Method for culturing wheat tissue capable of overcoming gene disturbance
A tissue culture and genotyping technology, applied in horticultural methods, botanical equipment and methods, plant phenotype improvement, etc. Effects of regeneration frequency, improving tissue culture efficiency, and overcoming genotypic barriers
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Embodiment 1
[0021] The young ear of embodiment 1 different development stages is to the response of in vitro culture
[0022] A plant material: 5 varieties (lines) of 6756, 8581, H89, 311 and 1772 were selected.
[0023] B sampling period: the two-edge stage (1mm), the glume primordium formation stage (2mm), the floret primordium formation stage (2.5mm), the pistil primordium formation stage (4mm), and the connective differentiation stage (6mm) and the young ears of the tetrad formation stage (10mm) stage are carried out in vitro culture, wherein, the young ears of the drug interval stage and the tetrad stage are cut into 2-3 sections for culture. 0.1% HgCl before inoculation 2 Disinfect for 8-10 minutes, rinse with sterile water 3-5 times, use tweezers and a dissecting needle to peel off the young ears, and plant them on the induction medium.
[0024] C medium
[0025] The induction medium is MS+2, 4-D (2mg / l);
[0026] The differentiation medium is MS basic medium;
[0027] Sprout ...
Embodiment 2
[0059] The response of different explants of embodiment 2 to in vitro culture
[0060] The material selection and cultivation method of A suitable young ear are the same as above;
[0061] B Immature Embryo Selection and Culture Method
[0062] Operation steps: a. Take immature embryos 14 days after flowering, and use 0.1% HgCl 2 Disinfect for 8-10 minutes, rinse with sterile water 3-5 times, use tweezers and dissecting needles to peel off immature embryos, inoculate on induction medium and culture in dark for 25-30 days; b. Transfer callus to differentiation medium Carry out differentiation (25-30 days); c. The green shoots are transferred to the strong root medium.
[0063] Medium and culture conditions: induction medium is MS+2, 4-D (2mg / l); differentiation medium is MS basic medium; strong root medium is 1 / 2MS+IAA2mg / l. In the callus induction period, culture in the dark at room temperature (25±1)°C; in the green seedling differentiation stage, culture in the room tempe...
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