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Cloning and characterization of a eukaryotic pantothenate kinase gene (panK) from Aspergillus nidulans

机译:构巢曲霉真核泛酸激酶基因(panK)的克隆与鉴定

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摘要

Pantothenate kinase (PanK) is the key regulatory enzyme in the CoA biosynthetic pathway. The PanK gene fromEscherichia coli (coaA) has been previously cloned and the enzyme biochemically characterized; highly related genes exist in other prokaryotes. We isolated a PanK cDNA clone from the eukaryotic fungus Aspergillus nidulans by functional complementation of a temperature-sensitive E. coli PanK mutant. The cDNA clone allowed the isolation of the genomic clone and the characterization of the A. nidulans gene designatedpanK. The panK gene is located on chromosome 3 (linkage group III), is interrupted by three small introns, and is expressed constitutively. The amino acid sequence of A. nidulans PanK (aPanK) predicted a subunit size of 46.9 kDa and bore little resemblance to its bacterial counterpart, whereas a highly related protein was detected in the genome of Saccharomyces cerevisiae. In contrast to E. coli PanK (bPanK), which is regulated by CoA and to a lesser extent by its thioesters, aPanK activity was selectively and potently inhibited by acetyl-CoA. Acetyl-CoA inhibition of aPanK was competitive with respect to ATP. Thus, the eukaryotic PanK has a distinct primary structure and unique regulatory properties that clearly distinguish it from its prokaryotic counterpart.
机译:泛酸激酶(PanK)是CoA生物合成途径中的关键调节酶。先前已克隆了来自大肠杆菌(coaA)的PanK基因,并对酶进行了生化鉴定。其他原核生物中存在高度相关的基因。我们通过对温度敏感的大肠杆菌PanK突变体的功能互补,从真核真菌构巢曲霉中分离出PanK cDNA克隆。 cDNA克隆允许分离基因组克隆和表征称为panK的构巢曲霉基因。 panK基因位于3号染色体上(连锁群III),被三个小内含子打断,并组成型表达。构巢曲霉PanK(aPanK)的氨基酸序列预测亚单位大小为46.9 kDa,与细菌的对应物几乎没有相似之处,而在酿酒酵母的基因组中检测到高度相关的蛋白质。与受CoA调节并受其硫酯影响程度较小的大肠杆菌PanK(bPanK)相反,乙酰辅酶AA选择性地并有效地抑制了aPanK活性。乙酰辅酶A对aPanK的抑制作用相对于ATP具有竞争性。因此,真核PanK具有独特的一级结构和独特的调控特性,从而使其与原核对应物明显区分开。

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