Method for efficiently producing cymbidium sinense tissue culture seedlings
A high-efficiency technology of Molan group, applied in the field of plant tissue culture, can solve the problem of low production efficiency of Molan tissue culture seedlings, and achieve the effect of commercialized high-efficiency production, obvious production advantages, and high production efficiency
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Embodiment 1
[0032] 1. Material: Wu Zicui.
[0033] 2. Selection and sterilization of explants: Select a healthy flowering Molan with vigorous growth and no pests and diseases as the mother plant. After artificial pollination, each mother plant will pollinate two flowers. During the fruit development stage, pay attention to control the suitable mother plant. The light, temperature and humidity conditions for plant growth, strengthen its fertilizer and water management and control of pests and diseases, so that the fruit is fully developed, and the capsule can be cut 180 days after pollination for disinfection and inoculation. , and then disinfected with 0.1% mercuric chloride solution for 15 minutes, and finally rinsed with sterile water for 5 times. The capsules washed and washed with sterile water were placed on sterilized filter paper to absorb water, the capsules were cut with a scalpel, and the seeds were evenly sown into the rhizome induction medium M1.
[0034] 3. Induction of rhiz...
Embodiment 2
[0040] This example is basically the same as Example 1, but has the following differences: the experimental material is white ink tissue culture seedlings, and the immersion time of the root-extracting vitality agent (an aqueous solution containing mass fraction of 0.2% potassium permanganate and 0.6% sodium chloride) is 20 minutes ; M1 composition in this example: Huabao No. 1 2.0g / L+ Huabao No. 2 2.0g / L+ banana 80g / L+ apple 20g / L+1.0mg / L 6-BA+1.0mg / LNAA+20g / L sucrose +Activated carbon 2.0g / L+5.0g / L agar, pH 5.4; M2 ingredients: Huabao No. 1 1.5g / L+ Huabao No. 2 1.5g / L+ Banana 80g / L+ Apple 20g / L+0.5mg / L 6- BA+2.0mg / LNAA+20g / L sucrose+activated carbon 2.0g / L+5.0g / L agar, pH 5.4; M3 component: MS+0.5mg / L6-BA+2.0mg / LNAA+20g / L sucrose, pH 5.4; M4 ingredients: Huabao No. 1 1.5g / L + Huabao No. 2 1.5g / L + banana 80g / L + apple 20g / L + 1.0mg / LTDZ + 0.5mg / L NAA + 20g / L sucrose + 5.0g / L Agar, pH 5.6; M5 composition: MS+1.0mg / L TDZ+0.5mg / LNAA+20g / L sucrose, pH 5.6; M6 composition: Huaba...
Embodiment 3
[0042] This example is basically the same as Example 1, except for the following differences: the experimental material is Huizhou Molan tissue culture seedlings, and the root-lifting activity agent (containing an aqueous solution of 0.15% potassium permanganate and 0.4% sodium chloride in mass fraction) soaking time It is 30min; M1 component in this example: Huabao No. 1 1.5g / L+ Huabao No. 2 1.5g / L+ banana 50g / L+ apple 10g / L+0.5mg / L 6-BA+0.5mg / L NAA+15g / L sucrose+activated carbon 0.5g / L+5.0g / L agar, pH 5.2. M2 component in this example: Huabao No. 1 1.0g / L + Huabao No. 2 1.0g / L+ banana 50g / L+ apple 10g / L+0.25mg / L 6-BA+1.0mg / LNAA+15g / L sucrose+ Activated carbon 1.0g / L+5.0g / L agar, pH 5.2; M3 composition: 1 / 2MS+0.25mg / L 6-BA+1.0mg / LNAA+15g / L sucrose, pH 5.2. M4 component in this example: Huabao No. 1 1.0g / L + Huabao No. 2 1.0g / L + banana 50g / L+ apple 10g / L+0.5mg / LTDZ+0.2mg / LNAA+15g / L sucrose+5.0g / L agar, pH 5.4; M5 composition: 1 / 2MS+0.5mg / L TDZ+0.2mg / LNAA+15g / L sucrose, pH...
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