Construction method of rapid Euonymus japonicus L.f. aureo-marginatus Rehd propagation system
A construction method and rapid propagation technology, applied in the field of plant cell engineering, can solve the problems of shortened plant life, susceptible to diseases, and infected diseases, and achieve the effects of low pollution rate, high germination rate, and short growth cycle.
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Embodiment 1
[0031] 1. Explant pretreatment and disinfection:
[0032] Select healthy, disease-free branches from the nursery, and select young shoot tips and stem segments with axillary buds as explants. Remove the mature leaves of the explants, soak them in 4°C washing powder water for 40 minutes, then rinse them with running water at 4°C for 1 hour, soak the explants in 75% alcohol for 30 seconds on an ultra-clean table, and rinse them with sterile water for 1 hour. Twice, and then soaked in 0.1% mercuric chloride solution at 4°C. The soaking time was set in five gradients of 4min, 6min, 8min, 15min and 25min. 1mL Tween-80 and sterile water were added to the mercuricl solution. Rinse 4 to 5 times, blot excess water with sterile filter paper; transfer to primary culture medium for culture.
[0033] In order to select the most suitable pretreatment conditions, the explants treated with different disinfection time were all inoculated on MS+6-BA2.5mg / L+NAA0.5mg / L+30g / L sucrose+8g / L agar+0....
Embodiment 2
[0047] 1. Explant pretreatment and disinfection:
[0048] Select the young stems of Buxus Phnom Penh without axillary buds as explants, soak them in 4°C washing powder water for 30 minutes, then wash them with 4°C running water for 1 hour, and place the explants on a super-clean bench with a mass fraction of 75% Soak in alcohol for 30s, rinse with sterile water once or twice, and then soak in 0.1% mercuric acid solution at 4°C. The soaking time is set to five gradients of 5min, 8min, 12min, 15min, and 25min, and 1mL of mercuricl solution needs to be added Tween-80, rinse with sterile water 4 to 5 times, and blot the excess water with sterile filter paper. The explants were all inoculated on the medium with the composition of MS+6-BA2.0+NAA0.5mg / L+30g / L sucrose+6g / L agar+0.2g / L activated carbon. The culture conditions were the same as in Example 1, and the pollution rate, browning rate and healing rate were counted in two weeks.
[0049] Table 3 Effects of different times of ...
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