首页> 美国卫生研究院文献>Journal of Bacteriology >The HP0165-HP0166 Two-Component System (ArsRS) Regulates Acid-Induced Expression of HP1186 α-Carbonic Anhydrase in Helicobacter pylori by Activating the pH-Dependent Promoter
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The HP0165-HP0166 Two-Component System (ArsRS) Regulates Acid-Induced Expression of HP1186 α-Carbonic Anhydrase in Helicobacter pylori by Activating the pH-Dependent Promoter

机译:HP0165-HP0166两组分系统(ArsRS)通过激活pH依赖型启动子来调节酸性诱导的HP1186α-碳酸酐酶在幽门螺杆菌中的表达

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摘要

The periplasmic α-carbonic anhydrase of Helicobacter pylori is essential for buffering the periplasm at acidic pH. This enzyme is an integral component of the acid acclimation response that allows this neutralophile to colonize the stomach. Transcription of the HP1186 α-carbonic anhydrase gene is upregulated in response to low environmental pH. A binding site for the HP0166 response regulator (ArsR) has been identified in the promoter region of the HP1186 gene. To investigate the mechanism that regulates the expression of HP1186 in response to low pH and the role of the HP0165-HP0166 two-component system (ArsRS) in this acid-inducible regulation, Northern blot analysis was performed with RNAs isolated from two different wild-type H. pylori strains (26695 and 43504) and mutants with HP0165 histidine kinase (ArsS) deletions, after exposure to either neutral pH or low pH (pH 4.5). ArsS-dependent upregulation of HP1186 α-carbonic anhydrase in response to low pH was found in both strains. Western blot analysis of H. pylori membrane proteins confirmed the regulatory role of ArsS in HP1186 expression in response to low pH. Analysis of the HP1186 promoter region revealed two possible transcription start points (TSP1 and TSP2) located 43 and 11 bp 5′ of the ATG start codon, respectively, suggesting that there are two promoters transcribing the HP1186 gene. Quantitative primer extension analysis showed that the promoter from TSP1 (43 bp 5′ of the ATG start codon) is a pH-dependent promoter and is regulated by ArsRS in combating environmental acidity, whereas the promoter from TSP2 may be responsible for control of the basal transcription of HP1186 α-carbonic anhydrase.
机译:幽门螺杆菌的周质α-碳酸酐酶对于在酸性pH下缓冲周质至关重要。该酶是酸适应反应的重要组成部分,它可使这种中性粒细胞在胃中定植。响应低环境pH值,HP1186α-碳酸酐酶基因的转录被上调。在HP1186基因的启动子区域中已经确定了HP0166反应调节因子(ArsR)的结合位点。为了研究响应低pH值调节HP1186表达的机制,以及HP0165-HP0166两组分系统(ArsRS)在这种酸诱导的调节中的作用,对从两种不同的野生型分离的RNA进行了RNA印迹分析在暴露于中性pH或低pH(pH 4.5)后,HP型H. pylori菌株(26695和43504)以及具有HP0165组氨酸激酶(ArsS)缺失的突变体。在两个菌株中均发现了响应低pH的ArsS依赖性HP1186α-碳酸酐酶的上调。幽门螺杆菌膜蛋白的蛋白质印迹分析证实了ArsS在响应低pH时在HP1186表达中的调节作用。对HP1186启动子区域的分析揭示了两个可能的转录起始点(TSP1和TSP2)分别位于ATG起始密码子的43和11 bp 5'处,表明存在两个转录HP1186基因的启动子。定量引物延伸分析表明,来自TSP1的启动子(ATG起始密码子的43 bp 5')是pH依赖型启动子,并受ArsRS调控以对抗环境酸性,而来自TSP2的启动子可能负责控制基础HP1186α-碳酸酐酶的转录

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