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过硫酸氢盐对大肠杆菌 O157:H7 和单核细胞增生李斯特菌的灭活效果。

Efficacy of activated persulfate in inactivating Escherichia coli O157:H7 and Listeria monocytogenes.

机构信息

Department of Food Science and Technology, University of Georgia, 1109 Experiment Street, Griffin, GA 30223, USA.

Department of Crop and Soil Sciences, University of Georgia, 1109 Experiment Street, Griffin, GA 30223, USA.

出版信息

Int J Food Microbiol. 2018 Nov 2;284:40-47. doi: 10.1016/j.ijfoodmicro.2018.06.021. Epub 2018 Jul 2.

Abstract

Concerns have been on the rise regarding the use of chlorine-based sanitizers for fresh produce sanitation due to the production of toxic disinfection by-products (DBPs). This study was undertaken to evaluate the efficacy of activated persulfate in inactivating Escherichia coli O157:H7 and Listeria monocytogenes in pure culture. The objectives were to study the effect of persulfate to activator ratios and determine the major contributing radical in pathogen inactivation. A five-strain cocktail of each pathogen was treated with sodium persulfate activated by ferrous sulfate or sodium hydroxide for 60 s or 120 s. Non-selective agars supplemented with sodium pyruvate were used for pathogen enumeration. The steady-state concentrations of free radicals were quantified using HPLC-DAD. Radical scavengers (tert-butanol, isopropanol, and benzoquinone) were used to determine the major contributing radical in pathogen inactivation. The results showed more than 7 log CFU/mL reductions can be achieved in 120 s for both pathogens at appropriate activation conditions. For ferrous activation, the persulfate to ferrous ratio played an important role in the overall inactivation efficacy. The maximum pathogen reduction (7.77 log CFU/mL for E. coli O157:H7 and 7.25 log CFU/mL for L. monocytogenes) was achieved at persulfate to ferrous molar ratio of 1:0.33 when the initial persulfate concentration was set at 40 mmol/L. Further increase or decrease of ferrous ratio always leads to lower pathogen reductions. For alkaline activation, the inactivation efficacy increased with more initial sodium hydroxide. The maximum reduction was achieved at 40 mmol/L persulfate with 30 mmol/L sodium hydroxide for E. coli O157:H7 (6.21 log CFU/mL reduction) and at 500 mmol/L persulfate with 350 mmol/L sodium hydroxide for L. monocytogenes (8.64 log CFU/mL reduction). Also, persulfate activated by sodium hydroxide always achieved significantly (P < 0.05) higher microbial reductions than sodium hydroxide or persulfate alone. L. monocytogenes was generally more resistant against the activated persulfate treatment compared with E. coli O157:H7, which might be due to the different cell envelop structures between Gram-positive and Gram-negative bacteria. Hydroxyl radical was demonstrated to be the major radical to inactivate both pathogens in ferrous activation while superoxide radical was demonstrated to be the major radical to inactivate both pathogens in alkaline activation.

摘要

人们越来越关注使用含氯消毒剂对新鲜农产品进行消毒,因为这会产生有毒的消毒副产物 (DBP)。本研究旨在评估过硫酸盐在纯培养物中灭活大肠杆菌 O157:H7 和李斯特菌的效果。目的是研究过硫酸盐与激活剂的比例的影响,并确定病原体失活的主要贡献自由基。用硫酸亚铁或氢氧化钠激活过硫酸钠,处理每一种病原体的五株混合菌,处理时间为 60 秒或 120 秒。用补充有丙酮酸的非选择性琼脂对病原体进行计数。使用 HPLC-DAD 定量自由基的稳态浓度。自由基清除剂(叔丁醇、异丙醇和苯醌)用于确定病原体失活的主要贡献自由基。结果表明,在适当的激活条件下,两种病原体在 120 秒内均可达到 7 个以上对数 CFU/mL 的减少。对于亚铁激活,过硫酸盐与亚铁的比例在整体失活效果中起着重要作用。当初始过硫酸盐浓度设定为 40mmol/L 时,过硫酸盐与亚铁的摩尔比为 1:0.33 时,最大病原体减少量(大肠杆菌 O157:H7 为 7.77 对数 CFU/mL,李斯特菌为 7.25 对数 CFU/mL)。亚铁比例的进一步增加或减少总是导致较低的病原体减少。对于碱性激活,随着初始氢氧化钠的增加,失活效果增加。在 40mmol/L 过硫酸盐和 30mmol/L 氢氧化钠下,大肠杆菌 O157:H7 的最大减少量为 6.21 对数 CFU/mL,在 500mmol/L 过硫酸盐和 350mmol/L 氢氧化钠下,李斯特菌的最大减少量为 8.64 对数 CFU/mL。此外,用氢氧化钠激活的过硫酸盐处理总是比单独用氢氧化钠或过硫酸盐处理显著(P < 0.05)更高的微生物减少量。与大肠杆菌 O157:H7 相比,李斯特菌通常对激活过硫酸盐处理更具抗性,这可能是由于革兰氏阳性菌和革兰氏阴性菌之间的不同细胞包膜结构所致。在亚铁激活中,羟基自由基被证明是灭活两种病原体的主要自由基,而在碱性激活中,超氧自由基被证明是灭活两种病原体的主要自由基。

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