vd Pol H, Veltkamp E, Nijkamp H J
Mol Gen Genet. 1980;178(3):535-40. doi: 10.1007/BF00337858.
The presence of plasmid Clo DF13 in Escherichia coli cells alters the response of these cells to infection with the double stranded DNA phages P1vir, lambda vir or T1. The multiplication of these phages is reduced in Clo DF13 harbouring cells, resulting in an altered burstsize and plaque morphology. The degree of reduction is correlated to the amount of particular Clo DF13 gene product(s) in the cell. The genetic information of Clo DF13 involved in this plasmid-phage interaction could be located, using insertion and deletion mutants of Clo DF13, between 29 an 62% on the Clo DF13 physical map. The genetic analysis of this region shows that at least two different genes, K and L, coding for polypeptides with a molecular weight of respectively 21 KD and 10.5 KD, are located in this region. The results presented, indicate that gene L and not gene K is involved in the interaction of Clo DF13 with the propagation of double stranded DNA phages.
大肠杆菌细胞中质粒Clo DF13的存在改变了这些细胞对双链DNA噬菌体P1vir、λvir或T1感染的反应。在含有Clo DF13的细胞中,这些噬菌体的增殖减少,导致爆发量和噬菌斑形态发生改变。减少的程度与细胞中特定Clo DF13基因产物的量相关。利用Clo DF13的插入和缺失突变体,参与这种质粒-噬菌体相互作用的Clo DF13的遗传信息可以定位在Clo DF13物理图谱上的29%至62%之间。对该区域的遗传分析表明,至少有两个不同的基因K和L位于该区域,它们分别编码分子量为21 KD和10.5 KD的多肽。给出的结果表明,基因L而非基因K参与了Clo DF13与双链DNA噬菌体繁殖的相互作用。