The relationship between membrane damage, release of protein and loss of viability in Escherichia coli exposed to high hydrostatic pressure

• Published in: International journal of food microbiology 2010-02, Vol.137 (2), p.214-220
• Main Authors: Klotz, Bernadette, Mañas, Pilar, Mackey, Bernard M.
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Buffers; Cell Membrane Permeability - physiology; cell membranes; Colony Count, Microbial; cytoplasm; E. coli; Escherichia coli; Escherichia coli - physiology; Escherichia coli Proteins - chemistry; Escherichia coli Proteins - metabolism; extracellular fluids; Fluorescent Dyes - metabolism; Food industries; Food microbiology; food pathogens; Fundamental and applied biological sciences. Psychology; high hydrostatic pressure; high pressure treatment; Hydrostatic Pressure; Membrane damage; Microbial Viability; Molecular Weight; pathogen survival; Propidium - metabolism; Protein leakage; proteins; Staining and Labeling; Temperature; viability
• ISSN: 0168-1605; 1879-3460
• DOI: 10.1016/j.ijfoodmicro.2009.11.020

The aim of this work was to examine a possible association between resistance of two Escherichia coli strains to high hydrostatic pressure and the susceptibility of their cell membranes to pressure-induced damage. Cells were exposed to pressures between 100 and 700 MPa at room temperature (∼ 20 °C) in phosphate-buffered-saline. In the more pressure-sensitive strain E. coli 8164, loss of viability occurred at pressures between 100 MPa and 300 MPa and coincided with irreversible loss of membrane integrity as indicated by uptake of propidium iodide (PI) and leakage of protein of molecular mass between 9 and 78 kDa from the cells. Protein release increased to a maximum at 400 MPa then decreased, possibly due to intracellular aggregation at the higher pressures. In the pressure-resistant strain E. coli J1, PI was taken up during pressure treatment but not after decompression indicating that cells were able to reseal their membranes. Loss of viability in strain J1 coincided with the transient loss of membrane integrity between approximately 200 MPa and 600 MPa. In E. coli J1 leakage of protein occurred before loss of viability and the released protein was of low molecular mass, between 8 and 11 kDa and may have been of periplasmic origin. In these two strains differences in pressure resistance appeared to be related to differences in the ability of their membranes to withstand disruption by pressure. However it appears that transient loss of membrane integrity during pressure can lead to cell death irrespective of whether cells can reseal their membranes afterwards.