Method for cultivating detoxification tissue culture bulb of hyacinth
A cultivation method and daffodil technology, applied in horticultural methods, botanical equipment and methods, cultivation, etc., can solve the problems of high virus carrying rate, difficulty in separation and purification, and low reproduction rate, so as to achieve rapid proliferation, ensure safety and quality, Eliminate the effect of carrying and spreading
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Embodiment 1
[0041] A method for cultivating the detoxified tissue-cultured bulbs of narcissus, carried out as follows:
[0042] (1) The preparation of the culture medium, including the basic medium and the components of the culture medium at each stage of tissue culture and the weight per liter are:
[0043] 1) Basic medium: MS medium for subbulb induction, proliferation and bulb growth medium, and 1 / 2 MS medium for rooting medium; wherein, the agar is 8g / L, and the pH is 5.7;
[0044]2) Daughter bulb induction medium: MS+BA 0.5mg / L and NAA 0.1mg / L of 30g / L sucrose;
[0045] 3) Daughter bulb proliferation medium: white sugar 40g / L MS+BA 0.1mg / L and NAA 0.5mg / L;
[0046] 4) Bulb growth medium: white sugar 40g / L MS+BA 0.05mg / L and NAA 0.1mg / L;
[0047] 5) Rooting medium: 1 / 2 MS+NAA 0.25mg / L of white sugar 20g / L.
[0048] (2) The cultivation of narcissus detoxified tissue culture bulbs:
[0049] 1) Bulb low-temperature treatment: the bulb is subjected to low-temperature treatment at 8°C ...
Embodiment 2
[0094] The agar in the basic medium of the present embodiment is 7g / L, and the pH is 5.6; the subbulb induction medium is: MS+BA 0.1mg / L and NAA 0.3mg / L of sucrose 20g / L; the subbulb proliferation medium is : white sugar 20g / L MS+BA 0.5mg / L and NAA 0.1mg / L; bulb growth medium: white sugar 30g / L MS+BA 0.02mg / L and NAA 0.25mg / L; rooting medium is: White sugar 40g / L 1 / 2 MS+NAA 0.45mg / L; bulbs were treated at 8°C for 2 weeks at low temperature; bulb shoots were soaked in 75% alcohol for 0.5 minutes, and 0.1% mercuric chloride aqueous solution for 10 minutes; induction, proliferation, The culture conditions of each stage of growth and rooting are: temperature 25±2° C., light intensity 1500 Lx, and light time 10 h / d;
Embodiment 3
[0096] The agar in the basic medium of this embodiment is 9g / L, and the pH is 5.8; the subbulb induction medium is: sucrose 40g / L MS+BA1mg / L and NAA 0.5mg / L; the subbulb proliferation medium is: white sugar 30g / L MS+BA 0.3mg / L and NAA 1mg / L; bulb growth medium: white sugar 20g / L MS+BA0.09mg / L and NAA 0.5mg / L; rooting medium: white sugar 30g / L 1 / 2 MS+NAA 0.1mg / L of L; the bulbs were treated at 8°C for 4 weeks at low temperature; the bulb shoots were soaked in 75% alcohol for 1.0 minutes, and 0.1% mercuric chloride aqueous solution for 15 minutes; induction, proliferation, growth, rooting The culture conditions of each stage are: temperature 25±2°C, light intensity 2500 Lx, light time 10h / d; other steps and processes are the same as in Example 1.
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