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用Tn916、Tn4001和整合质粒载体对鸡毒支原体进行转化。

Transformation of Mycoplasma gallisepticum with Tn916, Tn4001, and integrative plasmid vectors.

作者信息

Cao J, Kapke P A, Minion F C

机构信息

Department of Micrlbiology, Immunology and Preventive Medicine, Iowa State University, Ames 50011.

出版信息

J Bacteriol. 1994 Jul;176(14):4459-62. doi: 10.1128/jb.176.14.4459-4462.1994.

Abstract

Mycoplasma gallisepticum causes respiratory disease in avian species, but little is known about its mechanism(s) of pathogenesis. These studies were undertaken in order to develop genetic systems for analysis of potential virulence factors. M. gallisepticum was transformed with plasmids containing one of the gram-positive transposons Tn916 or Tn4001, which inserted randomly into the mycoplasmal chromosome. Plasmids containing cloned chromosomal DNA were also constructed and tested for integration into regions of DNA homology derived either from chromosomal fragments or from the gentamicin resistance marker from Tn4001. These studies demonstrate that M. gallisepticum is amenable to transformation with both transposons and integrative vectors.

摘要

鸡毒支原体可引起禽类呼吸道疾病,但其致病机制尚不清楚。开展这些研究是为了开发用于分析潜在毒力因子的遗传系统。用含有革兰氏阳性转座子Tn916或Tn4001之一的质粒转化鸡毒支原体,这些转座子随机插入支原体染色体。还构建了含有克隆染色体DNA的质粒,并测试其整合到来自染色体片段或Tn4001庆大霉素抗性标记的DNA同源区域。这些研究表明,鸡毒支原体适合用转座子和整合载体进行转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d9b/205662/9a4094508708/jbacter00032-0276-a.jpg

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