Cultivation method for keeping Guangxi Maytenus hookeri characteristics
A cultivation method and technology with characteristics, applied in the field of planting, can solve the problems of reduction, low seedling emergence rate and nursery rate of Guangxi Maydenwood, and achieve the effects of promoting germination factors, strong seed adaptability, and promoting seed germination.
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Embodiment 1
[0034] 1. Raw material preparation:
[0035] The culture substrate was prepared as follows:
[0036] (1) EM bacteria activation treatment: take the peeled banana, add slices into the same volume of water and stir into a mud; take the peeled sweet potato, slice into it, add the same volume of water and stir into a mud; peel the banana, slice it, dry it, pulverize it, and Spray water from the inlet of the conical flask into the conical flask while potato flour is added, banana powder and water are in a weight ratio of 1:5, then boil in a boiling water bath for 20 minutes, then filter with three layers of gauze to get the filtrate, Then the filtrate is centrifuged with a centrifuge, centrifuged at 3000rpm for 20S, the supernatant is taken, and then concentrated to a concentration of 30 ° of Pomi, and then the ethanol solution with a mass fraction of 75% is poured and stirred while pouring, and then produced A large number of flocculent precipitates are then frozen at a temperatu...
Embodiment 2
[0052] 1. Raw material preparation:
[0053] The culture substrate was prepared as follows:
[0054] (1) EM bacteria activation treatment: take the peeled banana, add slices into the same volume of water and stir into a mud; take the peeled sweet potato, slice into it, add the same volume of water and stir into a mud; peel the banana, slice it, dry it, pulverize it, and Spray water from the inlet of the conical flask into the conical flask while potato flour is added. Banana powder and water are in a weight ratio of 1:5, then cook in a boiling water bath for 30 minutes, and then filter with three layers of gauze to get the filtrate. Then the filtrate is centrifuged with a centrifuge, centrifuged at 3500rpm for 30S, the supernatant is taken, and then concentrated to a concentration of 30 ° of Pomi, and then the ethanol solution with a mass fraction of 75% is poured and stirred while pouring, and then produced A large number of flocculent precipitates are then frozen at a tempe...
Embodiment 3
[0070] 1. Raw material preparation:
[0071] The culture substrate was prepared as follows:
[0072] (1) EM bacteria activation treatment: take the peeled banana, add slices into the same volume of water and stir into a mud; take the peeled sweet potato, slice into it, add the same volume of water and stir into a mud; peel the banana, slice it, dry it, pulverize it, and Spray water from the inlet of the Erlenmeyer flask into the Erlenmeyer flask while potato flour is added. Banana powder and water are in a weight ratio of 1:5, and then boiled in a boiling water bath for 24 minutes, then filtered through three layers of gauze to get the filtrate. Then the filtrate is centrifuged with a centrifuge, centrifuged at 3450rpm for 25S, the supernatant is taken, and then concentrated to a concentration of 30 ° of Pomi degree, and then the ethanol solution with a mass fraction of 75% is poured and stirred while pouring, and then produced A large number of flocculent precipitates were t...
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