Two polyploid centella asiatica varieties and cultivation method thereof
A cultivation method and volume-doubling technology are applied to tetraploid and triple-volume Centella japonica varieties and their cultivation fields, which can solve the problems of tight supply of Centella asiatica raw materials, large input and output, etc., and achieve the effect of reducing nutrient consumption.
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Embodiment 1
[0026] 1) Cut off 2cm of terminal buds of adult Centella asiatica plants with strong growth potential, remove the outer leaves, rinse with water for 2-4 times, and then use 0.3% potassium permanganate solution under sterile conditions Soak for 20 minutes, wash with sterile water, then treat with 0.2% mercuric chloride for 5 minutes, and wash with sterile water for 6 times. Induced adventitious buds and callus respectively in conventional differentiation medium, and then transferred to conventional proliferation medium for subculture;
[0027] 2) Select the tissue-cultured subcultured seedlings with strong growth potential, cover the terminal buds or callus of the subcultured seedlings softly with sterilized cotton under aseptic conditions, and then use a sterile dropper to absorb 10 μmol.L of filter-sterilized -1 Amisulamide (chemical name: 3,5-dinitro-N4, N4-propylsulfonamide) solution soaked the cotton completely and cultured it in the dark at a low temperature of 5-10°C for...
Embodiment 2
[0034] 1) Cut off 2cm of terminal buds of adult Centella asiatica plants with strong growth potential, remove the outer leaves, rinse with water for 2-4 times, and then use 0.3% potassium permanganate solution under sterile conditions Soak for 20 minutes, wash with sterile water, then treat with 0.2% mercuric chloride for 5 minutes, and wash with sterile water for 6 times. Induced adventitious buds and callus were respectively connected to conventional differentiation medium, and then transferred to conventional proliferation medium for subculture;
[0035] 2) Select the tissue-cultured subcultured seedlings with strong growth potential and culture them in the dark for 5 days, gently peel off the outer leaves with tweezers under sterile conditions, and then transfer to MS solid culture with 12 μmol.L-1 amisulfurin solution Culture in dark medium at 5-10°C for 2-5 days, then transfer to conventional differentiation medium without amisulidine solution for light culture, light fo...
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