Method for tissue culture and rapid propagation by basal disc-free scales of Lycoris chinensis
A tissue culture rapid propagation and scale technology, which is applied in horticultural methods, botanical equipment and methods, applications, etc., can solve the problems of complex seed genetic background, restrictions on the popularization and application of pure Chinese Lycoris species, separation of progeny traits, and the like. Consistent genetic basis, significant competitive advantage, and uniform growth potential
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Embodiment 1
[0034] Embodiment 1: Select Chinese Lycoris bulbs with sufficient nutrition, remove external debris, soak in detergent for 10 minutes, rinse with running water for 2 hours, absorb the surface moisture and move to an aseptic operating table for disinfection; use a scalpel to cut the scales into The fragments of 1.0-1.5cm are inoculated on the culture medium; the inoculated materials are placed on the culture rack for cultivation, and after one and a half months, the differentiation of callus and small bulbs on the scales can be observed.
Embodiment 2
[0035] Embodiment 2:: select the upper half of the aseptic seedling bulblet without the base plate, remove the leaves, inoculate in the induction medium, place and cultivate under the same culture conditions as in Example 1, and it can be observed after 1 month The culture medium differentiates into calli.
Embodiment 3-5
[0036] Example 3-5: The induced callus is divided into several small pieces according to the size of 0.5×0.5cm, and transferred to the proliferation medium; the upper part of the induced bulblet is cut off, leaving the base The bottom of the dish was then transferred to proliferation medium. After a certain amount of propagation is reached, each small bulb is separated, and after the leaves are removed, it is inoculated in the strong seedling medium for 1 month to promote the growth of the bulb to a diameter of about 0.5 cm, and rooting culture can be carried out. The bulbs grow three strong fibrous roots of more than 1cm, and they can be domesticated and transplanted.
[0037] In the five examples in the above table, the success rate is above 76%. For the cultures that do not meet the requirements of the next growth stage, the culture time can be extended until a satisfactory effect is obtained.
[0038] In short, the key of this method is to grasp the selection and treatmen...
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