Tissue-culturing rapid propagation method of Actinidia macrosperma
A kiwifruit and tissue culture technology is applied in the field of tissue culture and rapid propagation of large-seeded kiwifruit, which can solve problems such as the tissue culture research report of large-seeded kiwifruit, which can eliminate the invasion of diseases and insect pests and pesticide residues, and the equipment is simple. Small footprint effect
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Embodiment 1
[0038] Selection of explants: Take the branches of large-seeded kiwifruit from Hangzhou and midsummer, wash them with tap water, rinse with running water for half an hour, cut into 1-2cm stem segments with buds, put them in a triangular flask, 75% alcohol Treated for 30sec, rinsed with sterile water, disinfected with 0.1% mercuric chloride for 12min, rinsed with sterile water for 4-5 times, and inoculated into the induction medium under aseptic conditions, with a contamination rate of 38%. Taking the branches from Hangzhou and winter, and disinfecting them according to the same disinfection method, the pollution rate is as high as 87%.
Embodiment 2
[0040] Take the branches of big-seeded kiwifruit from Fuyang Mountain in Hangzhou in midsummer, wash them with tap water, rinse with running water for half an hour, cut them into 1-2cm long sections with buds and stems, treat with 75% alcohol for 30sec, and then rinse with sterile water After sterilizing with 0.1% mercuric chloride for 12min, rinsed with sterile water for 4-5 times, inoculated in induction medium MS+BA 5μmol / L+NAA 1μmol / L under sterile conditions. The culture temperature is 24-26℃, the daily light time is 16h, and the light intensity is 35μmolm -2 s -1 , cultured for 10-15d. The germinated shoots obtained on the induction medium were cut off and transferred to the growth medium MS+BA 2μmol / L+GA 3μmol / L+ZT 4μmol / L, the culture temperature was 24-26℃, the daily light time was 16h, and the light intensity was 35μmolm -2 s -1 , cultured for 15-20d. The multiplication of buds reached 11.6 times, the average height of plants reached 9.28cm, but the leaves were y...
Embodiment example 3
[0042] Take the branches and leaves of the big-seeded kiwifruit from Hangzhou in midsummer, wash them with tap water, rinse with running water for half an hour, cut them into segments with buds, put them in a triangular flask, treat with 75% alcohol for 30 seconds, and then use no After rinsing with bacteria water, disinfect with 0.1% mercuric chloride for 12 minutes, rinse with sterile water for 4-5 times, and inoculate them in induction medium MS+BA 5μmol / L+NAA 1μmol / L under sterile conditions. The culture temperature is 24-26℃, the daily light time is 16h, and the light intensity is 35μmolm -2 s -1 , cultured for 10-15 days. The germinated shoots obtained on the induction medium were cut off and transferred to the proliferation medium MS+BA 6μmol / L+NAA 1μmol / L, the culture temperature was 24-26°C, the daily light time was 16h, and the light intensity was 35μmolm -2 s -1 , cultured for 15-20 days. The bud multiplication was 4.27, and the average seedling height was 3.85c...
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