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J Virol. 1972 May;9(5):776-84. doi: 10.1128/JVI.9.5.776-784.1972.
2
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J Virol. 1972 Dec;10(6):1170-8. doi: 10.1128/JVI.10.6.1170-1178.1972.

引用本文的文献

1
Mixed infections of Bacillus subtilis involving bacteriophage SPO2c 1 .枯草芽孢杆菌与噬菌体SPO2c 1的混合感染
J Virol. 1973 Jan;11(1):25-34. doi: 10.1128/JVI.11.1.25-34.1973.
2
Transcription during the development of bacteriophage phi 29: production of host- and phi 29-specific ribonucleic acid.噬菌体φ29发育过程中的转录:宿主特异性和φ29特异性核糖核酸的产生
J Virol. 1972 Dec;10(6):1170-8. doi: 10.1128/JVI.10.6.1170-1178.1972.
3
RNA polymerase from Bacillus amyloliquefaciens infected with phi29 bacteriophage.来自被phi29噬菌体感染的解淀粉芽孢杆菌的RNA聚合酶。
Proc Natl Acad Sci U S A. 1973 Aug;70(8):2234-7. doi: 10.1073/pnas.70.8.2234.
4
Abortive infection of lysogenic Bacillus subtilis 168(SPO2) by bacteriophage phi 1.噬菌体 phi 1 对溶源性枯草芽孢杆菌 168(SPO2) 的流产感染。
J Virol. 1974 Apr;13(4):870-80. doi: 10.1128/JVI.13.4.870-880.1974.
5
Isolation of a Bacillus thuringiensis RNA polymerase capable of transcribing crystal protein genes.一种能够转录晶体蛋白基因的苏云金芽孢杆菌RNA聚合酶的分离。
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4166-70. doi: 10.1073/pnas.85.12.4166.
6
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.

本文引用的文献

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CONTROL OF T2-SPECIFIC RNA SYNTHESIS.T2特异性RNA合成的调控
J Mol Biol. 1964 Jul;9:143-53. doi: 10.1016/s0022-2836(64)80096-6.
2
Membrane association by bacteriophage lambda-DNA: possible direct role of regulator gene N.噬菌体λ-DNA与膜的结合:调节基因N的可能直接作用
Nature. 1969 Sep 20;223(5212):1239-42. doi: 10.1038/2231239a0.
3
Process of infection with bacteriophage phiX174. XX. Attachment of the parental DNA of bacteriophage phiX174 to a fast-sedimenting cell component.噬菌体φX174的感染过程。XX. 噬菌体φX174的亲代DNA与快速沉降细胞成分的附着。
J Mol Biol. 1968 May 28;34(1):17-29. doi: 10.1016/0022-2836(68)90231-3.
4
Asymmetric distribution of the transcribing regions on the complementary strands of coliphage lambda DNA.大肠杆菌噬菌体λDNA互补链上转录区域的不对称分布。
Proc Natl Acad Sci U S A. 1967 Jun;57(6):1618-25. doi: 10.1073/pnas.57.6.1618.
5
RNA synthesis during bacteriophage SPO1 development: six classes of SPO1 RNA.噬菌体SPO1发育过程中的RNA合成:SPO1 RNA的六类
J Mol Biol. 1971 Apr 28;57(2):279-300. doi: 10.1016/0022-2836(71)90346-9.
6
Nucleic acid synthesis in Bacillus subtilis infected with bacteriophage beta-22.被噬菌体β - 22感染的枯草芽孢杆菌中的核酸合成。
J Virol. 1970 Oct;6(4):381-92. doi: 10.1128/JVI.6.4.381-392.1970.
7
Morphology and physiology of the intracellular development of Bacillus subtilis bacteriophage phi25.枯草芽孢杆菌噬菌体phi25细胞内发育的形态学与生理学
J Virol. 1970 Jul;6(1):114-24. doi: 10.1128/JVI.6.1.114-124.1970.
8
Differential expression of bacteriophage genomes in vegetative and sporulating cells of Bacillus subtilis.枯草芽孢杆菌营养细胞和芽孢形成细胞中噬菌体基因组的差异表达。
J Virol. 1967 Oct;1(5):935-47. doi: 10.1128/JVI.1.5.935-947.1967.
9
Isolation and properties of suppressor-sensitive mutants of Bacillus subtilis bacteriophage SP02.枯草芽孢杆菌噬菌体SP02抑制敏感突变体的分离与特性
J Virol. 1970 Jun;5(6):819-21. doi: 10.1128/JVI.5.6.819-821.1970.
10
Lack of nucleotide sequence relationship among the temperate bacteriophage SPO2, Bacillus subtilis, and virulent bacteriophages beta 3 and beta 22.温和噬菌体SPO2、枯草芽孢杆菌以及烈性噬菌体β3和β22之间不存在核苷酸序列关系。
J Virol. 1970 Jan;5(1):39-44. doi: 10.1128/JVI.5.1.39-44.1970.

噬菌体SPO2c 1感染的枯草芽孢杆菌中的核酸合成。

Nucleic acid synthesis in bacteriophage SPO2c 1 -infected Bacillus subtilis.

作者信息

Kolenbrander P E, Hemphill H E, Whiteley H R

出版信息

J Virol. 1972 May;9(5):776-84. doi: 10.1128/JVI.9.5.776-784.1972.

DOI:10.1128/JVI.9.5.776-784.1972
PMID:4623615
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC356373/
Abstract

The synthesis of host macromolecules was shut off very slowly and incompletely by bacteriophage SPO2c(1). No change in the rate of incorporation of radioactive precursors into protein and ribonucleic acid (RNA) could be detected after infection, and the rate of incorporation of thymidine was increased only slightly. The relative proportions of phage and host species of nucleic acids at various intervals in the latent period were determined by means of nucleic acid hybridization. Phage-specific RNA populations synthesized early were different from those synthesized late in the latent period. Host deoxyribonucleic acid (DNA) replication continued until 8 to 10 min after SPO2c(1) infection and then decreased markedly as phage-specific DNA synthesis was initiated. Host DNA was not degraded to trichloroacetic acid-soluble fragments, and its nucleotides were not found in either newly synthesized intracellular phage DNA or in progeny phage particles. The average burst size of SPO2c(1) was approximately 200 plaque-forming units per cell.

摘要

噬菌体SPO2c(1)能非常缓慢且不完全地阻断宿主大分子的合成。感染后,未检测到放射性前体掺入蛋白质和核糖核酸(RNA)的速率有变化,胸苷掺入速率仅略有增加。通过核酸杂交确定潜伏期不同时间间隔噬菌体和宿主核酸种类的相对比例。潜伏期早期合成的噬菌体特异性RNA群体与后期合成的不同。宿主脱氧核糖核酸(DNA)复制一直持续到SPO2c(1)感染后8至10分钟,然后随着噬菌体特异性DNA合成开始而显著下降。宿主DNA未降解为三氯乙酸可溶片段,其核苷酸也未出现在新合成的细胞内噬菌体DNA或子代噬菌体颗粒中。SPO2c(1)的平均裂解量约为每细胞200个噬菌斑形成单位。