A kind of rapid propagation method for the rejuvenation of Lvfengteng tea variety
A technology of phoenix vine and varieties, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems that viruses cannot be guaranteed and are difficult to survive, and achieve clustered buds and buds with high value-added coefficients, easy to master, and methods simple effect
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Embodiment 1
[0023] A kind of tissue culture rapid propagation method of Lvfengteng tea variety rejuvenation, its steps are:
[0024] 1) Selection and sterilization of explants:
[0025] Get the stem tips of 100 healthy young shoots of Lvfengteng tea, and use them for future use after surface sterilization.
[0026] Select 100 newly germinated shoots of 10 or 13 or 15 cm, cut off the leaves and tendrils, cut into 0.5 cm long stems with terminal buds, soak them in detergent for 5 or 8 or 10 minutes, then gently scrub them with a brush, Rinse with running water for about 3 hours, move to the ultra-clean workbench, wash with 70% (volume ratio) alcohol for about 30 seconds, wash with aseptic water for 3 or 4 or 5 times, and then put it into the mixture of mass (g) and volume (mL). Shock disinfection in 0.1% mercuric chloride solution for 7 minutes, rinsed with sterile water for 5 times, cut off 0.5mm shoot tips under a dissecting microscope, and inoculated them on the primary culture medium; ...
Embodiment 2
[0040] A kind of tissue culture rapid propagation method of Lvfengteng tea variety rejuvenation, its steps are:
[0041] 1) Selection and sterilization of explants:
[0042] Get the stem tips of 100 healthy young shoots of Lvfengteng tea, and use them for future use after surface sterilization.
[0043] Select 100 newly germinated shoots of 10 or 12 or 14 or 15 cm, cut off the leaves and tendrils, cut into 0.5 cm long stems with terminal buds, soak them in detergent for 5 or 7 or 10 minutes, and then gently scrub with a brush Clean it, rinse it with running water for about 3 hours, move it to the ultra-clean workbench, wash it with 70% alcohol for about 30 seconds, wash it with sterile water for 3 or 4 or 5 times, and then put it in 0.1% mercuric chloride solution for 7 minutes. After washing with bacterial water for 5 times, cut off the shoot tip of 0.5 mm under the dissecting microscope, and inoculate it on the primary culture medium;
[0044] 2) Preparation of culture med...
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