Rapid propagation method for tissue culture of moellendorf's spidemoss herb
A technology of tissue culture and cypress, applied in the field of plant tissue culture, can solve the problems of trait separation, unstable genetic traits, loss of good traits of parents, etc., and achieve the effect of long cycle, promoting industrialization development, and guaranteeing high-quality seedlings
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Embodiment 1
[0012] (1) Induction of adventitious buds: Select the annual jointed rattans of Dibaizhi as explants, sterilize them with 75% alcohol for 15 seconds, rinse them with sterile water for 6 times, and put them in 0.1% mercuric chloride solution for disinfection. After 18 minutes, wash it with sterile water for 7 times, dry it with sterile filter paper, cut it into 5 cm canes with joints, inoculate it on the induction medium, and culture it in the dark at 25°C for 21 days. It can induce the formation of adventitious buds, the pollution rate is as low as 3%, and the adventitious bud induction rate can reach 93%. The induction medium is: MS+0.3mg / LTDZ+1.5mg / L 6-BA+1.5mg / LNAA+28g / L sucrose+3.5g / L agar, pH is 5.6;
[0013] (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 16 hours a day after inoculation, the light intensity is 2100 lx, and the culture temperature is 2...
Embodiment 2
[0017] (1) Induction of adventitious buds: Select the annual jointed rattans of Dibaizhi as explants, sterilize them with 75% alcohol for 18 seconds, rinse them with sterile water for 6 times, and put them in 0.5% mercuric chloride solution for disinfection After 18 minutes, rinse with sterile water for 9 times, dry the water through sterile filter paper, cut into 7 cm canes with joints, inoculate them on the induction medium, and culture them in the dark at 26°C for 15 days. It can induce the formation of adventitious buds, the pollution rate is as low as 8%, and the adventitious bud induction rate can reach 96%. The induction medium is: MS+0.6mg / LTDZ+1.8mg / L 6-BA+0.5mg / LNAA+30g / L sucrose+6.0g / L agar, with a pH of 5.7.
[0018] (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 16 hours per day after inoculation, the light intensity is 2800 lx, and the cul...
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