首页> 美国卫生研究院文献>Journal of Bacteriology >The Escherichia coli stpA gene is transiently expressed during growth in rich medium and is induced in minimal medium and by stress conditions.
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The Escherichia coli stpA gene is transiently expressed during growth in rich medium and is induced in minimal medium and by stress conditions.

机译:大肠杆菌stpA基因在丰富的培养基中生长过程中瞬时表达并在最低培养基和压力条件下被诱导。

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摘要

The transcriptional regulation of the stpA gene, encoding the Escherichia coli H-NS-like protein StpA, has been studied as a function of a variety of environmental conditions, and its response to trans-acting factors has been characterized. Chromosomally located stpA is expressed primarily from a promoter immediately upstream of the gene which is severely repressed by the homologous nucleoid-associated protein H-NS. However, we show here that even in a strain containing functional H-NS, stpA is transiently induced during growth of a batch culture in rich medium. It can also be induced strongly by osmotic shock and, to a lesser extent, by an increase in growth temperature. Moreover, when cells are grown in minimal medium, we observe a more sustained induction of stpA which is dependent on the leucine-responsive regulatory protein (Lrp). This enhanced level of stpA transcription is virtually abolished in an H-NS-independent manner when the culture undergoes carbon starvation. A sensitivity of the stpA promoter to DNA topology may contribute to some of these responses. Results reported here show that cloned fragments of the stpA promoter region can confer H-NS and Lrp responsiveness upon a lacZ reporter gene and suggest that several hundred base pairs of DNA upstream of the transcriptional start may be required for regulation by these two proteins.
机译:已经研究了编码大肠杆菌H-NS样蛋白StpA的stpA基因的转录调控与多种环境条件的关系,并已表征了其对反式作用因子的响应。位于染色体上的stpA主要由紧接在该基因上游的启动子表达,该启动子被同源核苷相关蛋白H-NS严重抑制。但是,我们在这里表明,即使在含有功能性H-NS的菌株中,在丰富培养基中分批培养的生长过程中,stpA也会被瞬时诱导。它也可以被渗透压强烈地诱导,并且在较小程度上被生长温度的升高强烈诱导。此外,当细胞在基本培养基中生长时,我们观察到更持久的stpA诱导,这取决于亮氨酸反应性调节蛋白(Lrp)。当培养物遭受碳饥饿时,这种增强的stpA转录水平实际上会以H-NS独立的方式被消除。 stpA启动子对DNA拓扑结构的敏感性可能会导致其中一些响应。此处报道的结果表明,stpA启动子区域的克隆片段可赋予lacZ报告基因H-NS和Lrp响应性,并暗示转录起点上游的数百个碱基对的DNA可能需要这两个蛋白进行调控。

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