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Ⅱ型猪链球菌二元信号转导系统2148hk/rr基因敲除突变体的构建

Ⅱ型猪链球菌二元信号转导系统2148hk/rr基因敲除突变体的构建

ISSN:0253-2654
2008年第35卷第1期
医学微生物学
程功[1],李明[2],郑峰[2],王晶[2],王长军[2],潘秀珍[2],范红结[3],唐家琪[1] CHENG Gong[1],LI Ming[2],ZHENG Feng[2],WANG Jing[2],WANG Chang-Jun[2],PAN Xiu-Zhen[2],FAN Hong-Jie[3],TANG Jia-Qi[1]
  1. 南京农业大学动物医学院,南京,210095;南京军区军事医学研究所,南京,210002
  2. 南京军区军事医学研究所,南京,210002
  3. 南京农业大学动物医学院,南京,210095

构建猪链球菌2型(Streptococcus suis type 2)强毒株05ZYH33二元信号转导系统2148hk/rr基因敲除突变体.构建中间为壮观霉素抗性基因,两侧为2148hk/rr编码基因上、下游同源序列的基因敲除质粒,通过同源重组筛选2148hk/rr编码基因敲除突变体.PCR分析和Southern杂交结果均显示2148hk/rr编码基因完全被壮观霉素抗性基因替代,基因敲除突变体构建成功.筛选获得05ZYH33二元信号转导系统2148hk/rr基因敲除突变体,为阐明该调控系统在猪链球菌致病过程中的作用奠定了基础.

To construct gene knock-out mutant of a two-component signal transduction system named 2148hk/rr in Streptococcus suis type 2 virulent strain 05ZYH33. Recombinant gene knock-out vector was constructed consisting of Spcr cassette with flanking homology regions to the target genes, the isogenic 2148hk/rr-deficient mutant was screened by allelic replacement. PCR analysis and Southern hybridization confirmed that the coding genes of 2148hk/rr were replaced completely by spcr cassette. Conclusion The mutant of 05ZYH33 2148hk/rr system was successfully constructed, which laid the foundation for farther research on the role of this two-component signal transduction system during infection.

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ISSN:0253-2654
2008年第35卷第1期
医学微生物学

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