Tissue culture rapid propagation technique of moringa oleifera Lam.
A technology of tissue culture rapid propagation and Moringa oleifera, which is applied in the field of plant tissue culture, can solve problems such as no reports, and achieve the effect of solving the problem of supplying high-quality Moringa oleifera seedlings
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0017] (1) Collection and processing of explants: Select Moringa oleifera oleifera plants with plump shoots of the year, soak in washing powder water for 10 minutes after removing leaves, rinse with tap water for 1 hour after brushing, and cut into 1-3cm long branches with axillary buds Stem sections were first sterilized with 75% alcohol for 5 seconds, then washed 3 times with sterile water, then sterilized with 0.1% mercuric chloride solution for 10 minutes, washed 5 times with sterile water, and then used for later use.
[0018] (2) Bud induction: inoculate the stem section with axillary buds obtained from the treatment in step (1) on the bud induction medium, culture it in total darkness at 28°C for 3 days, and then place it in the light for 10 hours a day, with a light intensity of 1500~2000lx cultured for 18 days to form clustered buds, and the induction rate reached 87.4%. The bud induction medium is: MS+6-BA 4mg / L+sucrose 25g / L+agar 4g / L, pH is 5.8.
[0019] (3) Bud p...
Embodiment 2
[0023] (1) Collection and processing of explants: Select Moringa oleifera oleifera plants with plump shoots of the year, soak in washing powder water for 15 minutes after removing leaves, rinse with tap water for 3 hours after brushing, and cut into 1-3cm long branches with axillary buds Stem segments were first sterilized with 75% alcohol for 10 seconds, then washed 3 times with sterile water, then sterilized with 0.1% mercuric chloride solution for 15 minutes, washed 5 times with sterile water, and then set aside.
[0024] (2) Bud induction: inoculate the stem section with axillary buds obtained from the treatment in step (1) on the bud induction medium, and culture it in total darkness at 28°C for 3 days, and then put it in the light for 11 hours a day, and the light intensity is 1500~2000lx cultured for 21 days to form clustered buds, and the induction rate reached 94.1%. The bud induction medium is: MS+6-BA7mg / L+sucrose 30g / L+agar 5g / L, pH is 5.8.
[0025] (3) Bud p...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More