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通过电穿孔法对鳗弧菌和杀鱼巴斯德氏菌进行遗传转化。

Genetic transformation of Vibrio anguillarum and Pasteurella piscicida by electroporation.

作者信息

Cutrín J M, Toranzo A E, Barja J L

机构信息

Departamento de Microbiología y Parasitología, Facultad de Biología, Universidad de Santiago de Compostela, Spain.

出版信息

FEMS Microbiol Lett. 1995 Apr 15;128(1):75-80. doi: 10.1016/0378-1097(95)00086-k.

Abstract

Vibrio anguillarum and Pasteurella piscicida are Gram-negative bacteria which are pathogenic for marine fish and we report here the first successful transformation of these two bacteria by electroporation. The optimal conditions for electroporation included a field strength of 12.5 kV cm-1 and a time constant of 5 ms using 0.2-cm cuvettes. With these parameters, three plasmids (pSU2718, pCML, pEV3) with molecular sizes of 2.6, 5 and 13.7 kb, respectively were successfully transformed into both pathogens. V. anguillarum isolates belonging to serotypes O1 and O2 were transformed with greatest efficiency, 2.5 x 10(3) transformants per micrograms DNA, being achieved in the serotype O2 strains using plasmid pCML. Strains of serotype O3 were not transformed. In the case of P. piscicida the maximum efficiency achieved was 9.8 x 10(2) transformants per micrograms pCML plasmid DNA. This optimized system will allow development of procedures for the genetic manipulation of these pathogens.

摘要

鳗弧菌和杀鱼巴斯德氏菌是对海水鱼类致病的革兰氏阴性菌,我们在此报告首次通过电穿孔成功转化这两种细菌。电穿孔的最佳条件包括使用0.2厘米的比色杯,场强为12.5 kV cm-1,时间常数为5毫秒。利用这些参数,分别将分子大小为2.6、5和13.7 kb的三种质粒(pSU2718、pCML、pEV3)成功转化到这两种病原菌中。属于血清型O1和O2的鳗弧菌分离株转化效率最高,在使用质粒pCML的血清型O2菌株中,每微克DNA可获得2.5×10³个转化子。血清型O3的菌株未被转化。对于杀鱼巴斯德氏菌,每微克pCML质粒DNA获得的最大转化效率为9.8×10²个转化子。这个优化系统将有助于开发对这些病原菌进行基因操作的程序。

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