首页> 美国卫生研究院文献>Journal of Bacteriology >Lipoic acid metabolism in Escherichia coli: isolation of null mutants defective in lipoic acid biosynthesis molecular cloning and characterization of the E. coli lip locus and identification of the lipoylated protein of the glycine cleavage system.
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Lipoic acid metabolism in Escherichia coli: isolation of null mutants defective in lipoic acid biosynthesis molecular cloning and characterization of the E. coli lip locus and identification of the lipoylated protein of the glycine cleavage system.

机译:大肠杆菌中的硫辛酸代谢:分离在硫辛酸生物合成中无效的无效突变体大肠埃希菌嘴唇基因座的分子克隆和表征以及鉴定甘氨酸裂解系统的脂酰化蛋白。

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摘要

We report the isolation and genetic characterization of novel Tn10dTc and Tn1000dKn insertion mutations in and near the lip locus of the Escherichia coli chromosome. The Tn10dTc and Tn1000dKn mutations define two genes, lipA and lipB, involved in lipoic acid biosynthesis. Two representative alleles (lip-2 and lip-9) from the previously reported genetic class of lipoic acid auxotrophic mutants (A. A. Herbert and J. R. Guest, J. Gen. Microbiol. 53:363-381, 1968) were assigned to the lipA complementation group. We have cloned the E. coli lip locus and developed a recombinant plasmid-based genetic system for fine-structure physical-genetic mapping of mutations in this region of the E. coli chromosome. We also report that a recombinant plasmid containing a 5.2-kbp PvuII restriction fragment from the E. coli lip locus produced three proteins of approximately 8, 12, and 36 kDa by using either a maxicell or in vitro transcription translation expression system. The 36-kDa protein was identified as the gene product encoded by the lipA locus. Finally, we have identified a previously unreported lipoylated protein that functions in the glycine cleavage system of E. coli.
机译:我们报告了大肠杆菌染色体染色体的唇位及其附近的新型Tn10dTc和Tn1000dKn插入突变的分离和遗传特征。 Tn10dTc和Tn1000dKn突变定义了两个与硫辛酸生物合成有关的基因lipA和lipB。先前报道的硫辛酸营养缺陷型突变体的遗传分类(AA Herbert和JR Guest,J.Gen.Microbiol.53:363-381,1968)的两个代表性等位基因(lip-2和lip-9)被指定为lipA互补组。我们已经克隆了大肠杆菌的嘴唇基因座,并开发了一个基于重组质粒的遗传系统,用于在大肠杆菌染色体的这一区域进行突变的精细结构物理遗传映射。我们还报告说,通过使用maxicell或体外转录翻译表达系统,含有来自大肠杆菌嘴唇基因座的5.2-kbp PvuII限制性片段的重组质粒产生了大约8、12和36 kDa的三种蛋白质。该36kDa蛋白被鉴定为由lipA基因座编码的基因产物。最后,我们确定了以前未报道的脂酰化蛋白,该蛋白在大肠杆菌的甘氨酸裂解系统中起作用。

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