Tissue culture rapid propagation method for plukenetia volubilis L.
A technology of tissue culture and star oil vine, applied in the field of plant tissue culture, can solve the problems of prone to trait separation, unstable genetic traits, and long time consumption in offspring, and achieve the effect of rapid breeding and large-scale promotion and industrialization development
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Embodiment 1
[0016] (1) Induction of adventitious buds: select the explants of astragalus vines with joints in the same year, sterilize them with 75% alcohol for 12 seconds, rinse them with sterile water for 3 times, and put them in 0.1% mercuric chloride solution for disinfection After 15 minutes, wash it with sterile water for 5 times, dry it with sterile filter paper, cut it into 2-4cm canes with joints, inoculate it on the induction medium, and cultivate it in the dark at 25°C for 18 days. The formation of adventitious buds can be induced within a few days, the pollution rate is as low as 5%, and the adventitious bud induction rate can reach 92.7%. The induction medium is: MS+0.2mg / LTDZ+1.2mg / L 6-BA+0.5mg / LNAA+20g / L sucrose+4.5g / L agar, pH is 5.5;
[0017] (2) Subculture: cut off the adventitious buds obtained in step (1) from the base, inoculate them on the proliferation medium for subculture, and place them in the light for 13 hours a day after inoculation, the light intensity is 15...
Embodiment 2
[0021] (1) Induction of adventitious buds: select the explants of astragalus as the explants, sterilize them with 75% alcohol for 15 seconds, rinse them with sterile water for 4 times, and put them in 0.1% mercuric chloride solution for disinfection. After 15 minutes, rinse with sterile water for 6 times, dry the water through sterile filter paper, cut into 2-4cm canes with joints, and inoculate them on the induction medium, and cultivate them in the dark at 26°C for 14 The formation of adventitious buds can be induced within a few days, the pollution rate is as low as 7%, and the adventitious bud induction rate can reach 95.4%. The induction medium is: MS+0.4mg / LTDZ+1.6mg / L 6-BA+0.3mg / LNAA+20g / L sucrose+4.0g / L agar, with a pH of 5.8.
[0022] (2) Subculture: cut off the adventitious buds obtained in step (1) from the base, inoculate them on the proliferation medium for subculture, and place them in the light for 14 hours a day after inoculation, the light intensity is 2000 lx...
Embodiment 3
[0026] (1) Induction of adventitious buds: select the explants of astragalus as explants, sterilize them with 75% alcohol for 20 seconds, rinse them with sterile water for 4 times, and place them in 0.1% mercuric chloride solution for disinfection. After 30 minutes, rinse with sterile water for 6 times, dry the water through sterile filter paper, cut into 2-4cm canes with joints, inoculate them on the induction medium, and cultivate them in the dark at 28°C for 20 minutes. The formation of adventitious buds can be induced within a few days, the pollution rate is as low as 2%, and the adventitious bud induction rate can reach 87.9%. The induction medium is: MS+0.3mg / LTDZ+1.5mg / L 6-BA+0.3mg / LNAA+25g / L sucrose+4.5g / L agar, with a pH of 5.8.
[0027](2) Subculture: cut off the adventitious buds obtained in step (1) from the base, inoculate them on the proliferation medium for subculture, place them in the light for 15 hours a day after inoculation, the light intensity is 2000 lx,...
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