Rapid propagation method for sagittaria sagittifolia tissue culture seedling and culture medium
A technology of tissue culture seedlings and subculture medium, which is applied in the field of rapid propagation method and culture medium of sagittarius tissue culture seedlings, can solve the problems of intermittent submerged bioreactors and reduce the cultivation process, and achieve the purpose of inhibiting the growth of bacteria, Ensure normal growth and reduce the effect of man-made pollution
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0023] Take the tip of the stolon of Sagittarius sagittarius with a length of 1 cm, immerse it in water containing washing powder, wash it for 30 minutes, and after drying it, disinfect it with 75% ethanol for 30 seconds and 0.1% mercury liter for 10 minutes, and then rinse it with sterile water for 3 times; The explants of Sagittarius sagittarius were inoculated into solid medium and cultured for 3 weeks, wherein the formula of solid medium was: MS+6-BA2.0mg / L+NAA 0.5mg / L, sucrose concentration was 30g / L, agar 3.8g / L, and the pH value is 5.8; the culture conditions of the explants of Sagittarius sagittarius after detoxification in solid medium are: culture temperature 25°C, light 10h / d, dark 14h / d, light intensity 1000lx; The seedlings were inoculated into the intermittent submerged bioreactor, and the inoculation density was 8 plants / L; using the intermittent submerged culture method, the arrowhead explants were cultivated using liquid subculture medium, wherein the formula ...
Embodiment 2
[0025] Take the tip of the stolon of Sagittarius sagittarius with a length of 2cm, immerse it in water containing washing powder, wash it for 30 minutes, and after drying it, disinfect it with 75% ethanol for 30 seconds and 0.1% mercury liter for 10 minutes, and then rinse it with sterile water for 5 times; The explants of Sagittarius sagittarius were inoculated into solid medium and cultured for 3 weeks, wherein the formula of solid medium was: MS+6-BA 2.0mg / L+NAA 0.5mg / L, sucrose concentration was 30g / L, agar 3.8g / L, and the pH value is 6.2; the culture conditions of the explants of Sagittarius sagittarius after detoxification in solid medium are: culture temperature 28 ℃, light 10h, / d, dark 14h / d, light intensity 1500lx; The seedlings were inoculated into the intermittent submerged bioreactor, and the inoculation density was 15 plants / L; using the intermittent submerged culture method, the explants were cultivated using the liquid subculture medium, wherein the formula of ...
Embodiment 3
[0027] Take a 1.5cm-long stem tip of Arthia quinquefolium, immerse it in water containing washing powder, wash it for 30 minutes, and after drying, disinfect it with 75% ethanol for 30 seconds and 0.1% mercury liter for 10 minutes, and then rinse it with sterile water for 4 times; The explants of Sagittarius sagittarius were inoculated into solid medium and cultured for 3 weeks, wherein the formula of solid medium was: MS+6-BA 2.0mg / L+NAA 0.5mg / L, sucrose concentration was 30g / L, agar 3.8 g / L, and the pH value is 6.0; the culture conditions of the explants of Sagittarius sagittata after detoxification in solid medium are: culture temperature 26 ℃, light 10h / d, dark 14h / d, light intensity 1250lx; The seedlings were inoculated into the intermittent immersion bioreactor, and the inoculation density was 8 plants / L; using the intermittent immersion culture method, the arrowroot explants were cultivated using a liquid subculture medium, wherein the formula of the liquid subculture me...
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