Method for improving content of ergosterol in liquid fermentation products of phellinus igniarius
A technology for liquid fermentation and ergosterol, applied in the directions of microorganism-based methods, biochemical equipment and methods, fermentation, etc., to achieve high efficiency, good industrial application prospects, and good repeatability.
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Embodiment 1
[0038] 1. Material preparation
[0039] Pectinase (with an enzyme activity of 50,000 U / g) and cellulase (with an enzyme activity of 30,000 U / g) were provided by Guangxi Pangbo Bioengineering Co., Ltd.
[0040] PDA plate medium: potato 200g, glucose 20g and agar 15g, dilute to 1000ml with water, natural pH, sterilize at 121°C for 20min.
[0041] The Phellinus strains preserved on the slant were inoculated on the PDA plate medium, and activated culture was carried out at a culture temperature of 25° C. for 7 days to obtain activated Phellinus strains bacterial blocks.
[0042] The preparation method of Cyclocarya paliurus extract comprises: weighing a certain amount of Cyclocarya paliurus leaves, pulverizing through 100 meshes, first adding 70% ethanol aqueous solution at 60 Extract at ℃ for 1.0 h, filter to obtain the supernatant, concentrate the supernatant and vacuum freeze-dry to obtain the extract Ⅰ; add distilled water accounting for 10 times the weight of the leaves of C...
Embodiment 2
[0054] 1. Material preparation
[0055] Pectinase (enzyme activity: 30,000 U / g) and cellulase (enzyme activity: 20,000 U / g) were provided by Guangxi Pangbo Bioengineering Co., Ltd.
[0056] PDA plate medium: potato 200g, glucose 20g and agar 20g, dilute to 1000ml with water, natural pH, sterilize at 121°C for 20min.
[0057] The Phellinus strains preserved on the slant were inoculated on the PDA plate medium, and activated culture was carried out at a culture temperature of 28° C. for 9 days to obtain activated Phellinus strains bacterial blocks.
[0058] The preparation method of Cyclocarya paliurus extract comprises: weighing a certain amount of Cyclocarya paliurus leaves, pulverizing through 60 meshes, first adding 80% ethanol aqueous solution at 80 Extract at ℃ for 2 hours, filter to obtain the supernatant, concentrate the supernatant and vacuum freeze-dry to obtain the extract Ⅰ; add distilled water accounting for 20 times the weight of the Cyclocarya paliurus leaves to ...
Embodiment 3
[0070]1. Material preparation
[0071] Pectinase (enzyme activity: 40,000 U / g) and cellulase (enzyme activity: 20,000 U / g) were provided by Guangxi Pangbo Bioengineering Co., Ltd.
[0072] PDA plate medium: potato 200g, glucose 20g and agar 15g, dilute to 1000ml with water, natural pH, sterilize at 121°C for 20min.
[0073] The Phellinus strains preserved on the slant were inoculated on the PDA plate medium, and activated culture was carried out at a culture temperature of 30° C. for 4 days to obtain activated Phellinus strains bacterial blocks.
[0074] The preparation method of Cyclocarya paliurus extract comprises: weighing a certain amount of Cyclocarya paliurus leaves, pulverizing through 40 meshes, first adding 60% ethanol aqueous solution at 70 Extract at ℃ for 1.5h, filter to obtain the supernatant, concentrate the supernatant and vacuum freeze-dry to obtain the extract I; add distilled water accounting for 15 times the weight of the leaves of Cyclocarya paliurus to t...
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