Long-term multiplication and storage method for embryonic callus of sweet potatoes
A technology of embryogenic callus and sweet potato, which is applied in the field of plant tissue culture, can solve the problems of short embryogenic retention time of sweet potato embryogenic callus, small number of embryogenic callus expansion, loss of viability and space, etc., to achieve guaranteed Mass proliferation, great application value, and long storage time
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[0015] The present invention will be described in detail below in conjunction with examples.
[0016] 1) Induction of embryogenic callus: Disinfect the shoot tips of sweet potato variety Xu 55-2 with 70% alcohol for 30 seconds, and immediately transfer them to 0.1% HgCl 2 Sterilize in solution for 3 minutes and wash 4-5 times with sterile water. Under the dissecting microscope, cut the shoot tip tissue (with 1-2 leaf primordia) of about 0.5mm in length, and culture the shoot tip tissue on the 2.0mg / L 2,4-D MS solid medium, and the culture condition is 28 °C, dark. Induce embryogenic callus.
[0017] 2) The induced embryogenic callus was cut into small pieces, and transferred into 2.0 mg / L 2,4-D MS solid medium, and the culture condition was 22°C, dark. After 45 days, under the Leica EZ4D microscopic camera system, select the spherical embryos and heart-shaped embryos with bright yellow color and dense granules, and transfer them into fresh 2.0mg / L2, 4-D MS solid medium, and...
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