Method for creating new peanut specie in space breeding
A space breeding and new germplasm technology, applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve the problems of low beneficial mutation rate of mutagenesis, 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 space breeding to create new germplasm of peanuts. After the Huayu No. 20 peanuts are matured, 100 plump seeds are selected, firstly disinfected with 70% alcohol for 1 minute, and then 0.1% by mass. Sterilize with HgCl for 6 minutes, carry out surface disinfection, rinse with sterile water 4 times, take off the seed coat, and remove two cotyledons to obtain peanut embryos and cut off the front embryo growth point as the material for space breeding. Embryo growth points after mutagenesis carried by returnable spacecraft were inoculated on MSB5 medium supplemented with 1mg / L NAA and 4mg / L 6-BA to induce callus, and transferred to the medium supplemented with 1mg / L 6-BA and 0.5mg / L 6-BA 20 days later. / L KIN and 2mg / L NAA MSB5 shoot differentiation medium to obtain regenerated shoots. The tissue-cultured regenerated seedlings after embryonic growth point mutagenesis are scions with a seedling height of 2-2.5 cm. The regenerated seedlings are cut from the base ...
Embodiment 2
[0015] A method for space breeding to create new germplasm of peanuts. After the Huayu No. 20 peanuts are matured, 100 plump seeds are selected, firstly disinfected with 70% alcohol for 1 minute, and then 0.1% by mass. Sterilize with HgCl for 6 minutes, carry out surface disinfection, rinse with sterile water 4 times, take off the seed coat, and remove two cotyledons to obtain peanut embryos and cut off the front embryo growth point as the material for space breeding. Embryo growth points after mutagenesis carried by returnable spacecraft were inoculated on MSB5 medium supplemented with 1mg / L NAA and 4mg / L 6-BA to induce callus, and transferred to the medium supplemented with 1mg / L 6-BA and 0.5mg / L 6-BA 20 days later. / L KIN and 2mg / L NAA MSB5 shoot differentiation medium to obtain regenerated shoots. The tissue-cultured regenerated seedlings after embryo growth point mutagenesis were scions with a seedling height of 2.5 cm. The regenerated seedlings were cut from the base of ...
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