Wu K, Wood T K
Department of Chemical and Biochemical Engineering, University of California at Irvine, Irvine, California 92717-2575.
Biotechnol Bioeng. 1994 Oct;44(8):912-21. doi: 10.1002/bit.260440807.
The effectiveness of the hok/sok plasmid stability locus and mechanism of cloned-gene loss was evaluated in shake-flask cultures. Addition of the hok/sok locus dramitically increasedapparent plasmid segregational stability to the hok/sok(-) control. In terms of the number of generations before 10%of the population became plasmid-free, segregational stability was increased by 11- to 20-fold in different media in the absence of induction of the cloned-gene (hok/sok(+) plasmid stable for over 200 generations in all media tested). With constant expression of beta-galactosidase in the absence of an tibiotic, the segregational stability of the plasmid containing hok/sok was incresed more than 17- to 30-fold when beta-galactosidase was expressed at 7-15 wt % of total cell protein. Although the hok/sok system stabilized the plasmid well infour different media (Luria-Bertani (LB), LB glucose, M9C Trp, and a representative fedbatch medium), the ability of hok/sok to maintain the plasmid with induction of the cloned gene decreased as the complexity of the media increased. This result is better interpreted in terms of the influence of cloned-gene expression on plasmidmaintenance; plasmid segregational stability decreased linearly as specificbeta-galactosidase activity increased. (c) 1994 John Wiley & Sons, Inc.
在摇瓶培养中评估了hok/sok质粒稳定性位点的有效性以及克隆基因丢失的机制。添加hok/sok位点显著提高了相对于hok/sok(-)对照的表观质粒分离稳定性。就10%的群体变为无质粒之前的代数而言,在不诱导克隆基因的情况下,不同培养基中的分离稳定性提高了11至20倍(在所有测试培养基中,hok/sok(+)质粒稳定超过200代)。在无抗生素时β-半乳糖苷酶持续表达的情况下,当β-半乳糖苷酶表达量占总细胞蛋白的7 - 15 wt%时,含有hok/sok的质粒的分离稳定性提高了17至30倍以上。尽管hok/sok系统在四种不同培养基(Luria-Bertani(LB)、LB葡萄糖、M9C Trp和一种代表性的补料分批培养基)中能很好地稳定质粒,但随着培养基复杂性的增加,hok/sok在诱导克隆基因时维持质粒的能力下降。根据克隆基因表达对质粒维持的影响来解释这一结果会更好;随着特异性β-半乳糖苷酶活性的增加,质粒分离稳定性呈线性下降。(c) 1994 John Wiley & Sons, Inc.