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雄性特异性噬菌体在携带源自大肠杆菌的F基因型的巴斯德氏菌中的生长情况。

Growth of male-specific bacteriophage in Pasteurella harboring F-genotes derived from Escherichia coli.

作者信息

Molnar D M, Lawton W D

出版信息

J Virol. 1971 Jan;7(1):24-8. doi: 10.1128/JVI.7.1.24-28.1971.

Abstract

When either the F' lac or the F'Cm plasmid was transferred from Escherichia coli into Pasteurella pseudotuberculosis, the P. pseudotuberculosis (F') strains isolated formed plaques with both ribonucleic acid (RNA)-containing and deoxyribonucleic acid-containing male-specific phages. In contrast, strains of P. pestis harboring E. coli (F') plasmids did not form plaques with male-specific phages, although such strains permitted limited multiplication of phage MS2. The adsorption and burst size of MS2 were approximately the same in both species of Pasteurella, but the per cent of adsorbed MS2 that produced infective centers was much lower in P. pestis than it was in P. pseudotuberculosis. By use of a sib-selection technique of P. pestis (F') cells, we isolated a single clone that could form MS2 plaques. (32)P-labeled MS2 adsorbed equally to and its RNA penetrated equally into both the typical MS2-nonpermissive P. pestis cells and the MS2-permissive P. pestis cells. No host modification occurred after growth of MS2 in Pasteurella. Our data suggest that typical strains of P. pestis inhibit the intracellular development of phage MS2.

摘要

当F'lac或F'Cm质粒从大肠杆菌转移到假结核耶尔森氏菌中时,分离得到的假结核耶尔森氏菌(F')菌株能与含核糖核酸(RNA)和含脱氧核糖核酸的雄性特异性噬菌体形成噬菌斑。相比之下,携带大肠杆菌(F')质粒的鼠疫耶尔森氏菌菌株不能与雄性特异性噬菌体形成噬菌斑,尽管这类菌株能使噬菌体MS2有限增殖。MS2在两种耶尔森氏菌中的吸附和裂解量大致相同,但在鼠疫耶尔森氏菌中产生感染中心的吸附MS2的百分比远低于假结核耶尔森氏菌。通过对鼠疫耶尔森氏菌(F')细胞采用同胞选择技术,我们分离出了一个能形成MS2噬菌斑的单一克隆。用(32)P标记的MS2对典型的非MS2允许性鼠疫耶尔森氏菌细胞和MS2允许性鼠疫耶尔森氏菌细胞的吸附相同,其RNA的渗透也相同。MS2在耶尔森氏菌中生长后未发生宿主修饰。我们的数据表明,典型的鼠疫耶尔森氏菌菌株会抑制噬菌体MS2在细胞内的发育。

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本文引用的文献

2
[Transfer of the sex episome from Escherichia coli to Pasteurella pestis].
C R Hebd Seances Acad Sci. 1962 May 14;254:3589-90.
6
Sex hair (F-pili) mutants of E. coli.大肠杆菌的性菌毛(F菌毛)突变体
Biochem Biophys Res Commun. 1967 May 5;27(3):412-6. doi: 10.1016/s0006-291x(67)80115-3.

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