Danileĭchenko V V, Britskaia V S, Il'iashenko B N
Mol Gen Mikrobiol Virusol. 1990 Sep(9):23-6.
The plasmid RP4::Mu cts62 is transferred from Escherichia coli cells into a recipient strain Erwinia carotovora 268 by conjugation with the frequency 1.5-5 x 10(-7) per donor cell. The maximal frequencies of transfer are obtained by cultivation of donor and recipient cells for 3-5 h on the filters. Structural and functional validity of the plasmid in transconjugants is expressed in preservation of all antibiotic-resistant markers of RP4, thermosensitivity to growth at 42 degrees C as well as spontaneous and thermally-induced production and zygotic induction of bacteriophage determined by the genome of Mu cts62, total length of the plasmid restricts. Location and orientation of Mu cts62 genome in the plasmid restricts. Location and orientation of Mu cts62 genome in the plasmid RP4::Mu cts62 in Erwinia carotovora transconjugant cells has been determined. A single bacteriophage genome has been shown to transpose into the chromosome of the cell with the elimination of RP4 fragment under the conditions of thermal induction.
质粒RP4::Mu cts62通过接合作用从大肠杆菌细胞转移至受体菌株胡萝卜软腐欧文氏菌268,转移频率为每个供体细胞1.5 - 5×10⁻⁷。通过在滤膜上培养供体和受体细胞3 - 5小时可获得最大转移频率。转接合子中质粒的结构和功能有效性表现为保留RP4的所有抗生素抗性标记、对42℃生长的热敏感性以及由Mu cts62基因组决定的噬菌体的自发和热诱导产生及合子诱导,质粒全长受限。Mu cts62基因组在质粒中的位置和方向受限。已确定胡萝卜软腐欧文氏菌转接合子细胞中质粒RP4::Mu cts62内Mu cts62基因组的位置和方向。已表明在热诱导条件下,单个噬菌体基因组可转座至细胞染色体并消除RP4片段。