Method for preparing polysaccharide by using lucidum strain fermented laminaria leftover
A technology of kelp leftovers and ganoderma strains, applied in the direction of microorganism-based methods, biochemical equipment and methods, fermentation, etc., can solve the problems of terminal food safety hazards, single variety of polysaccharide products, secondary pollution, etc., and achieve broadened utilization efficiency, shorten fermentation time, and reduce pollution
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Embodiment 1
[0017] Weigh 140kg of kelp scraps after kelp hot water extraction of kelp juice, add 7000kg of water, after fully imbibition, add 1kg of cellulase, use 1M citric acid to adjust the pH value to 5.0, hydrolyze at 50°C for 10 hours, after the end of enzymatic hydrolysis Use 1M sodium bicarbonate solution to adjust to neutrality, control the temperature at 100°C for 10 minutes to inactivate the enzyme, use a desktop centrifuge at 4000 rpm, and centrifuge for 10 minutes to obtain sediment and kelp enzymatic hydrolysis solution. The sediment is dried and pulverized as feed. Take the supernatant of the kelp enzymatic hydrolysis solution and put it directly into the fermenter that has been sterilized, and then carry out the real sterilization. Enter the secondary Ganoderma lucidum strain, the secondary Ganoderma lucidum strain is 30 ℃, 160rpm liquid submerged secondary culture for 7 days, the inoculation amount is 8% of the kelp enzymatic hydrolysis supernatant, the pH value is contro...
Embodiment 2
[0019] Weigh 160kg of kelp scraps after soaking kelp juice in hot water, add 9600kg of water, after fully imbibed, add 1.5kg of cellulase, use 1M acetic acid to adjust the pH value to 6.0, hydrolyze at 60°C for 6 hours, after the enzymatic hydrolysis Adjust the solution to neutral with 1M sodium bicarbonate, control the temperature at 100°C for 10 minutes to inactivate the enzyme, and use a desktop centrifuge at 4000rpm to centrifuge for 10 minutes to obtain sediment and kelp enzymatic hydrolysis. The sediment is dried and pulverized as feed. Take the supernatant of the kelp enzymatic hydrolysis solution directly into the fermenter that has been sterilized, and then carry out the real sterilization. The temperature of both the sterilized and the real sterilized is 121°C, and the time is 20 minutes. After the temperature of the fermenter drops to 30°C Insert the second-grade ganoderma strains on the left and right sides. The second-grade ganoderma lucidum strains are formed by ...
Embodiment 3
[0021]Weigh 100kg of kelp scraps after soaking kelp juice in hot water, add 4000kg of water, add 1kg of cellulase after fully imbibed, use 1M acetic acid to adjust the pH value to 4.5, hydrolyze at 45°C for 12 hours, and use Adjust the 1M sodium bicarbonate solution to neutral, treat at 95°C for 15 minutes to inactivate the enzyme, use a desktop centrifuge at 4000rpm, and centrifuge for 10 minutes to obtain the sediment and kelp enzymatic solution. The sediment is dried and pulverized as feed, and the kelp enzyme is taken The supernatant of the solution is directly put into the fermentation tank that has been sterilized, and then the real sterilized. The temperature of both the sterilized and the real sterilized is 121°C, and the time is 20 minutes. When the temperature of the tank drops to about 30°C, it is connected to the second stage. Ganoderma lucidum strain, the second-level Ganoderma lucidum strain is obtained by submerged secondary culture at 30°C and 160rpm for a total...
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