Method for promoting rooting of alfalfa tissue culture seedlings
A technology for tissue cultured seedlings and alfalfa, applied in horticultural methods, botany equipment and methods, plant regeneration, etc., can solve the problem of long rooting period of alfalfa tissue cultured seedlings, affecting the efficiency of alfalfa tissue cultured seedlings, and low survival rate of transplanting and other problems, to achieve the effect of improving the speed and quality of reproduction, well-developed lateral roots, and good development
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Embodiment 1
[0035] A method for promoting rooting of alfalfa tissue culture seedlings, comprising the steps of:
[0036] Step (A), preparation such as figure 1 and figure 2 The solid rooting medium 1 of the hollow cylindrical shape shown;
[0037] Step (B), inoculate the rootless or a little rooted shoots obtained from the differentiation of alfalfa callus on the upper end surface of the solid rooting medium 1, and make the roots of the alfalfa seedlings grow along the hollow cylinder The inner wall of the body-shaped solid rooting medium 1 grows in a semi-suspension downward;
[0038] Step (C), seal with a sealing film after inoculation, put into the tissue culture room for rooting culture, after 1-2 weeks, when the roots of the alfalfa seedlings grow to more than 5cm, the seedlings are hardened and transplanted.
Embodiment 2
[0040] Step (A), preparation such as figure 1 and figure 2The solid rooting medium 1 of the hollow cylindrical shape shown;
[0041] Table 11 / 2 SH9 solid rooting medium formula
[0042] compound concentration MgSO 4 ·7H 2 o 0.375mM KNO 3 14mM (NH 4 )2SO 4 1.75mM CaCl 2 2H 2 o 0.55mM K H 2 PO 4 1.5mM MnSO 4 ·H 2 o 3μM
[0043] h 3 BO 3 40μM ZnSO 4 ·7H 2 o 1.75μM KI 3μM Na 2 MoO 4 2H 2 o 0.5μM CuSO 4 ·5H 2 o 0.4μM CoCl 2 ·6H 2 o 0.2μM niacin 20μM Vitamin B1 7.5μM Vitamin B6 12μM FeSO 4 0.19mM Inositol 0.275mM sucrose 1% agar 0.9%
[0044] The solid rooting medium 1 contains 1 mg / mL of indole butyric acid prepared with 75% alcohol, and the final concentration of indole butyric acid in the solid rooting medium 1 is 0.4 mg / L when it is in a high-temperature liquid state. The preparation meth...
Embodiment 3
[0050] The difference with Example 2 is: the final concentration of indolebutyric acid in solid rooting medium 1 is 0.2 mg / L when it is in a high-temperature liquid state, and the height of solid rooting medium 1 is 3 / 5 of the height of tissue culture tube 2 , on the solid rooting medium 1 in each tissue culture tube 2, inoculate 4 alfalfa seedlings to be rooted with a height of 1~2cm, and others are the same as in Example 2.
[0051] Table 2 is taking the rooting of Medicago truncatula tissue culture seedlings as an example, using the comparison of the inventive method and the conventional embedded rooting method;
[0052] Table 2 Comparison of the effects of two rooting methods after rooting culture of Medicago truncatula tissue culture seedlings for 2 weeks
[0053] rooting method Rooting rate root growth rate average root length Number of side roots Stem height Transplanting survival rate The method of the invention 95% 30mm / week 50mm 3~10...
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