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Tn7中的IntI2整合子整合酶

IntI2 integron integrase in Tn7.

作者信息

Hansson Karin, Sundström Lars, Pelletier Alex, Roy Paul H

机构信息

Department of Pharmaceutical Biosciences, Division of Microbiology, Uppsala University, Uppsala, Sweden.

出版信息

J Bacteriol. 2002 Mar;184(6):1712-21. doi: 10.1128/JB.184.6.1712-1721.2002.

Abstract

Integrons can insert and excise antibiotic resistance genes on plasmids in bacteria by site-specific recombination. Class 1 integrons code for an integrase, IntI1 (337 amino acids in length), and are generally borne on elements derived from Tn5090, such as that found in the central part of Tn21. A second class of integron is found on transposon Tn7 and its relatives. We have completed the sequence of the Tn7 integrase gene, intI2, which contains an internal stop codon. This codon was found to be conserved among intI2 genes on three other Tn7-like transposons harboring different cassettes. The predicted peptide sequence (IntI2*) is 325 amino acids long and is 46% identical to IntI1. In order to detect recombination activity, the internal stop codon at position 179 in the parental allele was changed to a triplet coding for glutamic acid. The sequences flanking the cassette arrays in the class 1 and 2 integrons are not closely related, but a common pool of mobile cassettes is used by the different integron classes; two of the three antibiotic resistance cassettes on Tn7 and its close relatives are also found in various class 1 integrons. We also observed a fourth excisable cassette downstream of those described previously in Tn7. The fourth cassette encodes a 165-amino-acid protein of unknown function with 6.5 contiguous repeats of a sequence coding for 7 amino acids. IntI2179E promoted site-specific excision of each of the cassettes in Tn7 at different frequencies. The integrases from Tn21 and Tn7 showed limited cross-specificity in that IntI1 could excise all cassettes from both Tn21 and Tn7. However, we did not observe a corresponding excision of the aadA1 cassette from Tn21 by IntI2179E.

摘要

整合子可通过位点特异性重组在细菌质粒上插入和切除抗生素抗性基因。1类整合子编码一种整合酶IntI1(长度为337个氨基酸),通常存在于源自Tn5090的元件上,比如在Tn21中部发现的元件。第二类整合子存在于转座子Tn7及其相关元件上。我们已完成了Tn7整合酶基因intI2的测序,该基因含有一个内部终止密码子。发现这个密码子在另外三个携带不同盒式元件的Tn7样转座子上的intI2基因中是保守的。预测的肽序列(IntI2*)长度为325个氨基酸,与IntI1的同源性为46%。为了检测重组活性,将亲本等位基因中第179位的内部终止密码子改为编码谷氨酸的三联体。1类和2类整合子中盒式元件阵列两侧的序列没有密切关系,但不同类别的整合子使用共同的可移动盒式元件库;Tn7及其近亲上的三个抗生素抗性盒式元件中的两个也存在于各种1类整合子中。我们还在Tn7中先前描述的那些盒式元件下游观察到了第四个可切除盒式元件。第四个盒式元件编码一种功能未知的165个氨基酸的蛋白质,该蛋白质具有编码7个氨基酸的序列的6.5个连续重复。IntI2179E以不同频率促进Tn7中每个盒式元件的位点特异性切除。来自Tn21和Tn7的整合酶表现出有限的交叉特异性,即IntI1可以切除Tn21和Tn7中的所有盒式元件。然而,我们没有观察到IntI2179E对Tn21上的aadA1盒式元件进行相应的切除。

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