Warnes A, Stephenson J R
Plasmid. 1986 Sep;16(2):116-23. doi: 10.1016/0147-619x(86)90070-3.
The stability of genetically engineered bacterial plasmids under continuous culture fermentation is of crucial importance in the application of microbiology to many processes of potential industrial importance. In order to determine the effect of inserting large pieces of foreign DNA on the stability of bacterial plasmids we have studied the behavior of pAT153 with DNA inserts of various sizes derived from cytomegalovirus. Foreign DNA up to 2 kb in length had no effect on stability, whereas the insertion of an 8-kb fragment resulted in a transient instability. This instability was overcome by the spontaneous appearance of leu+ cells in the culture. Insertion of a 21-kb DNA fragment resulted in a rapid loss of plasmid, which was not prevented by the appearance of leu+ cells. In all cases copy number analyses indicated that plasmid loss was due to segregational instability, probably because the plasmid placed an unacceptable metabolic load on the cell.
在连续培养发酵过程中,基因工程细菌质粒的稳定性对于微生物学在许多具有潜在工业重要性的过程中的应用至关重要。为了确定插入大片段外源DNA对细菌质粒稳定性的影响,我们研究了携带源自巨细胞病毒不同大小DNA插入片段的pAT153的行为。长度达2 kb的外源DNA对稳定性没有影响,而插入一个8 kb的片段导致了短暂的不稳定性。这种不稳定性通过培养物中亮氨酸营养缺陷型(leu⁺)细胞的自发出现而得以克服。插入一个21 kb的DNA片段导致质粒迅速丢失,亮氨酸营养缺陷型(leu⁺)细胞的出现并不能阻止这种情况。在所有情况下,拷贝数分析表明质粒丢失是由于分离不稳定性,这可能是因为质粒给细胞带来了不可接受的代谢负担。