Tissue culture and rapid propagation method of cynanchum glaucescens
A technology for tissue culture rapid propagation and staghorn fern, which is applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve the problems of lack of large-scale reproduction and cultivation, and achieves the improvement of survival rate and optimization of tissue culture technology. Effect
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Embodiment 1
[0045] The establishment of embodiment 1 Chlorospora staghorn tissue culture rapid propagation method
[0046] 1 Materials and methods
[0047] 1.1 Test material
[0048] The spores of staghorn fern were collected from the greenhouse of Southwest Forestry University. Put the sporophyll in a sulfuric acid paper bag, collect the spores in a centrifuge tube after they scatter naturally, and store them in a seed cabinet at 4°C for later use.
[0049] 1.2 Test method
[0050] 1.2.1 Spore germination and sporophyte induction
[0051] The spores were sterilized with 0.1% mercuric chloride solution for 5 minutes, rinsed with sterile water for 3 times, and inoculated on 1 / 2 MS medium. After the spores germinated until the dark green heart-shaped gametophytes appeared, they were transferred to MS, 1 / 2MS, 1 / 4MS, and improved Knops four kinds of media, agar 4g L -1 , pH 5.8. Inoculate 5 gametophytes per bottle, 5 bottles per treatment, and repeat 3 times. The growth of gametophytes a...
Embodiment 2 2
[0086] The optimization of embodiment 2 staghorn fern tissue culture rapid propagation technology
[0087] 1 Materials and methods
[0088] 1.1 Test material
[0089] The spores of staghorn fern were collected from the greenhouse of Southwest Forestry University. Put the sporophyll in a sulfuric acid paper bag, collect the spores in a centrifuge tube after they scatter naturally, and store them in a seed cabinet at 4°C for later use.
[0090] 1.2 Test method
[0091] 1.2.1 Spore germination and induction of GGB
[0092] The spores were sterilized with 5% sodium hypochlorite solution for 5 minutes, rinsed with sterile water for 5 times, and inoculated on 1 / 2 MS medium. After the spores germinated until dark green heart-shaped gametophytes appeared, they were subcultured until a small amount of sporophytes were induced. The sporozoites were transferred to the culture medium of 1 / 2MS+sucrose 15g / L+agar 4g / L, pH5.8. Add different types and concentrations of hormones, and dif...
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