Thin layer culture method of tulips
A thin-layer culture and tulip technology, applied in the field of plant tissue culture, can solve problems such as the limitation of the proliferation effect of bulb bulbs, and achieve the effects of efficient and stable genetic transformation system, robust growth, and increased bulb induction number
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example 1
[0011] The experimental group was set as 6 groups, and each group treated 60 explants. Adopt the method of the present invention: the tulip scale cross-cutting (tTCL) becomes thin layer (specific thickness sees Table 1), spreads on the culture medium; Induces the growth medium to add 6-BA per liter, NAA, 2,4- D (see Table 1 for the specific concentration), MS medium with 20 g of sucrose and 6 g of agar; the culture condition is a temperature of 23±2° C.; the light intensity is 1500-2000 Lx, and the light time is 16 h / d.
[0012] The control was set as follows: the whole piece of tulip tissue culture scale was inoculated on the MS medium supplemented with 6-BA 2.0mg / L, NAA 0.2mg / L, 30g / L sucrose and 6g / L agar per liter. The culture conditions are all at a temperature of 23±2°C; the light intensity is 1500-2000Lx, and the light time is 16h / d. 60 explants were processed.
[0013] Table 1 Multi-factor investigation on the effect of seed ball induction on the experimental group a...
example 2
[0017] The source and cutting mode of the scales in the method of the present invention are compared.
[0018] Taking tulip commercial bulbs as the source, the specific treatment method for the scales is: peel off the corky scales on the outer layer of the tulip commercial bulbs, take the healthy scales without disease spots, wash them with running water for 30 minutes, and use 70% of them on the ultra-clean work. Soak in ethanol solution for 30s, then soak in 2% sodium hypochlorite solution for 15min, rinse with sterile water 5 times. Using tulip tissue cultured bulbs as the source, the outer and middle scales are directly removed. Then the scales were cut longitudinally (TCL) or transversely (tTCL) into a thin layer with a thickness of 0.5 mm, and spread on the culture medium; the culture medium for inducing proliferation was supplemented with 6-BA 2.0 mg per liter, NAA 0.5 mg / L, 2 , 4-D 2.0mg, sucrose 20g and agar 6g MS medium. The culture conditions were the same as abov...
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