A probiotic composition for inhibiting Helicobacter pylori and its application
A technology of Helicobacter pylori and a composition is applied in the field of probiotic compositions for inhibiting Helicobacter pylori to achieve the effects of reducing cavitation damage, inhibiting growth, and reducing the number of
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[0024] In the probiotic composition of the present invention, the weight part of the Lactobacillus rhamnosus is preferably 15-25 parts, more preferably 20 parts. The Lactobacillus rhamnosus of the present invention preferably includes Lactobacillus rhamnosus LN56, and the preservation number is CGMCC No.17370. The number of viable bacteria in the bacterial powder of Lactobacillus rhamnosus LN56 of the present invention is preferably 1.0 × 10 10 ~3.0×10 11 CFU / g, more preferably 5.0×10 10 ~2.0×10 11 CFU / g, most preferably 8.0×10 10 CFU / g. The preparation method of the bacterial powder of the Lactobacillus rhamnosus LN56 in the present invention is not particularly limited, preferably comprising: 1) inoculating the Lactobacillus rhamnosus LN56 in the MRS culture fluid or the improved MRS culture fluid, at 36 Fermentation at ~38°C for 12 to 24 hours to obtain Lactobacillus rhamnosus LN56 fermentation liquid; the improved MRS culture liquid uses MRS culture liquid as a basal ...
Embodiment 1
[0039] Lactobacillus rhamnosus LN56, Lactobacillus plantarum LN66, Lactobacillus reuteri LN83 and Lactobacillus salivarius LN12 were used to activate facultative anaerobic culture in MSR medium at 37°C for 24 hours, then centrifuged at 10000rpm for 10min to remove bacteria The cell-free fermentation supernatant was obtained, and the inhibitory effects of the cell-free fermentation supernatant (CFS) of a single strain and the CFS composition of the four strains on Helicobacter pylori were detected respectively. Helicobacter pylori (Helicobacter pylori ATCC 43504) was purchased from the American Type Culture Collection. The solid culture of Helicobacter pylori was cultured on Colombian blood agar medium containing 10% sterile defibrinated sheep blood at 37°C under microaerophilic conditions for 3-4 days, and the liquid culture was cultured on Brucella broth medium containing 10% fetal bovine serum at 37°C. Cultivate at 80 rpm for 2-3 days under microaerobic conditions.
[0040]...
Embodiment 2
[0046] The composition of the cell-free fermentation supernatant (CFS) of Lactobacillus rhamnosus LN56, Lactobacillus plantarum LN66, Lactobacillus reuteri LN83, Lactobacillus salivarius LN12 obtained in Example 1 and the CFS of these 4 kinds of bacteria , to detect the effect on gene expression levels of Helicobacter pylori virulence factors CagA, VacA and Ure.
[0047] The specific detection method is as follows: culture Helicobacter pylori (Helicobacter pylori ATCC 43504) in 10% fetal bovine serum Brooke's broth medium for 48-72 hours microaerobically, dilute the bacterial solution with the broth until the bacterial density is 1×10 7 CFU / mL. Add 5mL LN56 CFS, 5mL LN66 CFS, 5mL LN83 CFS, 5mL LN12 CFS, and 5mL equal-proportion compositions (each 1.25mL) of the above four strains of CFS into different conical flasks, and then in each conical flask, respectively Add 5 mL of 10% fetal bovine serum Brucella broth medium and 10 mL of 1×10 7 CFU / mL of Hp bacteria liquid, 37 ℃ mic...
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