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pBaSysBioll: an integrative plasmid generating gfp transcriptional fusions for high-throughput analysis of gene expression in Bacillus subtilis

机译:pBaSysBioll:产生gfp转录融合蛋白的整合质粒,用于高通量分析枯草芽孢杆菌中的基因表达

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摘要

Plasmid pBaSysBioll was constructed for high-throughput analysis of gene expression in Bacillus subtilis. It is an integrative plasmid with a ligation-independent cloning (LIC) site, allowing the generation of transcriptional gfpmut3 fusions with desired promoters. Integration is by a Campbell-type event and is non-mutagenic, placing the fusion at the homologous chromosomal locus. Using phoA, murAA, gapB, ptsG and cggR promoters that are responsive to phosphate availability, growth rate and carbon source, we show that detailed profiles of promoter activity can be established, with responses to changing conditions being measurable within 1 min of the stimulus. This makes pBaSysBioll a highly versatile tool for real-time gene expression analysis in growing cells of B. subtilis.
机译:构建了质粒pBaSysBioll,用于高通量分析枯草芽孢杆菌中的基因表达。它是具有连接非依赖性克隆(LIC)位点的整合质粒,可生成具有所需启动子的转录gfpmut3融合体。整合是通过坎贝尔型事件进行的,并且是非诱变的,将融合置于同源染色体基因座上。使用对磷酸盐的可用性,生长速率和碳源有响应的phoA,murAA,gapB,ptsG和cggR启动子,我们显示可以建立启动子活性的详细情况,并且可以在刺激1分钟内测量对变化的条件的响应。这使pBaSysBioll成为用于枯草芽孢杆菌生长细胞中实时基因表达分析的高度通用的工具。

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