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1
Protease-sensitive transfection of Bacillus subtilis with bacteriophage GA-1 DNA: a probable case of heterologous transfection.用噬菌体GA-1 DNA对枯草芽孢杆菌进行蛋白酶敏感型转染:一个可能的异源转染案例。
J Virol. 1974 Mar;13(3):584-9. doi: 10.1128/JVI.13.3.584-589.1974.
2
Bacteriophage transformation of PBS2 in Bacillus subtilis.枯草芽孢杆菌中PBS2的噬菌体转化
J Virol. 1975 Jan;15(1):16-21. doi: 10.1128/JVI.15.1.16-21.1975.
3
Transfecting deoxyribonucleic acid of Bacillus bacteriophage phi 29 that is protease sensitive.转染对蛋白酶敏感的芽孢杆菌噬菌体 phi 29 的脱氧核糖核酸。
Proc Natl Acad Sci U S A. 1972 Jun;69(6):1555-9. doi: 10.1073/pnas.69.6.1555.
4
Characterization of temperate bacteriophages of Bacillus subtilis by the restriction endonuclease EcoRI: evidence for three different temperate bacteriophages.用限制性内切酶EcoRI对枯草芽孢杆菌的温和噬菌体进行鉴定:三种不同温和噬菌体的证据
J Virol. 1974 Oct;14(4):1013-6. doi: 10.1128/JVI.14.4.1013-1016.1974.
5
Structure of Bacillus subtilis bacteriophage phi25 and phi25 deoxyribonucleic acid.枯草芽孢杆菌噬菌体phi25及其脱氧核糖核酸的结构
J Virol. 1970 Jul;6(1):107-13. doi: 10.1128/JVI.6.1.107-113.1970.
6
Effect of lysogeny on transfection and transfection enhancement in Bacillus subtilis.溶源性对枯草芽孢杆菌中转染及转染增强的影响。
J Bacteriol. 1975 Jan;121(1):305-12. doi: 10.1128/jb.121.1.305-312.1975.
7
Molecular fate of heterologous bacterial DNA in competent Bacillus subtilis. I. Processing of B. pumilus and B. licheniformis DNA in B. subtilis.感受态枯草芽孢杆菌中异源细菌DNA的分子命运。I. 短小芽孢杆菌和地衣芽孢杆菌DNA在枯草芽孢杆菌中的加工处理
Genetics. 1982 Jun;101(2):179-88. doi: 10.1093/genetics/101.2.179.
8
Cotransduction and cotransformation of genetic markers in Bacillus subtilis and Bacillus licheniformis.枯草芽孢杆菌和地衣芽孢杆菌中遗传标记的共转导与共转化
J Bacteriol. 1969 Nov;100(2):1027-36. doi: 10.1128/jb.100.2.1027-1036.1969.
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INCORPORATION OF BACTERIOPHAGE GENOME BY SPORES OF BACILLUS SUBTILIS.枯草芽孢杆菌芽孢对噬菌体基因组的整合
J Bacteriol. 1964 Jun;87(6):1499-502. doi: 10.1128/jb.87.6.1499-1502.1964.
10
Transfection of Bacillus subtilis with bacteriophage H1 DNA: fate of transfecting DNA and transfection enhancement in B. subtilis uur+ and uur- strains.用噬菌体H1 DNA转染枯草芽孢杆菌:转染DNA的命运以及在枯草芽孢杆菌uur +和uur -菌株中转染增强情况
Mol Gen Genet. 1974;128(1):55-72. doi: 10.1007/BF00267294.

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In vivo DNA binding of bacteriophage GA-1 protein p6.噬菌体GA-1蛋白p6的体内DNA结合
J Bacteriol. 2007 Nov;189(22):8024-33. doi: 10.1128/JB.01047-07. Epub 2007 Sep 14.
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Analysis of early promoters of the Bacillus bacteriophage GA-1.芽孢杆菌噬菌体GA-1早期启动子的分析
J Bacteriol. 2001 Dec;183(23):6965-70. doi: 10.1128/JB.183.23.6965-6970.2001.
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Phi29 family of phages.Phi29噬菌体家族。
Microbiol Mol Biol Rev. 2001 Jun;65(2):261-87 ; second page, table of contents. doi: 10.1128/MMBR.65.2.261-287.2001.
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Differential functional behavior of viral phi29, Nf and GA-1 SSB proteins.病毒φ29、Nf和GA-1单链结合蛋白的差异功能行为。
Nucleic Acids Res. 2000 May 15;28(10):2034-42. doi: 10.1093/nar/28.10.2034.
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Terminal proteins and short inverted terminal repeats of the small Bacillus bacteriophage genomes.小型芽孢杆菌噬菌体基因组的末端蛋白和短反向末端重复序列
Proc Natl Acad Sci U S A. 1981 Apr;78(4):2596-600. doi: 10.1073/pnas.78.4.2596.
6
Protease-sensitive transfection of Streptococcus pneumoniae with bacteriophage Cp-1 DNA.用噬菌体Cp-1 DNA对肺炎链球菌进行蛋白酶敏感转染。
J Virol. 1983 Dec;48(3):721-30. doi: 10.1128/JVI.48.3.721-730.1983.
7
Physical arrangement of suppressor-sensitive mutations of Bacillus phage M2.芽孢杆菌噬菌体M2抑制敏感突变的物理排列
Mol Gen Genet. 1981;184(2):180-2. doi: 10.1007/BF00272902.
8
DNA-protein complex in circular DNA from Bacillus bacteriophage GA-1.来自芽孢杆菌噬菌体GA-1的环状DNA中的DNA-蛋白质复合物。
J Virol. 1976 May;18(2):783-4. doi: 10.1128/JVI.18.2.783-784.1976.
9
Bacteriophages of Bacillus subtilis.枯草芽孢杆菌噬菌体
Bacteriol Rev. 1975 Sep;39(3):257-315. doi: 10.1128/br.39.3.257-315.1975.
10
Bacteriophage phi29 terminal protein: its association with the 5' termini of the phi29 genome.噬菌体φ29末端蛋白:它与φ29基因组5'末端的关联
J Virol. 1978 Dec;28(3):895-904. doi: 10.1128/JVI.28.3.895-904.1978.

