Anthurium adndraeanum pollen culture method
A technology of pollen culture and anthurium, applied in the field of plant tissue culture, to achieve the effects of innovation of germplasm resources, short time to embryo formation, and great practical value
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Embodiment 1
[0019] A method for cultivating anthurium pollen, comprising the following steps,
[0020] 1) Inoculate 1000 grains of pollen from the mononuclear marginal stage into a callus induction medium, and culture to obtain a callus. The callus induction medium: WPM+NAA 0.3mg / L+6-BA 0.2mg / L L+2.4-D 0.4mg / L+Gibberellin 2.2mg / L+Agar 1500mg / L+Sucrose 600mg / L;
[0021] 2) inoculate the differentiation medium, cultivate and obtain test tube seedlings, and the described differentiation medium is WPM+6-BA 0.4mg / L+NAA 0.1mg / L+ZT 0.6mg / L+600mg / L sucrose;
[0022] 3) Inoculate the rooting medium and screen to obtain single plants. The rooting medium is 1 / 2WPM+IBA 0.1mg / L+NAA0.6mg / L+agar 600mg / L+sucrose 1400mg / L+activated carbon mass ratio 0.1%.
[0023] The culture conditions adopt the method of combining light culture and dark culture. The light culture light source adopts fluorescent lamps. The daytime temperature in the culture room is 28°C, the lighting is 12h, and the light intensity is 1...
Embodiment 2
[0026] A method for cultivating anthurium pollen, comprising the following steps,
[0027] 1) Inoculate the pollen at the marginal stage of mononuclei into the callus induction medium, and culture to obtain the callus. The callus induction medium: WPM+NAA0.5mg / L+6-BA0.4mg / L+ 2.4-D 0.7mg / L+ gibberellin 2.5mg / L + agar 1700mg / L+ sucrose 800mg / L;
[0028] 2) inoculate the differentiation medium, cultivate and obtain test tube seedlings, and the described differentiation medium is WPM+6-BA 0.6mg / L+NAA 0.3mg / L+ZT 1mg / L+800mg / L sucrose;
[0029] 3) Inoculate the rooting medium and screen to obtain single plants. The rooting medium is 1 / 2WPM+IBA 0.3mg / L+NAA 0.8mg / L+agar 800mg / L+sucrose 1600mg / L+activated carbon mass ratio 0.3%.
[0030] The culture conditions adopt the combination of light culture and dark culture. The light culture light source adopts fluorescent lamps. The daytime temperature in the culture room is 30°C, the lighting is 12h, and the light intensity is 20μmol.m -2 ...
Embodiment 3
[0033] A method for cultivating anthurium pollen, comprising the following steps,
[0034] 1) Inoculate the pollen at the marginal stage of mononuclei into the callus induction medium, and culture to obtain the callus. The callus induction medium: WPM+NAA 0.4mg / L+6-BA 0.3mg / L+ 2.4-D 0.6mg / L+ gibberellin 2.4mg / L + agar 1600mg / L+ sucrose 700mg / L;
[0035] 2) Inoculate the differentiation medium, cultivate and obtain the test tube seedlings, the differentiation medium is WPM+6-BA 0.5mg / L+NAA 0.2mg / L+ZT 0.8mg / L+700mg / L sucrose;
[0036] 3) Inoculate the rooting medium and screen to obtain single plants. The rooting medium is 1 / 2WPM+IBA 0.2mg / L+NAA0.7mg / L+agar 700mg / L+sucrose 1500mg / L+activated carbon mass ratio 0.2%.
[0037] The culture conditions adopt the combination of light culture and dark culture. The light culture light source adopts fluorescent lamps. The daytime temperature in the culture room is 29°C, the lighting is 12h, and the light intensity is 17μmol.m -2 .s -1 ...
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Abstract
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Application Information
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