A kind of high-efficiency induction method of Polygonatum chinensis in vitro rhizomes
A rhizome and in vitro technology, which is applied in the field of high-efficiency induction of Polygonatum rhizome in vitro, can solve problems such as cumbersome and complicated production process of Polygonatum tissue culture, unsuitability for large-scale production, and contradictory market demand, and achieve the application value of large-scale production and the survival rate High, strong proliferative effect
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Embodiment 1
[0025] Take the rhizomes with buds and wash them, scrub the surface with 75% ethanol, rinse with tap water, soak in 75% ethanol for 30s, rinse with sterilized deionized water twice, sterilize with 2.5% sodium hypochlorite for 5 minutes, rinse with sterilized deionized water for 2 Once again, sterilized with 2.5% sodium hypochlorite for 5 min, rinsed with deionized water for 5 times, blotted the surface moisture of the material with sterile filter paper, cut the material into bud tubers with a diameter of 0.5 cm and placed them on the adventitious bud induction medium (MS+ 6-BA 1.0mg / L+2,4-D 0.1mg / L+commercial white sugar 3%+agar powder 5g / L, pH 5.8~6.0), 25~27℃, light 1600Lx, light 12h / d. After 35 days, 90% of the explants had differentiated adventitious buds; the tubers with adventitious buds differentiated were cut into 0.5 cm in diameter and placed in adventitious bud growth medium (MS+6-BA0.5mg / L+2,4-D 0.1mg / L+ commercially available white sugar 3%+ agar powder 5g / L, pH 5....
Embodiment 2
[0027] Take the rhizomes with buds and wash them, scrub the surface with 75% ethanol, rinse with tap water, soak in 75% ethanol for 30s, rinse with sterilized deionized water twice, sterilize with 2.5% sodium hypochlorite for 5 minutes, rinse with sterilized deionized water for 2 Once again, sterilized with 2.5% sodium hypochlorite for 5 min, rinsed with deionized water for 5 times, blotted the surface moisture of the material with sterile filter paper, cut the material into bud tubers with a diameter of 0.5 cm and placed them on the adventitious bud induction medium (MS+ 6-BA 1.5mg / L+2,4-D 0.2mg / L+commercially available white sugar 3%+agar powder 5g / L, pH 5.8~6.0), 25~27℃, light 1600Lx, light 12h / d. After 35 days, 90% of the explants had differentiated adventitious buds; the tubers with differentiated adventitious buds were cut into 0.5 cm in diameter and placed in adventitious bud growth medium (MS+6-BA1.0mg / L+2,4-D 0.2mg / L + commercially available white sugar 3% + agar powd...
Embodiment 3
[0029] Take the rhizomes with buds and wash them, scrub the surface with 75% ethanol, rinse with tap water, soak in 75% ethanol for 30s, rinse with sterilized deionized water twice, sterilize with 2.5% sodium hypochlorite for 5 minutes, rinse with sterilized deionized water for 2 Once again, sterilized with 2.5% sodium hypochlorite for 5 min, rinsed with deionized water for 5 times, blotted the surface moisture of the material with sterile filter paper, cut the material into bud tubers with a diameter of 0.5 cm and placed them on the adventitious bud induction medium (MS+ 6-BA 2.0mg / L+2,4-D 0.5mg / L+commercially available white sugar 3%+agar powder 5g / L, pH 5.8~6.0), 25~27℃, light 1600Lx, light 12h / d. After 35 days, 90% of the explants differentiated into adventitious buds; the tubers with adventitious buds were cut into 0.5 cm in diameter and placed in adventitious bud growth medium (MS+6-BA1.5mg / L+2,4-D 0.2mg / L + commercially available white sugar 3% + agar powder 5g / L, pH 5....
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