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牛败血性大肠杆菌Vir质粒的遗传和分子特征

Genetic and molecular characteristics of Vir plasmids of bovine septicemic Escherichia coli.

作者信息

Lopez-Alvarez J, Gyles C L, Shipley P L, Falkow S

出版信息

J Bacteriol. 1980 Feb;141(2):758-69. doi: 10.1128/jb.141.2.758-769.1980.

Abstract

Three wild strains of bovine septicemic Escherichia coli were selected on the basis of their production of a toxin lethal for mice and chickens and their characteristic surface antigen. The transfer of these virulence (Vir) properties from two of the three to recipient E. coli was detected after mating. One Vir plasmid (pJL1) was derepressed for transfer and associated with mobilization of chromosomal markers. The other, pJL2, was repressed. Both plasmids were tagged with transposon Tn5 (kanamycin resistance), and transfer parameters of the tagged plasmids were studied. The Tn5 insertion in pJL2 usually increased transfer efficiency 100-fold. Plasmid pJL1 was classified as a member of the FIV incompatibility group. A pJL1::Tn5 derivative plasmid was incompatible with ColV1. Plasmid pJL2 behaved as an fi+ plasmid. Both plasmids pJL1 and pJL2 had a molecular weight of 92 x 10(6) and were present at about four copies per chromosome; their deoxyribonucleic acid (DNA) structures were not identical on the basis of restriction enzyme analysis. DNA-DNA hybridization revealed a polynucleotide sequence homology of at least 58% between the two plasmids. No plasmids could be detected in one wild or certain laboratory-derived Vir+ E. coli strains.

摘要

根据它们对小鼠和鸡产生致死毒素的能力以及其特征性表面抗原,挑选出三株牛败血性大肠杆菌野生菌株。在接合后检测到这三株中的两株的这些毒力(Vir)特性转移到了受体大肠杆菌中。一种Vir质粒(pJL1)在转移时去阻遏,并与染色体标记的移动有关。另一种,pJL2,被阻遏。两种质粒都用转座子Tn5(卡那霉素抗性)进行了标记,并研究了标记质粒的转移参数。pJL2中的Tn5插入通常使转移效率提高100倍。质粒pJL1被归类为FIV不相容群的成员。一种pJL1::Tn5衍生质粒与ColV1不相容。质粒pJL2表现为fi+质粒。质粒pJL1和pJL2的分子量均为92×10⁶,每条染色体上约有四个拷贝;根据限制性内切酶分析,它们的脱氧核糖核酸(DNA)结构不相同。DNA-DNA杂交显示两种质粒之间的多核苷酸序列同源性至少为58%。在一株野生或某些实验室衍生的Vir+大肠杆菌菌株中未检测到质粒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f273/293686/4a90b3d18ff6/jbacter00563-0335-a.jpg

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