O'Regan G T, Sternberg N L, Cohen G
Microbiology Department, Tel Aviv University, Ramat Aviv, Israel.
Gene. 1987;60(1):129-35. doi: 10.1016/0378-1119(87)90220-4.
A library of bacteriophage P1 DNA was constructed in the phage vector lambda D69. The DNA of some 150 randomly chosen lambda-P1 hybrid phages containing P1 DNA fragments 5-10 kb in size was analyzed by restriction endonuclease digestion using enzymes EcoRI, BglII, and BamHI that cleave P1 DNA at known positions on the physical map of P1. Approximately one third of the phages contained P1 DNA inserts having two or more restriction sites for any one of these enzymes, thus allowing the location of the insert to be determined with respect to the physical map. Genetic tests allowed detection of lambda-P1 hybrid phages possessing inserts with functional P1 ban and CmR genes. A subset of 18 phages was analyzed in more detail; their P1 DNA inserts comprise an ordered collection of overlapping P1 DNA fragments that cover almost 98% of the P1 genome.
在噬菌体载体λD69中构建了噬菌体P1 DNA文库。使用限制性内切酶EcoRI、BglII和BamHI对大约150个随机选择的含有大小为5 - 10 kb P1 DNA片段的λ-P1杂交噬菌体的DNA进行消化分析,这些酶在P1物理图谱上的已知位置切割P1 DNA。大约三分之一的噬菌体含有对这些酶中的任何一种都有两个或更多限制性位点的P1 DNA插入片段,从而可以相对于物理图谱确定插入片段的位置。遗传测试能够检测到具有带有功能性P1 ban和CmR基因插入片段的λ-P1杂交噬菌体。对18个噬菌体的一个子集进行了更详细的分析;它们的P1 DNA插入片段包含一个有序的重叠P1 DNA片段集合,覆盖了几乎98%的P1基因组。