Method for generating macrogametocyte by somatic cell of inducing undaria pinnatifida gynecogenic juvenile sporophyte
A technology of female gametophyte and parthenogenesis is applied in the field of inducing parthenogenetic young sporophyte somatic cells of Wakame to produce female gametophytes, which can solve the problems of limited number of male and female gametophytes, difficulty in meeting the requirements of the number of female gametophytes, etc. Solve the effect of insufficient number of female gametophytes and simple operation
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Embodiment 1
[0019] The male and female wakame gametophytes can be separated and separately preserved and cultivated according to the method for separating male and female in the prior art, and then carried out according to the following steps:
[0020] a. Take 10mg of preserved and cultured Wakame female gametophyte (wet weight), add 300ml of sterilized seawater, chop it into 190-210μm algae segments with a tissue mixer, and form female gametophyte body fluid, use a straw to culture female gametophyte body fluid at 1ml / time The dishes were moved to multiple petri dishes (diameter 9cm, the same below), added culture medium (sterilized seawater with nutrient salts added) and then moved to culture at a temperature of 20°C, a light intensity of 2000Lx, and a light time of 12 hours / day For 12 days, the culture medium was fully exchanged once every 3 days; the wet weight of the female gametophytes of Undaria pinnatae and the volume of added sterilized seawater can be adjusted according to the ra...
Embodiment 2
[0029] Other steps are all as embodiment 1, and the wakame female gametophyte that preserves culture as described in step a can obtain in the following manner:
[0030]f. During the breeding period of Undaria pinnatifida, take the mature spore leaves of algae cultivated on floating rafts, and put them into a beaker with sterilized seawater after being stimulated by drying in the shade. When it is observed that a large number of spores are released and the spore water is light brown, remove the spores Leaves, use a straw to get a small amount of spore water and move it to a petri dish added with culture solution (sterilized seawater with nutrient salt added). After 2 hours, it can be seen that round embryospores are attached to the bottom of the petri dish. Move the petri dish to a temperature of 20°C. Cultivate for 1 month under the conditions of ℃ and illuminance of 2000Lx, and exchange the culture medium once every 10 days;
[0031] After 2 days of culture, the undaria pinna...
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