首页> 外文期刊>Archives of microbiology >The kil gene of the ColE1 plasmid of Escherichia coli controlled by a growth-phase-dependent promoter mediates the secretion of a heterologous periplasmic protein during the stationary phase
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The kil gene of the ColE1 plasmid of Escherichia coli controlled by a growth-phase-dependent promoter mediates the secretion of a heterologous periplasmic protein during the stationary phase

机译:受生长期依赖性启动子控制的大肠杆菌ColE1质粒的kil基因在稳定期介导异源周质蛋白的分泌

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Heterologous gene products produced by Escherichia coli cells can be exported into the culture medium by the action of the kil gene of the ColE1 plasmid, which encodes a bacterial release protein. The kil gene was fused with the stationary-phase promoter of the fic gene of E. coli, and a secretion cassette (Kil-Km cassette) containing the regulated kil gene, the Km-resistance gene, and multiple cloning sites for the integration of target genes was constructed. Using the gene for beta-glucanase (bgl) as a target gene, it was shown that the protein produced was only secreted into the medium during the stationary phase. Quasi-lysis and lethality were not observed. The primary effect of the induction of the kil gene was the overproduction of beta-glucanase. The total amount produced per milliliter of bacterial culture was almost threefold higher than that of the corresponding Kil(-) control. The protein pattern of periplasm and culture medium was analyzed before and after induction of the kil gene expression, indicating that the release of periplasmic proteins is semiselective. This secretion system is the first to use a growth-phase-regulated promoter for the expression of the kil gene.
机译:由大肠杆菌细胞产生的异源基因产物可以通过ColE1质粒的kil基因的作用而输出到培养基中,该基因编码细菌释放蛋白。将kil基因与大肠杆菌fic基因的固定相启动子融合在一起,并与一个分泌盒(Kil-Km盒)融合,该分泌盒包含受调节的kil基因,Km抗性基因和多个克隆位点,用于整合靶基因被构建。使用β-葡聚糖酶(bgl)的基因作为靶标基因,表明产生的蛋白质仅在固定期分泌到培养基中。没有观察到准裂解和致死性。诱导kil​​基因的主要作用是β-葡聚糖酶的过量生产。每毫升细菌培养物产生的总量几乎比相应的Kil(-)对照高三倍。在诱导kil​​基因表达之前和之后分析周质和培养基的蛋白质模式,表明周质蛋白质的释放是半选择性的。该分泌系统是第一个使用生长阶段调控的启动子来表达kil基因的系统。

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