Method for significantly improving fir tissue culture production emergence rate
A technology of seedling emergence rate and Chinese fir, which is applied in the field of plant clone tissue culture, can solve the problems of low transplanting survival rate, low multiplication multiple, and uneven differentiation, so as to increase the multiplication multiple, overcome uneven growth, and promote transplanting of seedlings The effect of branches
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0025] 1. Bud proliferation induction culture
[0026] Inoculate aseptic single buds of Chinese fir about 1.5-2.5cm long on the proliferation induction medium for proliferation induction, and transfer to fresh proliferation induction medium when 2-5 buds germinate at the base, and remove the original buds when transferring Bud tops to promote the growth of new shoots, thus forming clusters of secondary seedlings.
[0027] The formulation of the proliferation-inducing medium is as follows, each liter contains: 1.0 mg of 6BA, 0.1 mg of NAA, 30 g of white granulated sugar, 3.2 g of agar powder, and the balance is MS medium, adjusting the pH value before sterilization 5.85 (the preparation method is to mix the above ingredients evenly, adjust the pH value, and then sterilize for later use, the same below); culture temperature 25±2°C, humidity 20%-40%, light time 12 hours / day, light intensity 2500Lx , cultivated for 35 days.
[0028] 2. Strong seedling cultivation
[0029]Transf...
Embodiment 2
[0038] 1. Bud proliferation induction culture
[0039] Inoculate aseptic single buds of Chinese fir about 1.5-2.5cm long on the proliferation induction medium for proliferation induction, and transfer to fresh proliferation induction medium when 2-5 buds germinate at the base, and remove the original buds when transferring Bud tops to promote the growth of new shoots, thus forming clusters of secondary seedlings.
[0040] The formula of the described proliferation-inducing medium is that every liter contains: 0.5mg of 6BA, 0.05mg of NAA, 30g of white granulated sugar, 3.2g of agar powder and the rest of the MS medium to adjust the pH before sterilization The value is 5.85; the culture temperature is 25±2°C, the humidity is 20%-40%, the light time is 12 hours / day, the light intensity is 2500Lx, and the culture is 35 days.
[0041] 2. Strong seedling cultivation
[0042] Transfer the clustered secondary seedlings to the strong seedling medium for rejuvenation before rooting. T...
Embodiment 3
[0051] 1. Bud proliferation induction culture
[0052] Inoculate aseptic single buds of Chinese fir about 1.5-2.5cm long on the proliferation induction medium for proliferation induction, and transfer to fresh proliferation induction medium when 2-5 buds germinate at the base, and remove the original buds when transferring Bud tops to promote the growth of new shoots, thus forming clusters of secondary seedlings.
[0053] The formula of the described proliferation-inducing medium contains per liter: 3.0mg of 6BA, 30g of white granulated sugar, 3.5g of agar powder and the rest of the MS medium, adjusting the pH value before sterilization to 5.8; the culture temperature 25±2°C, humidity 20%-40%, light time 12 hours / day, light intensity 3000Lx, culture for 35 days.
[0054] 2. Strong seedling cultivation
[0055] Transfer the clustered secondary seedlings to the strong seedling medium for rejuvenation before rooting. The strong seedling cultivation is mainly to promote the grow...
PUM
Property | Measurement | Unit |
---|---|---|
Diameter | 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