Sabelnikov A G, Cymbalyuk E S, Gongadze G, Borovyagin V L
All Union Research Institute of Protein Biosynthesis, Moscow, U.S.S.R.
Biochim Biophys Acta. 1991 Jul 1;1066(1):21-8. doi: 10.1016/0005-2736(91)90245-4.
Structural changes undergone by Escherichia coli cell envelope membranes under the conditions of electrically induced gene (DNA) transfer (exponential pulse of about 13 kV/cm, tau = 5 ms) were studied by freeze-fracture electron microscopy. Special device similar to that of Stenger and Hui [1986) J. Membr. Biol. 93, 43-53), that allowed cryofixation of samples almost simultaneously with application of electric pulse, was employed to examine the cells within a short time (less than or equal to 1 s) after the pulse. Extensive blebbing of cells was observed immediately after the pulse. At later times (30-40 s after the pulse) blebbing was not detected, instead infrequent cellular membrane fusion and formation of large membrane 'opening' or pores were observed. An attempt to relate the observed membrane changes with cellular viability and permeability to exogenous DNA failed. Challenge of cells with a plasmid DNA 10 s after the pulse application resulted in a dramatic loss (at least four orders of magnitude) of the number of transformants compared to cells pulsed in the presence of DNA. On the other hand the results on additional pulsing of cell prior to the main electrotransformation procedure suggested that the life-time of membrane defects is at least no less than 2 min. Possible ways to reconcile the results are suggested.
通过冷冻断裂电子显微镜研究了大肠杆菌细胞膜在电诱导基因(DNA)转移条件下(约13 kV/cm的指数脉冲,τ = 5 ms)所经历的结构变化。采用了一种类似于Stenger和Hui [1986年,《膜生物学杂志》93卷,43 - 53页] 所使用的特殊装置,该装置能在施加电脉冲的几乎同时对样品进行冷冻固定,以便在脉冲后短时间内(小于或等于1秒)检查细胞。脉冲后立即观察到细胞广泛出现泡状凸起。在随后的时间(脉冲后30 - 40秒)未检测到泡状凸起,相反,观察到细胞内膜偶尔融合以及形成大的膜“开口”或孔。将观察到的膜变化与细胞活力以及对外源DNA的通透性联系起来的尝试未成功。与在DNA存在下进行脉冲处理的细胞相比,在脉冲施加10秒后用质粒DNA对细胞进行挑战导致转化体数量急剧减少(至少四个数量级)。另一方面,在主要电转化程序之前对细胞进行额外脉冲处理的结果表明,膜缺陷的持续时间至少不少于2分钟。文中提出了协调这些结果的可能方法。