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赋予脯氨酸过量生产和渗透耐受性的重组质粒。

Recombinant plasmid conferring proline overproduction and osmotic tolerance.

作者信息

Jakowec M W, Smith L T, Dandekar A M

出版信息

Appl Environ Microbiol. 1985 Aug;50(2):441-6. doi: 10.1128/aem.50.2.441-446.1985.

Abstract

A recombinant plasmid carrying the proBA (pro-74) mutant allele which governs osmotic tolerance and proline overproduction was constructed by using the broad-host-range plasmid vector pQSR49. The physiological, biochemical, and genetic properties of strains carrying the pQSR49 derivatives pMJ101 and pMJ1, mutant and wild type, respectively, were investigated. pMJ101 conferred enhanced osmotolerance compared with strains carrying the wild type, pMJ1. These results are in contrast to those obtained previously with strains carrying recombinant plasmids based on pBR322 that failed to confer the osmotic tolerance phenotype. gamma-Glutamyl kinase (first step in proline biosynthesis) from strains carrying pMJ101 was 200-fold less sensitive to feedback inhibition than was the wild-type enzyme. As expected, the intracellular proline levels of strains carrying pMJ101 were more than an order of magnitude higher than those of the wild type. An analysis of copy number revealed that the pQSR49 constructs were present in the cell at a level six- to eightfold lower than those of the pBR322 recombinants, which may account for the difference in phenotype. We found that the genetic stability of the pQSR49 derivative in a variety of gram-negative bacteria was dependent on the insert orientation and the presence of foreign DNA on the plasmid. These factors may be significant in future studies aimed at expanding the osmotolerance phenotype to a broad range of gram-negative bacteria.

摘要

利用广宿主质粒载体pQSR49构建了携带proBA(pro-74)突变等位基因的重组质粒,该等位基因控制渗透耐受性和脯氨酸过量产生。分别对携带pQSR49衍生物pMJ101(突变型)和pMJ1(野生型)的菌株的生理、生化和遗传特性进行了研究。与携带野生型pMJ1的菌株相比,pMJ101赋予了增强的渗透耐受性。这些结果与先前用基于pBR322的重组质粒携带的菌株所获得的结果形成对比,后者未能赋予渗透耐受性表型。携带pMJ101的菌株中的γ-谷氨酰激酶(脯氨酸生物合成的第一步)对反馈抑制的敏感性比野生型酶低200倍。正如预期的那样,携带pMJ101的菌株的细胞内脯氨酸水平比野生型高出一个数量级以上。拷贝数分析表明,pQSR49构建体在细胞中的存在水平比pBR322重组体低6至8倍,这可能解释了表型上的差异。我们发现,pQSR49衍生物在多种革兰氏阴性细菌中的遗传稳定性取决于插入方向和质粒上外源DNA的存在。这些因素在未来旨在将渗透耐受性表型扩展到广泛的革兰氏阴性细菌的研究中可能具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/778a/238640/c1db3a475646/aem00143-0267-a.jpg

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