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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Genetic regulation of spy gene expression in Escherichia coli in the presence of protein unfolding agent ethanol
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Genetic regulation of spy gene expression in Escherichia coli in the presence of protein unfolding agent ethanol

机译:在蛋白质展开剂乙醇存在下大肠杆菌间谍基因表达的遗传调节

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摘要

In a living cell, folding of proteins is assisted by molecular chaperones and other folding helpers. In Escherichia coli (E. coli), recently an ATP independent chaperon 'Spy' was discovered which is highly up-regulated in the presence of protein unfolding agents like ethanol, butanol and tannic acid. Two response regulators; BaeR and CpxR have been recognized as transcriptional regulators of spy gene. However, the mechanism of genetic regulation of spy under protein denaturants like ethanol has not been studied in detail so far. Based on a combination of genetic, molecular biology and biochemical experimental data, we propose that BaeR protein is the primary regulator of spy gene in response to ethanol stress in E. coli. In addition, we expanded the experimental spectrum and validated that regulation of spy gene in the presence of zinc and copper metal stress is primarily via BaeR and CpxR regulators respectively. We also performed in-silico analysis to identify the homologs of Spy protein and their cognate regulatory elements in bacterial species belonging to enterobacteriaceae family. Based on the unique ATP-independent chaperone nature and genetic regulation of spy we also propose its importance in biosensor development and facilitated production of properly folded recombinant proteins.
机译:在活性细胞中,分子伴侣和其他折叠助剂辅助蛋白质的折叠。在大肠杆菌(大肠杆菌)中,最近发现了ATP独立伴侣'SPY',其在蛋白质展开试剂如乙醇,丁醇和单宁酸等蛋白质展开试剂存在上高度调节。两个反应调节器; Baer和CPXR已被认为是间谍基因的转录调节因子。然而,到目前为止,迄今为止尚未详细地研究蛋白质脱乙醇下蛋白质变性剂下的间谍遗传调节机制。基于遗传,分子生物学和生物化学实验数据的组合,我们提出了Baer蛋白是响应于大肠杆菌中乙醇胁迫的间谍基因的主要调节因子。此外,我们扩展了实验频谱,并验证了在锌和铜金属应力存在下的间谍基因的调节分别通过抗疱疹和CPXR调节剂。我们还进行了硅藻分析,以鉴定属于肠杆菌族的细菌物种中的间谍蛋白及其同源调节元件的同源物。基于独特的ATP独立的伴侣性和间谍的遗传调节,我们还提出了其在生物传感器开发中的重要性,并促进了适当折叠的重组蛋白的生产。

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