Tissue culture and rapid propagation method of striga asiatica
A tissue culture and Striga technology, applied in the field of plant tissue culture, can solve the problems of scarcity of wild Striga resources, tiny Striga seeds, and low germination rate, saving planting costs, improving reproductive capacity, and shortening seedling breeding. effect of time
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Embodiment 1
[0027] A tissue culture rapid propagation method of Striga is characterized in that, it is processed by the following steps:
[0028] 1) picking wild Striga plants, cutting into sections so that each section contains an axillary bud;
[0029] 2) put the sectioned plants containing axillary buds in step 1) into 0.1% mercuric chloride solution for disinfection for 8-10 minutes, and then wash them three times with sterile water, each time for 2-3 minutes;
[0030] 3) Inoculate the section plants containing axillary buds in step 2) into the induction medium for cultivation on the ultra-clean workbench, wherein the induction medium is composed of the following components: 1L MS medium is added with 3mg 6-BA and 0.1mg IBA, then use NaOH to adjust the pH of the induction medium to 5.5-6.2, and cultivate it under the artificial light intensity of 1900-2100Lx and the temperature of 25-35°C until adventitious buds grow, and then transfer the adventitious buds to Carry out multiple subc...
Embodiment 2
[0035] A tissue culture rapid propagation method of Striga is characterized in that, it is processed by the following steps:
[0036] 1) picking wild Striga plants, cutting them into sections so that each section contains a terminal bud;
[0037] 2) put the sectioned plant containing terminal buds in step 1) into 0.1% mercuric chloride solution for disinfection for 8-10 minutes, and then wash with sterile water three times, each time for 2-3 minutes;
[0038] 3) On the ultra-clean workbench, inoculate the sectioned plants containing terminal buds in step 2) into the induction medium for cultivation, wherein the induction medium is composed of the following components: 3mg 6-BA is added to 1L MS medium and 0.1mg IBA, then use NaOH to adjust the pH of the induction medium to 5.5-6.2, and cultivate it under the artificial light intensity of 1900-2100Lx and the temperature of 25-35°C until adventitious buds grow, and then transfer the adventitious buds Carry out multiple inductio...
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