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大肠杆菌核糖体蛋白操纵子中延伸因子Tu合成的一个次要启动子。

A secondary promoter for elongation factor Tu synthesis in the str ribosomal protein operon of Escherichia coli.

作者信息

Zengel J M, Lindahl L

出版信息

Mol Gen Genet. 1982;185(3):487-92. doi: 10.1007/BF00334145.

Abstract

The str operon of Escherichia coli contains genes for ribosomal proteins S12 and S7 and for elongation factors EF-G and EF-Tu (Jaskunas et al. 1975). We have subcloned various segments of DNA from this operon onto multicopy plasmids. We found that cells carrying a recombinant plasmid which lacks the major promoter for the str operon but contains the 5' portion of the EF-Tu gene synthesize a novel protein which we have identified as a truncated EF-Tu molecule. Moreover, cells carrying plasmids with an intact EF-Tu gene synthesize the elongation factor at a 3- to 5-fold higher rate than haploid cells. Thus the EF-Tu gene can be expressed in the absence of the major promoter for the str operon. This expression is not due to read-through from plasmid promoters, but it is dependent on the presence of the distal portion of the EF-G gene on the plasmids. These results indicate that there is a secondary promoter for EF-Tu expression, apparently located within the structural gene for elongation factor EF-G.

摘要

大肠杆菌的str操纵子包含核糖体蛋白S12和S7以及延伸因子EF - G和EF - Tu的基因(贾斯库纳斯等人,1975年)。我们已将该操纵子的不同DNA片段亚克隆到多拷贝质粒上。我们发现,携带重组质粒的细胞缺乏str操纵子的主要启动子,但含有EF - Tu基因的5'部分,这些细胞会合成一种新蛋白质,我们已将其鉴定为截短的EF - Tu分子。此外,携带完整EF - Tu基因质粒的细胞合成延伸因子的速率比单倍体细胞高3至5倍。因此,EF - Tu基因可以在缺乏str操纵子主要启动子的情况下表达。这种表达不是由于从质粒启动子通读所致,而是依赖于质粒上EF - G基因远端部分的存在。这些结果表明,存在一个用于EF - Tu表达的二级启动子,显然位于延伸因子EF - G的结构基因内。

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