Duchrow M, Giffhorn F
J Bacteriol. 1987 Sep;169(9):4410-4. doi: 10.1128/jb.169.9.4410-4414.1987.
We constructed a physical map of the 50-kilobase-pair (kb) DNA of the temperate Rhodobacter sphaeroides bacteriophage phi RsG1, with the relative positions of the cleavage sites for the nine restriction endonucleases KpnI, HindIII, XbaI, ClaI, BclI, EcoRV, EcoRI, BglII, and BamHI indicated. Using biotinylated phi RsG1 DNA as a probe in hybridization studies, we detected homologies with virus DNA and fragments of restriction endonuclease-digested host chromosomal DNA but not with plasmid DNA. This indicates that the prophage is integrated into the host chromosome. In addition, the use of specific probes such as the 10.4-kb BglII A fragment and the 2.65-kb BamHI H fragment allowed the determination of the position of phage attachment site (attP).
我们构建了温和型球形红细菌噬菌体 phi RsG1 的 50 千碱基对(kb)DNA 的物理图谱,标明了九种限制性内切酶 KpnI、HindIII、XbaI、ClaI、BclI、EcoRV、EcoRI、BglII 和 BamHI 的切割位点的相对位置。在杂交研究中,使用生物素化的 phi RsG1 DNA 作为探针,我们检测到与病毒 DNA 以及限制性内切酶消化的宿主染色体 DNA 片段具有同源性,但与质粒 DNA 没有同源性。这表明原噬菌体已整合到宿主染色体中。此外,使用特定探针,如 10.4 kb 的 BglII A 片段和 2.65 kb 的 BamHI H 片段,能够确定噬菌体附着位点(attP)的位置。