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几种原噬菌体对福氏痢疾杆菌遗传行为的影响。

The influence of several prophages on the genetic behavior of Flexner dysentery bacteria.

作者信息

Petrovskaia V G, Nevskaia N A

出版信息

Genetika. 1975;11(10):61-6.

PMID:773758
Abstract

In conjugation experiments of Escherichia coli K-12 Hfr strains and converted clones of Shigella flexneri var. y(-:3,4) that had acquired the capacity to synthesize type of antigens IV or V it is confirmed that the locus linked to lac-pro region in Sh. flexneri chromosome called Tp locus is a site of an attachment of prophages responsible for certain type specific antigens. Lac+ hybrids of the clone converted by phage IV lost the type specific antigen IV with the frequency comparable with the loss of the aforementioned antigen by wild strains of Sh. flexneri ser 4 in similar experiments carried out previously (90,8% and 97% respectively). Lac+ hybrids of the clones converted by phage V did not lose the type antigen that corresponded to the behaviour of wild strains of serotype 5b (V: 7,8) with double lysogenicity. It was shown that the clones converted by the aforementioned phage V had acquired an immunity not only to phage V, but to phage 7,8 as well. An independent segregation of immunity to phages V and 7,8 in lac+ hybrids of the converted clone was observed. It indicates that donor strain NTCC 595/52 carries two prophages, V and "defect" 7,8 (not expressing factor 7,8). A maintenance of antigen V observed in lac+ hybrids of the converted clone in this case confirms previous suggestions that an attachment of prophage 7,8 creates a state of some inhomology in this region disturbing the recombination process. The converting phage V isolated from the strain NTCC 595/52 is probably recombinant. An analysis of the hybrid classes allows to suggest the following approximate order of markers of the prophage on the chromosome of the converted clone: aV--imm V--imm 7,8--lac.

摘要

在大肠杆菌K-12 Hfr菌株与弗氏志贺氏菌变种y(-:3,4)的转化克隆进行的接合实验中,这些转化克隆已获得合成IV型或V型抗原的能力,结果证实,弗氏志贺氏菌染色体中与lac-pro区域相连的位点(称为Tp位点)是负责某些型特异性抗原的原噬菌体的附着位点。经噬菌体IV转化的克隆的Lac+杂种失去型特异性抗原IV的频率,与先前在类似实验中弗氏志贺氏菌血清型4的野生菌株失去上述抗原的频率相当(分别为90.8%和97%)。经噬菌体V转化的克隆的Lac+杂种没有失去与具有双重溶原性的血清型5b(V:7,8)野生菌株行为相对应的型抗原。结果表明,经上述噬菌体V转化的克隆不仅获得了对噬菌体V的免疫力,还获得了对噬菌体7,8的免疫力。在转化克隆的Lac+杂种中观察到对噬菌体V和7,8的免疫力独立分离。这表明供体菌株NTCC 595/52携带两种原噬菌体,V和“缺陷”7,8(不表达因子7,8)。在这种情况下,转化克隆的Lac+杂种中观察到的抗原V的维持证实了先前的推测,即原噬菌体7,8的附着在该区域产生了某种不同源状态,干扰了重组过程。从菌株NTCC 595/52分离出的转化噬菌体V可能是重组体。对杂种类别的分析表明,转化克隆染色体上原噬菌体标记的大致顺序如下:aV--免疫V--免疫7,8--lac。

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