Method for separating and screening anti-tumor active endophytic fungi of schisandra
An endophytic fungus, separation and screening technology, applied in the field of microorganisms, can solve the problems of increasing the volume of goods, unable to meet the demand of the market, and reducing the output of wild Schisandra chinensis, and achieve the effect of improving the success rate and efficiency.
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Embodiment 1
[0020] The stem tissue of Schisandra chinensis was collected from Shengli Nursery in Huanren, Liaoning, and the surface was sterilized according to the following procedure: the stem was cut into 2.0 cm small pieces, rinsed with sterile water, quickly rinsed in 75% ethanol for about 1 min, rinsed with sterile water for 3 times, and used Disinfect with 0.1% mercuric chloride for 8 minutes, and finally rinse with sterile water for 3 times, put it on a sterilized filter paper sheet, inoculate it on a PDA plate medium after the water is blotted dry, and incubate at 28°C for 3 to 5 days. The stem tissue on which the strain grows.
[0021] The aseptically tested stem tissue was cut into small pieces of about 0.5 cm × 0.5 cm under the ultra-clean workbench, and then the small pieces were planted on a PDA medium plate and cultured in a 28°C incubator. When hyphae obviously grew around the sample, the tip mycelia picking method was used to pick colonies with different shapes, and after ...
Embodiment 2
[0027] Take Schisandra cotyledons, and disinfect the surface according to the following procedures: rinse with sterile water, quickly rinse in 75% ethanol for about 1 min, rinse with sterile water for 3 times, then disinfect with 0.1% mercury liter for 5 min, and finally rinse with sterile water for 3 times, put On the sterilized filter paper sheet, inoculate it on the PDA plate culture medium after the water is blotted dry, culture at 28°C for 3-5 days, and select the leaf tissue without any bacteria growing on the surface.
[0028] The leaf tissue tested for sterility was cut into small pieces of about 0.5 cm × 0.5 cm under ultra-clean bench conditions, and then the small pieces were planted on PDA medium plates and cultured in an incubator at 28°C. When hyphae obviously grew around the sample, the tip mycelia picking method was used to pick colonies with different shapes, and after purification, they were transferred to PDA slant medium for future use.
[0029] The above-me...
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