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Sequence elements determining ampC promoter strength in E. coli.

机译:确定大肠杆菌中ampC启动子强度的序列元件。

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摘要

A number of spontaneous up-promoter mutations have been isolated in the ampC beta-lactamase gene of Escherichia coli. The mutants were analyzed by DNA sequencing, and the level of ampC gene expression was determined. Six mutants with a 21-fold increase in promoter strength compared with the wild-type were mutated in the -35 promoter region from TTGTCA to the consensus sequence TTGACA . The -10 region sequence TACAAT was mutated to the consensus sequence TATAAT in three mutants exhibiting an ampC promoter seven times stronger than the wild-type. We have previously described a 1-bp insertion mutant ( Jaurin et al., 1981) that changes the inter-region distance to the consensus 17 bp. Thus, all the up-mutations found in the ampC promoter represent corrections of the three major discrepancies between the ampC promoter and the consensus E. coli promoter. We conclude that the three consensus elements of E. coli promoters, the -35 and -10 regions and an optimal inter-region distance of 17 bp, are the main elements determining the promoter strength.
机译:在大肠杆菌的ampCβ-内酰胺酶基因中已经分离出许多自发的启动子突变。通过DNA测序分析突变体,并确定ampC基因表达水平。与野生型相比启动子强度增加21倍的六个突变体在-35启动子区域中从TTGTCA突变为共有序列TTGACA。在三个展示了比野生型强七倍的ampC启动子的突变体中,将-10区序列TACAAT突变为共有序列TATAAT。我们先前已经描述了一个1-bp插入突变体(Jaurin等,1981),该突变体将区域间距离更改为共有的17 bp。因此,在ampC启动子中发现的所有向上突变代表对ampC启动子和共有大肠杆菌启动子之间的三个主要差异的校正。我们得出的结论是,大肠杆菌启动子的三个共有元件-35和-10区域以及最佳区域间距离为17 bp是决定启动子强度的主要因素。

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