Messing J, Gronenborn B, Müller-Hill B, Hans Hopschneider P
Proc Natl Acad Sci U S A. 1977 Sep;74(9):3642-6. doi: 10.1073/pnas.74.9.3642.
A HindII restriction fragment comprising the Escherichia coli lac regulatory region and the genetic information for the alpha peptide of beta-galactosidase (beta-D-galactosidegalactohydrolase, EC. 3.2.1.23) has been inserted into 1 of the 10 Bsu I cleavage sites of M13 by blunt end ligation. A stable hybrid phage was isolated and identified by its ability to complement the lac alpha function. Further characterization of the hybrid phage includes retransformation studies, agarose gel electrophoresis, DNA-DNA hybridization, and heteroduplex mapping. The insertion point has been localized at 0.083 map unit on thewild-type circular map-i.e., within the intergenic region. The results prove that part of the intergenic region is nonessential and that the phage can be used as a cloning vehicle.
一个包含大肠杆菌乳糖调节区和β-半乳糖苷酶α肽(β-D-半乳糖苷半乳糖水解酶,EC. 3.2.1.23)遗传信息的HindII限制性片段,通过平端连接插入到M13的10个Bsu I切割位点中的1个。通过其互补乳糖α功能的能力分离并鉴定出一个稳定的杂交噬菌体。对杂交噬菌体的进一步表征包括再转化研究、琼脂糖凝胶电泳、DNA-DNA杂交和异源双链体作图。插入点已定位在野生型环状图谱上的0.083个图距单位处,即在基因间区域内。结果证明基因间区域的一部分是非必需的,并且该噬菌体可作为克隆载体。