首页> 美国卫生研究院文献>Journal of Bacteriology >Isolation of the hemF operon containing the gene for the Escherichia coli aerobic coproporphyrinogen III oxidase by in vivo complementation of a yeast HEM13 mutant.
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Isolation of the hemF operon containing the gene for the Escherichia coli aerobic coproporphyrinogen III oxidase by in vivo complementation of a yeast HEM13 mutant.

机译:通过酵母HEM13突变体的体内互补作用分离含有hemF操纵子的hemF操纵子该基因包含大肠杆菌的好氧原卟啉原III氧化酶。

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摘要

Coproporphyrinogen III oxidase, an enzyme involved in heme biosynthesis, catalyzes the oxidative decarboxylation of coproporphyrinogen III to form protoporphyrinogen IX. Genetic and biochemical studies suggested the presence of two different coproporphyrinogen III oxidases, one for aerobic and one for anaerobic conditions. Here we report the cloning of the hemF gene, encoding the aerobic coproporphyrinogen III oxidase from Escherichia coli, by functional complementation of a Saccharomyces cerevisiae HEM13 mutant. An open reading frame of 897 bp encoding a protein of 299 amino acids with a calculated molecular mass of 34.3 kDa was identified. Sequence comparisons revealed 43% amino acid sequence identity with the product of the S. cerevisiae HEM13 gene and 90% identity with the product of the recently cloned Salmonella typhimurium hemF gene, while a structural relationship to the proposed anaerobic enzyme from Rhodobacter sphaeroides was not obvious. The hemF gene is in an operon with an upstream open reading frame (orf1) encoding a 31.7-kDa protein with homology to an amidase involved in cell wall metabolism. The hemF gene was mapped to 52.6 min of the E. coli chromosome. Primer extension experiments revealed a strong transcription initiation site upstream of orf1. A weak signal, possibly indicative of a second promoter, was also identified just upstream of the hemF gene. A region containing bent DNA (Bent 111), previously mapped to 52.6 min of the E. coli chromosome, was discovered in the 5' region of orf1. Two potential integration host factor binding sites were found, one close to each transcription start site. An open reading frame (orf3) transcribed in a direction opposite that of the hemF gene was found downstream of the hemF gene. It encodes a protein of 40.2 kDa that showed significant homology to proteins of the XylS/AraC family of transcriptional regulators.
机译:辅助血卟啉原III氧化酶是一种参与血红素生物合成的酶,可催化辅助血卟啉原III的氧化脱羧反应,形成原卟啉原IX。遗传和生化研究表明存在两种不同的原卟啉原Ⅲ氧化酶,一种用于有氧条件,一种用于厌氧条件。在这里,我们报告了通过酿酒酵母HEM13突变体的功能互补,克隆了编码来自大肠杆菌的好氧原卟啉原III氧化酶的hemF基因的克隆。鉴定出一个897 bp的开放阅读框,该框编码299个氨基酸的蛋白质,计算的分子量为34.3 kDa。序列比较显示,与酿酒酵母HEM13基因的产物具有43%的氨基酸序列同一性,与最近克隆的鼠伤寒沙门氏菌hemF基因的产物具有90%的同一性,而与拟南芥球形厌氧酶的拟建厌氧酶之间的结构关系并不明显。 hemF基因位于操纵子中,上游操纵子可读框(orf1)编码31.7-kDa蛋白,与参与细胞壁代谢的酰胺酶同源。 hemF基因被定位到大肠杆菌染色体的52.6分钟。引物延伸实验显示了orf1上游的一个强大的转录起始位点。在hemF基因的上游还发现了一个可能指示第二个启动子的弱信号。在orf1的5'区域发现了一个包含弯曲DNA(Bent 111)的区域,该区域先前已映射到大肠杆菌染色体52.6分钟。发现了两个潜在的整合宿主因子结合位点,每个转录起始位点附近一个。在hemF基因的下游发现了一个以与hemF基因相反的方向转录的开放阅读框(orf3)。它编码一个40.2 kDa的蛋白,该蛋白与XylS / AraC家族的转录调节蛋白具有显着的同源性。

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