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首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Role of the rom protein in copy number control of plasmid pBR322 at different growth rates in Escherichia coli K-12.
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Role of the rom protein in copy number control of plasmid pBR322 at different growth rates in Escherichia coli K-12.

机译:rom蛋白在大肠杆菌K-12中以不同生长速率在质粒pBR322拷贝数控制中的作用。

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The copy number per cell mass of plasmid pBR322 and a rom- derivative was measured as a function of generation time. In fast growing cells the copy number per cell mass was virtually identical for rom+ and rom- derivatives. However, the copy number of pBR322 only increased 3- to 4-fold from a 20- to 80-min generation time, whereas the copy number of the rom- derivative increased 7- to 10-fold. The copy number stayed constant for the rom+ and rom- plasmids at generation times longer than 80-100 min. Thus, the presence of the rom gene decreased the copy number of plasmid pBR322 in slowly growing cells at least 2-fold when compared with the rom- plasmid. To study the effect of the rom gene in trans we cloned the gene into the compatible P15A-derived rom- plasmid pACYC184. In cells carrying both pACYC184 rom+ and pBR322 rom- the presence of the rom gene in trans had little effect on the copy number of pBR322 rom- at fast growth, but it decreased its copy number at slow growth to the same level as found for pBR322, i.e., complemented the pBR322 rom- plasmid. The pACYC184 plasmid and its rom+ derivatives showed copy numbers similar to those of pBR322 rom- and pBR322 itself, respectively, at fast and slow growth. We conclude that the rom gene product-the Rom protein-is an important element in copy number control of ColE1-type plasmids especially in slowly growing cells. Copyright 1999 Academic Press.
机译:测量质粒pBR322和rom-衍生物的每细胞质量的拷贝数作为产生时间的函数。在快速生长的细胞中,rom +和rom-衍生物的每细胞质量拷贝数实际上是相同的。但是,pBR322的拷贝数从20到80分钟的生成时间仅增加了3到4倍,而rom衍生物的拷贝数却增加了7到10倍。对于rom +和rom-质粒,在超过80-100分钟的生成时间,其拷贝数保持恒定。因此,与rom质粒相比,rom基因的存在使缓慢生长的细胞中质粒pBR322的拷贝数降低了至少2倍。为了研究rom基因的反式作用,我们将该基因克隆到了兼容的P15A衍生的rom质粒pACYC184中。在同时携带pACYC184 rom +和pBR322 rom的细胞中,反基因rom基因的存在对快速生长的pBR322 rom-的拷贝数影响不大,但在慢速生长时其拷贝数减少到与pBR322相同的水平。 ,即互补pBR322 rom-质粒。 pACYC184质粒及其rom +衍生物在快速和缓慢生长时分别显示出与pBR322 rom-和pBR322本身相似的拷贝数。我们得出结论,rom基因产物-Rom蛋白-是ColE1型质粒的拷贝数控制中的重要元素,尤其是在缓慢生长的细胞中。版权所有1999 Academic Press。

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