯草芽孢杆菌中表达的限制性片段。
J Bacteriol. 1981 Jun;146(3):1162-5. doi: 10.1128/jb.146.3.1162-1165.1981.
3
Cloning of the Bacillus subtilis recE+ gene and functional expression of recE+ in B. subtilis.枯草芽孢杆菌recE⁺基因的克隆及其在枯草芽孢杆菌中的功能表达。

本文引用的文献

1
A dye-buoyant-density method for the detection and isolation of closed circular duplex DNA: the closed circular DNA in HeLa cells.一种用于检测和分离闭环双链DNA的染料浮力密度法：HeLa细胞中的闭环DNA
Proc Natl Acad Sci U S A. 1967 May;57(5):1514-21. doi: 10.1073/pnas.57.5.1514.
2
Studies on the loss and the restoration of the transforming activity of the deoxyribonucleic acid of Bacillus subtilis.枯草芽孢杆菌脱氧核糖核酸转化活性的丧失与恢复研究
Biochim Biophys Acta. 1967 Nov 21;149(1):199-219. doi: 10.1016/0005-2787(67)90702-2.
3
General method for the isolation of plasmid deoxyribonucleic acid.
J Bacteriol. 1988 Jan;170(1):335-44. doi: 10.1128/jb.170.1.335-344.1988.
4
Bacteriophage SPO2-mediated plasmid transduction in transpositional mutagenesis within the genus Bacillus.
J Bacteriol. 1985 Dec;164(3):1283-7. doi: 10.1128/jb.164.3.1283-1287.1985.
5
The temperate B. subtilis phage phi 105 genome contains at least two distinct regions encoding superinfection immunity.温和型枯草芽孢杆菌噬菌体phi 105基因组包含至少两个编码超感染免疫的不同区域。
Mol Gen Genet. 1985;200(3):490-2. doi: 10.1007/BF00425736.
6
Nucleotide sequence and mutational analysis of an immunity repressor gene from Bacillus subtilis temperate phage phi 105.枯草芽孢杆菌温和噬菌体phi 105免疫抑制基因的核苷酸序列及突变分析
Nucleic Acids Res. 1985 Aug 12;13(15):5441-55. doi: 10.1093/nar/13.15.5441.
7
Thermoinducible transcription system for Bacillus subtilis that utilizes control elements from temperate phage phi 105.利用温和噬菌体phi 105控制元件的枯草芽孢杆菌热诱导转录系统。
J Bacteriol. 1985 Sep;163(3):1101-8. doi: 10.1128/jb.163.3.1101-1108.1985.
质粒脱氧核糖核酸的分离通用方法。
J Bacteriol. 1973 Nov;116(2):1064-6. doi: 10.1128/jb.116.2.1064-1066.1973.
4
Deletions and insertions in the immunity region of coliphage lambda: revised measurement of the promoter-startpoint distance.λ噬菌体免疫区域中的缺失和插入：启动子-起始点距离的修订测量
Virology. 1974 Dec;62(2):458-71. doi: 10.1016/0042-6822(74)90407-3.
5
Relationship between lysogeny, spontaneous induction, and transformation efficiencies in Bacillus subtilis.枯草芽孢杆菌中溶原性、自发诱导与转化效率之间的关系。
J Bacteriol. 1974 Dec;120(3):1256-9. doi: 10.1128/jb.120.3.1256-1259.1974.
6
Construction of a colicin E1-R factor composite plasmid in vitro: means for amplification of deoxyribonucleic acid.体外构建大肠杆菌素E1-R因子复合质粒：脱氧核糖核酸扩增方法
J Bacteriol. 1975 Jan;121(1):354-62. doi: 10.1128/jb.121.1.354-362.1975.
7
Molecular cloning of genetically active fragments of Bacillus DNA in Bacillus subtilis and properties of the vector plasmid pUB110.枯草芽孢杆菌中芽孢杆菌属DNA基因活性片段的分子克隆及载体质粒pUB110的特性
Proc Natl Acad Sci U S A. 1978 Mar;75(3):1423-7. doi: 10.1073/pnas.75.3.1423.
8
Characterization of Staphylococcus aureus plasmids introduced by transformation into Bacillus subtilis.通过转化导入枯草芽孢杆菌的金黄色葡萄球菌质粒的特性分析。
J Bacteriol. 1978 Apr;134(1):318-29. doi: 10.1128/jb.134.1.318-329.1978.
9
Fragmentation of Bacillus bacteriophage phi105 DNA by complementary single-stranded DNA in the cohesive ends of the molecule.芽孢杆菌噬菌体phi105 DNA在分子粘性末端被互补单链DNA片段化。
J Virol. 1977 Aug;23(2):377-83. doi: 10.1128/JVI.23.2.377-383.1977.
10
Specificity of substrate recognition by the EcoRI restriction endonuclease.EcoRI限制性内切核酸酶对底物识别的特异性
Proc Natl Acad Sci U S A. 1975 Sep;72(9):3310-4. doi: 10.1073/pnas.72.9.3310.