Hattermann D R, Stacey G
Department of Microbiology, University of Tennessee, Knoxville 37996-0845.
Appl Environ Microbiol. 1990 Apr;56(4):833-6. doi: 10.1128/aem.56.4.833-836.1990.
Intact cells of Bradyrhizobium japonicum USDA 110 were transformed with a 30-kilobase plasmid to efficiencies of 10(6) to 10(7) transformants per microgram by high-voltage electroporation. The technique was reliable and simple, with single colonies arising from transformed cells within 5 days of antibiotic selection. Plasmid DNA from B. japonicum transformed the Bradyrhizobium (Arachis) sp. with high efficiency, while the same plasmid extracted from Escherichia coli transformed B. japonicum at very low efficiency. The electrical conditions that resulted in the highest efficiencies were high voltage (10.5 to 12.5 kV/cm) and short pulse length (6 to 7 ms). A linear increase in the number of transformants was observed as DNA concentration was increased over 4 orders of magnitude; saturation appeared to begin between 120 ng/ml and 1.2 micrograms/ml. This novel method of transformation should enhance B. japonicum genetic research by providing a valuable alternative to conjugal mating, which is currently the only efficient, widely used means of introducing DNA into this organism.
用一个30千碱基的质粒通过高压电穿孔法转化日本慢生根瘤菌USDA 110的完整细胞,转化效率为每微克10⁶至10⁷个转化体。该技术可靠且简单,在抗生素选择后的5天内,转化细胞可形成单菌落。来自日本慢生根瘤菌的质粒DNA能高效转化慢生根瘤菌(花生)种,而从大肠杆菌中提取的相同质粒转化日本慢生根瘤菌的效率则非常低。产生最高转化效率的电参数是高电压(10.5至12.5 kV/cm)和短脉冲长度(6至7毫秒)。随着DNA浓度在4个数量级上增加,观察到转化体数量呈线性增加;饱和现象似乎在120 ng/ml至1.2 μg/ml之间开始出现。这种新型转化方法通过提供一种有价值的替代接合交配的方法,应该会加强日本慢生根瘤菌的遗传学研究,接合交配目前是将DNA导入该生物体的唯一有效且广泛使用的方法。