A Comprehensive Proteomics and Transcriptomics Analysis of<i>Bacillus subtilis</i>Salt Stress Adaptation

  • Hannes Hahne
    Institut für Mikrobiologie, Ernst-Moritz-Arndt Universität, Greifswald, Germany
  • Ulrike Mäder
    Interfaculty Institute for Genetics and Functional Genomics, Department of Functional Genomics, Ernst-Moritz-Arndt Universität, Greifswald, Germany
  • Andreas Otto
    Institut für Mikrobiologie, Ernst-Moritz-Arndt Universität, Greifswald, Germany
  • Florian Bonn
    Institut für Mikrobiologie, Ernst-Moritz-Arndt Universität, Greifswald, Germany
  • Leif Steil
    Interfaculty Institute for Genetics and Functional Genomics, Department of Functional Genomics, Ernst-Moritz-Arndt Universität, Greifswald, Germany
  • Erhard Bremer
    Laboratory for Microbiology, Department of Biology, Philipps-Universität, Marburg, Germany
  • Michael Hecker
    Institut für Mikrobiologie, Ernst-Moritz-Arndt Universität, Greifswald, Germany
  • Dörte Becher
    Institut für Mikrobiologie, Ernst-Moritz-Arndt Universität, Greifswald, Germany

書誌事項

公開日
2010-02
権利情報
  • https://journals.asm.org/non-commercial-tdm-license
DOI
  • 10.1128/jb.01106-09
公開者
American Society for Microbiology

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説明

<jats:title>ABSTRACT</jats:title><jats:p>In its natural habitats,<jats:italic>Bacillus subtilis</jats:italic>is exposed to changing osmolarity, necessitating adaptive stress responses. Transcriptomic and proteomic approaches can provide a picture of the dynamic changes occurring in salt-stressed<jats:italic>B. subtilis</jats:italic>cultures because these studies provide an unbiased view of cells coping with high salinity. We applied whole-genome microarray technology and metabolic labeling, combined with state-of-the-art proteomic techniques, to provide a global and time-resolved picture of the physiological response of<jats:italic>B. subtilis</jats:italic>cells exposed to a severe and sudden osmotic upshift. This combined experimental approach provided quantitative data for 3,961 mRNA transcription profiles, 590 expression profiles of proteins detected in the cytosol, and 383 expression profiles of proteins detected in the membrane fraction. Our study uncovered a well-coordinated induction of gene expression subsequent to an osmotic upshift that involves large parts of the SigB, SigW, SigM, and SigX regulons. Additionally osmotic upregulation of a large number of genes that do not belong to these regulons was observed. In total, osmotic upregulation of about 500<jats:italic>B. subtilis</jats:italic>genes was detected. Our data provide an unprecedented rich basis for further in-depth investigation of the physiological and genetic responses of<jats:italic>B. subtilis</jats:italic>to hyperosmotic stress.</jats:p>

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