Gentry D, Bengra C, Ikehara K, Cashel M
Section on Molecular Regulation, National Institutes of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1993 Jul 5;268(19):14316-21.
We have identified the gene gmk, in the same operon as rpoZ, spoT, and recG at about 82 minutes on the Escherichia coli chromosome. The gmk (GMP kinase) gene encodes a peptide of 23,592 Da, possessing extensive similarity to the amino acid sequence of guanylate kinase from yeast. To confirm that gmk truly encodes guanylate kinase and to explore some of its enzymatic features, we have overproduced the product of gmk and purified it to homogeneity. Unlike guanylate kinases purified from eukaryotic sources, E. coli guanylate kinase is multimeric, and ionic conditions dictate its protomeric state; under low ionic conditions it appears to be a tetramer while under high ionic conditions it is a dimer. Kinetic analysis reveals that guanylate kinase, again, unlike eukaryotic guanylate kinases, binds GMP cooperatively and that the observed cooperatively changes with ionic strength. These results indicate that, despite extensive sequence similarity to its eukaryotic counterparts, E. coli guanylate kinase is structurally and enzymatically different.
我们已经在大肠杆菌染色体上约82分钟处鉴定出了gmk基因,它与rpoZ、spoT和recG位于同一个操纵子中。gmk(GMP激酶)基因编码一个23,592 Da的肽段,与酵母鸟苷酸激酶的氨基酸序列具有广泛的相似性。为了证实gmk确实编码鸟苷酸激酶并探究其一些酶学特性,我们过量表达了gmk的产物并将其纯化至同质。与从真核生物来源纯化的鸟苷酸激酶不同,大肠杆菌鸟苷酸激酶是多聚体,离子条件决定其亚基状态;在低离子条件下它似乎是四聚体,而在高离子条件下它是二聚体。动力学分析表明,鸟苷酸激酶再次与真核生物鸟苷酸激酶不同,它协同结合GMP,并且观察到的协同作用随离子强度而变化。这些结果表明,尽管与真核生物对应物具有广泛的序列相似性,但大肠杆菌鸟苷酸激酶在结构和酶学上是不同的。