Cultivation method of stem tissues of shiny-leaved yellowhorn
A cultivation method, the technology of X. sorbifolium, which is applied in the field of plant tissue cultivation, can solve the problems of strong seed variability, possibility of weakening, low seed setting rate of X. sorbifolium, etc., and achieve the effect of high survival rate and fast tissue differentiation speed
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0022] A method for cultivating stem tissue of sorbifolium sorbifolium provided by the invention, the method comprises the following steps successively:
[0023] 1) Disinfection treatment
[0024] Collect the middle and lower stems of the dormant branches of Xanthos sorbifolium in the current year, trim them, subtract the dead branches and air-dried branches, clean them with sterile water, put them in a wide-mouthed bottle, drip 75% hydrogen peroxide on the leaf axils, and then use 75 % alcohol disinfection for 25s, rinsed, then disinfected with bromogeramine for 30-60s, and washed with sterile water;
[0025] 2) Primary culture
[0026] Remove the top and bottom of the clean branches after disinfection, cut the stem section with a 4-6cm length and one axillary bud obliquely into the primary culture medium at 24-26°C, cultivate in light for 12 / 12h, and incubate at a light intensity of 1000-1500lux for 15-17 sky;
[0027] Wherein: the first-generation medium is prepared by t...
Embodiment 2
[0034] Another method for cultivating the stem tissue of sorbifolium sorbifolium provided by the present invention, the method comprises the following steps successively:
[0035] 1) Disinfection treatment
[0036] Collect the middle and lower stems of the dormant branches of Xanthos sorbifolium in the current year, trim them, subtract the dead branches and air-dried branches, clean them with sterile water, put them in a wide-mouthed bottle, drip 75% hydrogen peroxide on the leaf axils, and then use 75 % alcohol disinfection for 20-40s, rinsed, then disinfected with bromogeramine for 60s, and washed with sterile water;
[0037] 2) Primary culture
[0038] Remove the top and bottom of the clean branch after disinfection, cut the stem section with a length of 4-6cm, and insert an axillary bud obliquely into the primary culture medium at 24°C, light culture for 12 / 12h, and light intensity 1000-1500lux for 15-17 days;
[0039] Wherein: the first-generation medium is prepared by ...
Embodiment 3
[0046] Another method for cultivating the stem tissue of sorbifolium sorbifolium provided by the present invention, the method comprises the following steps successively:
[0047] 1) Disinfection treatment
[0048] Collect the middle and lower stems of the dormant branches of Xanthos sorbifolium in the current year, trim them, subtract the dead branches and air-dried branches, clean them with sterile water, put them in a wide-mouthed bottle, drip 75% hydrogen peroxide on the leaf axils, and then use 75 % alcohol disinfection for 20s, rinsed, then disinfected with bromogeramine for 60s, and washed with sterile water;
[0049] 2) Primary culture
[0050] Remove the top and bottom of the clean branch after disinfection, cut the stem segment with a length of 6cm, and insert an axillary bud obliquely into the primary culture medium at 26°C, cultivate in light for 12 / 12h, and cultivate for 17 days with a light intensity of 1000-1500lux;
[0051]Wherein: the first-generation medium...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More