Tissue Culture Rapid Propagation Method of Ginger Lotus
A tissue culture, ginger lotus technology, applied in the field of plant tissue culture, can solve the problems of difficult operation of adventitious bud sub-generation division, low reproductive coefficient of adventitious buds, decreased quality of seedlings, etc., so as to shorten the proliferation culture period and improve tissue culture propagation. coefficient, the effect of accelerating the promotion speed
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Embodiment 1
[0026] The tissue culture rapid propagation method of Ginger Lotus, the method is carried out as follows:
[0027] (1) The preparation of the medium, including the basic medium and the components of the medium at each stage and the weight per liter:
[0028] 1) Basic medium: MS or 1 / 2MS medium is prepared according to the conventional formula;
[0029] 2) Sterile seedling medium: 1 / 2MS + sugar 20g / L + agar 8g / L, pH5.6;
[0030] 3) Adventitious bud induction medium: MS+6-BA1.0mg / L+NAA0.2mg / L+sugar 20g / L+agar 8g / L, pH5.6;
[0031] 4) Proliferation medium: MS+6-BA 2.0mg / L+NAA0.2mg / L+sugar 25g / L+agar 5g / L, pH5.6;
[0032] 5) Rooting medium: 1 / 2MS+NAA0.5mg / L+white sugar 30g / L+agar 8g / L, pH5.6;
[0033] (2) Cultivation and sterilization of root tubers and small buds: select healthy and plump ginger lotus tubers with no disease spots, no galls, put them in a biochemical incubator, and germinate them at 26-28°C under dark culture until they grow to 0.5-2.0cm Take small buds; wash ...
Embodiment 2
[0041] In this example, the preparation of step (1) culture medium, including the components of each stage culture medium and its contained weight per liter are:
[0042] 2) Aseptic medium: 1 / 2MS + sugar 25g / L + agar 5g / L, pH 5.7;
[0043] 3) Adventitious bud induction medium: MS+6-BA2.0mg / L+NAA0.1mg / L+sugar 30g / L+agar 5g / L, pH5.7;
[0044] 4) Proliferation medium: MS+6-BA3.0mg / L+NAA0.1mg / L+sugar 30g / L+agar 7g / L, pH5.7;
[0045] 5) The rooting medium is: 1 / 2MS+NAA1.0mg / L+white sugar 25g / L+agar 6g / L, pH5.7;
[0046] All the other steps, technology are the same as embodiment 1.
Embodiment 3
[0048]In this example, the preparation of step (1) culture medium, including the components of each stage culture medium and its contained weight per liter are:
[0049] 2) Sterile medium: 1 / 2MS + sugar 30g / L + agar 6g / L, pH 5.8;
[0050] 3) Adventitious bud induction medium: MS+6-BA3.0mg / L+NAA0.3mg / L+sugar 25g / L+agar 7g / L, pH5.8;
[0051] 4) Proliferation medium: MS+6-BA1.0mg / L+NAA0.3mg / L+white sugar 20g / L+agar 8g / L, pH5.8;
[0052] 5) Rooting medium: 1 / 2MS+NAA1.5mg / L+white sugar 20g / L+agar 5g / L, pH5.8;
[0053] All the other steps, technology are the same as embodiment 1.
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