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枯草芽孢杆菌与噬菌体SPO2c 1的混合感染

Mixed infections of Bacillus subtilis involving bacteriophage SPO2c 1 .

作者信息

Kolenbrander P E, Hemphill H E, Whiteley H R

出版信息

J Virol. 1973 Jan;11(1):25-34. doi: 10.1128/JVI.11.1.25-34.1973.

Abstract

The synthesis of ribonucleic acid (RNA) and deoxyribonucleic acid (DNA) was studied in Bacillus subtilis cells mixedly infected with phages SPO2c(1) and either SP82 or beta22. It was found that cells preinfected 5 min with either beta22 or SP82 could not support significant amounts of RNA or DNA synthesis from the genome of superinfecting SPO2c(1). Conversely, cells preinfected with SPO2c(1) remained susceptible to superinfection even at the midpoint of the latent period. When SP82 was added to cells preinfected 5 min with SPO2c(1), the former greatly inhibited the replication and transcription of the SPO2c(1), DNA, but if superinfection with SP82 was delayed until the 15th min of the SPO2c(1) latent period, RNA and DNA specific for both phages were synthesized. Both viral genomes were transcribed throughout the remainder of the lytic cycle when beta22 was added to cells preinfected either 5 or 15 min with SPO2c(1). In both the SPO2c(1)-SP82 and the SPO2c(1)-beta22 mixed infections, the types of phage-specific RNAs synthesized at a given time in the latent period were similar to those synthesized in single infections with each phage. The association of SPO2c(1) DNA with the host cell membrane in certain of the doubly infected cells was different from that observed in singly infected cells. In the SPO2c(1)-SP82 infection, SPO2c(1) DNA was not released from the membrane; in the SPO2c(1)-beta22 mixed infections, significantly less SPO2c(1) DNA was membrane-bound when beta22 was added before SPO2c(1). However, binding and release of SPO2c(1) DNA was normal in cells infected first with SPO2c(1) and then with beta22. The synthesis of phage-specific nucleic acids and the binding of phage DNA to the membrane are discussed with respect to dominance relationships among these phages.

摘要

对用噬菌体SPO2c(1)与SP82或β22混合感染的枯草芽孢杆菌细胞中的核糖核酸(RNA)和脱氧核糖核酸(DNA)合成进行了研究。发现用β22或SP82预感染5分钟的细胞不能支持来自超感染的SPO2c(1)基因组的大量RNA或DNA合成。相反,用SPO2c(1)预感染的细胞即使在潜伏期的中点仍易受超感染。当将SP82添加到用SPO2c(1)预感染5分钟的细胞中时,前者极大地抑制了SPO2c(1) DNA的复制和转录,但如果将SP82的超感染延迟到SPO2c(1)潜伏期的第15分钟,则会合成两种噬菌体特有的RNA和DNA。当将β22添加到用SPO2c(1)预感染5分钟或15分钟的细胞中时,两种病毒基因组在整个裂解周期的其余时间都进行转录。在SPO2c(1)-SP82和SPO2c(1)-β22混合感染中,在潜伏期给定时间合成的噬菌体特异性RNA类型与用每种噬菌体进行单一感染时合成的相似。在某些双重感染的细胞中,SPO2c(1) DNA与宿主细胞膜的结合与在单一感染细胞中观察到的不同。在SPO2c(1)-SP82感染中,SPO2c(1) DNA没有从膜上释放;在SPO2c(1)-β22混合感染中,当在SPO2c(1)之前添加β22时,与膜结合的SPO2c(1) DNA明显减少。然而,在先用SPO2c(1)感染然后用β22感染的细胞中,SPO2c(1) DNA的结合和释放是正常的。关于这些噬菌体之间的优势关系,讨论了噬菌体特异性核酸的合成以及噬菌体DNA与膜的结合。

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