Nakamura K, Katz-Wurtzel E T, Pirtle R M, Inouye M
J Bacteriol. 1979 Jun;138(3):715-20. doi: 10.1128/jb.138.3.715-720.1979.
The purified messenger ribonucleic acid (mRNA) for the lipoprotein of the Escherichia coli outer membrane was hybridized with fragments obtained by digestion of E. coli chromosomal deoxyribonucleic acid (DNA) with eight different restriction enzymes. For each restriction enzyme digestion, one specific fragment separated by agarose gel electrophoresis was found to hybridize with the lipoprotein mRNA. From the analysis of restriction fragments generated by double digestions with various combinations of restriction enzymes, cleavage sites for the restriction enzymes near the locus of the lipoprotein structural gene (lpp) were mapped. No restriction fragments of DNA from the E. coli lpp-2 mutant hybridized with the lipoprotein mRNA, confirming that the mutant has a deletion mutation in the vicinity of the lpp gene.
将大肠杆菌外膜脂蛋白的纯化信使核糖核酸(mRNA)与用八种不同限制酶消化大肠杆菌染色体脱氧核糖核酸(DNA)得到的片段进行杂交。对于每种限制酶消化,通过琼脂糖凝胶电泳分离出的一个特定片段被发现可与脂蛋白mRNA杂交。通过对用各种限制酶组合进行双酶切产生的限制片段的分析,绘制了脂蛋白结构基因(lpp)位点附近限制酶的切割位点图谱。来自大肠杆菌lpp - 2突变体的DNA没有限制片段与脂蛋白mRNA杂交,证实该突变体在lpp基因附近存在缺失突变。