A method for aseptic germination and rapid propagation of Michelia majestic seeds
A magnificent seed technology, applied in the field of aseptic germination and rapid propagation of Michelia grandis, can solve the problems of narrow distribution area, scarce population, insufficient seedlings, etc., and achieve easy seedling formation, simplified reproduction steps, and effective reproduction rate high effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0049] A method for aseptic germination of magnificent miraculous seeds, comprising the following steps:
[0050] Select the mature unsplit aggregate fruit of Magnificent Miracle, disinfect the surface with 75% alcohol on the ultra-clean bench, place it on sterile filter paper, dry the moisture on the surface, and take out the red fake fruit with sterile tweezers and blades. The seeds of the seed coat are explants.
[0051] Inoculate the seeds with red arils on the germination medium for germination culture, the medium is MS + no hormone; 1 / 2MS + no hormone; 1 / 3MS + no hormone; 1 / 4MS + no hormone; pure agar + no hormone, The pH values were all 5.8. One seed was inoculated per bottle, and a total of 10 seeds were inoculated for each treatment, repeated 3 times.
[0052] Table 1 The screening of the germination medium of Michelia grandis
[0053]
[0054] Cultivate under the conditions of no light and a temperature of 23-30°C. After 10 days, the seeds begin to germinate....
Embodiment 2
[0056] A method for rapid propagation of magnificent miraculous seeds, comprising the following steps:
[0057] The germinated nodal buds were inoculated on the proliferation and subculture medium for multiplication and subculture. A total of 10 germinated nodal buds were inoculated for each treatment, and repeated 3 times. Using MS medium as the basic medium for proliferation and subculture hormone screening, the cytokinin is 6-BA, and the concentration range is (0.1mg / L, 0.5mg / L, 0.8mg / L, 1.0mg / L, 1.2 mg / L, 1.5mg / L, 6 concentration gradients), the auxin concentrations were (0.1mg / L, 0.5mg / L, 1.0mg / L, 3 concentration gradients), using the uniform design method, the results are shown in Table 2.
[0058] Table 2 Proliferation medium hormone screening
[0059]
[0060] The proliferation and subculture medium is MS+1.0mg / L 6-BA+0.5mg / L IAA+sucrose 30g / L+agar 5g / L, pH value 5.8, light-dark cycle is 10:14, light intensity is 1500Lux, The temperature is 23-28° C. After 60 day...
Embodiment 3
[0062] A method for rapid propagation of magnificent miraculous seeds, comprising the following steps:
[0063] The proliferating seedlings prepared in Example 2 were inoculated onto the rooting medium, and the formulation of the rooting medium was shown in 4 formulations in Table 3, and the rooting medium was screened.
[0064] Table 3 Rooting Medium Hormone Screening Results
[0065]
[0066] The results are shown in Table 3. MS medium + 1.0mg / L IAA + 1.0mg / L IBA + sucrose 30g / L + agar 5g / L, pH 5.8 is the best formula, and the culture period is 30 days. Compared with other formulas, it has significant advantages, and the rooting rate reaches 93%. %.
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