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Insight into the proteome of the hyperthermophilic Crenarchaeon Ignicoccus hospitalis: the major cytosolic and membrane proteins

机译:深入了解嗜热克氏杆菌球菌医院的蛋白质组:主要的胞质和膜蛋白

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摘要

Ignicoccus hospitalis, a hyperthermophilic, chemolithoautotrophic Crenarchaeon, is the host of Nanoarchaeum equitans. Together, they form an intimate association, the first among Archaea. Membranes are of fundamental importance for the interaction of I. hospitalis and N. equitans, as they harbour the proteins necessary for the transport of macromolecules like lipids, amino acids, and cofactors between these organisms. Here, we investigated the protein inventory of I. hospitalis cells, and were able to identify 20 proteins in total. Experimental evidence and predictions let us conclude that 11 are soluble cytosolic proteins, eight membrane or membrane-associated proteins, and a single one extracellular. The quantitatively dominating proteins in the cytoplasm (peroxiredoxin; thermosome) antagonize oxidative and temperature stress which I. hospitalis cells are exposed to at optimal growth conditions. Three abundant membrane protein complexes are found: the major protein of the outer membrane, which might protect the cell against the hostile environment, forms oligomeric complexes with pores of unknown selectivity; two other complexes of the cytoplasmic membrane, the hydrogenase and the ATP synthase, play a key role in energy production and conversion.
机译:Ignicoccus hospitalis是一种嗜热性,嗜化学性自养的克雷纳查犬,它是马纳诺氏菌的宿主。他们共同组成了一个亲密的协会,这是古细菌中的第一个。膜对于I. Hospitalis和N. equitans的相互作用至关重要,因为它们具有在这些生物之间转运大分子(如脂质,氨基酸和辅因子)所需的蛋白质。在这里,我们调查了I. hospitalis细胞的蛋白质库存,并能够识别出总共20种蛋白质。实验证据和预测让我们得出结论,其中11种是可溶性胞质蛋白,8种膜或膜相关蛋白,以及1种是胞外蛋白。细胞质中占主导地位的蛋白质(过氧化物酶;体温体)可拮抗医院细菌细胞在最佳生长条件下暴露的氧化和温度胁迫。发现了三种丰富的膜蛋白复合物:外膜的主要蛋白可以保护细胞免受恶劣环境的影响,形成具有未知选择性孔的寡聚复合物。细胞质膜的另外两个复合物,氢化酶和ATP合酶,在能量产生和转化中起关键作用。

著录项

  • 来源
    《Archives of Microbiology》 |2008年第3期|379-394|共16页
  • 作者单位

    Centre for Electron Microscopy Faculty for Biology and Preclinical Medicine University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Centre for Electron Microscopy Faculty for Biology and Preclinical Medicine University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Centre for Electron Microscopy Faculty for Biology and Preclinical Medicine University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Institute for Microbiology University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Centre for Electron Microscopy Faculty for Biology and Preclinical Medicine University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Institute for Microbiology University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Institute for Biochemistry University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Institute for Biochemistry University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Membrane Biochemistry Max-Planck-Institute of Biochemistry Am Klopferspitz 18 82152 Martinsried Germany;

    Institute for Physical Biochemistry University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Institute for Microbiology University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Institute for Microbiology University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

    Centre for Electron Microscopy Faculty for Biology and Preclinical Medicine University of Regensburg Universitätsstraße 31 93053 Regensburg Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Crenarchaeota; Chemolithoautotrophy; Proteome; MALDI; Ignicoccus hospitalis;

    机译:EOMYCOTAY;化石自养;蛋白质组;MALDI;医院球菌;

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