Culture medium combination for tissue culture and rapid propagation of Lilium medogense, tissue culture and rapid propagation method and application
A technology of tissue culture and medium of lily, applied in the directions of medium, application, planting substrate, etc., to achieve the effects of rapid reproduction, solving sporadic distribution in the field, and simplifying steps
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Embodiment 1
[0060] Example 1 induced differentiation medium and screened embodiment
[0061] After taking on the scales of lily bulbs Motuo explants, washed first with tap water on the soil flakes, with 10% of the gold Wan spray disinfectant 8min, through the filtered water washed three times to get clean bench after disinfection with 75% alcohol 10s, sterile water 3 times, and then sterilized with 0.1% mercuric chloride for 7min, washed in sterile water 3-5 times to obtain explants sterilized aside.
[0062] The explants were inoculated in the sterilized following five kinds of induction and differentiation medium, the medium bottle a flat scales, concave upwardly. The above-mentioned five kinds of induction and differentiation medium were as follows: 1) modified MS medium (1x trace element) + 0.1mg / l 6-BA + 0.1mg / L NAA; 2) modified MS medium (Trace Elements plus 1x) + 0.2mg / l 6-BA + 0.2mg / LNAA; 3) modified MS medium (1x trace element) + 0.5mg / l 6-BA + 0.5mg / L NAA; 4) improvement...
Embodiment 2
[0067] Example 2 Screening proliferation embodiment subculture medium
[0068] (Same as Example 1 MS medium modified embodiment of the same) to modified MS medium for proliferation and minimal medium culture medium following screening hormone, cytokinin 6-BA 5 disposed gradients were 0.1mg / L , 0.5mg / L, 1.0mg / L, 1.5mg / L and 2.0mg / L, and NAA provided two gradients were 0.5mg / L and 1.0mg / L, for uniform design, selection of optimal proliferation and subculture medium. Each subculture medium added further with sucrose 45g / L, agar 5g / L, pH6.0. Following culture proliferation and conditions as follows: light intensity 1800LUX, a temperature of 25 ℃, photoperiod 10L: 24D, the culture period 50d. Statistical results are shown in Table 2.
[0069] Table 2 Screening of proliferation and subculture medium
[0070]
[0071] NOTE: "-" indicates no callus; "+" indicates callus 0.1cm or less; "++" indicates callus 0.1cm above.
[0072] From the results of Table 2, when the pro...
Embodiment 3
[0073] Screening seedling and rooting medium Example 3
[0074] (Modified MS medium identical with Example 1 of the embodiment) to be substantially modified MS medium medium medium seedling and rooting hormone screening, cytokinin 6-BA 2 gradient provided, respectively 0.5mg / L and 1.0mg / L, and NAA provided two gradients were 0.5mg / L and 1.0mg / L, and seedling screening a suitable rooting medium. Each seedling and rooting medium further contains sucrose 45g / L, agar 5g / L, pH6.0. Rooting seedlings and conditions as follows: light intensity 1500-2000LUX, a temperature of 25 ℃, photoperiod 5L: 19D, the culture period 50d. Statistical 50d shoots induced situation. Statistical results are shown in Table 3.
[0075] Table 3 seedlings and rooting medium screening
[0076]
[0077] NOTE: "-" indicates no callus; "+" indicates callus 0.1cm or less; "++" indicates callus 0.1cm above.
[0078] From the results in Table 3, when the seedling and rooting medium was modified MS medium...
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