Rooting induction method for tissue culture seedling of cork oak
A technology of Quercus variabilis and Quercus variabilis, applied in the field of rooting induction of Quercus cork tissue culture seedlings, can solve the problems of not thick roots, small number of roots, uneven rooting, etc., and achieve shortened rooting cycle, fast rooting speed, and many roots Effect
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Embodiment 1
[0022] Select subcultured buds of Quercus cork that have been cultured for 35-36 days in conventional tissue culture. After disinfecting the surface of the bottle, in the aseptic space on the ultra-clean workbench, select the subcultured buds that grow robustly and have a height of 1-2 cm. Single buds, cut at 2-3mm below the node, and remove the base leaves and petioles. The pruned single buds were inoculated in the pre-rooting medium, and placed under the conditions of temperature 20±1°C, humidity 40%, light intensity 2000lux, and light 16h / d for pre-rooting culture. The raw material content of the pre-rooting medium described therein is: 1 / 2 improved MS medium+NAA 1.0mg / L+activated carbon 6g / L++VC 15mg / L+sucrose 25g / L+agar 5.0g / L.
[0023] After 30-35 days of pre-rooting culture for single buds, transfer the single buds to the rooting medium and place them under the conditions of temperature 20±1°C, humidity 40%, light intensity 2000lux, and light 16h / d for rooting culture. ...
Embodiment 2
[0026] Select the secondary buds of Quercus cork that have been cultured for 36-37 days in the conventional tissue culture, and after disinfecting the surface of the bottle, select the vigorous growth of the secondary bud clusters with a height of 1-2 cm in the sterile space on the ultra-clean workbench. Single buds, cut at 2-3mm below the node, and remove the base leaves and petioles. The pruned single buds were inoculated in the pre-rooting medium, and placed under the conditions of temperature 20±1°C, humidity 40%, light intensity 2500lux, and light 15h / d for pre-rooting culture. The raw material content of the pre-rooting medium described therein is: 1 / 2 improved MS medium+NAA 1.5mg / L+activated carbon 6g / L++VC 15mg / L+sucrose 25g / L+agar 5.0g / L.
[0027] After 30-35 days of pre-rooting culture for single buds, transfer the single buds to the rooting medium and place them under the conditions of temperature 20±1°C, humidity 40%, light intensity 2500lux, and light 15h / d for ro...
Embodiment 3
[0030] Select the secondary buds of Quercus cork that have been cultured for 37-38 days in the conventional tissue culture, and after disinfecting the surface of the bottle, in the aseptic space on the ultra-clean workbench, select the vigorous growth of the secondary buds, with a height of 1-2 cm. Single buds, cut at 2-3mm below the node, and remove the base leaves and petioles. The pruned single buds were inoculated in the pre-rooting medium, and placed under the conditions of temperature 20±1°C, humidity 45%, light intensity 2000lux, and light 16h / d for pre-rooting culture. The raw material content of the pre-rooting medium described therein is: 1 / 2 improved MS medium+NAA 2.0mg / L+activated carbon 6g / L++VC 15mg / L+sucrose 25g / L+agar 5.0g / L.
[0031] After 30-35 days of pre-rooting culture for single buds, transfer the single buds into the rooting medium, and place them under the conditions of temperature 20±1°C, humidity 45%, light intensity 2000lux, and light 16h / d for rooti...
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