Tissue-culture rapid propagation method for succulents
A technology for rapid propagation of succulents and tissue culture, applied in botany equipment and methods, plant regeneration, horticultural methods, etc., can solve the problems of long breeding cycle, large site requirements, and high labor costs, and achieve short cultivation time and easy operation , a wide range of effects
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Embodiment 1
[0029] A method for tissue culture and rapid propagation of succulents described in this embodiment comprises the following steps:
[0030] (1) Selection and sterilization of explants: cut young leaves or stems of succulent plants, soak them in detergent solution for 10-30 minutes, then scrub the axillary buds with a brush, rinse them under running water overnight; On a sterile operating table, treat with 75% alcohol for 5-15 seconds, rinse with sterile water for 3-4 times, then treat with 0.1% mercuric chloride for 8-12 minutes, rinse with sterile water for 5-7 times, and dry That's it. Wherein, the time of mercuric chloride treatment is determined according to the degree of tenderness of the explant;
[0031] (2) Primary culture: Inoculate the explants obtained in step (1) on the primary culture medium for primary culture until the explants differentiate and sprout. The composition of the primary culture medium is: MS basic medium supplemented with 0.05 mg / LNAA, 4.0mg / L6-B...
Embodiment 2
[0036] The tissue culture rapid propagation method of a kind of succulent plant described in the present embodiment, differs from embodiment 1 in that:
[0037] In step (2), the composition of the primary medium is: MS basic medium, supplemented with 0.01mg / LNAA, 2.0mg / L6-BA, 0.1g / L hydrolyzed casein, 10g / L sucrose, and 2g / L agar;
[0038] In step (3), the composition of the proliferation medium is: MS basic medium, supplemented with 0.5mg / LKT, 0.1mg / L2, 4-D, 1.0mg / LGA3, 10g / L sucrose, 2g / L agar;
[0039] In step (4), the composition of the rooting medium is: 1 / 4MS basic medium supplemented with 0.08mg / L NAA, 50g / L sucrose, 10g / L agar, and 0.5mg / L activated carbon.
[0040] In the present embodiment, when the multiplication culture process was carried out to 15 days, new shoots germinated at the growth point, and the length of the new shoots reached 5 cm in 30 days, and the new shoots were strong; the rooting culture process began to take root when the rooting culture process ...
Embodiment 3
[0042] The tissue culture rapid propagation method of a kind of succulent plant described in the present embodiment, differs from embodiment 1 in that:
[0043] In step (2), the composition of the primary medium is: MS basic medium, supplemented with 0.08mg / LNAA, 5.0mg / L6-BA, 0.8g / L hydrolyzed casein, 50g / L sucrose, and 10g / L agar;
[0044] In step (3), the composition of the proliferation medium is: MS basic medium, supplemented with 2.0mg / LKT, 0.4mg / L2, 4-D, 5.0mg / LGA3, 50g / L sucrose, 10g / L agar;
[0045] In step (4), the composition of the rooting medium is: 1 / 4MS basic medium supplemented with 0.01mg / L NAA, 10g / L sucrose, 2g / L agar, and 0.1mg / L activated carbon.
[0046] In the present embodiment, when the multiplication culture process was carried out to 15 days, new shoots germinated at the growth point, and the length of the new shoots reached 5 cm in 28 days, and the new shoots were strong; the rooting culture process began to take root when the rooting culture process...
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