Peeled burdock liquid fermentation medium and method for fermenting agrocybe aegerita
A liquid fermentation and culture medium technology, applied in the direction of microorganism-based methods, fermentation, biochemical equipment and methods, etc., can solve the problems of long fermentation time, many steps, unfavorable separation and purification, etc., and achieve short product time and simple preparation method Effect
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Embodiment 1
[0048] Step 1, strain activation: inoculate the tea new mushroom strain (purchased from China General Microorganism Strain Collection and Management Center, strain number CGMCC No.5778) into the slant medium (potato dextrose agar slant medium), at 25 ° C Cultivate for 7 days until the hyphae cover the slope;
[0049] Step 2, preparation of liquid fermentation medium: the burdock root is washed and peeled; the peeled burdock root is cut into a size of 1.5cm×1.5cm, crushed and passed through a 40-mesh sieve, and the liquid fermentation medium consists of peeled burdock root and water, The weight ratio of material to water is 5% (w / v), the pH is natural (the pH is not adjusted), the pressure is 103.4KPa, and sterilized by high-pressure steam at 121°C for 20 minutes;
[0050] Step 3, liquid fermentation culture: inoculate the activated slant bacteria into a 250 mL culture bottle filled with 100 mL of the above liquid fermentation medium, ferment and culture at 24°C for 72 hours, a...
Embodiment 2
[0056] The difference from Example 1 is that the weight ratio of burdock and water is 1% (w / v), and the content of crude polysaccharide measured in liquid fermentation culture for 72 hours is 18.23 mg / ml.
[0057] Such as figure 2 As shown, according to the steps of Example 2, the liquid fermentation was cultivated for 72 hours, and the mycelial balls were covered with the culture medium.
Embodiment 3
[0059] The difference from Example 1 is that the weight ratio of burdock and water is 10% (w / v), and the crude polysaccharide content measured after 72 hours of liquid fermentation culture is 24.78mg / ml.
[0060] Such as image 3 As shown, according to the steps of Example 3, the liquid fermentation culture was carried out for 72 hours, and the mycelial balls were covered with the culture medium, and the density and polysaccharide content were higher than those of Examples 1 and 2.
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