Tissue culture technique of Chinese knotweed herb
A technology of tissue culture and fotan mother, which is applied in the field of plant tissue culture, can solve problems such as unfavorable protection of high-quality germplasm resources, restrictions on the promotion and planting of high-quality fiot mother, and separation of offspring traits of seed reproduction, so as to achieve the effect of accelerating promotion and resource development and utilization
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Embodiment 1
[0012] (1) Induction of clustered buds: select the budding stems of young trees that grow vigorously and have no diseases and insect pests in the current year as explants, soak them in an aqueous solution of detergent for 8 minutes, then rinse them with tap water for 13 minutes, dry the surface moisture and set aside. Soak in 75% ethanol for 8s in ultra-clean workbench, sterilize with 0.1% mercuric chloride solution for 11min, wash with sterile water for 6 times, dry and cut into 1.5cm-long stems and inoculate them on the induction medium. Cultivate in complete darkness at 28°C for 18 days, then place in light for 13 hours a day, light intensity 1500x, and culture temperature 27°C for 42 days to induce the formation of clustered buds, and the induction rate is 69%. The induction medium is MS+5mg / L6-BA+1.5mg / L NAA+0.2mmol / L La(NO 3 ) 2 +2.3% sucrose+0.6% agar+0.08% activated carbon, the pH value is 5.9.
[0013] (2) Proliferation culture: Transfer the clustered buds obtained ...
Embodiment 2
[0017] (1) Induction of clustered buds: Select the budding stems of young trees that grow vigorously and have no diseases and insect pests in the current year as explants, soak them in an aqueous solution of detergent for 10 minutes, then rinse them with tap water for 17 minutes, dry the surface moisture and set aside. Soak in 78% ethanol for 12s in an ultra-clean workbench, sterilize with 0.1% mercuric chloride solution for 12min, wash with sterile water for 6 times, dry and cut into 1.4cm-long stems and inoculate them on the induction medium. Cultivate in total darkness at 27°C for 24 days, then place in light for 16 hours a day, with light intensity of 1700x, and culture temperature at 27°C for 38 days to induce the formation of clustered buds, with an induction rate of 80%. The induction medium is MS+7mg / L6-BA+1.0mg / L NAA+1.3mmol / L La(NO 3 ) 2 +2.3% sucrose+0.5% agar+0.08% activated carbon, the pH value is 5.7.
[0018] (2) Proliferation culture: Transfer the clustered b...
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