Tissue culture rapid propagation method of prunus cerasifera
A technology of tissue culture and rapid propagation of cherries, applied in the field of agricultural biology, can solve the problems of low rooting rate of cherry plums and the inability to ensure the uniformity of seedlings, etc., and achieve the effects of easy to obtain strong seedlings, increase the effect of growth and multiplication, and increase the multiplication coefficient
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Embodiment 1
[0039] The establishment of embodiment 1 cherry plum tissue culture rapid propagation method
[0040] The present embodiment provides the rapid propagation method of cherry plum tissue culture, and its flow process is as follows figure 1 shown.
[0041] 1. Explant collection
[0042]Using the current-year-old stems of cherry plum seedlings as explants, the robust, semi-lignified middle stems of the current-year shoots were collected in June, and the leaves at the stem nodes were removed and rinsed with tap water. The upper part of the axillary bud is about 0.2 cm and the lower part is about 1.5 cm, respectively, and the stem section with the axillary bud is obtained, which is placed in a petri dish for later use;
[0043] 2. Disinfection of explants
[0044] Soak the stem section with axillary buds obtained on the ultra-clean workbench with 75% alcohol for 15 seconds, then soak for 15 minutes with 3% sodium hypochlorite, rinse 6 times with sterile water, and dry the moistur...
Embodiment 2
[0076] Example 2 Rapid Propagation of Cherry Plum Varieties "Senguo Honglu" and "Senguo Jiaren"
[0077] Utilize the Tissue Culture Rapid Propagation Method of Cherry Plum established in Example 1 to carry out rapid propagation respectively to Cherry Plum varieties "Senguo Honglu" and "Senguo Beauty", the specific methods are as follows:
[0078] The current year's stems of "Senguo Honglu" and "Senguo Jiaren" were taken as explants, and the robust, semi-lignified stems in the middle of the new shoots were collected, and the leaves at the stem nodes were removed and rinsed with tap water. Clean, cut off about 0.2 cm above and 1.5 cm below the axillary buds of each stem node to obtain stem segments with axillary buds, and put them in a petri dish for later use;
[0079] Step 1, soak the obtained stem section with axillary buds with 75% alcohol for 15 seconds, then soak it with 3% sodium hypochlorite for 15 minutes, rinse it with sterile water for 6 times, dry the surface moistur...
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