TY - JOUR
T1 - The inactivation of Escherichia coli O157:H7 during pulsed electric field (PEF) treatment in a static chamber
AU - Ravishankar, Sadhana
AU - Fleischman, Gregory J.
AU - Balasubramaniam, V. M.
N1 - Funding Information:
The ¢nancial support for this project was provided in part by a grant from US Army Natick Research Development Engineering Center, Natick, Massachusetts, USA and Collaborative Research and Development Agreement (CRA-DA) FD-000431 between US Food and Drug Administration and Illinois Institute of Technology. The authors are also grateful to Pure-Pulse Technologies (San Diego, California, USA) for the assistance of Mr Sam Lloyd, Ms C. McDonald, and Dr J. Dunn during the inception of this study; to Dr Rukma Reddy, FDA, Summit-Argo, Illinois, USA, for his suggestions concerning the microbiological aspects of this project; and, to Dr. Kenneth Ghiron of Magtherm Technologies, Emmaus, Pennsylvania, USA for his help with the electrostatic aspects of this project. References to commercial products and trade names are made with the understanding that no discrimination and no endorsement by Illinois Institute of Technology as well as Food and Drug Administration is implied.
PY - 2002/8
Y1 - 2002/8
N2 - The inactivation of Escherichia coli O157:H7 by pulsed electric field (PEF) processing as a function of electric field strength (15-30 kV cm-1), pulse number (1-20), temperature (5-65°C) and pH (3.5 and 6.8) was studied using a commercially available pulser, a static chamber and gellan gum gel as a suspension medium. The custom-designed static chamber achieved near-isothermal treatment conditions while eliminating flow field effects. Gellan gum gel was used to suspend the bacteria for treatment. It allowed uniform distribution of bacteria and neither inhibited nor promoted bacterial growth. The combination of equipment design and experimental protocol allowed the contribution of electrical (PEF) and thermal energy to be measured separately. In water-based gel, a maximum of 3 log reductions were achieved by PEF energy. Greater inactivation was observed at a treatment temperature of 55°C, but the additional inactivation was attributable entirely to thermal energy. Microbial injury was also observed at this temperature. At 60°C and above, complete inactivation was achieved, but this was attributable entirely to thermal energy. In water-based gellan gum gel adjusted to pH 3.5, again a 3 log reduction was achieved by PEF. In gel made from freshly squeezed apple juice naturally having the same pH, however, a maximum of 1.5 log reduction was observed.
AB - The inactivation of Escherichia coli O157:H7 by pulsed electric field (PEF) processing as a function of electric field strength (15-30 kV cm-1), pulse number (1-20), temperature (5-65°C) and pH (3.5 and 6.8) was studied using a commercially available pulser, a static chamber and gellan gum gel as a suspension medium. The custom-designed static chamber achieved near-isothermal treatment conditions while eliminating flow field effects. Gellan gum gel was used to suspend the bacteria for treatment. It allowed uniform distribution of bacteria and neither inhibited nor promoted bacterial growth. The combination of equipment design and experimental protocol allowed the contribution of electrical (PEF) and thermal energy to be measured separately. In water-based gel, a maximum of 3 log reductions were achieved by PEF energy. Greater inactivation was observed at a treatment temperature of 55°C, but the additional inactivation was attributable entirely to thermal energy. Microbial injury was also observed at this temperature. At 60°C and above, complete inactivation was achieved, but this was attributable entirely to thermal energy. In water-based gellan gum gel adjusted to pH 3.5, again a 3 log reduction was achieved by PEF. In gel made from freshly squeezed apple juice naturally having the same pH, however, a maximum of 1.5 log reduction was observed.
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U2 - 10.1006/fmic.2002.0484
DO - 10.1006/fmic.2002.0484
M3 - Article
AN - SCOPUS:0242500450
SN - 0740-0020
VL - 19
SP - 351
EP - 361
JO - Food Microbiology
JF - Food Microbiology
IS - 4
ER -