Kelp germplasm separation method
A separation method, the technology of kelp, applied in the direction of plant cells, etc., can solve the problems of low separation efficiency and easy contamination of kelp germplasm separation, and achieve the effect of improving separation efficiency, avoiding pollution, and satisfying rapid growth
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Embodiment 1
[0017] (1) Collect kelp leaves with mature sporangia when the seawater temperature reaches 16°C in the introduced sea area;
[0018] (2) Transport it indoors, cut small pieces of 20×20 cm with a blade, then wipe the kelp leaves with mature sporangia with sterile gauze, dry and stimulate in the shade for 1 hour, wrap them with gauze and 200-mesh sieve silk and put them in a container In the container of disinfected seawater, control the water temperature at 10-12°C to let the spores disperse;
[0019] (3) When the density of zoospores in seawater under microscope inspection is 5-10 / 100X, put them into slides.
[0020] (4) Continue to cultivate the slides after the spores attach, control the light intensity at 800-1000lx, light for 12 hours a day, control the water temperature at 10-12°C, and form gametophytes after 8 days of cultivation.
[0021] (5) Scrape the gametocytes on the glass slide into the embryo culture dish, add sterilized seawater to dilute 10 times, microscopica...
Embodiment 2
[0025] (1) Collect kelp leaves with mature sporangia when the seawater temperature reaches 15°C in the introduced sea area;
[0026] (2) Transport it indoors, cut small pieces of 30×30 cm with a blade, then wash the kelp leaves with mature sporangia with sterile gauze dipped in sterile sea water, dry in the shade and stimulate for 80 minutes, wrap it in gauze, and then use 200 Wrap the silk with a mesh sieve and put it into a container filled with sterilized seawater, and control the water temperature at 8-10°C to let the spores disperse;
[0027] (3) When the density of zoospores in the seawater under microscope inspection is 10-20 / 100X, put it into the glass slide.
[0028] (4) The slides after the spores attached were placed in a temperature-controlled light incubator for cultivation, the light intensity was controlled at 900-1100lx, the light was 12 hours a day, and the water temperature was controlled at 10-12°C. After 7 days of cultivation, gametophytes were formed.
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