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Tn5tac1在大肠杆菌中的插入极性

Tn5tac1 insertion polarity in Escherichia coli.

作者信息

Llosa M, Jubete Y, de la Cruz F

机构信息

Departamento de Biología Molecular, Universidad de Cantabria, Santander, Spain.

出版信息

Plasmid. 1991 Nov;26(3):222-4. doi: 10.1016/0147-619x(91)90045-x.

Abstract

The Tn5-derived transposon Tn5tac1 carries the strong tac promoter (Ptac) facing outward at one of its ends. Expression of Ptac is under the control of the lacIq gene, also contained within the transposon. By inserting Tn5tac1 upstream from a promoterless galK gene we determined the basal level of transcription from both ends of the transposon in the absence of IPTG to be about 4% relative to the lactose promoter (Plac). As a result, derivatives of strain N100 containing these plasmids produce red colonies in MacConkey-galactose plates. Deletion of the BamHI fragment including Ptac causes galactokinase levels to drop to less than 1% of Plac, enough to render white colonies in MacConkey-galactose plates. Thus, Tn5tac1 can be used for genetic analysis under conditions in which it shows no polarity (+ IPTG), low polarity (- IPTG), or strong polarity (delta Ptac).

摘要

源自Tn5的转座子Tn5tac1在其一端携带一个向外的强tac启动子(Ptac)。Ptac的表达受转座子中也含有的lacIq基因控制。通过将Tn5tac1插入无启动子的galK基因上游,我们确定在不存在异丙基-β-D-硫代半乳糖苷(IPTG)的情况下,转座子两端的基础转录水平相对于乳糖启动子(Plac)约为4%。因此,含有这些质粒的N100菌株衍生物在麦康凯 - 半乳糖平板上产生红色菌落。缺失包含Ptac的BamHI片段会导致半乳糖激酶水平降至Plac的1%以下,足以使麦康凯 - 半乳糖平板上的菌落变为白色。因此,Tn5tac1可用于在无极性(+IPTG)、低极性(-IPTG)或强极性(缺失Ptac)条件下的遗传分析。

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