Allan B J, Davies P, Carstens E B, Kropinski A M
Department of Microbiology and Immunology, Faculty of Medicine, Queen's University, Kingston, Ontario, Canada.
J Virol. 1989 Apr;63(4):1587-94. doi: 10.1128/JVI.63.4.1587-1594.1989.
The DNA of Pseudomonas aeruginosa rough-specific bacteriophage phi PLS27 was studied. The genome size as determined by summing the sizes of restriction fragments was 42.7 kilobase pairs. Of particular interest was the fact that the DNA was insensitive to certain common restriction endonucleases including EcoRI, BamHI, and HindIII. The ends of the phage DNA were cloned and sequenced, revealing direct repeats of 318 nucleotides. The left end of the genome when cloned into the promoter selection vector pKK232-8 exhibited promoter activity in Escherichia coli. Two promoters bearing greater than 70% sequence homology to the plasmid pNM74 TOL operon and PAK pilin promoters were identified.
对铜绿假单胞菌粗糙特异性噬菌体phi PLS27的DNA进行了研究。通过对限制片段大小求和确定的基因组大小为42.7千碱基对。特别令人感兴趣的是,该DNA对某些常见的限制内切酶不敏感,包括EcoRI、BamHI和HindIII。对噬菌体DNA的末端进行了克隆和测序,揭示了318个核苷酸的直接重复序列。当基因组的左端克隆到启动子选择载体pKK232-8中时,在大肠杆菌中表现出启动子活性。鉴定出了两个与质粒pNM74甲苯操纵子和PAK菌毛蛋白启动子具有大于70%序列同源性的启动子。