首页> 美国卫生研究院文献>Journal of Bacteriology >Comparison of tellurite resistance determinants from the IncP alpha plasmid RP4Ter and the IncHII plasmid pHH1508a.
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Comparison of tellurite resistance determinants from the IncP alpha plasmid RP4Ter and the IncHII plasmid pHH1508a.

机译:来自IncP alpha质粒RP4Ter和IncHII质粒pHH1508a的亚碲酸盐抗性决定簇的比较。

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摘要

The tellurite resistance (Ter) determinants of the IncHII plasmid pHH1508a and the broad host range IncP alpha plasmid RP4Ter were cloned into pUC8, creating plasmids pDT1364 and pDT1558, respectively. The Ter region of pDT1364 was localized to a 1.25-kilobase region by using Tn1000 insertion mutagenesis. Insertions of Tn1000 into pDT1558 which resulted in tellurite sensitivity spanned 1.75 kilobases of DNA. No similarity between the restriction maps of these two plasmids was observed, and no homology could be detected by DNA-DNA hybridization. Expression in an in vitro transcription-translation system showed that pDT1364 encoded two polypeptides with molecular masses of 23 and 12 kilodaltons (kDa) which were not expressed by pUC8. Some of the Tn1000 insertion mutants did not express the 23-kDa protein. pDT1558 encoded a 40-kDa polypeptide which was not expressed by pUC8. Both Ter determinants were expressed constitutively. Our findings suggest that the mechanisms of Ter encoded by these two plasmids are different.
机译:IncHII质粒pHH1508a和宽宿主范围IncP alpha质粒RP4Ter的亚碲酸盐抗性(Ter)决定簇被克隆到pUC8中,分别形成质粒pDT1364和pDT1558。通过使用Tn1000插入诱变,将pDT1364的Ter区定位在1.25碱基对的区域。将Tn1000插入pDT1558中会导致亚碲酸盐敏感性跨越1.75 kb的DNA。在这两个质粒的限制性酶切图之间未观察到相似性,并且通过DNA-DNA杂交未检测到同源性。在体外转录翻译系统中的表达表明,pDT1364编码了两种分子量分别为23和12千道尔顿(kDa)的多肽,而pUC8并未表达它们。一些Tn1000插入突变体不表达23 kDa蛋白。 pDT1558编码40kDa的多肽,pUC8不表达该多肽。两个Ter决定簇均组成性表达。我们的发现表明这两个质粒编码的Ter的机制是不同的。

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