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首页> 外文期刊>Applied and Environmental Microbiology >Genetic analysis of regions of the Lactococcus lactis subsp. lactis plasmid pRS01 involved in conjugative transfer.
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Genetic analysis of regions of the Lactococcus lactis subsp. lactis plasmid pRS01 involved in conjugative transfer.

机译:乳酸乳球菌亚种区域的遗传分析。乳酸质粒pRS01参与共轭转移。

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摘要

The genes responsible for conjugative transfer of the 48.4-kb Lactococcus lactis subsp. lactis ML3 plasmid pRS01 were localized by insertional mutagenesis. Integration of the IS946-containing plasmid pTRK28 into pRS01 generated a pool of stable cointegrates, including a number of plasmids altered in conjugative proficiency. Mapping of pTRK28 insertions and phenotypic analysis of cointegrate plasmids identified four distinct regions (Tra1, Tra2, Tra3, and Tra4) involved in pRS01 conjugative transfer. Tra3 corresponds closely to a region previously identified (D. G. Anderson and L. L. McKay, J. Bacteriol. 158:954-962, 1984). Another region (Tra4) was localized within an inversion sequence shown to correlate with a cell aggregation phenotype. Tra1 and Tra2, two previously unidentified regions, were located at a distance of 9 kb from Tra3. When provided in trans, a cloned portion of the Tra3 region complemented Tra3 mutants.
机译:负责48.4-kb乳酸乳球菌亚种的共轭转移的基因。通过插入诱变来定位乳酸菌ML3质粒pRS01。包含IS946的质粒pTRK28整合到pRS01中,产生了一组稳定的共整合体,其中包括许多结合能力发生了变化的质粒。 pTRK28插入的图谱和cointegrate质粒的表型分析确定了参与pRS01共轭转移的四个不同区域(Tra1,Tra2,Tra3和Tra4)。 Tra3紧密对应于先前鉴定的区域(D.G.Anderson和L.L.McKay,J.Bacteriol.158:954-962,1984)。另一个区域(Tra4)位于显示与细胞聚集表型相关的反向序列内。 Tra1和Tra2,这两个以前未识别的区域,位于距Tra3 9 kb的距离处。反式提供时,Tra3区域的克隆部分与Tra3突变体互补。

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