Method for preparing functional sugar-producing probiotic starter
A starter and probiotic technology, which is applied in the field of biological preparation, can solve the problems of not allowing subsequent use, restricting the development of lactic acid bacteria starter and fermented dairy products, etc., and achieves the effect of maintaining the activity of probiotics
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Embodiment 1
[0022] Lactobacillus plantarum was used as a fermentation strain, and 5% was inoculated into the proliferation medium of pH5.5. The concentration of each component in the proliferation medium is as follows: sucrose 10 g / L, glucose 10 g / L, yeast powder 1.5 g / L, tryptone 1.5 g / L, K 2 HPO 4 4.0 g / L, MgSO 4 ·7H 2 O 0.5 g / L, CaCl 2 0.02 g / L, Tween 80 1mL. The anaerobic fermentation was cultivated at 37° C. for 12 h, wherein glucose was added after 6 h of fermentation, and the glucose concentration was controlled at 5 g / L. The number of cells in the final medium reached 1.4×10 9 cfu / ml, centrifuge the fermentation broth under sterile conditions to obtain lactic acid bacteria cells. Then add the lyoprotectant in a ratio of 1:1, the concentration of each component in the lyoprotectant is as follows: skimmed milk powder 100g / L, sucrose 100g / L, glycerin 30ml / L, maltodextrin 50g / L, trehalose 100g / L, L-sodium glutamate 10g / L, L-cysteine 5g / L. After mixing evenly, pre-freeze a...
Embodiment 2
[0024] Lactobacillus gasseri was used as the fermentation strain, and 5% was inoculated into the proliferation medium of pH5.5. The concentration of each component in the proliferation medium is as follows: sucrose 10 g / L, glucose 10 g / L, yeast powder 1.5 g / L, tryptone 1.5 g / L, K 2 HPO 4 4.0 g / L, MgSO 4 ·7H 2 O 0.5 g / L, CaCl 2 0.02 g / L, Tween 80 1mL. The anaerobic fermentation was cultivated at 37° C. for 12 h, wherein glucose was added after 3 h of fermentation, and the glucose concentration was controlled at 5 g / L. The number of cells in the final medium reached 4.1×10 9 cfu / ml, centrifuge the fermentation broth under sterile conditions to obtain lactic acid bacteria cells. Then add the lyoprotectant in a ratio of 1:1, the concentration of each component in the lyoprotectant is as follows: skimmed milk powder 100g / L, sucrose 100g / L, glycerin 30ml / L, maltodextrin 50g / L, trehalose 100g / L, L-sodium glutamate 10g / L, L-cysteine 5g / L. After mixing evenly, pre-freeze a...
Embodiment 3
[0026] Lactobacillus reuteri was used as a fermentation strain, and was inoculated into the proliferation medium of pH5.5 at 5%. The concentration of each component in the proliferation medium is as follows: sucrose 10 g / L, glucose 10 g / L, yeast powder 1.5 g / L, tryptone 1.5 g / L, K 2 HPO 4 4.0 g / L, MgSO 4 ·7H 2 O 0.5 g / L, CaCl 2 0.02 g / L, Tween 80 1mL. The anaerobic fermentation was cultivated at 37° C. for 12 h, wherein glucose was added after 6 h of fermentation, and the glucose concentration was controlled at 5 g / L. The number of cells in the final medium reached 1.4×10 9 cfu / ml, centrifuge the fermentation broth under sterile conditions to obtain lactic acid bacteria cells. Then add the lyoprotectant in a ratio of 1:1, the concentration of each component in the lyoprotectant is as follows: skimmed milk powder 100g / L, sucrose 100g / L, glycerin 30ml / L, maltodextrin 50g / L, trehalose 100g / L, L-sodium glutamate 10g / L, L-cysteine 5g / L. After mixing evenly, pre-freeze ...
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