Production method of beta-glucan
A production method and glucan technology, applied in the production field of beta-glucan, can solve the problems of difficult post-processing of products, high cost of mushroom sources, and not too long cycle, and reduce uncontrollable factors and other metabolites. generation, meet the effect of large-scale industrial production, simplify the production process and equipment
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Embodiment 1
[0023] Step 1. Activation of Schizophyllum strains:
[0024] Under aseptic conditions, the Schizophyllum strains were inoculated on the plate medium and cultured in a 20°C incubator. The improved plate medium contained 200g / L of potato, 20g / L of glucose, and 10g / L of beef extract powder. , yeast extract powder 10g / L, agar 20g / L. After cultivating for 4 days, mycelium began to appear, and after 6 days, the mycelium was covered with solid medium, and a pure white, velvet flat mycelium was obtained.
[0025] Step two, seed activation:
[0026] The liquid culture medium that potato 200g / L, glucose 20g / L, beef extract powder 5g / L, yeast extract powder 5g / L are made is packed into shake flask, and the filling volume is 1 / 3. The plate mycelium obtained in step 1 was inoculated into the shake flask, and cultured in an incubator at a rotation speed of 180 rpm and a temperature of 18° C. for 10 days as a seed solution.
[0027] Step three, fermentation culture:
[0028] Mix glucose ...
Embodiment 2
[0036] Step 1. Activation of strains:
[0037] Under aseptic conditions, the Schizophyllum strains were inoculated on the plate culture medium and cultured in a 30°C incubator, where the plate medium contained 200 g / L of potato, 20 g / L of glucose, 5 g / L of beef extract powder, Yeast extract powder 5g / L, agar 15g / L. After culturing for 2 days, mycelium began to appear, and after 2 days, the mycelium was covered with solid medium, and a pure white, velvet flat mycelium was obtained.
[0038] Step two, seed activation:
[0039] The liquid culture medium that potato 200g / L, glucose 20g / L, beef extract powder 10g / L, yeast extract powder 10g / L are made is packed into shake flask, and the filling volume is 1 / 5. The plate mycelium obtained in step 1 was inoculated into the shake flask, and cultured in an incubator at a rotation speed of 90 rpm and a temperature of 30° C. for 4 days as a seed solution.
[0040] Step three, fermentation culture:
[0041] Glucose 30g / L, sorbitol 15g / ...
Embodiment 3
[0049] Step 1. Activation of strains:
[0050] Under aseptic conditions, the Schizophyllum strains were inoculated on the plate medium, and placed in a 28°C incubator for cultivation. The improved PDA plate medium contained 200g / L of potato, 20g / L of glucose, and 8g / L of beef extract powder. L, yeast extract powder 8g / L, agar 17.5g / L. After cultivating for 3 days, mycelium began to appear, and after 3 days, the mycelium was covered with solid medium, and a pure white, velvet flat mycelium was obtained.
[0051] Step two, seed activation:
[0052] The liquid culture medium that potato 200g / L, glucose 20g / L, beef extract powder 8g / L, yeast extract powder 8g / L are made is packed into shake flask, and the filling volume is 1 / 4. The plate mycelium obtained in step 1 was inoculated into the shake flask, and cultured in an incubator at a rotation speed of 150 rpm and a temperature of 28° C. for 7 days as a seed solution.
[0053] Step three, fermentation culture:
[0054] Mix glu...
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