In-vitro rapid propagation method for lycoris radiata
A technology of lycoris in vitro and in vitro is applied to the field of rapid in vitro propagation of lycoris, which can solve the problems of increased workload, repeated pollution, and bulb carrying bacteria, and achieves the effects of shortening the regeneration period, increasing the regeneration efficiency, and improving the induction rate.
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Embodiment 1
[0021] A method for rapid propagation of lycoris in vitro, comprising the steps of:
[0022] 1) Take Lycoris bulbs planted in the open field, disinfect them, remove the epiphytic seed bulbs near the cue bulb and plant them for 1 month;
[0023] 2) After disinfecting the bulbs obtained in step 1), remove the outer cortex, peel off the seed buds, place them flat on MS solid medium to induce growth of adventitious buds, and obtain tissue blocks with adventitious bud clusters;
[0024] 3) making the tissue block obtained in step 2) into a longitudinally divided tissue block, and carrying out bud elongation culture on the bud elongation medium;
[0025] 4) when the adventitious buds obtained in step 3) elongate to produce side buds, cut them;
[0026] 5) Putting the single stem cut in step 4) into the rooting medium to induce rooting culture to obtain Lycoris seedlings.
[0027] The MS solid medium is MS+BA1.8mg / L+NAA0.8mg / L, pH5.8, sucrose 28g / L, agar 4g / L.
[0028] The shoot e...
Embodiment 2
[0034] A method for rapid propagation of lycoris in vitro, comprising the steps of:
[0035] 1) Take Lycoris bulbs planted in the open field, disinfect them, remove the epiphytic seed bulbs near the cue bulb and plant them for 1.5 months;
[0036] 2) After disinfecting the bulbs obtained in step 1), remove the outer cortex, peel off the seed buds, place them flat on MS solid medium to induce growth of adventitious buds, and obtain tissue blocks with adventitious bud clusters;
[0037] 3) making the tissue block obtained in step 2) into a longitudinally divided tissue block, and carrying out bud elongation culture on the bud elongation medium;
[0038] 4) when the adventitious buds obtained in step 3) elongate to produce side buds, cut them;
[0039] 5) Putting the single stem cut in step 4) into the rooting medium to induce rooting culture to obtain Lycoris seedlings.
[0040] The MS solid medium is MS+BA2.2mg / L+NAA1.2mg / L, pH5.8, sucrose 32g / L, agar 6g / L.
[0041] The shoo...
Embodiment 3
[0047] A method for rapid propagation of lycoris in vitro, comprising the steps of:
[0048] 1) Take Lycoris bulbs planted in the open field, disinfect them, remove the epiphytic seed bulbs near the cue bulb and plant them for 2 months;
[0049] 2) After disinfecting the bulbs obtained in step 1), remove the outer cortex, peel off the seed buds, place them flat on MS solid medium to induce growth of adventitious buds, and obtain tissue blocks with adventitious bud clusters;
[0050] 3) making the tissue block obtained in step 2) into a longitudinally divided tissue block, and carrying out bud elongation culture on the bud elongation medium;
[0051] 4) when the adventitious buds obtained in step 3) elongate to produce side buds, cut them;
[0052] 5) Putting the single stem cut in step 4) into the rooting medium to induce rooting culture to obtain Lycoris seedlings.
[0053] The MS solid medium is MS+BA 2.0 mg / L+NAA 1.0 mg / L, pH 5.8, sucrose 30 g / L, agar 5 g / L.
[0054] The...
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