Pagan J, Senior A E
Department of Biochemistry, University of Rochester Medical Center, New York 14642.
Arch Biochem Biophys. 1990 Mar;277(2):283-9. doi: 10.1016/0003-9861(90)90580-r.
In order to generate mutants randomly in the Escherichia coli uncA gene (encoding the alpha-subunit of F1-ATPase), plasmids carrying uncA were treated in vitro with hydroxylamine. Restriction fragments of the mutated uncA gene were then reconstructed into plasmid pDP34, which expresses all of the F1F0 structural genes, and the reconstructed mutant plasmids were expressed in a strain carrying a deletion of chromosomal uncA. Each of the mutations was characterized by DNA sequencing, growth assays, and biochemical assays of membrane preparations. Three nonsense and one frameshift mutation were identified and their properties were studied briefly. Eight new missense mutations were identified and characterization of their properties is described. These eight mutations were R139H, A177V, R210C, R303C, A306V, T343I, G351S, and P370L.
为了在大肠杆菌uncA基因(编码F1 - ATP合酶的α亚基)中随机产生突变体,携带uncA的质粒在体外经羟胺处理。然后将突变的uncA基因的限制性片段重建到表达所有F1F0结构基因的质粒pDP34中,并将重建的突变体质粒在携带染色体uncA缺失的菌株中表达。通过DNA测序、生长测定以及膜制剂的生化测定对每个突变进行表征。鉴定出三个无义突变和一个移码突变,并对其性质进行了简要研究。鉴定出八个新的错义突变,并描述了其性质的表征。这八个突变分别是R139H、A177V、R210C、R303C、A306V、T343I、G351S和P370L。