Bifidobacterium and bacillus natto symbiotic culture device and method and application of method
A technology of Bacillus natto and bifidobacteria, which is applied in the directions of bifidobacteria, sterilization methods, microorganism-based methods, etc., can solve the problems of difficult preparation and long-term storage, high requirements for growth and nutrient conditions, and high difficulty in culture and proliferation. , to achieve the effect of improving growth performance and immune function, reasonable structure design and process arrangement, and avoiding external microbial infection
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Embodiment 1
[0036] 1. Bifidobacterium and Bacillus natto symbiotic culture device
[0037] See attached picture:
[0038] Bifidobacterium and Bacillus natto symbiotic culture device, including a fermenter 2 installed on a base 1, a rotating device 3 is arranged in the fermenter 2, and a culture container 4 for holding a symbiotic medium is placed on the rotating device 3 , the tank cover of the fermenter 2 is installed with a titration device 5 that extends into the top of the culture container and is used to hold the bifidobacteria. The titration device 5 can have a flow regulating valve;
[0039]Temperature sensor 6, oxygen sensor 7 are also arranged in fermentation tank 2; One side of fermentation tank fermenter is provided with hot blast supply device 8, and hot blast supply device 8 is installed on the upper end surface of base, and hot blast supply device 8 is connected with the fermenter by conveying pipeline 9. The upper part is connected, the conveying pipeline 9 is provided wit...
Embodiment 2
[0057] 1. Bifidobacterium and Bacillus natto symbiotic culture device
[0058] Exactly the same as Example 1
[0059] Two, bifidobacterium and bacillus natto symbiotic culture method
[0060] Specific steps are as follows:
[0061] (1) Preparation of symbiotic medium: symbiotic medium is made of the following raw materials in parts by weight: 22 parts of bean dregs, 11 parts of rice bran, 4 parts of NaCl, K 2 HPO 4 2 parts, NH 4 h 2 PO 4 3 parts, (NH 4 ) 2 SO 4 4 parts, MgSO 4 ·7H 2 O 4 parts, KNO 3 5 parts, vitamin B 1 13 parts, 10 parts of silkworm chrysalis powder, 225 parts of corn steep liquor, 14 parts of Tween-80, 9 parts of inulin oligosaccharide, 2 parts of Sophora flavescens powder, 2 parts of Radix Radix Radix;
[0062] The preparation method is as follows: a. Soak the bean dregs with 5 times of distilled water for 9 hours, grind and homogenize, the homogenization pressure is 140MPa, centrifuge, and take the supernatant;
[0063] b. Mix the unused ...
Embodiment 3
[0071] 1. Bifidobacterium and Bacillus natto symbiotic culture device
[0072] Exactly the same as Example 1
[0073] Two, bifidobacterium and bacillus natto symbiotic culture method
[0074] Specific steps are as follows:
[0075] (1) Prepare the symbiotic medium: the symbiotic medium is made of the following raw materials in parts by weight: 25 parts of bean dregs, 12 parts of rice bran, 6 parts of NaCl, K 2 HPO 4 3 parts, NH 4 h 2 PO 4 5 parts, (NH 4 ) 2 SO 4 5 parts, MgSO 4 ·7H 2 O 5 parts, KNO 3 6 parts, vitamin B 1 15 parts, 15 parts of silkworm chrysalis powder, 250 parts of corn steep liquor, 15 parts of Tween-80, 10 parts of inulin oligosaccharides, 3 parts of Sophora flavescens powder, 3 parts of Radix Radix Radix;
[0076] The preparation method is as follows: a. Soak the bean dregs with 5 times of distilled water for 10 hours, grind and homogenize, the homogenization pressure is 140MPa, centrifuge, and take the supernatant;
[0077] b. Mix the unu...
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