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Mechanism of Bacterial Inactivation by (+)-Limonene and Its Potential Use in Food Preservation Combined Processes

机译:(+)-柠檬烯细菌灭活的机理及其在食品保鲜组合工艺中的潜在应用

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摘要

This work explores the bactericidal effect of (+)-limonene, the major constituent of citrus fruits' essential oils, against E. coli. The degree of E. coli BJ4 inactivation achieved by (+)-limonene was influenced by the pH of the treatment medium, being more bactericidal at pH 4.0 than at pH 7.0. Deletion of rpoS and exposure to a sub-lethal heat or an acid shock did not modify E. coli BJ4 resistance to (+)-limonene. However, exposure to a sub-lethal cold shock decreased its resistance to (+)-limonene. Although no sub-lethal injury was detected in the cell envelopes after exposure to (+)-limonene by the selective-plating technique, the uptake of propidium iodide by inactivated E. coli BJ4 cells pointed out these structures as important targets in the mechanism of action. Attenuated Total Reflectance Infrared Microspectroscopy (ATR-IRMS) allowed identification of altered E. coli BJ4 structures after (+)-limonene treatments as a function of the treatment pH: β-sheet proteins at pH 4.0 and phosphodiester bonds at pH 7.0. The increased sensitivity to (+)-limonene observed at pH 4.0 in an E. coli MC4100 lptD4213 mutant with an increased outer membrane permeability along with the identification of altered β-sheet proteins by ATR-IRMS indicated the importance of this structure in the mechanism of action of (+)-limonene. The study of mechanism of inactivation by (+)-limonene led to the design of a synergistic combined process with heat for the inactivation of the pathogen E. coli O157:H7 in fruit juices. These results show the potential of (+)-limonene in food preservation, either acting alone or in combination with lethal heat treatments.
机译:这项工作探讨了(+)-柠檬烯(柑橘类水果精油的主要成分)对大肠杆菌的杀菌作用。通过(+)-柠檬烯实现的大肠杆菌BJ4灭活程度受处理介质的pH影响,在pH 4.0时比在pH 7.0时更具杀菌性。删除rpoS并暴露于亚致死热量或酸冲击下,都不会改变大肠杆菌BJ4对(+)-柠檬烯的抗性。但是,暴露于亚致死性冷冲击下会降低其对(+)-柠檬烯的抵抗力。尽管通过选择性铺板技术在暴露于(+)-柠檬烯后未在细胞膜中检测到亚致死性损伤,但灭活的大肠杆菌BJ4细胞对碘化丙锭的摄取指出,这些结构是其机制的重要靶标。行动。衰减的全反射红外光谱(ATR-IRMS)可以识别(+)-柠檬烯处理后随处理pH的变化的大肠杆菌BJ4结构:pH 4.0的β-折叠蛋白和pH 7.0的磷酸二酯键。在大肠杆菌MC4100 lptD4213突变体中,在pH 4.0下观察到的对(+)-柠檬烯的敏感性增加,外膜通透性增加,并且通过ATR-IRMS鉴定了改变的β-折叠蛋白,表明该结构在机理中的重要性(+)-柠檬烯的作用对(+)-柠檬烯灭活机理的研究导致设计了加热的协同联合过程,用于灭活果汁中的病原大肠杆菌O157:H7。这些结果显示了(+)-柠檬烯在食品保存中的潜力,无论是单独起作用还是与致死性热处理一起起作用。

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