Method for producing liquid edible fungus strains by using wastes from cordyceps militaris culture medium
A technology of medium and liquid strains of Cordyceps militaris, applied in the direction of botany equipment and methods, cultivation, application, etc., which can solve the problem of lack of reuse channels for medium waste, pollution of natural ecological environment and reproduction environment, and restriction of Cordyceps industry. Sustainable development and other issues to achieve the effect of facilitating large-scale factory production, high safety indicators, and low cost
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Embodiment 1
[0024] (1), crush the medium waste produced in the cultivation of Cordyceps militaris to 40-60 mesh, add water according to the ratio of material to water (mass volume ratio of medium waste to water) 1:8g / mL and stir well, boil water Gelatinization for 20min to obtain culture medium waste gelatinized material;
[0025] (2) Cool the medium waste gelatinized material to 60°C, adjust the pH value to 4.5 with dilute hydrochloric acid with a mass fraction of 18%, and add dual enzymes according to the amount of α-amylase 4U / g and glucoamylase 6U / g Mix and stir, wherein the mass ratio of α-amylase and glucoamylase is 1:1.8, perform double enzyme digestion at 60°C, react for 40min, raise the temperature to 90°C and maintain for 10min, to terminate the enzymatic reaction;
[0026] (3), be cooled to 55 ℃ of temperature, add water to the original volume of culture medium waste gelatinized material, the dilute hydrochloric acid of mass fraction 18% and NaOH solution adjust pH value to 7.0...
Embodiment 2
[0035] (1) Crush the culture medium waste produced in the planting of Cordyceps militaris to 40-60 mesh, add water according to the ratio of material to water 1:6g / mL and stir well, and gelatinize in boiling water for 20 minutes to obtain the culture medium waste gelatinized material ;
[0036] (2) Cool the medium waste gelatinized material to 55°C, adjust the pH value to 4.0 with dilute hydrochloric acid with a mass fraction of 18%, and add dual enzymes according to the amount of α-amylase 4U / g and glucoamylase 6U / g Mix and stir, wherein the mass ratio of α-amylase and glucoamylase is 1:1.5, perform double enzyme digestion at 55°C, react for 40 minutes, raise the temperature to 90°C for 5 minutes, and terminate the enzymatic reaction;
[0037] (3), be cooled to temperature 55 ℃, add water to the original volume of culture medium waste gelatinized material, the dilute hydrochloric acid of mass fraction 18% adjusts pH value 5.0, add and account for the papain of culture medium ...
Embodiment 3
[0046](1) Crush the culture medium waste produced in the cultivation of Cordyceps militaris to 40-60 mesh, add 7mL of water per gram of culture medium waste, that is, the ratio of material to water is 1:7g / mL, add water and stir well, and gelatinize in boiling water 20min, obtain medium waste gelatinized material;
[0047] (2) Cool the culture medium waste gelatinized material to 58°C, adjust the pH value to 4.2, add the double enzymes according to the amount of α-amylase 4U / g, glucoamylase 6U / g, mix and stir, wherein, α - The mass ratio of amylase and glucoamylase is 1:1.7, and double enzyme digestion is carried out at 58°C. After 40 minutes of reaction, the temperature is raised to 90°C and maintained for 8 minutes to terminate the enzymatic reaction;
[0048] (3), cooling to a temperature of 55° C., replenishing water to the original volume of the medium waste gelatinized material, adjusting the pH value to 6, adding papain accounting for 0.15% of the medium waste, and the ...
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