Method for constructing regeneration system of Magnolia officinalissubsp. biloba(Rehd. et Wils.) Law.
A kind of Magnolia officinalis and systemic technology, applied in the field of plant tissue culture, can solve the problems such as the unformed industrialized production mechanism, low natural reproduction rate, and difficulty in tissue culture, and achieve the effect of promoting the commercialization process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0020] (1) Establishment of a sterile system: Select mature, plump, complete and pest-free Magnolia officinalis seeds, and preliminarily wash them under tap water. Seeds were soaked in 0.1% potassium permanganate solution for 2 hours until the color of potassium permanganate solution became lighter to pink, rinsed with tap water, then sterilized in 75% ethanol solution for 5 minutes, rinsed with sterile water 4 times, and sterile filter paper Drain, manually remove the outer seed coat, and inoculate it on the germination medium to start the culture. The germination medium is 3 / 4B 5 + 0.3mg / L 6-BA+0.2mg / L NAA +3.5% sucrose+0.5% agar+0.1% activated carbon, the pH value is 5.8.
[0021] (2) Primary culture: Inoculate the aseptic seedlings with germinated cotyledons that have not fallen off from the aseptic system on the primary medium for cultivation. After inoculation, first culture in total darkness at 28°C for 10 days, and then place in light for 15 hours a day , the ligh...
Embodiment 2
[0027] (1) Establishment of a sterile system: Select mature, plump, complete and pest-free Magnolia officinalis seeds, and preliminarily wash them under tap water. Seeds were soaked in 0.3% potassium permanganate solution for 4 hours until the color of potassium permanganate solution became lighter to pink, rinsed with tap water, then sterilized in 75% ethanol solution for 5 minutes, rinsed with sterile water for 5 times, and washed with sterile filter paper. Drain, manually remove the outer seed coat, and inoculate it on the germination medium to start the culture. The germination medium is 3 / 4B 5 + 0.5mg / L 6-BA+0.4mg / L NAA +2.5% sucrose+0.5% agar+0.1% activated carbon, the pH value is 5.6.
[0028] (2) Primary culture: Inoculate the aseptic seedlings with germinated cotyledons that have not fallen off from the aseptic system on the primary medium for cultivation. After inoculation, first culture in total darkness at 28°C for 10 days, and then place in light for 13 hours a...
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