Smirnova N I, Eroshenko G A, Livanova L F, Mozharov O T, Fil'kova S L, Il'ina T S
Genetika. 1990 Feb;26(2):206-14.
Two replicons, pOX38 (in F-factor derivative lacking all IS elements) and pCT105 (containing cholera toxin operon cloned in pBR322) have been fused to produce recombinant plasmid, pCO109, which was then introduced into Vibrio cholerae eltor by conjugation. Restriction analysis showed pCO109 to dissociate in V. cholerae cells at a higher frequency than in Escherichia coli strains, its pOX38 component being lost, while the pCT105 component demonstrated relative stability. V. cholerae eltor RV79 (pCT105) produced 4-5 micrograms/ml of cholera toxin. Occasional insertion of cloned vctA, B operon into RV79 chromosome was also observed.
两个复制子,即pOX38(存在于缺乏所有插入序列元件的F因子衍生物中)和pCT105(含有克隆于pBR322中的霍乱毒素操纵子)已被融合以产生重组质粒pCO109,随后通过接合作用将其导入霍乱弧菌埃尔托生物型。限制性分析表明,pCO109在霍乱弧菌细胞中的解离频率高于在大肠杆菌菌株中的解离频率,其pOX38组分丢失,而pCT105组分表现出相对稳定性。霍乱弧菌埃尔托生物型RV79(pCT105)产生4 - 5微克/毫升的霍乱毒素。还观察到克隆的vctA、B操纵子偶尔插入RV79染色体。