Ohse M, Takahashi K, Kadowaki Y, Kusaoke H
Department of Applied Physics and Chemistry, Fukui University of Technology, Japan.
Biosci Biotechnol Biochem. 1995 Aug;59(8):1433-7. doi: 10.1271/bbb.59.1433.
Plasmid DNAs in the range from 2.9 to 12.6 kbp were transferred into Bacillus subtilis ISW1214 intact cells by the use of electroporation. The transformation efficiency (transformants per microgram plasmid DNA) decreased with increases of size of the DNA. However that of 2.0 x 10(3) transformants per microgram of DNA were done routinely, by using a plasmid with a large molecular size of 12.6 kbp. The size of plasmid DNA in the range of 3.7 to 12.6 kbp did not affect the molecular efficiency (transformants per molecule input DNA). The transformation efficiency as high as 9.3 x 10(4) transformants per microgram of purified plasmid pUB110 was obtained, using a cell concentration of 7.6 x 10(10) cells/ml and DNA concentration of 4 micrograms/ml in buffer containing 0.3 M sucrose, 1 mM CaCl2, and 1 mM sodium citrate (pH 6.0) under optimal pulse conditions of an electric field strength of 7 kV/cm and a duration of 500 mus with a single squared pulse at 0 degrees C. The gene expression for antibiotic resistance after electroporation was completed within 1.5 h. The transformants were confirmed to harbor the same intact plasmid by agarose gel electrophoretic analysis.
通过电穿孔法将2.9至12.6 kbp范围内的质粒DNA导入枯草芽孢杆菌ISW1214完整细胞中。转化效率(每微克质粒DNA的转化子数)随着DNA大小的增加而降低。然而,通过使用分子大小为12.6 kbp的大质粒,每微克DNA可常规获得2.0×10³个转化子。3.7至12.6 kbp范围内的质粒DNA大小不影响分子效率(每分子输入DNA的转化子数)。在含有0.3 M蔗糖、1 mM氯化钙和1 mM柠檬酸钠(pH 6.0)的缓冲液中,使用细胞浓度为7.6×10¹⁰个细胞/ml和DNA浓度为4微克/ml,在电场强度为7 kV/cm、持续时间为500微秒的最佳脉冲条件下于0℃进行单次方波脉冲处理,可获得每微克纯化质粒pUB110高达9.3×10⁴个转化子的转化效率。电穿孔后抗生素抗性的基因表达在1.5小时内完成。通过琼脂糖凝胶电泳分析确认转化子含有相同的完整质粒。