Tissue culture method of taxus chinensis
A technology of tissue cultivation and yew, which is applied in the field of plant cultivation, can solve the problems that the amount of yew resources cannot meet paclitaxel, the scarcity of paclitaxel drug sources cannot be solved, and the requirements for cultivation substrates are harsh, so as to achieve good water retention and ventilation. The incidence of pests and diseases, the amount of pesticide usage, and the effect of reducing cultivation costs
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0013] A method for tissue culture of Chinese yew, comprising the following steps:
[0014] ①Treatment of the culture bottle: Soak the culture bottle with 15mg / L nano-zinc oxide alcohol solution for 24 hours, then drain the culture bottle, and then irradiate with ultraviolet light for 40 minutes, and place it in a sterile environment for standby;
[0015] ②Callus cultivation: Select the middle layer cells of the new shoots of Taxus chinensis, process them into 2cm tissue slices, put them into a plant incubator with a wooden shell filled with medium, and cultivate them at 15°C for 15 days, and the light intensity is 10001x. 4 hours of light per day, until a 10cm callus is formed; the medium formula is: 15g / L sucrose, 600mg / L rice bran polysaccharide, 20mg / L γ-aminobutyric acid, 0.5mg / L gibberellin, 550mg / L L calcium hypochlorite, 400mg / L calcium hydroxide, 25mg / L osthole, 10mol / L L-glutamine, pH value is 5;
[0016] ③Rooting culture: select the middle 5cm callus, then steriliz...
Embodiment 2
[0018] A method for tissue culture of Chinese yew, comprising the following steps:
[0019] ①Treatment of the culture bottle: Soak the culture bottle with 15mg / L nano-zinc oxide alcohol solution for 24 hours, then drain the culture bottle, and then irradiate with ultraviolet light for 40 minutes, and place it in a sterile environment for standby;
[0020] ②Callus cultivation: Select the middle layer cells of the new branches of Taxus chinensis, process them into 2cm tissue slices, put them into a plant incubator with a wooden shell containing medium, and cultivate them at 18°C for 20 days, with a light intensity of 12001x. 4 hours of light every day, until a 12cm callus is formed; the medium formula is: 20g / L sucrose, 750mg / L rice bran polysaccharide, 25mg / L γ-aminobutyric acid, 1mg / L gibberellin, 750mg / L Calcium hypochlorite, 550mg / L calcium hydroxide, 32mg / L osthole, 12.5mol / L L-glutamine, pH value is 6.5;
[0021] ③Rooting culture: select the middle 6cm callus, then ster...
Embodiment 3
[0023] A method for tissue culture of Chinese yew, comprising the following steps:
[0024] ①Treatment of the culture bottle: Soak the culture bottle with 15mg / L nano-zinc oxide alcohol solution for 24 hours, then drain the culture bottle, and then irradiate with ultraviolet light for 40 minutes, and place it in a sterile environment for standby;
[0025] ②Callus cultivation: Select the middle layer cells of the new shoots of Taxus chinensis, process them into 2cm tissue slices, put them in a plant incubator with a wooden shell filled with medium, and cultivate them at 16°C for 18 days, and the light intensity is 11001x, Illuminated for 4 hours a day, until a callus of 11 cm was formed; the medium formula was: 17g / L sucrose, 650mg / L rice bran polysaccharide, 22mg / L γ-aminobutyric acid, 0.8mg / L gibberellin, 600mg / L L calcium hypochlorite, 450mg / L calcium hydroxide, 28mg / L osthole, 11.5mol / L L-glutamine, pH value is 5.5;
[0026] ③Rooting culture: select the middle 5.5cm callus...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com