A method for tissue culture and rapid propagation of Acer palmatum
A technology of Acer palmatum red division and tissue culture rapid propagation, which is applied in horticultural methods, botany equipment and methods, plant regeneration, etc., can solve the problem of not being able to quickly and efficiently meet the needs of scientific research and large-scale production, and the excellent traits cannot be well The maintenance of seedlings and the large variability of seed propagation plants can meet the needs of large-scale industrial seedling cultivation and industrialization development, with low cost and short cultivation time.
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Embodiment 1
[0032] The method for tissue culture and rapid propagation of Acer palmatum red division, including
[0033] Pretreatment: Take the current-year-old branches of Acer palmatum, remove the leaves, cut into budded stem segments with 1 to 2 buds, perform sterilization and cleaning treatment, and obtain sterilized explants;
[0034] Initiating culture: inoculate the sterilized explants in the initiating medium for initiating culture to obtain elongated axillary buds; the initiating medium includes: WPM salts and H organic, supplemented with 0.005-0.01mg / LTDZ, 0.05~0.1mg / LNAA, 0.1~0.4%PPM;
[0035] Proliferation culture: inoculate the axillary buds in the proliferation medium for proliferation culture to obtain sterile sprouts; the proliferation medium includes: WPM salts and H organic, supplemented with 0.15-0.25mg / LCPPU, 0.02-0.06mg / L2 ,4-D;
[0036] Rooting culture: after removing the callus from the base of the sterile sprouts, inoculate them on the rooting medium for rooting cu...
Embodiment 2
[0041] Effects of Components in Initiating Medium on Initiating Culture of Axillary Buds
[0042] Pretreatment: Take the branches of Acer palmatum in the same year, remove the leaves, cut into budded stems with 1-2 buds, sterilize with 75Vol% alcohol for 20-40s, wash with sterile water 1-3 times , 0.1wt% mercuric chloride sterilization treatment for 3 to 8 minutes, washed with sterile water for 5 to 6 times, to obtain explants after sterilization;
[0043] Initiating culture: inoculate the sterilized explants in the initiating medium for initiating culture to obtain elongated axillary buds with a length of 1-1.5 cm; the initiating medium includes: WPM salts and H organic, supplemented with TDZ, NAA, PPM, 20-30g / L sucrose, 4-6g / L agar. The pH value of the start-up medium is 5.5-5.8; the culture temperature of the start-up culture process is 24-26°C, the light intensity is 1500-2000Lx, and the light time is 12-14h / d;
[0044] According to the TDZ concentration, NAA concentrati...
Embodiment 3
[0049] Effects of Growth Hormone Concentration in Proliferation Medium on Proliferation of Axillary Buds
[0050] Pretreatment: Take the branches of Acer palmatum in the same year, remove the leaves, cut into budded stems with 1-2 buds, sterilize with 75Vol% alcohol for 20-40s, wash with sterile water 1-3 times , 0.1wt% mercuric chloride sterilization treatment for 3 to 8 minutes, washed with sterile water for 5 to 6 times, to obtain explants after sterilization;
[0051] Initiating culture: inoculate the sterilized explants in the initiating medium for initiating culture to obtain elongated axillary buds with a length of 1.0-1.5 cm; the initiating medium includes: WPM salts and H organic, supplemented with 0.005~0.01mg / LTDZ, 0.05mg / LNAA, 0.2%PPM, 20~30g / L sucrose, 4~6g / L agar;
[0052] Proliferation culture: inoculate the axillary buds in the proliferation medium for proliferation culture to obtain sterile sprouts with a plant height of 1.0-2.0 cm; the proliferation medium i...
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