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Proteomic analysis of Haloferax volcanii reveals salinity-mediated regulation of the stress response protein PspA

机译:火山嗜盐杆菌的蛋白质组学分析揭示了盐度介导的应激反应蛋白PspA的调节。

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摘要

A proteomic survey of the halophilic archaeon Haloferax volcanii was performed by comparative two-dimensional gel electrophoresis in order to determine the molecular effects of salt stress on the organism. Cells were grown under optimal (2.1 M) and high (3.5 M) NaCl conditions. From this analysis, over 44 protein spots responsive to these conditions were detected. These spots were excised, digested in-gel with trypsin, subjected to QSTAR tandem mass spectrometry (LC/MS/MS) analysis, and identified by comparing the MS/MS-derived peptide sequence to that deduced from the H. volcanii genome. Approximately 40 % of the proteins detected (18 in total) displayed differential abundance based on the detection of at least two peptide fragments per protein and overall MOWSE scores of ⩾ 75 per protein. All of these identified proteins were either uniquely present or 2.3- to 26-fold higher in abundance under one condition compared to the other. The majority of proteins identified in this study were preferentially displayed under optimal salinity and primarily involved in translation, transport and metabolism. However, one protein of interest whose transcript levels were confirmed in these studies to be upregulated under high salt conditions was identified as a homologue of the phage shock protein PspA. The pspA gene belongs to the psp stress-responsive regulon commonly found among Gram-negative bacteria where its transcription is stimulated by a wide variety of stressors, including heat shock, osmotic shock and prolonged stationary-phase incubation. Homologues of PspA are also found among the genomes of cyanobacteria, higher plants and other Archaea, suggesting that this protein may retain some aspects of functional conservation across the three domains of life. Given its integral role in sensing a variety of membrane stressors in bacteria, these results suggest that PspA may play an important role in hypersaline adaptation in H. volcanii.
机译:通过比较二维凝胶电泳对嗜盐古细菌Haloferax volcanii进行蛋白质组学研究,以确定盐胁迫对生物的分子影响。细胞在最佳(2.1 M)和高(3.5 M)NaCl条件下生长。通过该分析,检测到超过44种对这些条件有反应的蛋白质斑点。切下这些斑点,用胰蛋白酶在凝胶中消化,进行QSTAR串联质谱分析(LC / MS / MS),并通过比较MS / MS衍生的肽序列与从火山嗜血杆菌基因组推导的肽序列进行鉴定。基于每个蛋白质至少两个肽片段的检测以及每个蛋白质⩾75的总体MOWSE得分,大约40%的蛋白质(总共18个)显示出不同的丰度。在一个条件下,所有这些鉴定出的蛋白质要么独特地存在,要么丰度高出2.3至26倍。本研究中鉴定出的大多数蛋白质优先显示在最佳盐度下,并且主要参与翻译,转运和代谢。但是,在这些研究中证实其转录水平在高盐条件下被上调的一种目标蛋白被鉴定为噬菌体休克蛋白PspA的同源物。 pspA基因属于在革兰氏阴性细菌中常见的psp应激反应性调节子,其转录受多种应激源刺激,包括热休克,渗透压休克和长期固定相孵育。在蓝细菌,高等植物和其他古细菌的基因组中也发现了PspA的同源物,这表明该蛋白可能在生命的三个域中保留某些功能保守性。鉴于其在检测细菌中各种膜应激源中所起的重要作用,这些结果表明PspA可能在火山嗜血杆菌的高盐适应中发挥重要作用。

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