Method for obtaining poinsettia filial generation through utilizing young embryo rescue
A technology of immature embryo rescue and first-class products, applied in the field of biotechnology breeding, to overcome the difficulty of obtaining hybrids, shorten the growth cycle, and improve the success rate
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Embodiment 1
[0022] The method for rescuing immature ovule embryos after embodiment one poinsettia artificial hybridization pollination 15d
[0023] 1. Artificial cross-pollination: Select and determine the hybrid parents of poinsettia, and control the flowering period and keep the flowering period consistent through shading or supplementary light adjustment. Pollination is carried out between 11:00 and 12:00 in the morning on a sunny day. Fresh pollen collected from the male parent's stigma on the same day is gently transferred to the inverted "eight"-shaped stigma of the female parent with a brush; pollination is repeated once the next day. The ambient temperature of the greenhouse should not be lower than 25°C and should be managed normally.
[0024] 2. Stripping of hybrid ovules and induction culture: take poinsettia ovaries that have developed 15 days after cross-pollination, wash them under running water for 5 minutes, soak them in ethanol with a volume ratio of 75% for 1 minute unde...
Embodiment 2
[0027] The ovule immature embryo rescue method after embodiment two poinsettia artificial hybridization pollination 22d
[0028] 1 item is the same as embodiment one.
[0029] 2. Extraction of hybrid ovules and induction culture: take poinsettia hybrid ovary developed 22 days after pollination, wash it under running water for 5 minutes, soak it in ethanol with a volume ratio of 75% for 1 minute under sterile conditions, and then use a mass percentage of 0.1% Disinfect in mercuric solution for 10 minutes, rinse with sterile water for 4 to 5 times, tear off the ovary wall with tweezers, gently peel off the ovules, and quickly inoculate them with MS+NAA 0.5mg / L+6-BA 0.5mg / L for culture Cultivate on medium, medium pH 5.6-5.8, sucrose 60g / L, agar 6g / L, at a temperature of 20-25°C, a photoperiod of 10-12h / d, and a light intensity of 1500-2000lux. Culture directly induces germination of immature embryos.
[0030]3. Subculture, proliferation and rooting culture: After 30 days, trans...
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