Diet fiber and its producing method
A technology of dietary fiber and bacterial strains, applied in the field of dietary fiber, can solve problems such as unfavorable human health, complex process, organic chlorine residue, etc., achieve the effect of increasing the acidic environment in the intestine, simple production process, and preventing hyperlipidemia
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Embodiment 1
[0026] Mix 70kg of bagasse, 15kg of crushed bran, 10kg of bean dregs and 1kg of edible calcium sulfate, add 90kg of water and 0.5-1% citric acid to adjust the pH value to 5.0-5.5, moisten the material for 2-3 hours, and adjust the water content of the medium At 62% is appropriate. Pack the wet raw materials into high temperature resistant plastic bags, each bag weighing 1kg. Put the plastic bag in a sterilizing pot at 105-120°C for 1 hour to sterilize. Under sterile conditions, insert 2-3% of the secondary species of Ganoderma lucidum into the sterilized culture medium, and cultivate them for 35-45 days under the conditions of 80-85% humidity and 20-28°C. Dried and crushed into fine powder above 100 mesh to obtain 72kg of yellow product. The tested product quality indicators meet the food hygiene standards.
Embodiment 2
[0028] Mix 100kg of bagasse, 40kg of bran, 20kg of bean dregs, 2kg of edible calcium sulfate, and 1kg of ferrous sulfate, add 130kg of water and 0.5-1% citric acid to adjust the pH value to 5.0-5.5, moisten the material for 2-3 hours, and culture medium The water content is preferably 62%. Pack the wet raw materials into high temperature resistant plastic bags, each bag weighing 1kg. Place the plastic bag in a sterilizer at 120°C for 1 hour to sterilize. Under sterile conditions, insert 2-3% of the secondary mushroom species into the sterilized culture medium, and cultivate for 35-45 days under the condition of 80-85% humidity and 20-28°C. Dried at 60-80°C, crushed into a fine powder above 100 mesh to obtain 145kg of yellow product. The tested product quality indicators meet the food hygiene standards.
Embodiment 3
[0030]Mix 70kg of bagasse, 15kg of bran, 12kg of bean dregs, 1kg of edible calcium sulfate, and 1kg of zinc phosphate, add 70kg of water and 0.5-1% citric acid to adjust the pH value to 5.0-5.5, and moisten the material for 2-3 hours. The amount of water is preferably 62%. Pack the wet raw materials into high temperature resistant plastic bags, each bag weighing 1kg. Place the plastic bag in a sterilizer at 110°C for 1 hour to sterilize. Under sterile conditions, insert 2-3% secondary species of shiitake mushrooms into the sterilized culture medium, and cultivate them for 30-35 days under the condition of 80-85% humidity and 20-28°C. Dried at 60-80°C, crushed into a fine powder above 100 mesh to obtain 71kg of yellow product. The tested product quality indicators meet the food hygiene standards.
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