益生菌发酵乳中的活菌数是保证其功能特性的关键因素,为提高益生菌发酵乳中的活菌总数,以干酪乳杆菌和双歧杆菌复合菌种为试验对象,以发酵过程中的pH值和吸光度平均值OD值为试验指标,在单因素试验的基础上,利用Box-Benhnken中心组合试验和响应面分析法研究了接种量、益生菌接种比例、发酵温度、葡萄糖添加量以及大豆多肽添加量对发酵乳pH值和活菌数的影响,并建立了复合益生菌发酵模型。响应面优化试验结果表明复合益生菌发酵的最佳工艺条件是脱脂乳乳固体质量分数为12%,接种量为6%,干酪乳杆菌:双歧杆菌接种体积比为3:1,葡萄糖添加量为2.9%,大豆多肽添加量为0.8%,发酵温度为34℃,在此条件下OD预测值为1.076,验证试验得到实际OD值为1.087,与理论预测值相比,相对误差为1.0%。发酵乳最大活菌数为4.1×1011cfu/mL,与已有研究相比,活菌数提高了1~2个对数级。在4℃条件下贮藏21d后,发酵乳的活菌数仍然保持在4.7×1010cfu/mL。研究结果为工业化生产高活菌数的益生菌饮料提供参考。
The viable probiotic count is the key factor to functionality of fermented milk. It is very important for the milk industry to improve the number of viable bacteria in its final products. Lactobacillus casei and Bifidobacterium were blended using them as a starter culture for fermented milk to achieve a high viable probiotic count. Lactobacillus casei and Bifidobacterium were studied and a high density culture technology of Lactobacillus was applied to increase the number of viable bacteria in the fermentation system. Determination of the absorbance method was used to assess the viable count of probiotics in fermented milk in which the calcium ion would combine with salt under alkaline conditions to make fermented milk dispersed evenly in a solution state. Ethylenediamine Tetraacetic Acid (EDTA) was selected as a chelating agent to chelate the calcium ion in the fermented milk, and to make the solution clarify. The OD value of the bacteria did not change significantly after entering the stable phase, and the number of viable probiotics count in the fermented milk achieved the maximum. The OD value of fermented milk in this study did not change significantly from the second day of fermentation. On this basis, OD value was measured for three consecutive days from the second day, and the average OD value was used as indicator of the viable probiotic count. Inoculation volume, ratio of probiotics strains, added glucose,, added soybean peptide, and fermentation temperature were studied as a single factor affecting the number of viable bacterium in the fermented milk. Results show that the average OD value at different inoculation volume was not significant (P〈0.01) while the other four factors were highly significant (P〉0.01). The ratio ofprobiotics strains in blend culture, glucose level, soybean peptide level, and fermentation temperature were further studied using a Box-Benhnken design to optimize the fermentation technology. The results were analyzed with the software Design Expert to 8.0. Results