Universidad de Buenos Aires, FCEyN, Department de Química Biológica, Bs As, Argentina.
J Microbiol Methods. 2010 Nov;83(2):164-7. doi: 10.1016/j.mimet.2010.08.017. Epub 2010 Aug 31.
We here describe a new method for electroporation of Lactobacillus species, obligately homofermentative and facultatively heterofermentative, based on the cell-wall weakening resulting from growth in high-salt media. For L. casei, optimum transformation efficiency of up to 10(5) transformants per microgram of plasmid DNA was achieved following growth in the presence of 0.9 M NaCl. Plasmids of different sizes and replication origins were also similarly transformed. These competent cells could be used either directly or stored frozen, up to 1 month, for future use, with similar efficiency. This protocol was assayed with different Lactobacillus species: L. delbrueckii subsp. lactis, L. paracasei, L. plantarum and L. acidophilus, and it was found that they were transformed with similar efficiency.
我们在这里描述了一种基于高盐环境下生长导致细胞壁弱化的新型电穿孔方法,可用于同型发酵和兼性异型发酵的乳杆菌属细菌。对于干酪乳杆菌,在 0.9 M NaCl 存在的情况下生长时,其最佳转化效率高达每微克质粒 DNA 10(5)个转化体。不同大小和复制起点的质粒也可以同样转化。这些感受态细胞可以直接使用或冷冻保存长达 1 个月,用于未来的使用,效率相似。该方案已在不同的乳杆菌属物种中进行了检测:德氏乳杆菌亚种乳亚种、副干酪乳杆菌、植物乳杆菌和嗜酸乳杆菌,发现它们的转化效率相似。