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Advances in Bacterial Spores Inactivation in Thermal Treatments Under Pressure

机译:细菌孢子在压力下热处理中的灭活进展

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The effect of heat treatments coupled with high pressure on Clostridium sporogenes putrefactive anae4robe spores in a model system was stuided. A meat broth used as model system was sterilised and inoculated with spores of Clostridium sporogenes putrefactive anaerobe 3679 ATCC 7955 (2 x 10~6 spores/ml). The inoculated meat broth (2.5 ml) was packaged in sterilised PE vials. The vials were kept at 0 deg C until processed. The packages were subjected to pressures from 600 to 800 MPa and the processing time was up to 20 min using an experimental press (the ABB QFP 15000 high pressure food processor). The temperatures of the samples (from 90 to 110 deg C) were kept constant during the process using an internal control system placed into the press vessel. The processed samples were aseptically opened and the surviving spores were counted using TSC Agar Base (OXOID). The plates were incubated at 30 deg C for 7 d under anaerobic conditions. "D" and "z" values were calculated for various processing pressures (600, 700 and 800 MPa). The "D" values decreased from 1.28 to 0.69 min as the processing pressure increased from 600 to 800 MPa. The "z" values increased from 16 to 17.9 deg C as the processing pressure increased from 600 to 800 MPa. The heat treatment in combination with high pressure appears to be as effective or better than thermal processing alone (D_(120)=1.9', z=11.8 deg C at ambient pressure). From these results it has been possible to establish a relation between time, temperature and pressure. This relation is able to calculate the D value at known pressure and temperature in a predictive way. This relation seems to have a good correlation with reality. Its use will allow the calculation and prediction of the effect of any processing at high pressure conditions for Clostridium sporogenes putrefactive anaerobe 3679 ATCC 7955. Further studies are performed to verify and optimise the relation founded.
机译:促使了在模型系统中与梭菌孢子蛋白孢子蛋白孢子料腐烂的Anae4孢子孢子的效果。用作模型系统的肉汤被灭菌并接种梭菌孢子料孢子素腐蚀性Anaerobe 3679 ATCC 7955(2×10〜6孢子/ mL)。将接种的肉汤(2.5mL)包装在灭菌的PE小瓶中。将小瓶保持在0℃直至加工。将封装从600至800MPa的压力进行压力,并且使用实验压机(ABB QFP 15000高压食品加工机)的加工时间最多20分钟。使用放置在压力容器中的内部控制系统期间,样品的温度(从90至110℃)保持恒定。无菌地打开处理的样品,使用TSC琼脂碱(Okoid)计算存活的孢子。在厌氧条件下在30℃下在30℃下温育。为各种处理压力(600,700和800MPa)计算“D”和“Z”值。随着处理压力从600到800MPa增加,“D”值从1.28降至0.69分钟。随着处理压力从600增加到800MPa,“Z”值从16到17.9℃增加增加。与高压组合的热处理似乎与单独的热处理一样有效或更好(在环境压力下D_(120)= 1.9',Z = 11.8℃)。通过这些结果,已经可以在时间,温度和压力之间建立关系。该关系能够以预测的方式计算已知的压力和温度的D值。这一关系似乎与现实具有良好的相关性。它的使用将允许计算和预测任何处理的梭菌孢子育术的高压条件的效果,腐败厌氧3679 ATCC 7955.进行进一步的研究以验证和优化成立的关系。

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