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促进蜡样芽胞杆菌孢子发芽,然后用温和的热处理将其灭活。

Promoting Bacillus cereus spore germination for subsequent inactivation by mild heat treatment.

机构信息

Nofima AS, Department of Process Technology, P.O. Box 8034, N-4068 Stavanger, Norway.

出版信息

J Food Prot. 2011 Dec;74(12):2079-89. doi: 10.4315/0362-028X.JFP-11-292.

Abstract

Sublethal heat treatment may activate dormant spores and thereby potentiate the conversion of spores to vegetative cells. As the germinated spore is known to possess lower heat resistance than its dormant counterpart, it has been postulated that double heat treatment, i.e., spore heat activation followed by germination and then by heat inactivation, can be used to control spores in foods. Production of refrigerated processed foods of extended durability often includes more than one heat treatment of the food components. This work simulates conventional heat treatment procedures and evaluates double heat treatment as a method to improve spore control in model food matrixes of meat broth and cream sauce. Bacillus cereus NVH 1230-88 spores were supplemented in food model matrixes and heat activated at 70°C and then heat inactivated at 80 or 90°C. The samples were held at 29 to 30°C for 1 h between primary and secondary heat treatments, to allow spore germination. Nutrients naturally present in the food matrixes, e.g., amino acids and inosine, could act as germinants that induce germination. The levels of germinants could be too low to produce effective germination within 1 h. Following primary heat treatment, some samples were therefore supplemented with a combination of L-alanine and inosine, a germinant mixture known to be effective for B. cereus spores. In both matrixes, a combination of double heat treatment (heat activation, germination, and inactivation) and addition of germinants gave a reduction in spore counts equivalent to or greater than that obtained with a single heat treatment for 12 min at 90°C. Addition of germinants was essential to induce effective germination in cream sauce during 1 h at 29 to 30°C, and germinants were therefore a crucial supplement to obtain an effect of double heat treatment in this matrix. These data will be valuable when setting up temperature-time-germinant combinations for an optimized spore reduction in mild-heat-treated foods.

摘要

亚致死热处理可能会激活休眠孢子,从而促进孢子向营养细胞的转化。由于已发现萌发的孢子比休眠的孢子具有更低的耐热性,因此有人假设可以使用双重热处理,即孢子热激活后发芽,然后再热失活,来控制食品中的孢子。生产保质期更长的冷藏加工食品通常包括对食品成分进行多次热处理。本工作模拟了常规热处理程序,并评估了双重热处理作为一种控制肉汁和奶油酱模型食品基质中孢子的方法。将蜡样芽孢杆菌 NVH 1230-88 孢子添加到食品模型基质中,并在 70°C 下进行热激活,然后在 80 或 90°C 下进行热失活。在主、次热处理之间,将样品在 29 至 30°C 下保持 1 小时,以允许孢子发芽。食品基质中存在的天然营养物质,例如氨基酸和肌苷,可以作为诱导发芽的发芽剂。发芽剂的水平可能太低,无法在 1 小时内产生有效发芽。在主热处理后,一些样品因此补充了 L-丙氨酸和肌苷的混合物,这是一种已知对蜡样芽孢杆菌孢子有效的发芽剂混合物。在两种基质中,双重热处理(热激活、发芽和失活)与添加发芽剂的组合可使孢子计数减少的程度与在 90°C 下进行 12 分钟的单次热处理相当或更大。在 29 至 30°C 下 1 小时内,添加发芽剂对于奶油酱中有效发芽至关重要,因此发芽剂是在该基质中获得双重热处理效果的关键补充剂。在设置优化的低热处理食品中孢子减少的温度-时间-发芽剂组合时,这些数据将非常有价值。

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