Armillaria mellea YN01 (WT) and application thereof
A typical technology of Armillaria mellea, applied in the field of microorganisms, can solve the problems of unfavorable artificial cultivation of Gastrodia elata, unknown sources of commercial species, unfavorable Armillaria mellea resources, etc., and achieve the effects of increasing the yield of Gastrodia elata, shortening the cultivation period, and shortening the co-cultivation time
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Embodiment 1
[0040] Embodiment 1: Collection, isolation and identification of Armillaria armillaria
[0041] 1. Collect wild Gastrodia elata from Dazhaizi Township, Buluqi, Zhaotong City, wash it clean, soak it in alcohol with a volume concentration of 75% in an ultra-clean workbench and sterilize it, take the symbiotic part of Gastrodia elata and Armillaria mellea, and inoculate it on the ampicillin-containing On PDA medium, cultivate in the dark at 18°C; during this period, transfer the hyphae with germinated mycelia to PDA medium without antibiotics and culture in the dark at 25°C for 2 weeks. If there are morphological differences, a second separation is performed. The bacterial cords of the obtained strains were detected, and if blue-green fluorescence could be emitted at 530nm, the isolated strains could be preliminarily determined to be Armillaria armillaria. Afterwards, molecular identification was carried out, DNA was extracted by CTAB method, rDNA-IGS sequence amplification was ...
Embodiment 2
[0078] Embodiment 2: Armillaria armillaria strain seed dressing cultivation experiment
[0079] (1) Preparation of primary strains: Put 200mL PDA liquid medium after removing agar into a 500mL Erlenmeyer flask, sterilize and cool for later use, and insert the 0.5cm tip of the strain into the liquid medium (each bottle is connected with Into the 3 segment cable), in the dark at 25 ° C, 180r / min shaker culture 10d.
[0080] (2) Preparation of cultivars: Add branches with a diameter of 1-2 cm in a 380mL culture bottle as fungus materials, and add nutrient solution to the 2 / 3 of the bottle according to the ratio of 20% starch and 2% glucose, and submerge the culture solution. The bacterial material is made into a bottled liquid medium with a natural pH; transfer the first-grade liquid bacteria to the sterilized bottled liquid medium according to the aseptic operation process, put it in a room temperature of 25°C, and cultivate it in the dark for 30 days, and then it can be cultiva...
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