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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

Inactive Publication Date: 2019-03-01
江苏艺轩园林景观工程有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In order to maintain the specificity of the mutated Donghong fruit, when using conventional tissue culture techniques to breed the mutated Donghong fruit, the obtained seedlings have obvious character separation, and the excellent specific characters of the mutated Donghong fruit cannot be stably maintained. Therefore, in the field There is an urgent need to solve the difficult problem of tissue culture and breeding of mutated Donghong fruit, so that the specific characters of mutated Donghong fruit can be stably maintained, and the fruiting rate should also be improved.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

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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Abstract

The invention discloses a bonsai-type ornamental plant variation malus spectabilis tissue culture and breeding method. The method includes first treating a variation malus spectabilis plant with gibberellin, cutting a newly-extracted branch as an explants, washing and disinfecting, cutting a stem segment of 1-3cm, culturing the stem segment on a culture medium 1 / 2MS+6-BA0.2mg / L+0.1g / L activated carbon, grafting the selected lateral buds to a first medium 1 / 2MS+6-BA5mg / L, conducting subculture for 20 days and then grafting to a second medium 1 / 2MS+6-BA1.0mg / L, conducting culture for 20 days, then grafting to a third medium MS+6-BA0.4mg / L, conducting culture for 25 days, grafting the twig with the length of 2cm or more to a rooting medium 1 / 2MS+0.5IBA for culture, and finally forming a matrix according to the ratio of peat: perlite = 1:1, and covering a film and a shading net for refining a seedling. The obtained variation malus spectabilis tissue culture seedling has the rooting percentage of 95% or more, and the breeding speed is fast.

Description

technical field [0001] The invention belongs to the field of plant tissue breeding, and particularly relates to a tissue culture and breeding technology of bonsai ornamental plant winter red fruit, in particular to a tissue culture breeding method of variant winter red fruit. Background technique [0002] Donghongguo belongs to the Rosaceae apple genus. The flowers are light pink. They open in spring and bear fruit immediately. The fruit matures in autumn. It does not fall until February to March of the second year. The ripe fruit weighs 10 to 20g, and the single ripe fruit is spherical or oblate. At the same time, the plant of winter red fruit is short and compact, so the ornamental value is extremely high. [0003] At present, one of the most commonly used techniques in plant production is the rapid propagation of excellent varieties through tissue culture. Tissue culture methods generally include explant selection and disinfection, medium culture, rooting culture, and see...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A01H4/00
CPCA01H4/001A01H4/008
Inventor 王醒陈蕾韩林芝潘楠楠欧阳嘉晖岳阳韦晨余炻
Owner 江苏艺轩园林景观工程有限公司
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