Method for creating new peanut specie in space breeding
A technology of aerospace breeding and new germplasm, applied in horticultural methods, botany equipment and methods, plant regeneration, etc., can solve the problems of low mutagenesis beneficial mutation rate, difficult selection, high cost of carrying, etc. The method is simple and easy to master , low loading cost, low selection difficulty
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Embodiment 1
[0013] A method for aerospace breeding to create new peanut germplasm. After selecting Huayu No. 20 peanuts mature, select 100 full seeds, first disinfect them with 70% alcohol for 1 minute, and then use 0.1% by mass Sterilize with HgCl for 6 minutes, perform surface disinfection, rinse with sterile water 4 times, remove the seed coat, remove two cotyledons, and obtain the peanut embryo cut off the front embryo growth point as a material for space breeding. The embryo growth point after mutagenesis on the return spacecraft was inoculated on MSB5 medium supplemented with 1mg / L NAA and 4mg / L 6-BA to induce callus, and transferred to the supplemented with 1mg / L 6-BA, 0.5mg after 20 days. Regenerated shoots were obtained on the MSB5 bud differentiation medium containing 2 mg / L KIN and 2 mg / L NAA. The tissue culture regenerated seedling after the embryo growth point mutagenesis is a scion, the height of the seedling is 2-2.5 cm, the regenerated seedling is cut from the base of the b...
Embodiment 2
[0015] A method for aerospace breeding to create new peanut germplasm. After selecting Huayu No. 20 peanuts mature, select 100 full seeds, first disinfect them with 70% alcohol for 1 minute, and then use 0.1% by mass Sterilize with HgCl for 6 minutes, perform surface disinfection, rinse with sterile water 4 times, remove the seed coat, remove two cotyledons, and obtain the peanut embryo cut off the front embryo growth point as a material for space breeding. The embryo growth point after mutagenesis on the return spacecraft was inoculated on MSB5 medium supplemented with 1mg / L NAA and 4mg / L 6-BA to induce callus, and transferred to the supplemented with 1mg / L 6-BA, 0.5mg after 20 days. Regenerated shoots were obtained on the MSB5 bud differentiation medium containing 2 mg / L KIN and 2 mg / L NAA. The tissue culture regenerated seedling after the embryo growth point mutation is a scion, the seedling height is 2.5 cm, the regenerated seedling is cut from the base of the bud cluster, ...
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