Comparison of intense pulsed light- and ultraviolet (UVC)-induced cell damage in Listeria monocytogenes and Escherichia coli O157:H7

被引:95
作者
Cheigh, Chan-Ick [2 ]
Park, Mi-Hyun [1 ]
Chung, Myong-Soo [2 ]
Shin, Jung-Kue [3 ]
Park, Young-Seo [1 ]
机构
[1] Kyungwon Univ, Dept Food Sci & Biotechnol, Gyeonggi Do 461701, Seongnam, South Korea
[2] Ewha Womans Univ, Dept Food Sci & Engn, Seoul 120750, South Korea
[3] Jeonju Univ, Dept Korean Tradit Food Culture, Jeonju 560759, South Korea
关键词
Intense pulsed light (IPL); UVC; Listeria monocytogenes; Escherichia coli O157:H7; Cell damage; CYCLOBUTANE PYRIMIDINE DIMERS; CRYPTOSPORIDIUM-PARVUM; UV-LIGHT; INACTIVATION; COLI; FOOD; RADIATION; DNA;
D O I
10.1016/j.foodcont.2011.11.032
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The purpose of this study was to compare the degree of microbial inactivation and cell damage induced by intense pulsed light (IPL) and short-wavelength ultraviolet (UVC) in Listeria monocytogenes and Escherichia coli O157:H7. The viability of the food-borne pathogens treated with IPL and UVC (254 nm) decreased exponentially with treatment time. Particularly dramatic reductions in L monocytogenes and E. coli O157:H7 were observed for IPL treatments at energy densities of 376 and 455 W/m(2), with an approximately 7-log reduction for a treatment time of 60-180 s. Also, a 4-fog reduction of L monocytogenes and a 5-log reduction of E. coli O157:H7 were achieved with UVC irradiation for 1200 s. The types and amounts of IPL- and UVC-induced DNA damage in both microorganisms were determined and compared. DNAs from cells irradiated with either IPL or UVC accumulated double-strand breaks (DSBs), single-strand breaks, and cyclobutane pyrimidine dimers, and with a similar pattern: however, more DSBs were detected following UVC than following IPL in both types of microorganism. Transmission electron microscopy observations of IPL- and UVC-induced cell damage clearly indicate that bacterial cell structures were destroyed by IPL treatment but not by UVC treatment. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:654 / 659
页数:6
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