A kind of tissue culture rapid propagation method of Hibiscus hibiscus
A technology for tissue culture and rapid propagation and Hibiscus can be applied to horticultural methods, botanical equipment and methods, plant regeneration and other directions, which can solve the problems of long breeding time, lack of promotion, low survival rate and the like, and achieve short and shortened cultivation time. The effect of reproductive cycle and high survival rate
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Embodiment 1
[0033] The tissue culture rapid propagation method of a kind of hibiscus hibiscus described in the present embodiment, comprises the following steps:
[0034] (1) Bud induction culture: cut the stem section with bud point of Hibiscus hibiscus as explant, after cleaning, first treat it with 75% alcohol for 30 seconds, wash it twice with sterile water, and then treat it with 0.1% mercuric chloride for 9 minutes, Wash 4 times with sterile water, and finally absorb the water with sterile filter paper, inoculate it into the induction medium after adjusting the pH to 6.0 and sterilize, and cultivate until the upper axillary buds of the explants germinate and grow to a certain length, wherein The composition of the induction medium is: MS basic medium, supplemented with 0.2mg / L 6-BA, 0.1mg / L NAA, 20g / L sucrose, 6g / L agar;
[0035] (2) Rooting culture: cut out the axillary buds described in step (1), inoculate them into the rooting medium and cultivate them until the base of the axill...
Embodiment 2
[0041] The tissue culture rapid propagation method of a kind of hibiscus hibiscus described in the present embodiment, the difference with embodiment 1 is:
[0042] The composition of step (1) induction medium is: MS minimal medium, supplemented with 0.1mg / L 6-BA, 0.05mg / LNAA, 10g / L sucrose, 4g / L agar;
[0043] The composition of step (2) rooting medium is: 1 / 2MS minimal medium, supplemented with 0.1mg / L NAA, 0.05mg / L6-BA, 10g / L sucrose, 4g / L agar;
[0044] The composition of the proliferation medium in step (3) is: 1 / 2 MS basic medium supplemented with 0.1 mg / L NAA, 0.05 mg / L 6-BA, 10 g / L sucrose, and 4 g / L agar.
[0045] In the present embodiment, after step (1) bud induction culture for 2 weeks, the axillary buds germinated on the explants grow to 1-2 cm; after step (2) rooting culture for 10 days, the base of the axillary buds take root, and the root length is 2-2 cm after 3 weeks. 3cm, the rooting rate is 100%, and the upper axillary buds can be extended to 4cm, and afte...
Embodiment 3
[0047] The tissue culture rapid propagation method of a kind of hibiscus hibiscus described in the present embodiment, the difference with embodiment 1 is:
[0048] The composition of step (1) induction medium is: MS minimal medium, supplemented with 0.5mg / L 6-BA, 0.15mg / LNAA, 30g / L sucrose, 6g / L agar;
[0049] The composition of step (2) rooting medium is: 1 / 2MS basic medium, supplemented with 0.5mg / L NAA, 0.15mg / L6-BA, 30g / L sucrose, 6g / L agar;
[0050] The composition of the proliferation medium in step (3) is: 1 / 2 MS basic medium supplemented with 0.5 mg / L NAA, 0.15 mg / L 6-BA, 30 g / L sucrose, and 6 g / L agar.
[0051] In this example, after step (1) bud induction culture for 2 weeks, the axillary buds germinated on the explants grew to 2 cm; step (2) after rooting culture for 1 week, the base of the axillary buds took root, and the root length was 2-4 cm after 3 weeks , the rooting rate is 100%, and the upper axillary buds can be extended to 4cm, and the axillary buds can ...
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