Production method of single-cell protein
A single-cell protein and production method technology, applied in the direction of single-cell algae, fungi, etc., can solve the problems of high production cost of single-cell protein, high quality of single-cell protein, low production cost, etc., to solve food shortage, enzymatic hydrolysis, etc. High efficiency and the effect of improving production efficiency
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Embodiment 1
[0022] The oil-rich Chlorella algae were inoculated into sterile f / 2 medium through aseptic operation, and placed in a light incubator for cultivation at a cultivation temperature of 25°C and a light intensity of 2000lx for 10 days. Inoculate the strains of Rhodotorula viscosus rich in oil into the sterilized shake flask culture solution through aseptic operation: 1000mL of potato extract (200g potatoes are peeled, cut into small pieces, add water and boil for 1 hour, filter with 5 layers of gauze, and dilute to 1000mL ) and glucose 20,000 mg / L, cultured in a shaker with a rotation speed of 150 rpm and a culture temperature of 37°C for 72 hours. 50g of oil-rich Chlorella grown in a light incubator and 50g of oil-rich Rhodotorula viscose fermented in a shaker were collected by centrifugation (8000 rpm, 10 minutes) to obtain biomass, and washed 5 times with distilled water . Pretreatment with lysozyme L6876: oil-rich microorganisms (dry matter) and lysozyme L6876 were mixed at ...
Embodiment 2
[0026]The oil-rich Nannochloropsis species were inoculated into sterile f / 2 medium through aseptic operation, and placed in a light incubator for cultivation at a cultivation temperature of 25°C and a light intensity of 2000 lx for 10 days. Inoculate the strains of Rhodotorula viscosus rich in oil into the sterilized shake flask culture solution through aseptic operation: 1000mL of potato extract (200g potatoes are peeled, cut into small pieces, add water and boil for 1 hour, filter with 5 layers of gauze, and dilute to 1000mL ) and glucose 20,000 mg / L, cultured in a shaker with a rotation speed of 150 rpm and a culture temperature of 37°C for 72 hours. Respectively, 50 g of oil-rich Nannochloropsis grown in a light incubator and 50 g of oil-rich Rhodotorula viscosum fermented in a shaker were collected by centrifugation (8000 rpm, 10 minutes) to obtain biomass, and washed with distilled water for 5 Second-rate. Pretreatment with lysozyme L7651: oil-rich microorganisms (dry m...
Embodiment 3
[0030] The oil-rich Chlorella algae were inoculated into sterile f / 2 medium through aseptic operation, and placed in a light incubator for cultivation at a cultivation temperature of 25°C and a light intensity of 2000lx for 10 days. Inoculate the strains of Rhodotorula viscosus rich in oil into the sterilized shake flask culture solution through aseptic operation: 1000mL of potato extract (200g potatoes are peeled, cut into small pieces, add water and boil for 1 hour, filter with 5 layers of gauze, and dilute to 1000mL ) and glucose 20,000 mg / L, cultured in a shaker with a rotation speed of 150 rpm and a culture temperature of 37°C for 72 hours. 50g of oil-rich Chlorella grown in a light incubator and 50g of oil-rich Rhodotorula viscose fermented in a shaker were collected by centrifugation (8000 rpm, 10 minutes) to obtain biomass, and washed 5 times with distilled water . Pretreatment with lysozyme L2879: oil-rich microorganisms (dry matter) and lysozyme L2879 were mixed at ...
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