期刊
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY
卷 131, 期 2-3, 页码 240-245出版社
ELSEVIER
DOI: 10.1016/j.ijfoodmicro.2009.03.005
关键词
Allyl isothiocyanate; E. coli O157:H7; Enzymatic inhibition; Decomposition products
资金
- Natural Science and Engineering Research Council of Canada (NSERC)
- Manitoba Graduate Scholarship
- Canadian Meat Science Association
- Percy Gitelman Memorial Scholarship
Allyl isothiocyanate (AIT) is derived from the glucosinolate sinigrin found in plants of the family Brassicaceae. It is a well-recognized antimicrobial agent against a variety of organisms. including foodborne pathogens such as Escherichia coli O157:H7. The efficiency of this natural agent in reducing E. coli O157:H7 numbers in food products have been reported. However. few have examined the mechanism by which AIT and perhaps most of the isothiocyanates, kill E. coli O157:H7. In the present report, AIT showed greater antimicrobial activity at low pH values. For example, at pH 4.5 and 5.5 the MIC was 25 mu L/L, while at pH 8.5, 500 mu L/L was required to inhibit bacterial growth. This mustard-derived compound exhibited a high decomposition rate in water at 37 degrees C. Its degradation profile contained 3 major products and of these, diallylthiourea represented the largest (similar to 80%) component. The decomposition products did not show antimicrobial activity towards E. coli O157:H7, even when combined with a sub-lethal dose of AIT (10 mu L/L). AIT may only be antimicrobial in its original form and any further degradation in water is undesirable. AIT interactions with thioredoxin reductase and acetate kinase were also subjects of this study. AIT at 10 to 100 mu L/L was able to significantly inhibit both enzymes, but only 1 mu L/L was needed to decrease the activity of thioredoxin reductase. From these results, it can be postulated that: 1) AIT is a more effective antimicrobial at low pH values and its degradation reduces this activity; 2) decomposition products in water might not participate in the antimicrobial action of AIT; and 3) AIT seems to have a multi-targeted mechanism of action, perhaps inhibiting several metabolic pathways and damaging cellular structures. (C) 2009 Elsevier B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据