Tissue culture and rapid propagation method for lobularia maritima
A tissue culture fast propagation and fragrant snowball technology, applied in the field of plant tissue culture, can solve problems such as rot, difficulty in collecting seeds, and cuttings are easily infected by pathogens, and achieve the effect of promoting commercialization and enhancing reproduction coefficient.
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Embodiment 1
[0018] (1) Obtaining sterile seedlings: select full-bodied seeds of Aurantium aurantium, first soak them in deionized water for 3 hours, filter the water, disinfect them with 75% alcohol on an ultra-clean workbench for 30 seconds, then disinfect them with 0.1% mercuric chloride solution for 8 minutes, and finally Rinse 3 times with sterile water. After disinfection, the seeds were inoculated in the germination medium for seed germination culture. After inoculation, it was placed under the condition of 12 hours of light per day, the light intensity was 2000lx, the culture temperature was 25°C, and the relative air humidity was 75% and the germination rate reached 96% after 30 days of cultivation. The germination medium is: 1 / 2MS+0.02mg / L NAA+15g / L sucrose+3.5g / L agar, with a pH of 5.4.
[0019] (2) Induction culture: inoculate the stem segment of about 1 cm of sterile seedlings on the induction medium for induction culture. After inoculation, it was placed in the light fo...
Embodiment 2
[0024] (1) Acquisition of sterile seedlings: select the plump seeds of Snowball, soak them in deionized water for 5 hours, filter out the water, disinfect them with 75% alcohol on the ultra-clean workbench for 40 seconds, then disinfect them with 0.1% mercuric chloride solution for 10 minutes, and finally Rinse 3 times with sterile water. After disinfection, the seeds were inoculated in the germination medium for seed germination culture. After inoculation, it is placed under the conditions of 12 hours of light per day, the light intensity is 2000lx, the culture temperature is 27°C, and the relative air humidity is 75% and the germination rate reaches 100% after 30 days of cultivation. The germination medium is: 1 / 2MS+0.05mg / L NAA+15g / L sucrose+3.5g / L agar, with a pH of 5.7.
[0025] (2) Induction culture: inoculate the stem segment of about 1 cm of sterile seedlings on the induction medium for induction culture. After inoculation, it was placed in the light for 14 hours...
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