Fan Q, Li S, Fu J, Zhai C, Chen Y, Liu B
Hua Xi Yi Ke Da Xue Xue Bao. 1992 Sep;23(3):293-6.
Shuttle vector plasmid pZ189 was used as a molecular tool and the SupF inserted in the plasmid was worked as a target gene for mutagenesis study. The host cells (E. coli MBM 7070) with pZ189 were treated with ethylmethane sulfonate (EMS) and plated on the selective media containing X-gal (5-bromo-4-chloro-3-indolyl-beta-D-galactoside) and IPTG (isopropyl-beta-D-thiogalactoside). The SupF and the LacZ amber mutant carried by the host cells complemented each other and thus made the colonies blue on the selective media. However the colonies derived from the SupF mutants changed the colour from blue to white. The mutant frequencies in a series of experiments with different concentrations of EMS were estimated. Furthermore, the DNA isolated from 5 SupF mutants was digested with restruiction enzyme Hha I. It suggests that the 214 bp Hha I fragments containing mutant SupF could be distinguished from their wild type counterparts by temperature-gradient gel electrophoresis under optimal conditions.
穿梭载体质粒pZ189被用作分子工具,插入质粒中的SupF作为诱变研究的靶基因。用甲磺酸乙酯(EMS)处理携带pZ189的宿主细胞(大肠杆菌MBM 7070),并接种在含有X-gal(5-溴-4-氯-3-吲哚基-β-D-半乳糖苷)和IPTG(异丙基-β-D-硫代半乳糖苷)的选择性培养基上。宿主细胞携带的SupF和LacZ琥珀突变体相互互补,因此在选择性培养基上菌落呈蓝色。然而,来自SupF突变体的菌落颜色从蓝色变为白色。估计了一系列不同浓度EMS实验中的突变频率。此外,从5个SupF突变体中分离的DNA用限制性内切酶Hha I消化。这表明在最佳条件下,通过温度梯度凝胶电泳,含有突变SupF的214 bp Hha I片段可以与其野生型对应物区分开来。