C. tertii and its cultivation method
A technology of C. tertii and its cultivation method, which is applied in the field of C. tertii and its cultivation, can solve the problems of cultivating fruit bodies that have not yet obtained sexual spores, and achieve stable production in large quantities, good economic benefits and Social benefits, effects of strong antioxidant capacity
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Embodiment 1
[0040] 1. Production of mother species
[0041] 1.1 Isolation of strains
[0042] The comprehensive PDA (20wt% of potato, 2wt% of glucose, 2wt% of agar, 0.3wt% of potassium dihydrogen phosphate, 0.15wt% of magnesium sulfate, vitamin B1 10ppm, the balance is water) is divided into test tubes, at 0.11MPa atmospheric pressure, 121 ℃ High temperature and high pressure damp heat sterilization for 30 minutes, take out and cool and place on an inclined plane. CCTCC NO: M2015746 The fruiting body of C. tertii is wiped with 75% alcohol on the surface under aseptic conditions, then torn apart, and the internal bacterial tissue of 0.2-0.5mm × 0.2-0.5mm is connected to the comprehensive PDA slope. Place it in an incubator at 25°C for constant temperature and dark cultivation. After the mycelia cover the slope, the transfer can be carried out. The time for the mycelium to grow is about 10-15 days.
[0043] 1.2 Purified strains
[0044] Red Bengal culture medium (peptone (peptone) 0.5wt...
Embodiment 2
[0062] Example 2 Determination of antioxidant activity
[0063] 6.1 Preparation of medium PDA solid medium contains 200g potato, 20g glucose, 20g agar, 1000mL water; PDA liquid medium contains 200g potato, 20g glucose, 1000mL water.
[0064] 6.2 Preparation of fermentation broth and mycelia extract. Transfer the strain of C. tertii CCTCC NO: M2015746 into a slant test tube, place it in a constant temperature incubator at 28°C for 5-7 days, and connect 5 pieces after the tube is full (0.5cm×0.5cm) into a 250mL Erlenmeyer flask containing 100mL of medium, placed in a constant temperature shaker at 25°C, at 110r·min -1 Vibrating culture, after the fermentation broth is clarified, take it out, filter with a filter cloth (100 mesh) to obtain the fermentation broth and mycelia respectively, and set aside.
[0065] The mycelium was blotted dry with filter paper and dried at 60°C to constant weight. After grinding with liquid nitrogen, 1.5 g was extracted with distilled water and abs...
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