首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Broad-Host-Range Shuttle Vectors for Screening of Regulated Promoter Activity in Viridans Group Streptococci: Isolation of a pH-Regulated Promoter
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Broad-Host-Range Shuttle Vectors for Screening of Regulated Promoter Activity in Viridans Group Streptococci: Isolation of a pH-Regulated Promoter

机译:筛选Viridans链球菌中调控启动子活性的广泛宿主区间穿梭载体:pH调控启动子的分离

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摘要

Viridans group streptococci are major constituents of the normal human oral flora and are also identified as the predominant pathogenic bacteria in native valve infective endocarditis. Little information is available regarding the regulation of gene expression in viridans group streptococci, either in response to changes in the oral environment or during development of endocarditis. We therefore constructed a set of broad-host-range vectors for the isolation of promoters from viridans group streptococci that are activated by specific environmental stimuli in vitro or in vivo. A genomic library of Streptococcus gordonii strain CH1 was constructed in one of the new vectors, and this library was introduced into a homologous bacterium by using an optimized electroporation protocol for viridans group streptococci. Because viridans group streptococci entering the bloodstream from the oral cavity encounter an increase in pH, we selected promoters upregulated by this specific stimulus. One of the selected promoter sequences showed homology to the promoter region of the hydA gene from Clostridium acetobutylicum, the expression of which is known to be regulated by the environmental pH. The isolation of this pH-regulated promoter shows that S. gordonii can sense an increase in the environmental pH, which serves as a signal for bacterial gene activation. Furthermore, this demonstrates the usefulness of these new selection vectors in research on adaptive gene expression of viridans group streptococci and possibly also of other gram-positive bacteria.
机译:Viridans组链球菌是正常人口腔菌群的主要成分,也被确定为天然瓣膜感染性心内膜炎的主要致病菌。关于弧菌链球菌中基因表达调控的信息很少,无论是对口腔环境的变化还是在心内膜炎的发展过程中。因此,我们构建了一套宽宿主范围的载体,用于从体外或体内被特定环境刺激激活的vi族链球菌中分离出启动子。在其中一种新载体中构建了戈登链球菌菌株CH1的基因组文库,并通过使用针对viridis组链球菌的优化电穿孔方案将该文库引入同源细菌。由于vi虫类链球菌从口腔进入血流时会导致pH值升高,因此我们选择了受此特定刺激上调的启动子。所选的启动子序列之一显示出与来自丙酮丁醇梭菌的hydA基因的启动子区域同源,已知其表达受环境pH调节。分离此受pH调节的启动子表明,戈登酵母可以检测到环境pH的升高,这是细菌基因激活的信号。此外,这证明了这些新的选择载体在研究绿豆类链球菌以及可能还有其他革兰氏阳性细菌的适应性基因表达方面的有用性。

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