4.6 Article

DnaK and GroEL chaperones are recruited to the Bacillus subtilis membrane after short-term ethanol stress

期刊

JOURNAL OF APPLIED MICROBIOLOGY
卷 112, 期 4, 页码 765-774

出版社

WILEY
DOI: 10.1111/j.1365-2672.2012.05238.x

关键词

Bacillus subtilis; ethanol stress; membrane; molecular chaperones; phospholipids

资金

  1. Grant Agency of Charles University in Prague [156/2006]
  2. MSMT [113100256]
  3. Ministry of Education, Youth and Sports of the Czech Republic [LC07017]
  4. Institutional Research Concepts [MSM0021620858, AV0Z50200510]

向作者/读者索取更多资源

Aims: To find out membrane tolerance strategy to ethanol in Bacillus subtilis that possesses a powerful system of protection against environmental stresses. Methods and Results: Cytoplasmic membranes of B. subtilis were severely affected by even short-term exposure to 3% (v / v) ethanol: the growth rate and membrane protein synthesis were markedly reduced, and no adaptive alterations in phospholipids were detected. Simultaneously, steady-state DPH fluorescence anisotropy (rss) showed that the membrane rigidity increased substantially. Analysis of the membrane phosphoproteome using in vitro labelling with [c-32 P] ATP revealed the association of DnaK and GroEL chaperones with membrane, indicating a stress induction process. Upon a long-term 3% (v / v) ethanol stress, the cell growth accelerated slightly and the composition of polar head groups and fatty acids of membrane phospholipids underwent an extensive reconstruction. Correspondingly, membrane fluidity turned back to the original rss values of the control cells. Conclusions: In B. subtilis, the adaptive response to short-term ethanol stress comprises the recruitment of molecular chaperones on the impaired membrane structure; consequently, the phospholipid synthesis is restored and membrane fluidity adapts properly to the continuing ethanol stress. Significance and Impact of the Study: These findings underline the role of membrane lipids in establishing tolerance towards ethanol and also suggest the contribution of molecular chaperones to the membrane and cell recovery.

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