Method for ultralow-temperature storage and renewal cultivation of wild rice stem tips
A technology for cryopreservation and recovery cultivation, which is applied to plant preservation, horticultural methods, botanical equipment and methods, etc. It can solve the problems of small shoot tip meristems, damage, and difficulty in surviving, and achieve good growth recovery , reduce damage and simplify operation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0020] Example 1 Obtaining of Aseptic Seedlings of Wild Rice
[0021] refer to figure 1 As shown, the induction and subculture steps of wild rice aseptic seedlings are as follows: take the stem section of the underground stem of wild rice with germinated buds, wash it repeatedly for about 1 hour under running water, and then disinfect it with 70% alcohol for 1 minute, 0.1% alcohol Mercury chloride disinfection for 15 minutes, rinsed several times with sterile water, stripped about 2mm shoot tips under the dissecting microscope, and inoculated them with 4mg·L -1 BA and 0.5mg·L -1 Cluster shoots were induced on MS medium with NAA. The culture temperature is 25±2℃, and the light is 12h·d -1 , light intensity 36μmolm -2 the s -1 . After the clustered shoots were induced, the clustered shoots were cut off and inoculated in a medium containing 2 mg·L -1 BA and 0.5mg·L -1 NAA was subcultured on MS medium. Subculture every 3 months.
Embodiment 2
[0022] Example 2 Gradient preculture of wild rice
[0023] refer to figure 1 As shown in the gradient domestication culture of sterile seedlings, the steps of peeling off the shoot tip and shoot tip pre-cultivation are: get the tissue culture seedling obtained in Example 1, cut off the upper plant, leave about 3 cm of the base, and put about 1 cm of the root into the plant that does not contain After 7 days of culture in the MS medium of hormones, take the buds that sprout 1 cm from the base, and transfer them to 0.3 molL sucrose -1 and abscisic acid 5mgL -1 cultured on culture medium. After 7 days, transfer to 0.7molL -1 and abscisic acid 5mgL -1 pre-cultured on medium for 5 days. Strip off the shoot tip of 2-3mm under the dissecting microscope, and add 0.4molL -1 and glycerol 2moL -1 , without NH4 + Pre-culture on MS solid medium for 16 hours.
Embodiment 3
[0024] Example 3 Device fixation of wild rice stem tips
[0025] refer to figure 1 with Figure 5 As shown, the shoot tip is fixed to the loading strip and the steps of pretreatment and vitrification are: use tweezers to lightly dip the shoot tip pre-cultured in Example 2 in 2-4% calcium ion-free sodium alginate solution , that is, neatly placed on a 5mm×20mm metal mesh loading strip, with 10 stem tips on each loading strip. Dip the loading strips with shoot tips in a solution containing 0.2% CaCl, 0.4molL -1 Sucrose and 2moL -1 Glycerin, NH4 free +After being fixed for 20 min in MS liquid medium, place the loading strip on sterile filter paper to absorb excess liquid.
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