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首页> 外文期刊>Applied and Environmental Microbiology >The pH-Dependent Expression of the Urease Operon in Streptococcus salivarius Is Mediated by CodY
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The pH-Dependent Expression of the Urease Operon in Streptococcus salivarius Is Mediated by CodY

机译:CodY介导唾液链球菌尿素酶操纵子的pH依赖表达。

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摘要

Urease gene expression in Streptococcus salivarius 57.I, a strain of one of the major alkali producers in the mouth, is induced by acidic pH and excess amounts of carbohydrate. Expression is controlled primarily at the transcriptional level from a promoter, pureI. Recent sequencing analysis revealed a CodY box located 2 bases 5′ to the ?35 element of pureI. Using continuous chemostat culture, transcription from pureI was shown to be repressed by CodY, and at pH 7 the repression was more pronounced than that in cells grown at pH 5.5 under both 20 and 100 mM glucose. The direct binding of CodY to pureI was demonstrated by electrophoretic mobility shift assay and chromatin immunoprecipitation (ChIP)–quantitative real-time PCR (qPCR). The result of ChIP-qPCR also confirmed that the regulation of CodY is indeed modulated by pH and the binding of CodY at neutral pH is further enhanced by a limited supply of glucose (20 mM). In the absence of CodY, the C-terminal domain of the RNA polymerase (RNAP) α subunit interacted with the AT tracks within the CodY box, indicating that CodY and RNAP compete for the same binding region. Such regulation could ensure optimal urease expression when the enzyme is most required, i.e., at an acidic growth pH with an excess amount of carbon nutrients.
机译:唾液链球菌57.I中的脲酶基因表达是口腔中一种主要的碱产生剂,它是由酸性pH和过量碳水化合物诱导的。表达主要受启动子p ureI 的转录水平控制。最近的测序分析揭示了一个CodY盒,位于p ureI 的?35元素的5个碱基的2个碱基处。使用连续化学恒温器培养,显示pd ureI 的转录受CodY抑制,在pH 7时,抑制作用比在pH 5.5下生长的细胞更明显。 20和100 mM葡萄糖。电泳迁移率变动分析和染色质免疫沉淀(ChIP)-实时定量PCR(qPCR)证明了CodY与p ureI 的直接结合。 ChIP-qPCR的结果还证实,pH确实调节了CodY的调节,而葡萄糖的限量供应(20 mM)进一步增强了CodY在中性pH下的结合。在缺少CodY的情况下,RNA聚合酶(RNAP)α亚基的C末端结构域与CodY框内的AT轨道相互作用,表明CodY和RNAP竞争相同的结合区。当最需要酶时,即在酸性生长pH下,具有过量的碳营养素时,这种调节可以确保最佳的脲酶表达。

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