Abduction method for Camptotheca acuminata Decne polyploid
A technology of polyploidy and tetraploidy, applied in horticultural methods, botanical equipment and methods, material inspection products, etc., can solve the problem of low camptothecin content, achieve high active ingredient content, high efficiency, and improve genetic Effect
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Embodiment 1
[0016] (1) Processing of explants: collect the young and tender stems of Campylodon chinensis as explants, disinfect them with 70% alcohol for 30 seconds, rinse them with sterile water for 3 times, and then use 0.1% mercuric chloride After 30 minutes of disinfection, rinse with sterile water 5 times, and then dry the water with sterile filter paper;
[0017] (2) Callus culture: cut the sterilized stems into 2cm lengths and inoculate them in B 5 +NAA1mg / L+2,4-D0.5mg / L+KT0.5mg / L callus culture medium;
[0018] (3) Polyploid induction: Soak the callus in the colchicine solution that has been filtered and sterilized for 40 hours, the solution concentration is 400 mg / L, then rinse with sterile water for 3 to 4 times, and then transfer to a place without Colchicine MS+6-BA 1mg / L+NAA0.2mg / L bud differentiation medium cultured in the dark for 7 days, then transferred to light culture, the light intensity was 1500-2000Lx, and the light was 12 hours a day;
[0019] (4) Identification ...
Embodiment 2
[0024] (1) Treatment of explants: collect the young and tender leaves of Campylodon chinensis as explants, disinfect them with 75% alcohol for 5 seconds, rinse them with sterile water for 3 times, and then use 0.1% mercuric chloride After 5 minutes of disinfection, rinse with sterile water 5 times, and then dry the water with sterile filter paper;
[0025] (2) Callus culture: Cut the sterilized young leaves in half and inoculate them in B 5 +2,4-D1.5mg / L+KT0.5mg / L callus culture medium;
[0026] (3) Polyploid induction: Soak the callus in the colchicine solution that has been filtered and sterilized for 30 hours. Colchicine MS+6-BA0.5mg / L+NAA0.2mg / L bud differentiation medium cultured in the dark for 7 days, then transferred to light culture, the light intensity was 1500-2000Lx, and the light was 12 hours a day;
[0027] (4) Polyploid identification: the adventitious buds after 50 days of growth were pretreated in a 0.2% colchicine solution for 2.3 hours, washed with water, ...
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