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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

Active Publication Date: 2016-01-20
NINGBO XINUOYA MARINE BIOTECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although the raw material cost of the first method is low, the extraction process is complicated and inefficient, and the obtained β-glucan has low branching degree, small molecular weight, poor water solubility and structural stability, and its application value is greatly reduced; although the obtained β-glucan obtained by the second method - The branching degree, molecular weight, water solubility and structural stability of dextran are relatively high, but the source cost of mushrooms is high, the cycle is long, the production space is large, the output is low, the post-processing of the product is difficult, and impurities are easy to remain; the third method The cycle is relatively short, and the branching degree, molecular weight, water solubility and other properties of the product can be selected by selecting different strains and controlling the fermentation conditions, but it takes a lot of research to determine the optimal conditions for fermentation
[0004] However, no matter which of the above methods, a large amount of pigments with complex components will be produced in the production process, and the decolorization step must be performed to improve the purity and product quality
Taking into account many factors such as maintaining the biological activity of β-glucan, the cycle should not be too long, the environment is friendly and the use of too many organic solvents should not be used, and the production cost should be low. At present, the only practical decolorization method is to use activated carbon or resin adsorption.
However, the principles of these two methods are all physical adsorption, and the product β-glucan will be adsorbed at the same time when the pigment is removed, so that the loss rate of the product is very large, and the yield is greatly reduced.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

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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Abstract

The invention discloses a production method of beta-glucan. The production method comprises the following steps of (1) schizophyllum commune activation; (2) seed activation; (3) fermentation culture; (4) coarse extraction; (5) purification. A colorless liquid culture medium prepared from 25 to 30g / L of glucose, 10 to 15g / L of sorbitol, 0.2 to 0.8g / L of monopotassium phosphate, 3 to 5g / L of epsom salt, 0.5 to 1g / L of ammonium sulphate, 0.1 to 0.5g / L of triethylamine hydrochloride, 1 to 2.2ml / L of trace element mixed solution and water is used as a fermentation culture medium for performing deep layer liquid fermentation culture on strains to obtain the colorless fermentation liquid. No pigment exists in the whole process; a decoloring step is not needed; loss due to adsorption is reduced; the problem of beta-glucan separation purification is overcome; high-purity white beta-glucan is obtained; the production method is suitable for mass industrial production.

Description

technical field [0001] The invention relates to a production method of β-glucan. Background technique [0002] Glucans are natural polysaccharides found in oats, barley, wheat, yeast and fungi, including 1,3-glucan, 1,4-glucan (with branched chains) and 1,6-glucans (unbranched), they may be alpha or beta. A large number of studies have shown that β-glucan is a good immune enhancer, which can effectively stimulate immune cells, not only enhance the specific immune response of the organism, but also improve the non-specific immune response. In addition, β-glucan can also enable organisms to resist infection by bacteria, fungi, viruses and parasites, and inhibit the growth of tumors, and has been well clinically applied abroad. Due to the huge application value of β-glucan in biology, medicine, health care and food, how to effectively obtain high-purity β-glucan, especially the biologically active β-glucan that can meet the injection standard Dextran has become a key directi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12P19/08C12R1/645
Inventor 贾艳诸辉
Owner NINGBO XINUOYA MARINE BIOTECH CO LTD
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