Rieger Begonia tissue culture quick replication method
A tissue culture and rapid technology, applied in the field of bioengineering, can solve the problems of long induction time, low seedling induction rate, and inability to adapt to market demand, etc., and achieve the effect of convenient induction and cultivation and good effect
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example 1
[0030] 1. Treatment of explant materials: including cleaning, disinfection and cutting of explant materials to prepare explants that meet the requirements. Specifically: take the young leaves of Rieger Begonia with red flowers, wash them with tap water for 20-30 minutes, and then soak them with detergent-added water for 20-30 minutes. After cleaning, carry out disinfection treatment on the ultra-clean workbench, soak in 70% alcohol for 20 seconds, and then soak in 10% (V / V) sodium hypochlorite (available chlorine ≥ 7.5%) solution with Tween-20 for 10 minutes After the leaves are sterilized, put them into sterile bottles for later use. When necessary, the leaves are taken out from the aseptic bottle, and after removing the edge and petiole of the leaves on the ultra-clean workbench, they are then cut into leaf pieces of 0.5-1 cm×0.5-1 cm in size to form explants.
[0031] 2. Inducing budding: inoculate the leaf pieces as explants on the medium with the formula MS+6-benzylamino...
example 2
[0034] Get the young leaves of Rieger Begonia with pink flowers, and process them in the same way as Example 1 to obtain explants. Then the explants are inoculated on the same medium as in Example 1, placed under the light of 100~200lx and cultivated for 14 days, and then moved to the light of 1100~1200lx and cultivated. After 18 days, the induction rate of clustered buds reaches 99%. After 21 days, the induction rate of clustered buds reached 100%.
example 3
[0036] Get the young leaves of Rieger Begonia with red flowers, and process them in the same way as example one to obtain explants. Then the explants were inoculated on the medium whose formula was MS+6-benzylaminopterin 0.6mg / l+ naphthalene acetic acid 0.3mg / l+ sucrose 30g+ agar 6g, first cultured under 100~200lx light conditions for 14 days, and then transplanted When cultivated under the light condition of 1100~1200lx, the induction rate of clustered buds reaches 90% after 18 days, and the induction rate of clustered buds reaches 100% after 28 days.
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