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首页> 外文期刊>Applied and Environmental Microbiology >Reactivation of Insertionally Inactivated Shiga Toxin 2 Genes of Escherichia coli O157:H7 Caused by Nonreplicative Transposition of the Insertion Sequence
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Reactivation of Insertionally Inactivated Shiga Toxin 2 Genes of Escherichia coli O157:H7 Caused by Nonreplicative Transposition of the Insertion Sequence

机译:由插入序列的非复制性转座引起的大肠杆菌O157:H7插入失活志贺毒素2基因的重新激活

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IS1203v is an insertion sequence which has been found in inactivated Shiga toxin 2 genes of Escherichia coliO157:H7. We analyzed the transpositional mechanism of IS1203v in order to investigate whether the Shiga toxin 2 genes inactivated by IS1203v could revert to the wild type. When the transposase activity of IS1203v was enhanced by artificial frameshifting, IS1203v was obviously excised from the Shiga toxin 2 gene in a circular form. The IS1203v circle consisted of the entire IS1203v, but an extra 3-bp sequence (ATC) intervened between the 5′ and 3′ ends of IS1203v. The extra 3-bp sequence was identical to a direct repeat which was probably generated upon insertion. Moreover, we detected the Shiga toxin 2 gene with a precise excision of IS1203v. In the wild-type situation, the transposition products of IS1203v could be observed by PCR amplification. These results show that IS1203v can transpose in a nonreplicative manner and that the Shiga toxin gene inactivated by this insertion sequence can revert to the wild type.
机译:IS1203v是在大肠杆菌O157:H7的灭活的志贺毒素2基因中发现的插入序列。为了分析被IS1203v灭活的志贺毒素2基因是否可以回复到野生型,我们分析了IS1203v的转座机制。当通过人工移码增强IS1203v的转座酶活性时,IS1203v显然以环状形式从志贺毒素2基因中切除。 IS1203v圈由整个IS1203v组成,但在IS1203v的5'和3'末端之间插入了一个额外的3 bp序列(ATC)。额外的3-bp序列与可能在插入时产生的直接重复相同。此外,我们通过精确切除IS1203v检测到了志贺毒素2基因。在野生型情况下,通过PCR扩增可以观察到IS1203v的转座产物。这些结果表明IS1203v可以以非复制方式转座,并且被该插入序列灭活的志贺毒素基因可以恢复为野生型。

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