A method for somatic embryogenesis and plant regeneration of Pinus tabulaeformis
A technology of somatic embryos and pine tabulaeformis, applied in the directions of plant regeneration, botanical equipment and methods, horticultural methods, etc., can solve the difficulty of cutting, the seedling propagation technology cannot meet the needs of large-scale afforestation, and the natural seed-setting rate of tabuliformis is low. and other problems, to achieve the effect of improving survival rate and growth, maintaining rapid proliferation ability, and promoting division
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Embodiment 1
[0059] 1. Test materials
[0060] 1. Immature zygotic embryos of Pinus tabulaeformis
[0061] The present invention uses Beijing Forestry University forest farm (Haidian District, Beijing, longitude: 116.34, latitude: 40.00) good, mature, healthy, without pests, and 10 Chinese pine trees with high seed setting rate as material resources, from early May to June 2013 During the last ten days of the month, the cones of Pinus tabulaeformis in the 4-11th week after collecting loose powder were collected every 7 days. 30 cones were collected from each tree, and a total of 300 cones were collected each time. The cones collected on the day were stored in an ice box at low temperature and brought back to the laboratory, and then refrigerated in a refrigerator at 0‐4°C for 1-2 hours. month, spare.
[0062] 2. Plant growth regulator
[0063] The plant growth regulating substance used in the present invention adopts domestic 6-benzylaminoadenine (6-BA), 2,4-dichlorophenoxyacetic acid (...
Embodiment 2
[0086] 1. Sterilization of explants
[0087] The 30th, 37th, 44th, 51st, 58th, 65th, 72nd, and 79th days after the loose powder was stored at 0-4°C for 1 month, the cones of Pinus tabulaeformis were first washed with detergent to remove the oil on the surface of the cones, and then After washing with tap water, the cones were cut open, and the seeds were taken out; then on the ultra-clean workbench, the pine cone seeds were soaked in alcohol with a volume percentage concentration of 75% for 1 min, and then the seeds were soaked with 0.1% HgCl 2 Soak the pine cone seeds in the solution for 3-10min (preferably 5min), then rinse several times (3-6 times) with sterile water; then put the pine cone seeds on sterile dry filter paper to absorb the surface moisture Then peel off the seed coat in a sterile state to obtain immature zygote embryos, and obtain surface-sterilized immature zygote of Pinus tabulaeformis on the 30th, 37th, 44th, 51st, 58th, 65th, 72nd, and 79th days after flo...
Embodiment 3
[0100] 1. Sterilization of explants
[0101] The pinus tabulaeformis cones stored at 0-4°C for 1 month on the 51st day after loose powder were treated according to the explant sterilization method in Example 2 to obtain sterilized immature zygotic embryos of Pinus tabulaeformis;
[0102] 2. Embryogenic callus induction culture
[0103] In the ultra-clean workbench, inoculate the whole immature zygotic embryos of Pinus tabulaeformis 51 days after flowering and powder sterilized on the surface as explants in the embryogenic callus induction medium, and conduct embryogenic callus under dark conditions Induction culture, subculture once every 20 days, that is, take out the sterilized immature zygotic embryos after culture for 20 days, and place them in another fresh embryogenic callus induction medium to continue the induction of embryogenic callus In order to maintain sufficient nutrients and water in the medium, the culture temperature is (25±2)°C, the 2,4‐D used in the embryog...
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