Butterfly orchid induction culture medium and asexual propagation method of butterfly orchid
An induction medium and asexual reproduction technology, applied in the field of plant tissue culture, can solve the problems of damaging the female parent, wasting internodes of pedicels, etc., and achieve the effects of fast growth, cost saving, and short induction time
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Embodiment 1
[0032] Example 1: Preparation of induction medium
[0033] (1) Prepare the basal mother solution of the Phalaenopsis induction medium according to the composition and concentration of the standard N6 medium, and divide it into 9 Erlenmeyer flasks, and label them respectively. No. 1 to No. 8 triangular flasks are the Phalaenopsis induction medium experimental group added with plant growth regulators and organic additives of the present invention, and No. 9 bottle is the medium control group only added with agar, white granulated sugar and activated carbon.
[0034] (2) According to Table 1, add 6-bean aminoadenine BA mother solution, tomato juice and activated carbon into each Erlenmeyer flask and mix with N6 basic mother solution to the desired concentration.
[0035] (3) Take a certain amount of tap water (replacing distilled water) and boil it. According to the concentration in Table 1, use an electronic balance to take agar and white sugar, pour the agar into boiling water ...
Embodiment 2
[0038] Embodiment 2: Inoculation and cultivation between pedicel internodes
[0039] Carry out inoculation in a sterile ultra-clean workbench, use a sterilized scalpel to cut off the incision where the two ends of the pedicel are in contact with the disinfectant, take the tender part between the two pedicel nodes, cut it into 2-3mm sections, and inoculate quickly Into each induction medium prepared in Example 1, seal with a sterilized bottle stopper after inoculation.
[0040] After inoculation, the culture bottle was placed in an artificial culture room, and the environmental parameters of the culture bottle were as follows:
[0041] Culture conditions: temperature 25±1°C, light intensity 1500-1800lx, light-dark alternation 12h / 12h.
[0042] After culturing for 50 days, the induction rate, induction time and growth of protocorms in each culture flask were recorded (see Table 1 for experimental data).
[0043] Table 1 Concentration of each component of induction medium and e...
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