4.7 Article

Analysis of Escherichia coli cell damage induced by HPCD using microscopies and fluorescent staining

期刊

INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY
卷 144, 期 1, 页码 169-176

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijfoodmicro.2010.09.017

关键词

E. coli; Outer membrane; Cytoplasmic membrane; Membrane fluidity; Fluorescence

资金

  1. Science and Technology Support of China [2006BAD05A02]
  2. Program for New Century Excellent Talents in University [NCET-06-0109]
  3. 863 High-Tech Plan of China [2007AA100405]

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20Cellular damage of Escherichia coli (E. coli) induced by high pressure carbon dioxide (HPCD) at 37-57 degrees C and 10-30 MPa for 5-75 min was investigated using scanning electronic microscopy (SEM), transmission electronic microscopy (TEM), confocal laser scanning microscopy (CLSM), and fluorospectrophotometer (FSM). HPCD-induced alterations in the morphology and the intracellular organization of E. coli cells was more susceptible to HPCD. A vast majority of HPCD-treated E. coli cells with seemingly intact morphology sustained severe damage in their intracellular organization. CLSM suggested that initial disruption of the outer membrane and later permeabilization of the cytoplasmic membrane of HPCD-treated E. coli cells was a consecutive and progressive process. These results were confirmed by FSM with the probes PI and SYTO 9. The membrane fluidity of HPCD-treated E. coli cells decreased as suggested by increased fluorescence polarization using FSM with the probe 1,6-diphenyl-1,3,5-hexatriene (DPH). The temperatures of 37,42 and 47 degrees C alone showed no impact on the outer membrane and membrane fluidity of E. coli cells whereas 57 degrees C alone had greater impact on them. Combined with HPCD, the temperatures of 37, 42 and 47 degrees C disrupted the outer membrane of E. coli cells without damage to the cytoplasmic membrane and of 57 degrees C damaged the cytoplasmic membrane, but all these temperatures decreased the membrane fluidity of E. coli cells. Higher temperature increased HPCD-induced outer membrane disruption and the cytoplasmic membrane damage and decreased the membrane fluidity. (C) 2010 Elsevier B.V. All rights reserved.

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