Li Shan-Hu, Wang Jian, Li Jie-Zhi, Huang Cui-Fen, Zhou Jian-Guang
Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100850, China.
Sheng Wu Gong Cheng Xue Bao. 2005 Jul;21(4):520-3.
A new neo/E counterselection technique was set up using Red recombination, which could be used in constructing recombinant plasmid. Firstly, linear targeting cassettes were amplified by PCR; secondly, two steps of homology recombination occurred in vivo: (1) The neo/E counterselection targeting cassette, consisting of a unique endonuclease recognition site and an antibiotic resistance gene, was introduced into the targeted region. (2) The neo/E cassette was replaced in the second round of recombination by another linear targeting cassettes DNA fragment carrying the targeted gene. For selecting a correct recombinant plasmid from the mixture of nonrecombinant and recombinant clones, the unique endonuclease recognition site in the nonrecombinant clones was cut by endonuclease and then transformed into the E. coli competent cells, up to 20% correct recombinants were yielded. A recombinant plasmid of pGL3-Basic PC1900T was successfully constructed in this way. Application of this technique offers a new and highly efficient way for recombinant plasmids construction.
利用Red重组建立了一种新的neo/E反选择技术,该技术可用于构建重组质粒。首先,通过PCR扩增线性靶向盒;其次,在体内发生两步同源重组:(1)由独特的核酸内切酶识别位点和抗生素抗性基因组成的neo/E反选择靶向盒被引入到目标区域。(2)在第二轮重组中,neo/E盒被携带目标基因的另一个线性靶向盒DNA片段取代。为了从非重组和重组克隆的混合物中筛选出正确的重组质粒,用核酸内切酶切割非重组克隆中的独特核酸内切酶识别位点,然后转化到大肠杆菌感受态细胞中,可产生高达20%的正确重组体。通过这种方法成功构建了pGL3-Basic PC1900T重组质粒。该技术的应用为重组质粒的构建提供了一种新的高效方法。