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乳酸乳球菌乳酸亚种MG1363中不存在的一种宿主因子是接合转座所必需的。

A host factor absent from Lactococcus lactis subspecies lactis MG1363 is required for conjugative transposition.

作者信息

Bringel F, Van Alstine G L, Scott J R

机构信息

Department of Microbiology and Immunology, Emory University Health Sciences Center, Atlanta, Georgia 30322.

出版信息

Mol Microbiol. 1991 Dec;5(12):2983-93. doi: 10.1111/j.1365-2958.1991.tb01858.x.

Abstract

In matings between Lactococcus lactis strains, the conjugative transposons Tn916 and Tn919 are found in the chromosome of the transconjugants in the same place as in the chromosome of the donor, indicating that no transposition has occurred. In agreement with this, the frequency of L. lactis transconjugants from intraspecies matings is the same whether the donor contains the wild-type form of the transposon or the mutant Tn916-int1, which has an insertion in the transposon's integrase gene. However, in intergeneric crosses with Bacillus subtilis or Enterococcus faecalis donors, Tn916 and Tn919 transpose to different locations on the chromosome of the L. lactis transconjugants. Moreover, Tn916 and Tn919 could not be transferred by conjugation from L. lactis and B. subtilis, E. faecalis or Streptococcus pyogenes. This suggests that excision of these elements does not occur in L. lactis. When cloned into E. coli with adjacent chromosomal DNA from L. lactis, the conjugative transposons were able to excise, transpose and promote conjugation. Therefore, the inability of these elements to excise in L. lactis is not caused by a permanent structural alteration in the transposon. We conclude that L. lactis lacks a factor required for excision of conjugative transposons.

摘要

在乳酸乳球菌菌株之间的交配中,接合转座子Tn916和Tn919在转接合子的染色体中位于与供体染色体相同的位置,这表明未发生转座。与此一致的是,无论供体含有转座子的野生型形式还是在转座子整合酶基因中有插入的突变体Tn916-int1,种内交配产生的乳酸乳球菌转接合子的频率都是相同的。然而,在与枯草芽孢杆菌或粪肠球菌供体的属间杂交中,Tn916和Tn919会转座到乳酸乳球菌转接合子染色体上的不同位置。此外,Tn916和Tn919不能通过接合从乳酸乳球菌与枯草芽孢杆菌、粪肠球菌或化脓性链球菌进行转移。这表明这些元件在乳酸乳球菌中不会发生切除。当与来自乳酸乳球菌的相邻染色体DNA一起克隆到大肠杆菌中时,接合转座子能够切除、转座并促进接合。因此,这些元件在乳酸乳球菌中无法切除不是由转座子的永久性结构改变引起的。我们得出结论,乳酸乳球菌缺乏切除接合转座子所需的因子。

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