Mar'ina O V, Gerasimova T V, Bekkarevich A O, Khrenova E A, Ianenko A S
Genetika. 1992 Oct;28(10):48-57.
Plasmid DNA transduction with mini-D3112 delta H, deletion derivative of phage D3112, which lost the genes essential for phage growth but retained the sites required for transposition and packaging was studied. Unlike D3112, mini-D3112 delta H element can transduce plasmids and plasmid markers at frequencies of 10(-5)-10(-8) in rec+ cells of Pseudomonas aeruginosa. Plasmids R1162 and R388 of the size smaller than phage genome were transduced intact. Large plasmids, like RP4 and R151, were deleted under transduction. By this way, we isolated deletion derivatives of RP4. The smallest derivative pN2 contained a 4.5 kb fragment of RP4. Unlike the latter, pN2 plasmid had narrow host range and did not maintain in Escherichia coli cells.
研究了用噬菌体D3112的缺失衍生物mini-D3112 delta H进行质粒DNA转导,该衍生物失去了噬菌体生长所必需的基因,但保留了转座和包装所需的位点。与D3112不同,mini-D3112 delta H元件能在铜绿假单胞菌的rec+细胞中以10(-5)-10(-8)的频率转导质粒和质粒标记。小于噬菌体基因组大小的质粒R1162和R388被完整转导。像RP4和R151这样的大质粒在转导过程中被缺失。通过这种方式,我们分离出了RP4的缺失衍生物。最小的衍生物pN2包含RP4的一个4.5 kb片段。与后者不同,pN2质粒宿主范围狭窄,不能在大肠杆菌细胞中维持。