Variation malus spectabilis tissue culture and breeding method
A tissue culture and red fruit technology, applied in horticultural methods, botanical equipment and methods, horticulture and other directions, can solve the problems of stable maintenance of the excellent and specific characteristics of the invariable winter red fruit, prevent seedlings from being injured and sick, and reduce the subculture cycle. , the effect of increasing the value-added ratio
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Embodiment 1
[0032] This embodiment sequentially includes eight stages: pre-treatment of explants, selection and cleaning of explants, disinfection of explants, initiation of culture, subculture, rooting culture, seedling washing, and seedling hardening:
[0033] Pre-treatment stage of explants: In spring, gibberellin with a concentration of 50 mg / l was used to perform pre-explant treatment on mutant winter red fruit plants.
[0034] Explant selection and washing stage: The newly extracted shoots with low degree of lignification were cut as explants, and washed with tap water for 5 minutes.
[0035] Explant disinfection stage: disinfect it with 0.1% mercuric chloride solution for 5 minutes, and then rinse the sterilized explants with sterile water for 3 times, each time for 1 minute.
[0036] Start the culture phase: put the sterilized and rinsed explants on a sterile workbench, cut 1 cm of the stem section and put them on the medium 1 / 2MS+6-BA 0.2mg / L+0.1g / L activated carbon for culture, ...
Embodiment 2
[0043] This embodiment sequentially includes eight stages of pre-treatment of explants, selection and cleaning of explants, disinfection of explants, initiation culture, subculture, rooting culture, seedling washing, and seedling hardening. The only difference from Example 1 is:
[0044] During the explant selection and washing stage, the explants were rinsed with running water for 10 minutes.
[0045] In the explant disinfection stage, the disinfection time with a concentration of 0.1% mercuric chloride solution was 8 minutes, and the sterilized explants were rinsed 5 times with sterile water, and each rinse time was 2 minutes.
[0046] In the start-up culture stage, cut 2cm stem segments and put them on medium 1 / 2MS+6-BA0.2mg / L+0.1g / L activated carbon for culture
[0047] In the rooting culture stage, the young shoots were inserted into the rooting medium 1 / 2MS+0.5IBA and cultivated for 10 days.
[0048] In the seedling washing stage, the mass ratio of water and carbendazim ...
Embodiment 3
[0053] The only difference between this embodiment and embodiment 2 is:
[0054] During the explant selection and washing stage, the explants were rinsed with running water for 15 minutes.
[0055] In the explant disinfection stage, the disinfection time with a concentration of 0.1% mercuric chloride solution was 10 minutes, and the sterilized explants were rinsed 6 times with sterile water, and each rinse time was 1 minute.
[0056] In the start-up culture stage, 3 cm of stem segments were cut and cultured on medium 1 / 2MS+6-BA0.2mg / L+0.1g / L activated carbon.
[0057] In the rooting culture stage, the young shoots were inserted into the rooting medium 1 / 2MS+0.5IBA and cultivated for 15 days.
[0058] In the seedling washing stage, the mass ratio of water and carbendazim was 1000:1.
[0059] During the hardening stage, keep the air humidity at 80% and the temperature at 30 degrees.
[0060] The pH value of the medium used in the three stages of initiation culture, subculture...
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