Construction method of cashew regeneration system
A system and technology of cashew nuts, applied in the field of cashew regeneration system construction, can solve the problems of unformed industrialized production mechanism, low natural reproduction rate, low reproduction coefficient, etc., and achieve the effect of promoting the commercialization process
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Embodiment 1
[0015] (1) Establishment of a sterile system: Select mature, plump, complete cashew seeds without pests and diseases, and preliminarily wash them under tap water. Seeds were soaked in 0.1% potassium permanganate solution for 4 hours until the color of potassium permanganate solution became lighter to pink, rinsed with tap water, then sterilized in 75% ethanol solution for 9 minutes, rinsed with sterile water for 5 times, and washed with sterile filter paper. Drain, manually remove the outer seed coat, and inoculate it on the germination medium to start the culture. The germination medium is 3 / 4B 5 + 0.5mg / L 6-BA+0.4mg / L NAA4.5% sucrose+0.4% agar+0.3% activated carbon, the pH value is 5.6.
[0016] (2) Primary culture: Inoculate the aseptic seedlings with germinated cotyledons that have not fallen off from the aseptic system on the primary medium for cultivation. After inoculation, first culture in total darkness at 24°C for 10 days, and then place in light for 15 hours a day...
Embodiment 2
[0022] (1) Establishment of a sterile system: Select mature, plump, complete cashew seeds without pests and diseases, and preliminarily wash them under tap water. Seeds were soaked in 0.3% potassium permanganate solution for 3 hours until the color of potassium permanganate solution became lighter to pink, rinsed with tap water, then sterilized in 75% ethanol solution for 5 minutes, rinsed with sterile water for 3 times, and washed with sterile filter paper. Drain, manually remove the outer seed coat, and inoculate it on the germination medium to start the culture. The germination medium is 3 / 4B 5 + 0.6mg / L 6-BA+0.5mg / L NAA +3.8% sucrose+0.5% agar+0.1% activated carbon, the pH value is 5.8.
[0023] (2) Primary culture: Inoculate the aseptic seedlings with germinated cotyledons that have not fallen off from the aseptic system on the primary medium for cultivation. After inoculation, first culture in total darkness at 24°C for 13 days, and then place in light for 16 hours a d...
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