Nasri M, Berry F, Sayadi S, Thomas D, Barbotin J N
Laboratoire de Technologie Enzymatique, UA Numero 523 du Centre National de la Recherche Scientifique, Université de Technologie de Compiègne, France.
J Gen Microbiol. 1988 Aug;134(8):2325-31. doi: 10.1099/00221287-134-8-2325.
The maintenance of the plasmid vectors pTG201 and pTG206 (which both carry the Pseudomonas putida xylE gene) and pB lambda H3 in Escherichia coli hosts was studied in free and immobilized continuous cultures. pTG201, containing the strong lambda PR promoter, was more quickly lost than plasmid pTG206, containing the tetracycline resistance gene promoter. The instability of pTG201 seems to be related to high expression of the cloned xylE genet. Fluctuations in the proportion of pTG201-containing cells were observed in the free system, suggesting the appearance of adaptive descendants (with and without plasmid) from the initial strains. The loss of plasmid vectors from E. coli cells and the fluctuations in the proportion of plasmid-containing cells could be prevented by immobilizing plasmid-containing bacteria in carrageenan gel beads.
在游离和固定化连续培养中研究了质粒载体pTG201和pTG206(二者均携带恶臭假单胞菌木糖异构酶基因)以及pB λ H3在大肠杆菌宿主中的维持情况。含有强λ PR启动子的pTG201比含有四环素抗性基因启动子的质粒pTG206更快丢失。pTG201的不稳定性似乎与克隆的木糖异构酶基因的高表达有关。在游离系统中观察到含pTG201细胞比例的波动,表明初始菌株出现了适应性后代(有质粒和无质粒)。通过将含质粒的细菌固定在角叉菜胶凝胶珠中,可以防止大肠杆菌细胞中质粒载体的丢失以及含质粒细胞比例的波动。