Method for obtaining hedychium coronarium tetraploid plants by slice culture technology
A white ginger flower and tetraploid technology is applied in the field of obtaining a white ginger flower tetraploid plant by using a thin slice culture technology, which can solve the problems of successful induction of polyploid plants without the white ginger flower thin plate culture technology, and achieves easy popularization and reliability. The effect of promotion, strong operability, and simplified screening process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0063] (1) Disinfection of explants and induction of adventitious buds: Get the new shoots germinated from the rhizomes of Hedychium coronarium (commercially available routine. The same below), rinse them with tap water and soak them in detergent for 30 minutes. Minutes, then rinsed with tap water for 30 minutes, then sterilized the surface with 70wt% alcohol for 60 seconds, and finally sterilized with 0.1wt% mercury chloride for 18 minutes, cut 0.5cm buds on the ultra-clean workbench as explants, and inoculated the buds Cultivate in induction medium A, and induce adventitious buds after 20 days of cultivation; the described bud induction medium A is MS medium + 3mg L -1 6-BA+0.2mg·L -1 NAA+30g·L -1 Sucrose+7g·L -1 Agar;
[0064] (2) Adventitious buds become seedlings: the adventitious buds induced by step (1) are transferred to the seedling medium to promote the rooting and maturation of the seedlings, and after 15 days of cultivation, strong test-tube plantlets with a hei...
Embodiment 2
[0081] (1) Disinfection of explants and induction of adventitious buds: Take the new shoots germinated from the rhizomes of Hedychium coronarium, rinse them with tap water, soak them in detergent for 28 minutes, and then rinse them with tap water for 28 minutes. Minutes later, carry out surface disinfection with 75wt% alcohol for 75 seconds, and finally sterilize with 0.1wt% mercuric chloride for 15 minutes, cut 1.0cm buds on the ultra-clean workbench as explants, inoculate them into bud induction medium A and cultivate them. After 30 days of cultivation, adventitious buds can be induced; the bud induction medium A is MS medium+4mg L -1 6-BA+0.1mg·L -1 NAA+30g·L -1 Sucrose+7g·L -1 Agar;
[0082] (2) Adventitious buds become seedlings: the adventitious buds induced by step (1) are transferred to the seedling medium to promote the rooting and maturation of the seedlings, and cultivate for 30 days to obtain strong test-tube plantlets with a height of more than 6 cm; described ...
Embodiment 3
[0092] (1) Disinfection of explants and induction of adventitious buds: Take the new shoots germinated from the rhizomes of Hedychium coronarium, wash them with tap water, soak them in detergent for 25 minutes, and then rinse them with tap water for 25 minutes. Minutes later, carry out surface disinfection with 72wt% alcohol for 90 seconds, and finally disinfect with 0.1wt% mercuric chloride for 20 minutes, cut 1.5cm buds on the ultra-clean workbench as explants, inoculate them into bud induction medium A and cultivate them. Adventitious buds were induced after 40 days of cultivation; the bud induction medium A was MS medium+5mg L -1 6-BA+0.15mg·L -1 NAA+30g·L -1 Sucrose+7g·L -1 Agar;
[0093] (2) Adventitious buds become seedlings: the adventitious buds induced by step (1) are transferred to the seedling medium to promote the rooting and maturation of the seedlings, and they can be cultivated for 45 days to obtain strong test-tube plantlets with a height of more than 6 cm;...
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