Hansen F G, von Meyenburg K
Mol Gen Genet. 1979 Sep;175(2):135-44. doi: 10.1007/BF00425529.
Specialized transducing phages lambda tna (tryptophanase) harboring chromosomal DNA and genetic markers from the dnaA region of the Escherichia coli chromosome were isolated. Transductional analysis showed that some of these tnaA transducing phages carry two genes important in DNA replication, namely the dnaA gene (initiation of chromosome replication) and the gyrB gene (subunit B of DNA gyrase), formerly designated couR. The following clockwise order of genetic markers was found: uhp, gyrB, dnaA, rimA, tnaA, bglB. The gene-protein relationship was established by the determination of the gene products encoded on the chromosomal DNA of the different lambda tna. A 54 kD and a 91 kD polypeptide appear to be coded for by the dnaA and gyrB genes, respectively; the 91 kD protein is encoded on a region in which coumermycin sensitivity maps and is with respect to electrophoretic behavior identical to subunit B of DNA gyrase. The 54 kD protein is encoded on the region in which different independently isolated dnaA(Ts) mutations (dnaA5, dnaA46, dnaA167, dnaA203, dnaA204, dnaA205, dnaA211, dnaA508) are located. Additional genes which code for polypeptides with hitherto unknown functions were identified and mapped. The acriflavin sensitivity mutation acrB1 was found to be an allele of the gyrB gene (see "Note Added in Proof").
分离出了携带大肠杆菌染色体dnaA区域的染色体DNA和遗传标记的特异性转导噬菌体λtna(色氨酸酶)。转导分析表明,其中一些tnaA转导噬菌体携带两个对DNA复制很重要的基因,即dnaA基因(染色体复制起始)和gyrB基因(DNA回旋酶的B亚基,以前称为couR)。发现了以下顺时针方向的遗传标记顺序:uhp、gyrB、dnaA、rimA、tnaA、bglB。通过确定不同λtna染色体DNA上编码的基因产物,建立了基因与蛋白质的关系。一个54kD和一个91kD的多肽似乎分别由dnaA和gyrB基因编码;91kD蛋白质在香豆霉素敏感性图谱所在的区域编码,并且在电泳行为上与DNA回旋酶的B亚基相同。54kD蛋白质在不同独立分离的dnaA(Ts)突变(dnaA5、dnaA46、dnaA167、dnaA203、dnaA204、dnaA205、dnaA211、dnaA508)所在的区域编码。鉴定并定位了编码迄今功能未知的多肽的其他基因。发现吖啶黄素敏感性突变acrB1是gyrB基因的一个等位基因(见“校样中补充说明”)。