Gorbunova S A, Ianenko A S, Akhverdian V Z, Reulets M A, Krylov V N
Genetika. 1985 Sep;21(9):1455-63.
Expression of transposable phages (TP) of Pseudomonas aeruginosa in the cells of P. putida was studied. The high efficiency of phage lytic development was shown both as a consequence of zygotic induction after transfer of the RP4::TPc+ plasmid into nonlysogenic recipients, and as a result of heat induction of lysogens PpG1 (D3112cts15). The high phage yield (20-25 particles of D3112cts phage per one cell of P. putida) is an evidence for a high level of transposition in the cells of this bacterial species. Plasmids RP4::TP are transferred into cells of PpG1 and PAO1 with similar frequency. However, the efficiency of establishment of the lysogenic state is lower in PpG1. Transposable phages of P. aeruginosa can integrate into the chromosome of PpG1 producing stable inducible lysogens. The presence of RP4 in the P. putida cells is not necessary for expression of transposable phages. The transposable phage D3112cts15 can be used in experiments of interspecies transduction of plasmids and chromosomal genes.
研究了铜绿假单胞菌的转座噬菌体(TP)在恶臭假单胞菌细胞中的表达。无论是将RP4::TPc +质粒转移到非溶源受体后通过合子诱导,还是通过溶源菌PpG1(D3112cts15)的热诱导,都显示出噬菌体裂解发育的高效率。高噬菌体产量(每一个恶臭假单胞菌细胞产生20 - 25个D3112cts噬菌体颗粒)证明了该细菌物种细胞中的转座水平很高。质粒RP4::TP以相似的频率转移到PpG1和PAO1细胞中。然而,在PpG1中建立溶源状态的效率较低。铜绿假单胞菌的转座噬菌体可以整合到PpG1的染色体中,产生稳定的可诱导溶源菌。恶臭假单胞菌细胞中RP4的存在对于转座噬菌体的表达不是必需的。转座噬菌体D3112cts15可用于质粒和染色体基因的种间转导实验。