Method for improving culture efficiency of anther of filial generation of Oryza rufipogon
A culture method and technology of culture efficiency, applied in the field of plant tissue culture, can solve the problems of low anther culture efficiency, achieve the effect of speeding up the rice breeding process, improving the breeding efficiency, and improving the callus induction rate and seedling rate
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Embodiment 1
[0019] Example 1: Suspension Culture of Anthers of Common Wild Rice Japonica Hybrid Progeny in Yuanjiang, Yunnan
[0020] In this example, the japonica hybrid progeny F1-24 of Yuanjiang common wild rice in Yunnan was used as the test material, and haploid plants were obtained by the method of the present invention. The implementation process is as follows:
[0021] 1) Selection of explants: Take the young ears in the field where the dew is not dry in the morning on a sunny day, select the rice ears with a distance of 5 cm between the flag leaf ring and the next leaf ring, the ears are not broken, keep two leaves and leaf sheaths, and use volume Wipe the leaves and leaf sheaths with 70% alcohol cotton balls, then wrap the young ears with plastic wrap according to different strains, and place them in a 6°C refrigerator for low-temperature pretreatment for 7 days. Select the branch stalk whose spikelet anther is in the mononuclear stage, that is: the anther is light yellow, and ...
Embodiment 2
[0029] Embodiment 2: Suspension culture of anthers of common wild rice indica type hybrid progeny in Yuanjiang, Yunnan
[0030] In this example, SP13 and SP15, the indica hybrid progenies of common wild rice in Yuanjiang, Yunnan, were used as test materials, and haploid plants were obtained by using the method of the present invention. The implementation process is basically the same as in Embodiment 1, the difference is that:
[0031] 1) During the selection of the explant, choose the distance between the flag leaf annulus and the next leaf annulus to be 7cm rice ears, and select the branches whose anthers of the spikelets are in the single-nucleus stage, that is: the anthers are light yellow, and the length of the stamens in the glume is long. Anther callus induction was carried out on rice ears close to 2 / 5 of the glume length.
[0032]2) The induction time of anther callus in liquid suspension is 20 days.
[0033] 3) It takes 30 days for anther callus differentiated seed...
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