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中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2010, Vol. 30 Issue (09): 62-67    DOI: Q785
技术与方法     
利用T载体克隆快速构建布鲁氏菌缺失突变株
白耀霞1,2,杨毅2,王玉飞2,王同坤2,于爽2,陈燕芬2,付思美2,黄留玉2,田晋红1**,陈泽良2**
1.西南大学药学院 重庆 400716
2.军事医学科学院疾病预防控制所 北京 100071
Construction of Brucella Deletion Mutant by Using T Cloning Vector
BAI Yao-xia1,2,YANG Yi2,WANG Yu-fei2,WANG Tong-kun2,YU Shuang2,CHEN Yan-fen2,FU Si-mei2,HUANG Liu-yu2,TIAN Jin-hong1,CHENG Ze-liang2
1.College of Pharmaceutical Science, Southwest University, Chongqing 400716,China
2.Institute of Disease Control and Prevention, Academy of Military Medical Science, Beijing 100071,China
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摘要:

目的:建立一种基于T载体快速克隆构建布鲁氏菌突变株的方法,提高布鲁氏菌突变株构建的效率;方法:采用融合PCR的方法,将待缺失基因上下游的同源臂与卡那霉素抗性基因融合起来,构建突变盒,然后将突变盒直接与T载体连接,构建突变载体,将载体转入布鲁氏菌感受态细胞并筛选抗性克隆,进而获得布鲁氏菌的缺失突变株。结果:结合融合PCR和T载体快速克隆,能够在48h之内构建好突变载体,与传统的酶切连接相比,效率高、周期短。结论:基于T载体快速克隆是一种非常高效的构建突变株的方法,为布鲁氏菌突变株的构建提供了一种新方法。

关键词: 布鲁氏菌T载体突变株构建    
Abstract:

Control and Prevention, Academy of Military Medical Science, Beijing, 100071) Abstract: Construction of mutant strain is an essential method in pathogenesis researches. In the present study, the Brucella deletion mutant was constructed by using T cloning vector. At first, the homology arms of upstream and downstream of the target gene were fused with kanamycin resistance gene by fusion PCR. Then, the mutant cassette was ligated with T vector, resulted in the mutant plasmid. And the mutant plasmid was transformed into recombination competent cells and recombinants were selected by kanamycin resistance. As the results showed, the mutant construction was convenient and the mutant could be generated by only one round of selection with high efficiency. Therefore, this recombinational cloning strategy provides us a new method to construct the Brucella mutant and would accelerate gene function analysis of Brucella.

Key words: Brucella    T vector    Mutant construction
收稿日期: 2010-05-04 出版日期: 2010-08-25
基金资助:

国家自然科学基金(30901071)、“十一五”国家科技重大专项子课题(2008ZX1004015)、国家“973”计划(2009CB522602)资助项目

通讯作者: 田晋红;陈泽良     E-mail: zeliangchen@yahoo.com;13896057119@163.com
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白耀霞
杨毅
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于爽
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付思美
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陈泽良

引用本文:

白耀霞 杨毅 王玉飞 王同坤 于爽 陈燕芬 付思美 黄留玉 田晋红 陈泽良. 利用T载体克隆快速构建布鲁氏菌缺失突变株[J]. 中国生物工程杂志, 2010, 30(09): 62-67.

BAI Yao-Xia, YANG Yi, WANG Yu-Fei, WANG Tong-Kun, XU Shuang, CHEN Yan-Fen, FU Sai-Mei, HUANG Liu-Yu, TIAN Jin-Gong, CHEN Ze-Liang. Construction of Brucella Deletion Mutant by Using T Cloning Vector. China Biotechnology, 2010, 30(09): 62-67.

链接本文:

https://manu60.magtech.com.cn/biotech/CN/Q785        https://manu60.magtech.com.cn/biotech/CN/Y2010/V30/I09/62

[1] Boschiroli M L, Foulongne V, O’Callaghan D. Brucellosis: a worldwide zoonosis. Curr Opin Microbiol, 2001, 4: 5864. 
[2] Cutler S J, Whatmore A M, Commander NJ. Brucellosis—new aspects of an old disease. J Appl Microbiol, 2005, 98: 12701281. 
[3] den Hartigh A B, Sun Y H, Sondervan D, et al. Differential requirements for VirB1 and VirB2 during Brucella abortus infection. Infect Immun, 2004, 72: 51435149. 
[4] Ugalde J E, Comerci D J, Leguizamon M S, et al. Evaluation of Brucella abortus phosphoglucomutase (pgm) mutant as a new live roughphenotype vaccine. Infect Immun, 2003, 71: 62646269. 
[5] 乔凤, 陈泽良, 王玉飞, 等. pUC19K质粒的构建及其在布鲁氏菌突变株构建中的应用. 中国生物工程杂志, 2007, 27: 15. Qiao F,Chen Z L,Wang Y F, et al. China Biotechnology, 2007, 27: 15. 
[6] Boschiroli M L, OuahraniBettache S, Foulongne V, et al. The Brucella suis virB operon is induced intracellularly in macrophages. PNAS, 2002, 99: 1544 1549. 
[7] Boschiroli M L, OuahraniBettache S, Foulongne V, et al. Type IV secretion and Brucella virulence. Vet Microbiol, 2002, 90: 341348. 
[8] OrtizMartin I, Macho A P, Lambersten L, et al. Suicide vectors for antibiotic marker exchange and rapid generation of multiple knockout mutants by allelic exchange in Gramnegative bacteria. J Microbiol Methods, 2006, 67: 395407.

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