Dendrobium officinale sprout rapid propagation method with high efficiency
A technology for Dendrobium officinale and seedlings, which is applied in the field of high-efficiency and rapid propagation of Dendrobium officinale seedlings, can solve the problems of low root induction efficiency, low multiplication coefficient, and limited germplasm sources, so as to achieve unrestricted germplasm sources, Improve the reproduction coefficient, the effect of a wide range of sources
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0020] Select the bud tip of Dendrobium officinale with a height of 0.5cm~1.5cm, and inoculate it in the pseudoprotocorm induction medium: 1 / 2MS+sucrose 30g / L+agar 10g / L+TDZ0.5mg / L+NAA1mg / L+2,4-D0. 5mg / L, the formation of pseudoprotocorms can be seen after 12 days of culture, and the incidence rate reaches 92%. The protocorms are inoculated on the original induction medium for proliferation and culture, and the subculture cycle is 30 days.
[0021] Inoculate the pseudoprotocorm after proliferation culture in the pseudoprotocorm differentiation medium: MS medium + sucrose 20g / L + agar 10g / L + NAA2mg / L + 6-BA10mg / L, after 28 days, it can be differentiated into 1cm ~ 2cm Clusters of buds, with an average of 45 buds / 0.1g pseudoprotocorms.
[0022] Divide the differentiated clusters of buds into 1-2 buds / plant and inoculate them into rooting and strong seedling medium; 1 / 2MS medium + sucrose 20g / L + agar 10g / L + 6-BA1mg / L + NAA1mg / L + IBA6mg / L+potato extract 200g / L+2g / L activated...
Embodiment 2
[0028] Select stem tips or sterile seedlings of Dendrobium officinale seedlings with a height of 0.5cm to 1.0cm, and inoculate them in pseudoprotocorm induction medium: MS+sucrose 20g / L+agar 12g / L+TDZ1mg / L+NAA4mg / L+2,4-D0 .5mg / L, pseudoprotocorms can be seen to form after 10 days of culture, and the incidence rate reaches 98%. The protocorms are inoculated on the original induction medium for proliferation and culture, and the subculture cycle is 30 days.
[0029] Inoculate the pseudoprotocorm after proliferation culture in the differentiation medium of pseudoprotocorm: MS medium + sucrose 30g / L + agar 8g / L + NAA0.5mg / L + 6-BA4mg / L, after 30 days, it can be differentiated into 1cm~ 2cm clusters of buds, about 50 buds / / 0.1g pseudoprotocorms.
[0030] Divide the differentiated bud clusters into 1-2 buds / plant, and inoculate them into rooting and strong seedling medium; 3 / 4MS medium + sucrose 25g / L + agar 12g / L + 6-BA0.5mg / L + NAA1mg / L + IBA3mg / L+potato extract 100g / L+3g / L activ...
Embodiment 3
[0036] Select stem tips or sterile seedlings of Dendrobium officinale with a height of 0.5cm to 1.5cm, and inoculate them in pseudoprotocorm induction medium: 1 / 4MS+sucrose 30g / L+agar 8g / L+TDZ1mg / L+NAA1mg / L+2,4- D1mg / L, after 12 days of culture, pseudoprotocorms can be seen to form, and the incidence rate reaches 96%. The protocorms are inoculated on the original induction medium for proliferation and culture, and the subculture cycle is 30 days.
[0037] Inoculate the pseudoprotocorm after proliferation culture in the differentiation medium of pseudoprotocorm: MS medium + sucrose 30g / L + agar 12g / L + NAA1mg / L + 6-BA5mg / L, after 25 days, it can be differentiated into 1cm ~ 2cm Clusters of buds, about 40 buds / / 0.1g pseudoprotocorms.
[0038] Divide the differentiated bud clusters into 1-2 buds / plant and inoculate them into rooting and strong seedling medium; 1 / 4MS medium+sucrose 20g / L+agar 8g / L+6-BA3mg / L+NAA2mg / L+IBA3mg / L+potato extract 100g / L+4g / L activated carbon, cultivate...
PUM
Property | Measurement | Unit |
---|---|---|
Length and width | aaaaa | aaaaa |
Particle size | aaaaa | aaaaa |
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