Method for preparing cell protein through fermentation of liquid waste in ginkgo leaf extract production
A cell protein and extract technology, applied in the field of waste resource utilization and agricultural product processing, to achieve good social and environmental benefits, low cost, and simple preparation methods
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Embodiment 1
[0035] Implementation of the first option
[0036] Collect 85 kg of waste liquid from the production of Ginkgo biloba extract after absorbing ginkgo flavonoids with macroporous adsorption resin, put it into a fermenter, heat and boil for 2 hours to sterilize, and when the temperature is lowered to 25-30°C, use dilute phosphoric acid (98% Dilute 1.5L of concentrated phosphoric acid with water to 40L), adjust the pH to 4.8, heat and boil for 1 hour to sterilize, and when the temperature drops to 36-38°C, add Aspergillus niger, Bacillus subtilis and brewer’s yeast in a weight ratio of 1:1 : 3 (ie 3 kg of Aspergillus niger, 3 kg of Bacillus subtilis, 9 kg of brewer's yeast) 15 kg of compound microbial bacterial starter, at a temperature of 36°C and a ventilation rate of 1:0.6v / v / min 1. Under the condition of stirring speed of 35r / min, after 22 hours of culture and fermentation, the culture and fermentation broth was dehydrated by disc centrifuge with a set speed of 6000r / min for 2...
Embodiment 2
[0038] Implementation of the second option
[0039] Collect 78.745 kg of waste liquid after absorbing ginkgo flavonoids by macroporous adsorption resin in the production of ginkgo leaf extract, put it into a fermenter, heat and boil for 2 hours to sterilize, and when the temperature is lowered to 25-30°C, add 5 kg of wort juice, 1 kg of ammonium sulfate, 0.015 kg of ferrous sulfate tetrahydrate, 0.04 kg of magnesium sulfate heptahydrate, 0.2 kg of calcium chloride dihydrate, stir evenly, and adjust the pH to 5.0 with dilute phosphoric acid (1.5L of 98% concentrated phosphoric acid is diluted with water to 40L) , then heated and boiled for 1 hour to sterilize, and when the temperature was lowered to 36-38°C, the composite microbial bacteria mixed with Aspergillus niger, Bacillus cereus and Candida tropicalis in a weight ratio of 1:1:3 were added 15 kg of starter, under the conditions of temperature 38°C, ventilation rate 1:0.6v / v / min, and stirring speed 40r / min, after 20 hours ...
Embodiment 3
[0041] Implementation of the third option
[0042] Collect 73 kg of waste liquid after the Ginkgo biloba flavonoids are absorbed by the macroporous adsorption resin in the production of Ginkgo biloba extract, put it into a fermenter, heat and boil for 2 hours to sterilize, and when the temperature drops to 25-30°C, add 12 kg of bran powder , stir evenly, adjust the pH to 4.8 with dilute phosphoric acid (1.5L of 98% concentrated phosphoric acid and dilute to 40L with water), heat and boil for 1 hour to sterilize, and when the temperature is lowered to 36-38°C, add Aspergillus niger and Bacillus licheniformis 15 kg of compound microbial bacterial starter mixed with Candida utilis in a weight ratio of 1:1:3, at a temperature of 37°C, a ventilation rate of 1:0.6v / v / min, and a stirring speed of 45r After 22 hours of culture and fermentation under the condition of 1 / min, the culture fermentation liquid was dehydrated by disc centrifuge with a set speed of 8000r / min for 18 minutes, a...
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