A medium for promoting rooting of tetraploid paulownia tissue cultured seedlings and its application
A rooting medium and medium technology, applied in the biological field, can solve the problems of low rooting rate and irregular rooting of tetraploid Paulownia tissue culture seedlings, and achieve the effects of improving the survival rate of seedlings, promoting rooting, and high rooting rate
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Embodiment 1
[0021] Under sterile conditions, cut off the subcultured plant height of about 2cm, with more than 2 pairs of leaves with budding stems, cut into individual plants, and inoculate them into the rooting medium. The composition of the rooting medium is MS+IBA0. 1mg / L+IAA 0.05mg / L+NAA0.1mg / L+agar 4.0g / L+20g / L sucrose (pH 5.8), the culture conditions are daytime temperature 25°C, night temperature 18°C, light intensity 2500Lx, light time 13h / d. Cultivate for about 12 days to form root primordia, and grow tender roots from the root primordium in about 14 days. After 20 days of cultivation, seedlings can be hardened and transplanted. The number of roots is 5-7, the root length is 0.5-1.5cm, and the rooting rate is 100%.
Embodiment 2
[0023] Under sterile conditions, cut off the subcultured shoots with a height of about 2 cm, with more than 2 pairs of leaves, cut into individual plants, and inoculate them into the rooting medium. The composition of the rooting medium is MS+IBA 1.5 mg / L+IAA 0.5mg / L+NAA 0.3mg / L+agar 4.5g / L+20g / L sucrose (pH 5.8), the culture conditions are daytime temperature 25°C, night temperature 18°C, light intensity 2500Lx, light time 13h / d. Cultivate for about 10 days to form root primordia, and grow tender roots from the root primordia in about 11 days. After 20 days of cultivation, seedlings can be hardened and transplanted. The number of roots is 5-18, the root length is 1.5-3.0cm, and the rooting rate is 100%.
Embodiment 3
[0025] Under sterile conditions, cut off the subcultured shoots with a height of about 2cm and more than 2 pairs of leaves, cut into individual plants, and inoculate them into the rooting medium. The composition of the rooting medium is MS+IBA 4.0 mg / L+IAA 2.0mg / L+NAA 2.0mg / L+agar 6.0g / L+20g / L sucrose (pH 5.8), the culture conditions are daytime temperature 25°C, night temperature 18°C, light intensity 2500Lx, light time 13h / d. Cultivate for about 10 days to form root primordia, and grow tender roots from the root primordium in about 13 days. After 20 days of cultivation, seedlings can be hardened and transplanted. The number of roots is 5-12, the root length is 1.0-2.0cm, and the rooting rate is 100%.
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