Konrad M
Max-Planck-Institut for Biophysical Chemistry, Department of Molecular Genetics, Göttingen, Germany.
J Biol Chem. 1992 Dec 25;267(36):25652-5.
Guanylate kinase catalyzes the reversible transfer of the terminal phosphoryl group of ATP to the acceptor molecule GMP. Detailed analysis of the in vivo function of this enzyme has been limited by the lack of any genetic data. Using oligonucleotides based on amino acid sequence information of the yeast enzyme, the Saccharomyces cerevisiae gene, GUK1, was isolated and characterized. The gene is present in single copy and maps to chromosome IV. Insertional mutagenesis of the GUK1 locus caused recessive lethality, indicating that this enzyme is necessary for vegetative cell growth. Using inducible expression systems, guanylate kinase was produced in large amounts both in S. cerevisiae and in Escherichia coli.
鸟苷酸激酶催化ATP末端磷酸基团可逆地转移至受体分子GMP上。由于缺乏任何遗传数据,对该酶体内功能的详细分析受到了限制。利用基于酵母酶氨基酸序列信息的寡核苷酸,分离并鉴定了酿酒酵母基因GUK1。该基因以单拷贝形式存在,定位于第四条染色体上。GUK1基因座的插入诱变导致隐性致死,表明该酶是营养细胞生长所必需的。利用诱导表达系统,在酿酒酵母和大肠杆菌中均大量产生了鸟苷酸激酶。