Fonshteĭn M Iu, Iankovskiĭ N K
Genetika. 1986 Aug;22(8):2042-7.
Circular monomeric lambda DNA molecules were used as a substrate for packaging reaction in vitro. For obtaining lambda DNA in circular monomeric form only, Escherichia coli recA plasmid bearing cells were used. This hybrid DNA molecule which we designated phasmid lambda pMYF11, is the pBR322 plasmid in which lambda 47.1 DNA was introduced in vitro. The phasmid can exist in the plasmid form or as a non-defective phage. The efficiency of packaging reaction in vitro proved to be similar for monomeric circular and linear form of phasmid DNA molecules. The cI- variant of the phasmid is not able to exist as a plasmid even in the cells containing homoimmune prophage. Still, cI+ phasmid variants capable of lysogenizing arise with low frequency, as a result of recombination between the resident cI+ prophage and infecting cI- phasmid.
环状单体λ DNA 分子被用作体外包装反应的底物。为了仅获得环状单体形式的λ DNA,使用了携带大肠杆菌recA 质粒的细胞。我们将这种杂合 DNA 分子命名为噬菌粒λ pMYF11,它是在体外引入了λ 47.1 DNA 的 pBR322 质粒。该噬菌粒可以以质粒形式存在,也可以作为无缺陷噬菌体存在。事实证明,噬菌粒 DNA 分子的单体环状和线性形式在体外包装反应中的效率相似。即使在含有同源免疫原噬菌体的细胞中,噬菌粒的 cI-变体也不能以质粒形式存在。不过,由于常驻 cI+原噬菌体与感染性 cI-噬菌粒之间的重组,能够进行溶原化的 cI+噬菌粒变体仍以低频率出现。