Anti-aging probiotic preparation and preparation method thereof
A probiotic preparation and anti-aging technology, applied in biochemical equipment and methods, methods based on microorganisms, anti-toxic agents, etc., can solve the problems of probiotics with less anti-aging functions, and achieve strong tolerance, simple preparation, and broad The effect of market prospects
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Embodiment 1
[0035] Example 1 Preparation of anti-aging probiotic powder
[0036] S1. Activate Bifidobacterium longum BL21 and Lactobacillus plantarum Lp90 in a test tube respectively to obtain a first-grade seed solution, and then transfer the first-grade seed solution to the seed medium to obtain a second-grade seed solution. 40°C, anaerobic culture for 8-24 hours; the secondary seed liquid is respectively connected to the fermentation medium for high-density fermentation, the inoculum amount of the secondary seed liquid connected to the fermentation medium is 1%-5%, and the culture condition is 30-40°C, anaerobic culture for 8-18 hours, until the cell density in the fermentation liquid reaches 10 9 , respectively collect the fermentation broth;
[0037] Wherein, the seed culture medium is MRS liquid medium, the pH value of MRS liquid medium is 6.5~6.8, and MRS liquid medium comprises: 2% lactose, 1% peptone, 0.5% yeast extract, 0.5 % sodium acetate, 0.2% diammonium hydrogen citrate, 0...
Embodiment 2
[0041] Example 2 In vitro acid resistance and bile salt resistance test of probiotics
[0042] A. Determination of acid resistance of strains
[0043] Method: The bacterial powder was inserted into the simulated artificial gastric juice (pH=2.5) for 3 hours according to the inoculum amount of 1% (w / v), and the samples were taken to count plate colonies, and the number of viable bacteria at 0 hours was used as a control to calculate the survival rate of the strains .
[0044] B. Determination of strain tolerance to bile salts
[0045] Method: The bacterial powder was inoculated into the simulated artificial intestinal fluid (0.3% bile salt concentration) according to the inoculum amount of 1% (w / v) and cultivated for 3 hours, and the plate colonies were counted by sampling. Rate.
[0046] The result is as figure 1 As shown, the survival rate of Bifidobacterium longum BL21 and Lactobacillus plantarum Lp90 after acidification and bile salt treatment were all above 60%, and th...
Embodiment 3
[0047] Example 3 Determination of Free Radical Scavenging Ability and Superoxide Dismutase (SOD) Activity
[0048] A. Materials
[0049] SOD kit, H 2 o 2 , FeSO 4 , Pyrogallol, O-phenanthroline and other reagents are analytical reagents.
[0050] B. Method
[0051] 1) Preparation of cell-free extract
[0052] Two strains (Bifidobacterium longum BL21, Lactobacillus plantarum Lp90) were continuously cultured in MRS medium at 37°C for 3 generations, collected by centrifugation at 8000r / min for 20min, washed 3 times with PBS buffer and resuspended in PBS buffer , the number of live bacteria is adjusted to 10 10 cfu / mL, break the cells in an ultrasonic cell disruptor in an ice bath, and collect the supernatant after centrifugation at 4°C for 30 min.
[0053] 2) 2 strains are sensitive to superoxide free radicals (O 2 - ) Determination of scavenging capacity
[0054] Pyrogallol autoxidation colorimetric analysis method was adopted, the Tris-HCl buffer solution with a conce...
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