Method for improving embryonic induction rate of free microspores of medicago sativa l
A technology of spore emergence rate and alfalfa, applied in the field of biological science, can solve problems such as low embryo rate, and achieve the effects of improving embryo rate, improving selection efficiency and shortening breeding cycle
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Embodiment 1
[0016] Embodiment one: a kind of method that the present invention improves the free microspore germination rate of alfalfa, the method comprises in the blooming stage of alfalfa, from the donor plant, selects robust flower buds without damage by diseases and insect pests, selects free microspores to be in the mononuclear habitat The step of cultivating flower buds in the middle stage. During the blooming period of alfalfa, the time to extract healthy and pest-free flower buds from the donor plant is to extract from the donor plant at 8:00-10:00 in the morning on a sunny day.
[0017] Show through part of experiment below, the present invention selects free microspore to be in the flower bud of uninucleate middle stage and cultivates and can improve microspore embryo rate, has compared the influence of the microspore development period on the free microspore embryo rate of alfalfa, including single The results showed that the embryonic rate of free microspores at the single-nu...
Embodiment 2
[0020] Embodiment two: a kind of method that the present invention improves the free microspore germination rate of alfalfa, the method comprises in the blooming stage of alfalfa, from the donor plant, selects robust and pest-free flower buds, and selects free microspores to be in the mononuclear habitat The step of cultivating flower buds in the middle stage. During the blooming period of alfalfa, the time to extract healthy and pest-free flower buds from the donor plant is to extract from the donor plant at 8:00-10:00 in the morning on a sunny day.
[0021] Further, before culturing the flower buds, the flower buds were first sterilized with 75% alcohol for 30 seconds, then sterilized with 8% sodium hypochlorite for 12 minutes, rinsed with sterile water for 5 times, and then placed in a sterile mortar.
[0022] The culture method comprises adding half an amount of MS liquid medium and B5 liquid medium in a sterile mortar, the volume ratio of MS liquid medium and B5 liquid me...
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