Inonotus obliquus extracellular and intracellular mixing crude polysaccharide with function of strengthening immunity
A technology of Inonotus obliquus and external mixing, applied in the field of medicine, can solve the problems of the limitation of development and utilization of Inonotus obliquus, the high price of Inonotus obliquus, etc.
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Embodiment 1
[0093] Embodiment 1 Preparation of tablet of the present invention
[0094] 1. Under sterile conditions, take the slant strains and insert them into a plate of fresh comprehensive solid medium, culture at 26°C, and cultivate for 240 hours; the comprehensive solid medium formula (g / 100ml): potato 16, glucose 1.2, agar 1.5, MgSO 4 0.12, KH 2 PO 4 0.28, VB 1 Add 0.8mg of water to dissolve to the required volume, and the pH value is natural;
[0095] 2. Primary fermentation: under aseptic conditions, use a 6mm hole puncher to punch holes at the edge of the colony, use an inoculation shovel to pick up 6 pieces of bacterial cakes and insert them into a 250ml shaker flask containing 100ml of liquid medium, and place at 26°C , the rotating speed is in the shaker of 120rpm / min, after 210 hours of constant temperature cultivation, carry out secondary fermentation culture; the liquid medium formula (g / 100ml): potato 16, glucose 1.2, MgSO 4 0.12, KH 2 PO 4 0.28, VB 1 Add 0.8mg of ...
Embodiment 2
[0099] Embodiment 2: the preparation of granule of the present invention
[0100] 1. Under aseptic conditions, take the slant strains and insert them into a plate of fresh comprehensive solid medium, culture at 28°C, and cultivate for 300 hours; the comprehensive solid medium formula (g / 100ml): potato 21, glucose 2.4, agar 2.0, MgSO 4 0.16, KH 2 PO 4 0.31, VB 1 Add 1.0mg of water to dissolve to the required volume, and the pH value is natural.
[0101] 2. Primary fermentation: under aseptic conditions, use a 6mm hole puncher to punch holes at the edge of the colony, use an inoculation shovel to pick up 8 pieces of bacterial cakes and insert them into a 250ml shaker flask containing 120ml of liquid medium, and place at 28°C , the rotating speed is in the shaker of 150rpm / min, after 260 hours of constant temperature cultivation, the secondary fermentation culture is carried out; the liquid medium formula (g / 100ml): potato 21, glucose 2.4, MgSO 4 0.16, KH 2 PO 4 0.31, VB ...
Embodiment 3
[0105] The preparation of embodiment 3 capsules of the present invention
[0106] 1. Under sterile conditions, take the slant strains and insert them into a plate of fresh comprehensive solid medium, culture at 29°C, and cultivate for 360 hours; the comprehensive solid medium formula (g / 100ml): potato 26, glucose 3.2, agar 2.5, MgSO 4 0.2, KH 2 PO 4 0.35, VB 1 Add 1.2mg of water to dissolve to the required volume, and the pH value is natural;
[0107] 2. Primary fermentation: Under sterile conditions, use a 6mm hole puncher to punch holes at the edge of the colony, use an inoculation shovel to pick up 10 pieces of bacterial cakes and insert them into a 250ml shaker flask containing 150ml of liquid medium, and place at 29°C , rotating speed is in the shaker of 185rpm / min, carry out secondary fermentation culture after 300 hours of constant temperature cultivation; The formula of this liquid culture medium (g / 100ml): Potato 26, glucose 3.2, MgSO 4 0.2, KH 2 PO 4 0.35, VB ...
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