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猪肉午餐肉中蜡样芽孢杆菌和产气荚膜梭菌营养细胞及芽孢的热灭活

Thermal inactivation of Bacillus cereus and Clostridium perfringens vegetative cells and spores in pork luncheon roll.

作者信息

Byrne B, Dunne G, Bolton D J

机构信息

Ashtown Food Research Centre, Teagasc, Ashtown, Dublin, Ireland.

出版信息

Food Microbiol. 2006 Dec;23(8):803-8. doi: 10.1016/j.fm.2006.02.002. Epub 2006 May 2.

Abstract

The aim of this study was to design a thermal treatment(s) for pork luncheon roll, which would destroy Bacillus cereus and Clostridium perfringens vegetative cells and spores. B. cereus and C. perfringens vegetative and spore cocktails were used to inoculate luncheon meat. Samples were subjected to different temperatures and removal times. The decimal-reduction times (D-values) were calculated by linear regression analysis (D = -1/slope of a plot of log surviving cells versus time). The log(10) of the resulting D-values were plotted against their corresponding temperatures to calculate (-1/slope of the curve) the thermal resistance (z-values) of each cocktail. The D-values for vegetative cells ranged from 1 min (60 degrees C) to 33.2 min (50 degrees C) for B. cereus and from 0.9 min (65 degrees C) to 16.3 min (55 degrees C) for C. perfringens. The D-values for B. cereus spores ranged from 2.0 min (95 degrees C) to 32.1 min (85 degrees C) and from 2.2 min (100 degrees C) to 34.2 min (90 degrees C) for C. perfringens. The z-values were calculated to be 6.6 and 8.5 degrees C for B. cereus vegetative and spores, respectively, and 7.8 and 8.4 degrees C for C. perfringens vegetative cells and spores, respectively. The D-values of B. cereus and C. perfringens suggest that a mild cook of 70 degrees C for 12s and 1.3 min would achieve a 6 log reduction of B. cereus and C. perfringens vegetative cells, respectively. The equivalent reduction of B. cereus and C. perfringens spores would require the pork luncheon meat to be heated for 36 s at 105 and 110 degrees C, respectively. The results of this study provide the thermal inactivation data necessary to design a cooking protocol for pork luncheon roll that would inactivate B. cereus and C. perfringens vegetative cells and spores. The data may also be used in future risk assessment studies.

摘要

本研究的目的是设计一种针对猪肉午餐肉卷的热处理方法,该方法能杀灭蜡样芽孢杆菌和产气荚膜梭菌的营养细胞及芽孢。使用蜡样芽孢杆菌和产气荚膜梭菌的营养细胞及芽孢混合菌液接种午餐肉。对样品进行不同温度和处理时间的处理。通过线性回归分析计算十进制减少时间(D值)(D = -1/对数存活细胞与时间关系图的斜率)。将所得D值的对数(10)与其相应温度作图,以计算每种混合菌液的热阻(z值)(-曲线斜率)。蜡样芽孢杆菌营养细胞的D值范围为1分钟(60℃)至33.2分钟(50℃),产气荚膜梭菌营养细胞的D值范围为0.9分钟(65℃)至16.3分钟(55℃)。蜡样芽孢杆菌芽孢的D值范围为2.0分钟(95℃)至32.1分钟(85℃),产气荚膜梭菌芽孢的D值范围为2.2分钟(100℃)至34.2分钟(90℃)。蜡样芽孢杆菌营养细胞和芽孢的z值分别计算为6.6℃和8.5℃,产气荚膜梭菌营养细胞和芽孢的z值分别为7.8℃和8.4℃。蜡样芽孢杆菌和产气荚膜梭菌的D值表明,70℃温和烹饪12秒和1.3分钟将分别使蜡样芽孢杆菌和产气荚膜梭菌的营养细胞减少6个对数级。要使蜡样芽孢杆菌和产气荚膜梭菌的芽孢等量减少,猪肉午餐肉卷分别需要在105℃和110℃加热36秒。本研究结果提供了设计猪肉午餐肉卷烹饪方案所需的热灭活数据,该方案可灭活蜡样芽孢杆菌和产气荚膜梭菌的营养细胞及芽孢。这些数据也可用于未来的风险评估研究。

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