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大肠杆菌苯丙氨酰 - tRNA合成酶操纵子:多拷贝质粒上分离出的突变的特征分析

Escherichia coli phenylalanyl-tRNA synthetase operon: characterization of mutations isolated on multicopy plasmids.

作者信息

Plumbridge J A, Springer M

出版信息

J Bacteriol. 1982 Nov;152(2):650-60. doi: 10.1128/jb.152.2.650-660.1982.

Abstract

Plasmid pB1 carries the genes for threonyl-tRNA synthetase, phenylalanyl-tRNA synthetase, and translation initiation factor IF3. Strains carrying this plasmid overproduce phenylalanyl-tRNA synthetase about 100-fold. Spontaneous mutant plasmids were obtained which no longer caused the overproduction of the enzyme. Three classes of mutations were found. (i) Deletion mutations were found, some of which had the interesting property of fusing different genes together, e.g., putting phenylalanyl-tRNA synthetase under the control of the threonyl-tRNA synthetase promoter. (ii) Insertion mutations were found; one insertion in particular was studied. This insertion is located in front of the structural gene for phenylalanyl-tRNA synthetase and is shown to interrupt a cis-acting regulatory region. (iii) Mutations that showed no major change in DNA structure were found. One of these mutations is apparently purely structural, as it produces a small subunit of phenylalanyl-tRNA synthetase with a reduced molecular weight. This protein is less stable than the wild-type enzyme. These mutations represent useful tools to investigate how the phenylalanyl-tRNA synthetase operon is regulated.

摘要

质粒pB1携带着苏氨酰 - tRNA合成酶、苯丙氨酰 - tRNA合成酶以及翻译起始因子IF3的基因。携带该质粒的菌株会使苯丙氨酰 - tRNA合成酶过量产生约100倍。获得了不再导致该酶过量产生的自发突变质粒。发现了三类突变。(i)发现了缺失突变,其中一些具有将不同基因融合在一起的有趣特性,例如,使苯丙氨酰 - tRNA合成酶受苏氨酰 - tRNA合成酶启动子的控制。(ii)发现了插入突变;特别研究了其中一个插入突变。该插入位于苯丙氨酰 - tRNA合成酶结构基因的前面,并且显示出中断了一个顺式作用调节区域。(iii)发现了DNA结构没有重大变化的突变。其中一个突变显然纯粹是结构性的,因为它产生了一种分子量降低的苯丙氨酰 - tRNA合成酶小亚基。这种蛋白质比野生型酶更不稳定。这些突变是研究苯丙氨酰 - tRNA合成酶操纵子如何被调控的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c41/221512/8ffa37b29414/jbacter00252-0110-a.jpg

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