Culturing method for mycelia of Antrodia camphorata

A kind of technology of Antrodia cinnamomea mycelium and cultivation method, which is applied in the field of cultivation of Antrodia cinnamomea mycelium, can solve the problems of long cultivation period, low success rate and low medicinal value of Antrodia cintrodia mycelium, and achieve the goal of overcoming the long period and overcoming success Low rate, overcome the effect of low medicinal value

Inactive Publication Date: 2018-01-16
殷东林 +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patented technology uses two methods - one involves mixing an organic acid solution into water or another solvent containing other substances like sugars (such as citric acids) before adding it back together again after being mixed with this mixture. By doing these steps, we create tiny crystals called Amanita nibrobalanica mushroom cells instead of traditional culturing techniques used on natural sources such as enzymes. These small cellular structures have unique properties making them ideal candidates for use in medicine because they may be more effective at treating diseases than any existing drugs currently available due to their high content of flavonoids found within certain plants.

Problems solved by technology

This patented technical problem addressed in this patents relates to growing Aeolia Camphora for its commercial potential due to poor nutritional values obtained during conventional processes used for producing these plants.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] Prepare each raw material to prepare slant medium according to the following formula:

[0029] Potato 100g / L, glucose 10g / L, corn flour 10g / L, peptone 2g / L, magnesium sulfate 0.1g / L, potassium dihydrogen phosphate 0.2g / L, VB 1 10mg / L, agar powder 16g / L;

[0030] Inoculate the strain of Antrodia camphorata on the slant medium prepared above for activation and purification, and the culture temperature is 25°C to obtain the activated mother species;

[0031] Prepare each raw material according to the following formula to prepare liquid shake flask culture medium:

[0032] Potato juice 10g / 100mL, glucose 1g / 100mL, corn flour 1g / 100mL, peptone 0.2g / 100mL, magnesium sulfate 0.01g / 100mL, potassium dihydrogen phosphate 0.02g / 100mL, VB 1 0.001g / 100mL and agar powder 0.05g / 100mL;

[0033] Inoculate the above-mentioned activated mother species into the liquid shake flask culture medium for shake flask culture. The culture temperature of the above s

Embodiment 2

[0043] Prepare each raw material to prepare slant medium according to the following formula:

[0044] Potato 200g / L, glucose 15g / L, corn flour 30g / L, peptone 4g / L, magnesium sulfate 0.5g / L, potassium dihydrogen phosphate 1g / L, VB 1 30mg / L, agar powder 18g / L;

[0045] Inoculate the strains of Antrodia camphorata on the slant medium prepared above for activation and purification, and the culture temperature is 28°C to obtain the activated mother species;

[0046] Prepare each raw material according to the following formula to prepare liquid shake flask culture medium:

[0047] Potato juice 20g / 100mL, glucose 1g / 100mL, corn flour 3g / 100mL, peptone 1g / 100mL, magnesium sulfate 0.05g / 100mL, potassium dihydrogen phosphate 0.1g / 100mL, VB 1 0.005g / 100mL and agar powder 0.1g / 100mL;

[0048] Inoculate the above-mentioned activated mother species into the liquid shake flask culture medium for shake flask culture. The culture temperature of the above shake

Embodiment 3

[0059] Prepare each raw material to prepare slant medium according to the following formula:

[0060] Potato 200g / L, glucose 20g / L, corn flour 50g / L, peptone 5g / L, magnesium sulfate 1g / L, potassium dihydrogen phosphate 2g / L, VB 1 50mg / L, agar 20g / L;

[0061] Inoculate the strains of Antrodia camphorata on the slant medium prepared above for activation and purification, and the culture temperature is 30°C to obtain the activated mother species;

[0062] Prepare each raw material according to the following formula to prepare liquid shake flask culture medium:

[0063] Potato juice 50g / 100mL, glucose 4g / 100mL, corn flour 5g / 100mL, peptone 1g / 100mL, magnesium sulfate 0.1g / 100mL, potassium dihydrogen phosphate 0.2g / 100mL, VB 1 0.01g / 100mL and agar powder 0.15g / 100mL;

[0064] Inoculate the above-mentioned activated mother species into the liquid shake flask culture medium for shake flask culture. The culture temperature of the above shake flask cult

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Abstract

The invention discloses a culturing method for the mycelia of Antrodia camphorata, belonging to the field of biological fermentation technology. The method of the invention comprises the following steps: inoculating a slant culture medium with a Antrodia camphorata strain for activation and purification so as to obtain an activated mother strain; inoculating a liquid shake-flask culture medium with the activated mother strain for static culture, and carrying out stirring culture after mycelia germinate and are free of pollution so as to obtain a shake-flask strain; inoculating a fermentation medium with the shake-flask strain for fermentation culture so as to obtain fermented mycelia; and inoculating a artificially synthesized solid culture medium with the fermented mycelia which are usedas a liquid strain and carrying out fermentation for 30 to 90 days so as to obtain the mycelia of Antrodia camphorata. The method of the invention has the advantages of a short cultivation period forthe mycelia of Antrodia camphorata, a high culture success rate of and high medicinal value of the mycelia.

Description

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Claims

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Application Information

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Owner 殷东林
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