Konrad M
Department of Molecular Genetics, Max-Planck-Institute for Biophysical Chemistry, Götting, Germany.
Biochim Biophys Acta. 1993 Feb 20;1172(1-2):12-6. doi: 10.1016/0167-4781(93)90262-c.
Screening for genes homologous to adenylate kinase in the yeast Saccharomyces cerevisiae resulted in the isolation of a homolog of the previously characterized ADK1. The derived protein sequence is most closely related to mammalian GTP:AMP phosphotransferase (adenylate kinase isozyme 3; AK3); this novel gene is therefore named ADK3. Its deletion from the yeast genome does not lead to an observable change in cellular phenotype. A strain defective for both ADK1 and ADK3 is viable. When introduced on a multicopy plasmid into an ADK1-deficient yeast strain, which shows a reduced proliferation rate, ADK3 did not rescue this growth defect. The protein was also highly overexpressed in E. coli cells. However, no change in enzymatic activity was detected in cellular extracts of yeast or bacteria.
在酿酒酵母中筛选与腺苷酸激酶同源的基因,结果分离出了先前已鉴定的ADK1的一个同源物。推导的蛋白质序列与哺乳动物的GTP:AMP磷酸转移酶(腺苷酸激酶同工酶3;AK3)关系最为密切;因此,这个新基因被命名为ADK3。从酵母基因组中删除该基因不会导致细胞表型出现可观察到的变化。ADK1和ADK3双缺陷的菌株是可存活的。当将其导入多拷贝质粒到增殖速率降低的ADK1缺陷酵母菌株中时,ADK3并不能挽救这种生长缺陷。该蛋白在大肠杆菌细胞中也高度过表达。然而,在酵母或细菌的细胞提取物中未检测到酶活性的变化。