Schmieger H, Buch U
Mol Gen Genet. 1975 Sep 29;140(2):111-22. doi: 10.1007/BF00329779.
The kinetics of production of transducing particles for different bacterial markers were followed by premature lysis of Salmonella typhimurium cells infected with P22 phages. The were compared for cells infected with wild type phage or with HT-mutants which show increased transduction frequencies. Measuring the sedimentation velocity of bacterial DNA of cells infected with wild type or HT-phages, it was shown that: a) there is no cutting of DNA at random; b) original fragments necessary for packaging host DNA into transducing particles cannot be smaller than 10 phage-genome lengths; c) cutting of transducing fragments leads immediately to the right length; d) there is no loss of precipitable DNA due to phage infection.
通过对感染P22噬菌体的鼠伤寒沙门氏菌细胞进行过早裂解,追踪了不同细菌标记转导颗粒的产生动力学。对感染野生型噬菌体或转导频率增加的HT突变体的细胞进行了比较。通过测量感染野生型或HT噬菌体的细胞中细菌DNA的沉降速度,结果表明:a)DNA不是随机切割的;b)将宿主DNA包装到转导颗粒中所需的原始片段不能小于10个噬菌体基因组长度;c)转导片段的切割会立即产生合适的长度;d)噬菌体感染不会导致可沉淀DNA的损失。