Oka A
J Bacteriol. 1978 Feb;133(2):916-24. doi: 10.1128/jb.133.2.916-924.1978.
A small plasmid (pAO2, 1 megadalton) carrying genes responsible for replication and colicin E1 immunity has been constructed from colicin E1 plasmid (A. Oka, K. Sugimoto, and M. Takanami, Proc. Mol. Biol. Jpn., p. 113-115, 1976). pAO2 DNA was cleaved into unique fragments with seven restriction endonucleases (R.HaeII,R.HaeIII,R.HapII,R.HhaI,R.AluI,R.HgaI, and R.HinfI). R.HaeII cleaved pAO2 DNA at two sites, R.HaeIII at four sites, R.HapII at nine sites, R.HhaI at eight sites, R-AluI at nine sites, R.HgaI at two sites, and R.HinfI at four sites, respectively. The order of HaeIII fragments of pAO2 was deduced from the physical map of colicin E1 plasmid previously reported (A. Oka and M. Takanami, Nature (London) 264:193-196, 1976). HapII, HhaI, and AluI fragments of pAO2 were assigned by analyzing overlapping sets of fragments arising upon digestion of individual HaeIII fragments with one of R.HapII, R.HhaI, or R.AluI, and upon their reciprocal digestion. The cleavage sites for R.HaeII, R.HgaI, and R.HinfI were localized on HapII, HhaI, and AluI fragments by combined digestion. On the basis of these data and estimates of the size of each fragment, a fine cleavage map of pAO2 was constructed.
一种携带负责复制和大肠杆菌素E1免疫相关基因的小质粒(pAO2,1兆道尔顿)已从大肠杆菌素E1质粒构建而成(A. 冈、K. 杉本和M. 高波,《日本分子生物学学报》,第113 - 115页,1976年)。用七种限制性内切酶(R.HaeII、R.HaeIII、R.HapII、R.HhaI、R.AluI、R.HgaI和R.HinfI)将pAO2 DNA切割成独特的片段。R.HaeII在两个位点切割pAO2 DNA,R.HaeIII在四个位点切割,R.HapII在九个位点切割,R.HhaI在八个位点切割,R - AluI在九个位点切割,R.HgaI在两个位点切割,R.HinfI在四个位点切割。pAO2的HaeIII片段顺序是根据先前报道的大肠杆菌素E1质粒的物理图谱推导出来的(A. 冈和M. 高波,《自然》(伦敦)264:193 - 196,1976年)。通过分析用R.HapII、R.HhaI或R.AluI之一消化单个HaeIII片段时产生的重叠片段组以及它们的相互消化情况,确定了pAO2的HapII、HhaI和AluI片段。通过联合消化将R.HaeII、R.HgaI和R.HinfI的切割位点定位在HapII、HhaI和AluI片段上。基于这些数据和每个片段大小的估计,构建了pAO2的精细切割图谱。