Kufer B, Backhaus H, Schmieger H
Mol Gen Genet. 1982;187(3):510-5. doi: 10.1007/BF00332636.
P22 lysates were grown on Salmonella strains carrying P22 prophages deleted to various extents. Transducing bacterial markers at both sides of the prophage insertion site it could be shown that: (i) transduction of markers can be enhanced by the prophage pac site; (ii) the recognition signal pac is in the area of gene 3 on the phage genome and thus close to the cutting site(s); (iii) transposon Tn10 may also act as a signal for packaging initiation; (iv) (at least) Tn10 initiates packaging sequences in both directions.
P22裂解物在携带不同程度缺失P22原噬菌体的沙门氏菌菌株上生长。通过转导原噬菌体插入位点两侧的细菌标记,可以证明:(i)原噬菌体pac位点可增强标记的转导;(ii)识别信号pac位于噬菌体基因组上基因3的区域,因此靠近切割位点;(iii)转座子Tn10也可作为包装起始的信号;(iv)(至少)Tn10在两个方向上启动包装序列。