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Characterization of Temperate Bacillus Bacteriophage phi105.温和型芽孢杆菌噬菌体phi105的特性分析
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TRANSFORMATION OF BIOCHEMICALLY DEFICIENT STRAINS OF BACILLUS SUBTILIS BY DEOXYRIBONUCLEATE.脱氧核糖核酸对枯草芽孢杆菌生化缺陷菌株的转化
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Determination of the base composition of deoxyribonucleic acid from its buoyant density in CsCl.根据脱氧核糖核酸在氯化铯中的浮力密度测定其碱基组成。
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Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperature.根据热变性温度确定脱氧核糖核酸的碱基组成
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BACTERIOPHAGE DEOXYRIBONUCLEATE INFECTION OF COMPETENT BACILLUS SUBTILIS.感受态枯草芽孢杆菌的噬菌体脱氧核糖核酸感染
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CONFIGURATION OF TRANSFORMING DEOXYRIBONUCLEIC ACID DURING ENTRY INTO BACILLUS SUBTILIS.转化脱氧核糖核酸进入枯草芽孢杆菌过程中的构型
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POLYOMA VIRUS: PRODUCTION IN BACILLUS SUBTILIS.多瘤病毒:在枯草芽孢杆菌中的产生
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TRANSDUCTION OF BACILLUS LICHENIFORMIS AND BACILLUS SUBTILIS BY EACH OF TWO PHAGES.两种噬菌体对地衣芽孢杆菌和枯草芽孢杆菌的转导作用
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Factors affecting transformation of Bacillus licheniformis.影响地衣芽孢杆菌转化的因素。
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10
Reexamination of the association between melting point, buoyant density, and chemical base composition of deoxyribonucleic acid.对脱氧核糖核酸的熔点、浮力密度和化学碱基组成之间关联的重新审视。
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用噬菌体GA-1 DNA对枯草芽孢杆菌进行蛋白酶敏感型转染:一个可能的异源转染案例。

Protease-sensitive transfection of Bacillus subtilis with bacteriophage GA-1 DNA: a probable case of heterologous transfection.

作者信息

Arwert F, Venema G

出版信息

J Virol. 1974 Mar;13(3):584-9. doi: 10.1128/JVI.13.3.584-589.1974.

DOI:10.1128/JVI.13.3.584-589.1974
PMID:4207247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC355341/
Abstract

The host bacterium of bacteriophage GA-1, Bacillus sp. G1R, was compared with respect to its taxonomic relationship to Bacillus subtilis, B. licheniformis, and B. pumilis. The physiological-biochemical properties of Bacillus sp. G1R are equal to those of B. licheniformis, but the thermal denaturation midpoint of G1R DNA differs by 3 C and the buoyant density by 0.005 g/cm(3) from that of B. licheniformis. Transformation with G1R donor DNA was neither observed in B. licheniformis nor in B. subtilis-competent recipients. Bacteriophage GA-1 shows neither infectivity on B. licheniformis nor on B. subtilis. However, infection of competent B. subtilis cultures with phenol-extracted GA-1 DNA results in the production of infective GA-1 particles. The transfecting activity of GA-1 DNA is destroyed by treatment with proteolytic enzymes. Resistance of transfecting DNA to inactivation by trypsin develops earlier than that to inactivation by DNase. Protease-treated GA-1 DNA competes with transforming DNA to approximately the same extent as does untreated GA-1 DNA, suggesting that uptake of GA-1 DNA is not affected by protease treatment. CsCl density gradient centrifugation reveals that the density of trypsinized GA-1 DNA is 0.004 g/cm(3) greater than that of untreated DNA.

摘要

噬菌体GA - 1的宿主细菌芽孢杆菌属G1R,就其与枯草芽孢杆菌、地衣芽孢杆菌和短小芽孢杆菌的分类关系进行了比较。芽孢杆菌属G1R的生理生化特性与地衣芽孢杆菌相同,但G1R DNA的热变性中点与地衣芽孢杆菌相差3℃,浮力密度相差0.005 g/cm³。在地衣芽孢杆菌和枯草芽孢杆菌感受态受体中均未观察到用G1R供体DNA进行的转化。噬菌体GA - 1对地衣芽孢杆菌和枯草芽孢杆菌均无感染性。然而,用酚提取的GA - 1 DNA感染枯草芽孢杆菌感受态培养物会导致产生有感染性的GA - 1颗粒。GA - 1 DNA的转染活性经蛋白水解酶处理后被破坏。转染DNA对胰蛋白酶失活的抗性比对DNA酶失活的抗性出现得更早。经蛋白酶处理的GA - 1 DNA与转化DNA的竞争程度与未处理的GA - 1 DNA大致相同,这表明GA - 1 DNA的摄取不受蛋白酶处理的影响。氯化铯密度梯度离心显示,经胰蛋白酶处理的GA - 1 DNA的密度比未处理的DNA高0.004 g/cm³。