Dendrobium officinale rapid breeding method through root tip tissue culture
A technology of dendrobium candidum and root tip is applied in the field of rapid propagation of dendrobium candidum root tip tissue culture to achieve the effects of short culture time, good resistance and maintaining growth characteristics
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experiment example 1
[0018] Select robust Dendrobium officinale seedlings, take about 1.5cm root tip and wash it with running water for about 1 hour, then disinfect it with 75% ethanol solution for 40 seconds, then rinse it twice with sterile water, then put the material into a beaker and wash it with 0.1% ethanol solution. Soak in mercuric chloride for 8 minutes, then rinse with sterile water 4-5 times, take 0.3-0.5mm root tips and inoculate them into differentiation induction medium: MS medium (100 parts) + NAA0.4mg / L (3.5 parts ) + banana juice 10% (6.4 parts) + agar 5.7g / L (3.7 parts) + sucrose 30g / L (28 parts), at a temperature of 25°C, a light intensity of 1800lx, and a light time of 12 hours, cultivate two moon. Post-transplant proliferation medium: MS medium (100 parts) + NAA1.0mg / L (1.5 parts) + 6-BA0.2 mg / L (1.2 parts) + potato juice 10% (7.3 parts) + agar 5.7 g / L (1.8 parts) + 30 g / L sucrose (14.3 parts), cultivated for one and a half months at a temperature of 25°C, a light intensity ...
Embodiment 2
[0020] Disinfection of root tips: Select robust Dendrobium officinale seedlings, take 1~1.5cm root tips, wash them with running water for 1 hour, sterilize with 75% ethanol solution for 40 seconds, rinse them with sterile water twice, put the root tips into the container, and use Soak in 0.1% mercuric chloride for 8 minutes, then rinse with sterile water 4-5 times to obtain the root tip to be inoculated;
[0021] Root tip differentiation: Cut out 0.3-0.5 mm of the root tip to be inoculated, insert it into the induction differentiation medium, and cultivate it for 45 days under the conditions of temperature 25°C, light intensity 1800 lx, and daily light time 12 hours to obtain differentiation root tip; the induction differentiation medium is 100 parts of MS medium, 5.5 parts of 0.4mg / L NAA, mass fraction is 1-10 parts of 10% banana juice, 0.5-5 parts of 5.7g / L agar, 30g / L A mixture of 18 parts of sucrose, 12.5 parts of pine pollen, and 6 parts of diatom powder.
[0022] Proli...
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