Departments of Food Science and Microbiology, Southeast Dairy Foods Research Center, North Carolina State University, Raleigh, North Carolina 27695-7625.
Appl Environ Microbiol. 1991 Jan;57(1):283-8. doi: 10.1128/aem.57.1.283-288.1991.
We present a rapid method to isolate and analyze bacteriophage DNA. Cells are infected and phage replication is allowed to proceed normally for 30 to 60 min. Prior to DNA packaging and cell bursts, the infected cells (1 ml) are harvested and lysed by using a combination of lysozyme and sodium dodecyl sulfate treatments. The total DNA recovered is enriched for phage genomes, and restriction fragments of the phage DNA can be readily visualized on agarose gels. This method was used to grossly compare the genomes of nine lactococcal phages isolated from different cheese plants at different times. The method was also used to visualize the inhibitory effects of pTR2030-induced abortive infection on the replication of phage nck202.31 in its homologous host, Lactococcus lactis NCK203.
我们提出了一种快速分离和分析噬菌体 DNA 的方法。让细胞感染并使噬菌体复制正常进行 30 到 60 分钟。在 DNA 包装和细胞破裂之前,收获感染的细胞(1 毫升),并用溶菌酶和十二烷基硫酸钠处理进行裂解。回收的总 DNA 富含噬菌体基因组,并且噬菌体 DNA 的限制片段可以在琼脂糖凝胶上轻松可视化。该方法用于粗略比较从不同奶酪厂在不同时间分离的九种乳球菌噬菌体的基因组。该方法还用于可视化 pTR2030 诱导的流产感染对其同源宿主乳球菌 lactis NCK203 中噬菌体 nck202.31 复制的抑制作用。