Vaccinium australe tissue culture and rapid propagation method
A technology of tissue culture rapid propagation and induction medium, which is applied in the field of tissue culture rapid propagation of Nangao Congyue, can solve the problems of limited rapid propagation and new variety selection, low reproduction coefficient, high cost, etc., and achieves strong stress resistance, The effect of fast growth and high yield
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Embodiment 1
[0017] (1) Disinfection of explants: Collect the healthy plants of Nangao Congyue with buds and stems, gently scrub with a soft brush dipped in washing powder water, rinse with tap water for 3 hours, put them in an ultra-clean workbench, and disinfect with 75% ethanol for 20 seconds After that, wash 4 times with sterile water, then sterilize with 0.1% mercuric chloride solution for 9 minutes, rinse 6 times with sterile water, and then dry the water drops on the surface with sterile filter paper before use.
[0018] (2) Induction culture: inoculate the budded stem segments treated in step (1) in the induction medium to induce clustered buds. After inoculation, they were first cultured in total darkness at 27°C for 12 days, and then placed in light for 14 hours a day with a light intensity of 3000 lx and cultured at a culture temperature of 27°C. The induction rate was 78.56%. The induction medium is: WPM+1.5mg / L ZT+3.0mg / L 6-BA+0.2mg / L NAA+18g / L sucrose+3.6g / L agar, with a pH o...
Embodiment 2
[0023] (1) Disinfection of explants: Collect the healthy plants of Nangao Congyue with buds and stems, gently scrub with a soft brush dipped in washing powder water, rinse with tap water for 2 hours, put them in an ultra-clean workbench, and disinfect with 75% ethanol for 15 seconds After that, wash 4 times with sterile water, then disinfect with 0.1% mercuric chloride solution for 5 minutes, rinse 6 times with sterile water, and then dry the water drops on the surface with sterile filter paper before use.
[0024] (2) Induction culture: inoculate the budded stem segments treated in step (1) in the induction medium to induce clustered buds. After inoculation, it was cultured in total darkness at 25°C for 10 days, and then placed in light for 13 hours a day, with a light intensity of 2000 lx, and cultured at a culture temperature of 25°C, and the induction rate was 83.47%. The induction medium is: WPM+1.2mg / L ZT+2.4mg / L 6-BA+0.4mg / L NAA+18g / L sucrose+3.6g / L agar, with a pH of 5...
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