Induced culture method of tender shoots of aronia melanocarpa
The technology of a kind of Sorbus nigrutica and its cultivation method is applied in horticultural methods, botanical equipment and methods, horticulture, etc., and can solve the problems such as the shortage of seedlings restricting the development of Sorbus nigrutica, and achieve the benefits of popularization and production, The effect of simple materials and controllable culture conditions
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Embodiment 1
[0020] A method for inducing and cultivating young shoots of Arana nigruta, comprising the steps of:
[0021] The Sorbus adenocarpus plant to be multiplied is selected as the mother tree for collecting explants, and the 20 cm long branch of the top tip is cut during the growth period, rinsed under running water, cut into 3 cm long sections, and placed in an ultra-clean workbench , under aseptic conditions, cut the young shoots, with less branch xylem, disinfect in alcohol for 20 seconds, then soak in glutaraldehyde solution for 10 minutes, rinse with sterile water, inoculate into the medium, MS+sucrose 30g / L+agar powder 6g / L+6-BA (6-benzylpurine) 2.0g / L+NAA (naphthaleneacetic acid) 0.2g / L, induction culture was carried out in an intelligent incubator for 20 days.
Embodiment 2
[0023] A method for inducing and cultivating young shoots of Arana nigruta, comprising the steps of:
[0024] Select the Sorbus adenocarpus plant to be multiplied as the mother tree for collecting explants, cut 1-year-old branches with a length of 30 cm during the dormant period, and move them into the greenhouse for water insertion culture. The plastic film canopy is used to keep heat and keep moisture, and wait for the new buds to germinate Then cut it off, rinse it under running water, immerse it in sterile water and put it in an ultra-clean workbench. Under aseptic conditions, peel off the young shoots, with less xylem, disinfect them in alcohol for 20 seconds, and then put them in glutaraldehyde solution Soak in medium for 10 minutes, rinse with sterile water, inoculate into the culture medium, MS + sucrose 30g / L + agar powder 6g / L + 6-BA (6-benzylpurine) 2.0g / L + NAA (naphthaleneacetic acid) 0.2g / L , and induced culture for 20 days in an intelligent incubator.
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