Nakashima Y, Ikeda H, Kakita Y, Miake F, Watanabe K
Microbiology Laboratory, Faculty of Pharmaceutical Sciences, Fukuoka University, Japan.
J Gen Virol. 1994 Sep;75 ( Pt 9):2537-41. doi: 10.1099/0022-1317-75-9-2537.
A restriction map of the genomic DNA of Lactobacillus casei phage PL-1 was constructed using the restriction endonucleases BamHI, EcoRI, HindIII, KpnI, NruI and XhoI. The PL-1 genome was 42.2 kb in size and had complementary cohesive ends forming a ring-like monomer. The cohesive ends, analysed with exonuclease III and S1 nuclease, were 3'-terminated single strands protruding from both ends. The nucleotide sequence of the cohesive ends, determined by the dideoxynucleotide method, comprised four A + T and 10 G + C pairs: 5' GAGGCCGACCGTTC 3'/3' CTCCGGCTGGCAAG 5'. Thus, the cohesive ends of PL-1 DNA were higher in G + C content than those of other known bacteriophage DNAs.
使用限制性内切酶BamHI、EcoRI、HindIII、KpnI、NruI和XhoI构建了干酪乳杆菌噬菌体PL-1基因组DNA的限制性图谱。PL-1基因组大小为42.2 kb,具有互补的粘性末端,形成环状单体。用核酸外切酶III和S1核酸酶分析的粘性末端是从两端突出的3'-末端单链。通过双脱氧核苷酸法测定的粘性末端的核苷酸序列由四个A + T和10个G + C对组成:5' GAGGCCGACCGTTC 3'/3' CTCCGGCTGGCAAG 5'。因此,PL-1 DNA的粘性末端的G + C含量高于其他已知噬菌体DNA的粘性末端。