Construction of recombinant plasmid using Neo/E Technology.
- Author:
Shan-Hu LI
1
;
Jian WANG
;
Jie-Zhi LI
;
Cui-Fen HUANG
;
Jian-Guang ZHOU
Author Information
1. Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100850, China.
- Publication Type:Journal Article
- MeSH:
Bacteriophage lambda;
genetics;
DNA, Recombinant;
genetics;
Escherichia coli;
genetics;
Genetic Engineering;
Plasmids;
genetics;
Rec A Recombinases;
genetics;
metabolism;
Recombinant Proteins;
biosynthesis;
genetics
- From:Chinese Journal of Biotechnology
2005;21(4):520-523
- CountryChina
- Language:Chinese
-
Abstract:
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.
