Domestic fungus liquid spawn culture method and medium thereof
A strain culture medium and liquid strain technology, which is applied in the field of edible fungus liquid strain culture and edible fungus liquid strain culture medium, and can solve the problems that the influence of micro-nano bubble water on the growth of edible fungi has not been reported.
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Embodiment 1
[0093] Embodiment 1, DO value 10mg / L micronano bubble water carries out Pleurotus eryngii liquid strain culture
[0094] Provide a predetermined amount of micro-nano bubble water with a DO value of 10 mg / L, and a predetermined amount of tap water with a DO value of 6 mg / L. Provide two media raw materials, which respectively include: white sugar 20g / L, soybean meal powder 3g / L, MgSO 4 0.6g / L, K 2 HPO 4 0.6g / L, respectively use micro-nano bubble water and tap water to dissolve to a constant volume to form two strain culture media.
[0095] Inject the same amount of Pleurotus eryngii strains into two strain culture media respectively. After 7 days of shaking culture at a constant temperature at 25°C, take 150ml of the culture solution from the above two culture solutions and filter out the bacteria balls with filter paper, wash them several times, then put them in a drying oven, dry them at 105°C for 2 hours, and dry them. Dry, weigh after cooling to determine the biomass of ...
Embodiment 2
[0098] Embodiment 2, DO value 15mg / L micro-nano bubble water carries out Pleurotus eryngii liquid strain culture
[0099] Provide a predetermined amount of micro-nano bubble water with a DO value of 15 mg / L, and a predetermined amount of tap water with a DO value of 6 mg / L. Provide two media raw materials, which respectively include: white sugar 20g / L, soybean meal powder 3g / L, MgSO 4 0.6g / L, K 2 HPO 4 0.6g / L, respectively use micro-nano bubble water and tap water to dissolve to a constant volume to form two strain culture media.
[0100] Inject the same amount of Pleurotus eryngii strains into two strain culture media respectively. After 7 days of shaking culture at a constant temperature at 25°C, take 150ml of the culture solution from the above two culture solutions and filter out the bacteria balls with filter paper, wash them several times, then put them in a drying oven, dry them at 105°C for 2 hours, and dry them. Dry, weigh after cooling to determine the biomass of...
Embodiment 3
[0104] Embodiment 3, DO value 15mg / L micro-nano bubble water carries out the Pleurotus eryngii liquid strain cultivation of different time
[0105] Provide a predetermined amount of micro-nano bubble water with a DO value of 15 mg / L, and a predetermined amount of tap water with a DO value of 6 mg / L. Provide two media raw materials, which respectively include: white sugar 20g / L, soybean meal powder 3g / L, MgSO 4 0.6g / L, K 2 HPO 4 0.6g / L, respectively use micro-nano bubble water and tap water to dissolve to a constant volume to form two strain culture media.
[0106] Inject the same amount of Pleurotus eryngii strains into two strain culture media respectively. After constant temperature shaking culture at 25°C for 6 days and 7 days respectively, take 150ml of the culture liquid from the above two culture liquids and filter out the bacterial balls with filter paper, wash them several times, then put them into a drying oven, and dry them at 105°C for 2 hours , dried it, weighe...
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