Specific molecular marker of pleurotus eryngii NX2-O strain as well as acquisition method and application of specific molecular marker
A molecular marker, the technology of eryngium eryngii, applied in the directions of biochemical equipment and methods, DNA preparation, recombinant DNA technology, etc., can solve the influence of cultivation and production enthusiasm, the damage of the development of the eryngium eryngii industry, the loss of mushroom farmers and manufacturers, etc. problem, to achieve the effect of good application prospect, short detection time and high accuracy
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[0032] 1. Materials: The Pleurotus eryngii Pleurotus eryngii strain used in the experiment was preserved by the Edible Fungus Branch Center of the China Agricultural Microbiology Collection Center. The DX25 strain is a monokaryotic strain isolated from the protoplasts of the Pleurotus eryngii strain.
[0033] 2. The synthesis of PCR primers was completed by Shanghai Jierui Bioengineering Co., Ltd.
[0034] Table 1 PCR primers for amplifying pyrF gene
[0035]
[0036] 3. Culture medium: Potato glucose medium (PD medium): 20g potato, 20g glucose, add water to 1L, use after sterilization.
[0037] 4. Mycelia culture: the Pleurotus eryngii strain was transferred to the potato glucose medium, cultured in a dark shake flask at 25°C, and the mycelium was collected after 4 days.
[0038] 5. Using the CTAB (cetyltrimethylammonium bromide) method to extract the genomic DNA of Pleurotus eryngii strains:
[0039] (1) Grind the Pleurotus eryngii mycelium which was freeze-dried in liqui...
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