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首页> 外文期刊>The biochemical journal >Conserved amphiphilic feature is essential for periplasmic chaperone HdeA to support acid resistance in enteric bacteria
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Conserved amphiphilic feature is essential for periplasmic chaperone HdeA to support acid resistance in enteric bacteria

机译:保守的两亲性特征对于周质伴侣HdeA支持肠细菌的抗酸性至关重要

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pThe extremely acidic environment of the mammalian stomach (pH 1–3) represents a stressful challenge for enteric pathogenic bacteria, including iEscherichia coli/i, iShigella/i and iBrucella/i. The ihdeA/i (ihns/i-dependent expression A) gene was found to be crucial for the survival of these enteric bacteria under extremely low pH conditions. We recently demonstrated that HdeA is able to exhibit chaperone-like activity exclusively within the stomach pH range by transforming from a well-folded conformation at higher pH values (above pH 3) into an unfolded conformation at extremely low pH values (below pH 3). This study was performed to characterize the action mechanisms and underlying specific structural features for HdeA to function in this unfolded conformation. In the present study, we demonstrate that the conserved ‘amphiphilic’ feature of HdeA, i.e. the exposure of the conserved hydrophobic region and highly charged terminal regions, is essential for exhibiting chaperone-like activity under extremely low pH conditions. Mutations that disrupt this amphiphilic feature markedly reduced the chaperone-like activity of HdeA. The results also strongly suggest that this acid-induced chaperone-like activity of HdeA is crucial for acid resistance of the enteric bacteria. Moreover, our new understanding of this amphiphilic structural feature of HdeA helps to better interpret how this unfolded (disordered) conformation could be functionally active./p
机译:>哺乳动物胃的极端酸性环境(pH值为1-3)代表了对肠道致病菌(包括大肠杆菌,志贺氏菌和志贺氏菌)的压力挑战。布鲁切拉。发现 hdeA (依赖hns的表达A)基因对于这些肠道细菌在极低pH条件下的存活至关重要。我们最近证明,HdeA能够通过从较高pH值(高于pH 3)的折叠良好的构象转变为极低pH值(低于pH 3)的未折叠构象,而仅在胃pH范围内表现出伴侣状活性。 3)。进行这项研究来表征HdeA在这种展开构象中起作用的作用机制和潜在的特定结构特征。在本研究中,我们证明了HdeA的保守的“两亲”特征,即保守的疏水区域和高电荷末端区域的暴露,对于在极低的pH条件下表现出类似伴侣的活性至关重要。破坏该两亲性特征的突变显着降低了HdeA的分子伴侣样活性。结果也强烈表明,HdeA的这种酸诱导的伴侣样活性对于肠细菌的抗酸性至关重要。此外,我们对HdeA的两亲结构特征的新理解有助于更好地解释这种未折叠(无序)构象如何发挥功能活性。

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