Tissue culture method for early-maturing pear stem section and culture medium
A technology for tissue culture and inoculation of medium, applied in the field of plant cell molecular biology, can solve the problems of average rooting rate, low average root number, low proliferation coefficient of test-tube plantlets, low reproduction coefficient, etc., to reduce browning rate, shorten Growth time, effect of increasing proliferation coefficient
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Embodiment 1
[0048] Tissue culture of pear stem segments of 'Su Cui No. 1' and 'Su Cui No. 2' was carried out as follows.
[0049] Collection and disinfection of explants: From October to December of the previous year, annual shoots were collected from the orchard and stored in a 4°C refrigerator. From late February to early March of that year, the branches were taken and inserted into sterile water, at 22°C-25°C, 8 hours of light per day, 16 hours of darkness, light intensity of 1500-2000lx, germination was accelerated, and fresh sterile water was changed every 7 days. In early and mid-April, after the buds germinate, take multiple stem sections with buds, cut them into 1-1.5cm high stem sections with one bud, and perform the following disinfection treatment: use 100mg / L carbenzyl carboxybenzyl After soaking in tap water with penicillin for 2.5 hours, vortex for 5-8 minutes with a mixed disinfectant solution, then peel off the bracts, and perform secondary disinfection with a mixed disinf...
Embodiment 2
[0081] Example 2 Adopt conventional tissue culture rapid propagation method to cultivate 'Su Cui No. 1' and 'Su Cui No. 2'
[0082] The following methods were used to cultivate 'Su Cui No. 1' and 'Su Cui No. 2':
[0083] 1) Collection and disinfection of explants: select robust annual branches from the field, cut young branches as explants, rinse with washing powder, and rinse with tap water for 30 minutes. On the ultra-clean workbench, the treated explants were sterilized with 75% alcohol for 20 seconds, 0.1% mercuric chloride for 8-10 minutes, and rinsed with sterile water for 4-5 times. The scales were removed with a scalpel, and the naked buds were cut and inoculated on the induction medium, and 3 explants were inoculated in each bottle. The induction medium is: add 6-BA, IBA, GA to 1 / 2MS medium 3 , sucrose and agar, wherein the final concentration of 6-BA is 1.0mg / L, the final concentration of IBA is 0.2mg / L, GA 3 The final concentration of sucrose is 2.0mg / L, the fina...
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