McClements J M, Patterson M F, Linton M
Department of Agriculture and Rural Development for Northern Ireland, Belfast.
J Food Prot. 2001 Apr;64(4):514-22. doi: 10.4315/0362-028x-64.4.514.
The effect of high hydrostatic pressure on the survival of the psychrotrophic organisms Listeria monocytogenes, Bacillus cereus, and Pseudomonas fluorescens was investigated in ultrahigh-temperature milk. Variation in pressure resistance between two strains of each organism were studied. The effect of growth stage (exponential and stationary phase), growth temperature (8 and 30 degrees C) on pressure resistance, and sublethal pressure injury were investigated. Exponential-phase cells were significantly less resistant to pressure than stationary-phase cells for all of the three species studied (P < 0.05). Growth temperature was found to have a significant effect at the two growth stages studied. Exponential cells grown at 8 degrees C were more resistant than those grown at 30 degrees C, but for stationary-phase cells the reverse was true. B. cereus stationary-phase cells grown at 30 degrees C were the most pressure resistant studied. L. monocytogenes showed the most sublethal damage compared to B. cereus and P. fluorescens. B. cereus spores were more resistant to pressure than vegetative cells. Pressure treatment at 400 MPa for 25 min at 30 degrees C gave a 0.45-log inactivation. Pressure treatment at 8 degrees C induced significantly less spore germination than at 30 degrees C. This study indicates the importance of the history of a bacterial culture prior to pressure treatment and that bacterial spores require more severe pressure treatments, probably in combination with other preservation techniques, to ensure inactivation.
研究了超高温灭菌乳中高静水压对嗜冷菌单核细胞增生李斯特菌、蜡样芽孢杆菌和荧光假单胞菌存活的影响。研究了每种微生物的两株菌株之间耐压性的差异。研究了生长阶段(指数期和稳定期)、生长温度(8℃和30℃)对耐压性的影响以及亚致死压力损伤。在所研究的所有三个物种中,指数期细胞对压力的耐受性明显低于稳定期细胞(P<0.05)。发现在所研究的两个生长阶段,生长温度有显著影响。在8℃下生长的指数期细胞比在30℃下生长的细胞更耐压,但对于稳定期细胞则相反。在30℃下生长的蜡样芽孢杆菌稳定期细胞是所研究的最耐压的。与蜡样芽孢杆菌和荧光假单胞菌相比,单核细胞增生李斯特菌的亚致死损伤最大。蜡样芽孢杆菌芽孢比营养细胞更耐压。在30℃下400MPa处理25分钟可使芽孢失活0.45个对数。8℃下的压力处理比30℃下诱导的芽孢萌发明显更少。这项研究表明了压力处理前细菌培养历史的重要性,并且细菌芽孢需要更严格的压力处理,可能与其他保存技术结合使用,以确保失活。