Method for obtaining regeneration plants of petunia hybrida by anther culture
A technology for regenerating petunia plants, applied in the agricultural field, can solve the problems of low regeneration rate and no regenerated petunia plants, and achieve the effect of improving breeding efficiency and shortening the period of hybrid breeding
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Embodiment 1
[0030] Embodiment 1, a kind of method that obtains petunia regenerated plant by anther culture, carries out following steps successively:
[0031] A) low temperature pretreatment and disinfection, the following steps are carried out successively:
[0032] 1) The selected petunia material is the red color of the Meilin series, sow seedlings in December, and start in late April of the following year. In the morning on a sunny day, select flower buds with a longitudinal diameter of 0.8cm-1.3cm (the flower buds in this period Most of them are in the single-core marginal stage),
[0033] 2), put the above-mentioned flower buds into plastic bags, and put them into a refrigerator at 5°C for low-temperature pretreatment for 2 days;
[0034]3), the flower buds after the above-mentioned low-temperature pretreatment are first placed under tap water and rinsed for 5 minutes, then rinsed with distilled water for 3 times, and then blotted with absorbent paper; Sterilize for 1 min; then ri...
Embodiment 2
[0050] Embodiment 2, a kind of method that obtains petunia regenerated plant by anther culture, carries out following steps successively:
[0051] A), low temperature pretreatment and disinfection, carry out the following steps successively:
[0052] 1), the selected petunia material is Meilin series blue, sow seedlings in December, and start in late April of the following year. In the morning on a sunny day, select flower buds with a longitudinal diameter of 0.8cm-1.3cm (the The flower buds are mostly in the uninucleate stage),
[0053] 2), put the above-mentioned flower buds into a plastic bag, and put them into a refrigerator at 5°C for low-temperature pretreatment for 3 days;
[0054] 3), the flower buds after the above-mentioned low-temperature pretreatment are first placed under tap water and rinsed for 5 minutes, then rinsed with distilled water for 3 times, and then blotted with absorbent paper; Sterilize for 1 min; then rinse with sterile distilled water for 3 times...
Embodiment 3
[0068] Example 3. Change the differentiation medium in step C of Example 1 to: Nitsch basic medium + 7g / L agar + 20g / L maltose + 0.1mg / L IBA + 1.0mg / L 6-BA + hydrolyzed casein 0.5 g / L, the pH value is 5.8. Change 1.0mg / LTDZ to 1.0mg / L 6-BA. All the other are with embodiment 1.
[0069] The result is:
[0070] In this case, the callus induction rate can reach 40%, and the callus differentiation rate can reach 33%. The survival rate can reach more than 70%.
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