Membrane permeabilization and cellular death of Escherichia coli, Listeria monocytogenes and Saccharomyces cerevisiae as induced by high pressure carbon dioxide treatment

被引:55
|
作者
Garcia-Gonzalez, L. [1 ,2 ]
Geeraerd, A. H. [4 ,5 ]
Mast, J. [6 ]
Briers, Y. [7 ]
Elst, K. [2 ]
Van Ginneken, L. [2 ]
Van Impe, J. F. [3 ]
Devlieghere, F. [1 ]
机构
[1] Univ Ghent, Lab Food Microbiol & Food Preservat, Dept Food Safety & Food Qual, B-9000 Ghent, Belgium
[2] Flemish Inst Technol Res VITO, Business Unit Separat & Convers Technol, B-2400 Mol, Belgium
[3] Katholieke Univ Leuven, Dept Chem Engn, B-3001 Leuven, Belgium
[4] Katholieke Univ Leuven, Dept Biosyst BIOSYST MeBioS, B-3001 Leuven, Belgium
[5] Katholieke Univ Leuven, Leuven Ctr Biosci Bioengn & Biotechnol BioSCENTre, B-3001 Leuven, Belgium
[6] Vet & Agrochem Res Ctr, Dept Biocontrol, B-1180 Uccle, Belgium
[7] Katholieke Univ Leuven, Dept Biosyst, Lab Gene Technol, B-3001 Louvain, Belgium
关键词
High pressure carbon dioxide; Membrane permeabilization; Propidium iodide; Escherichia coli; Listeria monocytogenes; Saccharomyces cerevisiae; LACTOBACILLUS-PLANTARUM; INACTIVATION; MICROORGANISMS; SURVIVAL; MODEL; CO2; KINETICS; TIME;
D O I
10.1016/j.fm.2009.12.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In this study, the relationship between (irreversible) membrane permeabilization and loss of viability in Escherichia coli, Listeria monocytogenes and Saccharomyces cerevisiae cells subjected to high pressure carbon dioxide (HPCD) treatment at different process conditions including temperature (35-45 degrees C), pressure (10.5-21.0 MPa) and treatment time (0-60 min) was examined. Loss of membrane integrity was measured as increased uptake of the fluorescent dye propidium iodide (PI) with spectrofluorometry, while cell inactivation was determined by viable cell count. Uptake of PI by all three strains indicated that membrane damage is involved in the mechanism of HPCD inactivation of vegetative cells. The extent of membrane permeabilization and cellular death increased with the severity of the HPCD treatment. The resistance of the three tested organisms to HPCD treatment changed as a function of treatment time, leading to significant tailing in the survival curves, and was dependent on pressure and temperature. The results in this study also indicated a HPCD-induced damage on nucleic acids during cell inactivation. Transmission electron microscopy showed that HPCD treatment had a profound effect on the intracellular organization of the micro-organisms and influenced the permeability of the bacterial cells by introducing pores in the cell wall. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:541 / 549
页数:9
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