hirae肠球菌
电穿孔
穿梭机载体
大肠杆菌
质粒
转化(遗传学)
多克隆站点
PBR322电话
生物
克隆(编程)
微生物学
分子生物学
DNA
肠球菌
重组DNA
化学
表达式向量
载体(分子生物学)
遗传学
基因
计算机科学
程序设计语言
抗生素
作者
Marc Solioz,Marco Waser
出处
期刊:Biochimie
[Elsevier]
日期:1990-04-01
卷期号:72 (4): 279-283
被引量:28
标识
DOI:10.1016/0300-9084(90)90084-t
摘要
In the present study, an Enterococcus-Escherichia coli shuttle vector, pC3, was constructed that allows efficient transformation by electroporation of Enterococcus hirae ATCC9790. 5 x 10(6) transformants per microgram of plasmid DNA were obtained, using a commercial capacitor discharge device with an improved circuitry and a home-made electrode assembly, delivering pulses of 24 kV/cm across the cell suspension. The transformants were stable without selective pressure and plasmid DNA reisolated from transformed cells displayed no alterations in restriction enzyme analysis. Chromosomal DNA from E coli or E hirae, carried by pC3, was stably maintained in E hirae, making cloning and genetic manipulation in this organism feasible.
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