期刊文献+

杜氏利什曼原虫遗传转化中潮霉素及嘌呤霉素适宜浓度的筛选 被引量:2

STUDY ON THE OPTIMAL MASS CONCENTRATION OF HYGROMYCIN AND PUROMYCIN IN LEISHMANIA DONOVANI TRANSFORMATION
下载PDF
导出
摘要 通过基因打靶构建基因缺失株是利什曼原虫分子水平研究的有效方法,而筛选特定的转化体是研究成功的第1步。筛选转化体常用抗生素筛选法。本文通过观察潮霉素和嘌呤霉素不同质量浓度对杜氏利什曼原虫四川分离株的生长抑制情况,确定了在抗性基因转化的阳性克隆筛选中,潮霉素及嘌呤霉素的适宜筛选浓度分别为32和10μg/mL。本实验的结果为下一步筛选杜氏利什曼原虫基因缺失株提供了可靠的实验依据。 Generation of gene deletion mutant by gene targeting is an effective method on Leishmania research on molecular level and screen of specific transformant is an important step. The popular method for transformant selection is to add antibiotics. The selection effects on Leishmania donovani with different mass concentration of hygromycin and puromycin were determinded. The results showed that the optimal mass concentration of hygromycin and puromycin was 32 μg/mL and 10 μg/mL respectively, which could provide a credible experimental data for selection of gene deletion mutant of Leishmania donovani.
出处 《寄生虫与医学昆虫学报》 CAS 2008年第2期120-122,共3页 Acta Parasitologica et Medica Entomologica Sinica
基金 国家自然科学基金资助项目(No.30500422)
关键词 杜氏利什曼原虫 潮霉素 嘌呤霉素 浓度 转化 Leishmania donovani Hygromycin Puromycin Concentration Transformation
  • 相关文献

参考文献5

  • 1Beverley, S. M. 2003 Protozomics: trypanosomatid parasite genetics comes of age. Nat. Rev. Genet., 4 (1): 11-19.
  • 2Bilang, R., S. lida, A. Peterhas, et al. 1991 The 3'-terminal region of the hygromycin-B-resistance gene is important for its activity in Escherichia coil and Nicotiana tabacum. Gene, 100: 247-250.
  • 3Burchmore, R. J., D. Rodriguez-Contreras, K. McBride, et al. 2003 Genetic characterization of glncose transporter function in Leishmania mexicana. Proc. Natl. Acad Sci. USA, 100 (7) : 3 901-3 906.
  • 4Gritz, L., and J. Davies. 1983 Plasmid-eneoded hygromyein B resistance: the sequence of hygromycin B phosphotransferase gene and its expression in Escherichia coli and Saecharomyces cerevisiae. Gene, 25 (2-3): 179-188.
  • 5Ilg, T. 2000 Lipophosphoglycan is not required for infection of macrophages or mice by Leishmania mexicana. EMBO J., 19 (9) : 1 953-1 962.

同被引文献115

引证文献2

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部