A kind of rooting method of safrole type camphor tree tissue culture bud
A technology of sassafras oil and camphor tree, which is applied in the field of plant propagation, can solve the problems of difficult rooting of subculture buds, easy blackening of the root system, and long initial rooting time, so as to improve the rooting rate and transplanting survival rate, and shorten the rooting cycle , the effect of high rooting rate
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Embodiment 1
[0024] Select the safrole-type camphor tree secondary buds that have been cultured for 35 days in conventional tissue culture. After disinfecting the surface of the bottle, in the sterile space on the ultra-clean workbench, select the secondary buds that grow robustly and have a height of ≥ 2cm. Cut the single bud at 1-2mm below the node, and remove the base leaves and petioles. Then insert the 0.4-0.5cm of the base of the lower end of the bud stem of the single bud into ascorbic acid (VC) 50mg / L sterile solution and soak for 1.5h to perform rooting pretreatment.
[0025] Insert pretreated single shoots vertically into rooting medium. The formula of described rooting medium is: improved ER+NAA 2-3mg / L+ABT 1 0.5-1mg / L + ascorbic acid (VC) 30mg / L + sucrose 15g / L + agar powder 5.8g / L. Among them, the formulation of the improved ER medium is: NH 4 NO 3 1200mg / L + KNO 3 1900mg / L + CaCl 2 .2H 2 O440mg / L + MgSO 4. .7H 2 O 370mg / L + KH 2 PO 4 340mg / L + H 3 BO 3 0.63m...
Embodiment 2
[0029] Select the secondary buds of safrole-type camphor tree that have been cultured for 36 days in the conventional tissue culture. After the surface of the bottle is disinfected, in the sterile space on the ultra-clean workbench, select the secondary buds that grow robustly and have a height of ≥ 2cm. Cut the single bud at 1-2mm below the node, and remove the base leaves and petioles. Then insert the 0.4-0.5cm of the base of the lower end of the bud stem of the single bud into ascorbic acid (VC) 50mg / L sterile solution and soak for 1.5h to perform rooting pretreatment.
[0030] Insert pretreated single shoots vertically into rooting medium. The formula of described rooting medium is: improved ER+NAA 2-3mg / L+ABT 1 0.5-1mg / L + ascorbic acid (VC) 30mg / L + sucrose 15g / L + agar powder 5.8g / L. Among them, the formulation of the improved ER medium is: NH 4 NO 3 1200mg / L + KNO 3 1900mg / L + CaCl 2 .2H 2 O440mg / L + MgSO 4. .7H 2 O 370mg / L + KH 2 PO 4 340mg / L + H 3 BO ...
Embodiment 3
[0034] Select the secondary buds of sassafras type camphor tree that have been cultured for 38 days in the strong buds of conventional tissue culture. After disinfecting the surface of the bottle, in the sterile space on the ultra-clean workbench, select the secondary buds that grow robustly and have a height of ≥ 2cm. Cut the single bud at 1-2mm below the node, and remove the base leaves and petioles. Then insert the 0.4-0.5 cm of the base of the lower end of the single bud stem into ascorbic acid (VC) 50 mg / L sterile solution and soak for 2 hours to perform rooting pretreatment.
[0035] Insert pretreated single shoots vertically into rooting medium. The formula of described rooting medium is: improved ER+NAA 2-3mg / L+ABT 1 0.5-1mg / L + ascorbic acid (VC) 30mg / L + sucrose 15g / L + agar powder 5.8g / L. Among them, the formulation of the improved ER medium is: NH 4 NO 3 1200mg / L + KNO 3 1900mg / L + CaCl 2 .2H 2 O440mg / L + MgSO 4. .7H 2 O 370mg / L + KH 2 PO 4 340mg / L +...
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