Tissue culture technique of aquilaria sinensis
A technology of tissue culture and arborina, 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 arborina, 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
[0016] (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 5 minutes, then rinse them with tap water for 10 minutes, dry the surface moisture and set aside. Soak in 75% ethanol for 5 seconds in an ultra-clean workbench, sterilize with 0.1% mercuric chloride solution for 8 minutes, wash with sterile water for 3 times, cut into stems with a length of 0.5-1.2 cm and inoculate them on the induction medium after drying. Cultivate in total darkness at 25°C for 15 days, then place in light for 10 hours a day, light intensity 1000x, and culture temperature 25°C for 39 days to induce the formation of clustered buds, with an induction rate of 68.5%. The induction medium is MS+2mg / L6-BA+0.5mg / L NAA+0.1mmol / L La(NO 3 ) 2 +2.0% sucrose+0.35% agar+0.05% activated carbon, the pH value is 5.8.
[0017] (2) Proliferation culture: T...
Embodiment 2
[0021] (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 15 minutes, dry the surface moisture and set aside. Soak in 78% ethanol for 10 seconds in an ultra-clean workbench, sterilize with 0.1% mercuric chloride solution for 10 minutes, wash with sterile water for 4 times, cut into stems with a length of 0.5-1.2 cm and inoculate them on the induction medium after drying. Cultivate in complete darkness at 28°C for 18 days, then place in light for 12 hours a day, light intensity 1500x, and culture temperature 28°C for 36 days to induce the formation of clustered buds, and the induction rate is 74.9%. The induction medium is MS+4mg / L6-BA+0.9mg / L NAA+0.3mmol / L La(NO 3 ) 2 +2.0% sucrose+0.35% agar+0.05% activated carbon, the pH value is 5.8.
[0022] (2) Proliferation cultu...
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