Composite probiotic preparation capable of relieving non-alcoholic fatty liver, preparation method and application thereof
A compound probiotic, non-alcoholic technology, applied in the field of microorganisms, can solve the problems of unclear treatment effect and mechanism of NAFLD, and achieve the effect of reducing the swelling degree, number and weight of liver cells.
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Embodiment 1
[0043] Example 1: Preparation of Bifidobacterium animalis subsp. lactisBLa80 freeze-dried powder
[0044] Inoculate Bifidobacterium animalis subsp. lactis BLa80 into the culture medium according to the inoculum amount accounting for 3% of the total mass of the culture medium, and cultivate it at 37°C for 18 hours to obtain a culture medium; centrifuge the culture medium to obtain bacteria ; Resuspend the trehalose lyoprotectant with a trehalose concentration of 100g / L (the mass ratio of the lyoprotectant to the bacteria is 2:1) to obtain a resuspension; vacuum freeze the resuspension Freeze-drying is carried out to obtain Bifidobacterium animalis subsp. lactis BLa80 freeze-dried powder.
Embodiment 2
[0045] Embodiment 2: Preparation of Lactobacillus rhamnosus LRa05 freeze-dried powder
[0046] Lactobacillus rhamnosus LRa05 was inoculated into the medium according to the inoculum amount accounting for 3% of the total mass of the medium, and cultured at 37°C for 18 hours to obtain a culture medium; the culture medium was centrifuged to obtain the cells; the cells were used The trehalose lyoprotectant with a trehalose concentration of 100g / L was resuspended (the mass ratio of the lyoprotectant to the bacteria was 2:1) to obtain a resuspension; the resuspension was lyophilized by vacuum freezing, The freeze-dried powder of Lactobacillus rhamnosusLRa05 was obtained.
Embodiment 3
[0047] Embodiment 3: Preparation of Lactobacillus plantarum Lp90 freeze-dried powder
[0048] Lactobacillus plantarum Lp90 was inoculated into the culture medium according to the inoculum amount accounting for 3% of the total mass of the culture medium, and cultured at 37°C for 18 hours to obtain a culture solution; the culture solution was centrifuged to obtain bacteria; the bacteria were treated with trehalose Trehalose lyoprotectant with a concentration of 100g / L was resuspended (the mass ratio of lyoprotectant to bacteria was 2:1) to obtain a resuspension; the resuspension was lyophilized by vacuum freezing to obtain a plant Lactobacillus plantarum Lp90 freeze-dried powder.
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