A method for rapid propagation of Striga in tissue culture
A technology of tissue culture and Striga, which is applied in the field of plant tissue culture, can solve the problems of low germination rate, scarce wild Striga resources, and small Striga seeds, so as to shorten the seedling time, save planting costs, and improve reproduction effect of ability
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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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