Production method of antrodia camphorata stock seeds
A production method and the technology of the original seed are applied in the field of making the original seed of Antrodia camphorata, and can solve the problems such as the limitation of domestication and cultivation of Antrodia camphorata
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Embodiment 1
[0018] Experimental strain: Antrodia camphorata
[0019] Experimental steps:
[0020] 1. Preparation of activated slant medium:
[0021] Raw materials per liter of medium: 200 grams of potatoes (peeled), 20 grams of glucose, 20 grams of agar, 100 grams of camphor wood chips. Boil potatoes and camphor wood chips in water (20-30min), filter with gauze to obtain the filtrate, add glucose and agar to the filtrate, then make up to 1L with water, sterilize at 121°C for 30min, then pour it into a test tube, and make it 18mm×180mm test tube slant medium.
[0022] 2. Transfer tube activation of Antrodia camphorata parent species: Inoculate under sterile conditions, cut a piece of bacteria about 5mm×5mm thick about 2mm from the original Antrodia camphorata strain, transfer to the activated slant culture prepared in step 1 medium; conventional PDA medium was used as a control. There were 5 replicates for the two media respectively.
Embodiment 2
[0035] Experimental strain: Antrodia camphorata
[0036] Experimental steps:
[0037] 1. Preparation of activated slant medium:
[0038] Raw materials per liter of medium: 200 grams of potatoes (peeled), 20 grams of glucose, 20 grams of agar, 100 grams of camphor wood chips. Boil potatoes and camphor wood chips in water (20-30min), filter with gauze to obtain the filtrate, add glucose and agar to the filtrate, then make up to 1L with water, sterilize at 121°C for 30min, then pour it into a test tube, and make it 18mm×180mm test tube slant medium.
[0039] 2. Transfer tube activation of Antrodia camphorata parent species: Inoculate under sterile conditions, cut a piece of bacteria about 5mm×5mm thick about 2mm from the original Antrodia camphorata strain, transfer to the activated slant culture prepared in step 1 medium; conventional PDA medium was used as a control. There were 5 replicates for the two media respectively.
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