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来自大肠杆菌α-溶血素质粒的新插入序列IS91的特性分析。

Characterization of the new insertion sequence IS91 from an alpha-hemolysin plasmid of Escherichia coli.

作者信息

Diaz-Aroca E, de la Cruz F, Zabala J C, Ortiz J M

出版信息

Mol Gen Genet. 1984;193(3):493-9. doi: 10.1007/BF00382089.

Abstract

IS91 is a 1.85 kb insertion sequence originally resident in the alpha-hemolytic plasmid pSU233. The element was transposed sequentially from this plasmid to pACYC184, to R388, and to pBR322. Both cointegrates and simple insertions of the element were obtained. A detailed restriction enzyme map of the element is presented. This does not bear any relationship to the maps of previously described insertion sequences. Furthermore, hybridization between these sequences and IS91 could not be demonstrated. Deletion derivatives of IS91 were constructed which are unable to transpose. However, their transposition can be complemented in trans by wild-type elements. One of these deletion derivatives has been genetically labeled with a kanamycin resistance marker from Tn5. When this new element was complemented for transposition, only about 2% of the transposition products were cointegrates. Thus, the behavior of IS91 is better explained by transposition models that allow direct transposition.

摘要

IS91是一个1.85 kb的插入序列,最初存在于α-溶血性质粒pSU233中。该元件依次从这个质粒转座到pACYC184、R388和pBR322。获得了该元件的共整合体和简单插入体。给出了该元件的详细限制性酶切图谱。这与先前描述的插入序列图谱没有任何关系。此外,无法证明这些序列与IS91之间的杂交。构建了不能转座的IS91缺失衍生物。然而,它们的转座可以被野生型元件反式互补。这些缺失衍生物之一已用来自Tn5的卡那霉素抗性标记进行了遗传标记。当这个新元件的转座得到互补时,只有约2%的转座产物是共整合体。因此,通过允许直接转座的转座模型可以更好地解释IS91的行为。

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