In-vitro culture method of asiatic toddalia root
A technique for in vitro culture of dragon palm blood, applied in the field of plant tissue culture, can solve problems such as hindering the large-scale use of dragon palm blood and research improvement.
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Embodiment 1
[0032] (1) explant collection: collect with scissors the sprouting tiller at the rhizome junction of the year's life Pterodactyl palmatum rhizome that is good in physiological state and free from damage by diseases and insect pests as explants;
[0033] (2) First-generation induction culture: the explants collected in step (1) were rinsed under tap water for 3 hours, placed in a clean bench and sterilized twice in 70% ethanol solution for 30 seconds each time, and then added 1-2 drops of Tween-20 0.1% HgCI 2 Stir and sterilize for 10 minutes, and finally rinse with sterile water for 7 times, blot dry with sterile filter paper, remove part of the leaflets, cut into 1.0-1.5cm long stems and inoculate them into the primary induction medium, place at 20°C and fully Adventitious buds can be induced to form after dark culture for 25 days, and the induction rate reaches 93%.
[0034] The induction medium is: Miller medium+3.0mg / L Vc+0.5mg / L PVP+0.1mg / L ZT+0.1mg / L IBA+0.5mg / L activat...
Embodiment 2
[0042] (1) Explant collection: collect with scissors the sprouting tillers at the joints of the rhizomes and rhizomes of the year-old Pterodactyl palmatum with good physiological state and no damage by diseases and insect pests as explants;
[0043] (2) First-generation induction culture: the explants collected in step (1) were rinsed under tap water for 3 hours, placed in a clean bench and sterilized twice in 70% ethanol solution, each time for 30 seconds, and then used With 0.1% HgCI adding 1-2 drops of Tween-20 2 Stir and sterilize for 10 minutes, finally rinse with sterile water for 5 times, then blot dry with sterile filter paper, remove part of the leaflets, cut into 1.0-1.5cm long stems and inoculate them into the primary induction medium, place at 20°C and fully Adventitious buds can be induced to form after dark culture for 30 days, and the induction rate reaches 91%.
[0044] The induction medium is: Miller medium+2.0mg / L Vc+0.3mg / L PVP+0.08mg / L ZT+0.05mg / L IBA+0.3m...
Embodiment 3
[0052] (1) explant collection: collect with scissors the sprouting tiller at the rhizome junction of the year's life Pterodactyl palmatum rhizome that is good in physiological state and free from damage by diseases and insect pests as explants;
[0053] (2) First-generation induction culture: the explants collected in step (1) were rinsed under tap water for 3 hours, placed in a clean bench and sterilized twice in 70% ethanol solution for 30 seconds each time, and then added 1-2 drops of Tween-20 0.1% HgCI 2 Stir and sterilize for 10 minutes, and finally rinse with sterile water for 6 times, blot dry with sterile filter paper, remove part of the leaflets, cut into 1.0-1.5cm long stems and inoculate them into the primary induction medium, place at 20°C and fully Adventitious buds can be induced to form after dark culture for 35 days, and the induction rate reaches 85%.
[0054] The induction medium is: Miller medium+1.0mg / L Vc+0.1mg / L PVP+0.05mg / L ZT+0.01mg / L IBA+0.1mg / L activ...
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