A kind of genetic transformation method of larch embryogenic cells
A genetic transformation method, embryogenic cell technology, applied in sterilization methods, biochemical equipment and methods, methods of supporting/immobilizing microorganisms, etc., can solve the lack of systematicness, slow progress in genetic transformation research, and lack of regeneration systems question
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Embodiment 1
[0080] Example 1, Construction of recombinant plasmid pSuper::MIR156 and preparation of recombinant Agrobacterium GV3101 / MIR156
[0081] 1. Construction of recombinant plasmid pSuper::MIR156
[0082] 1. Design primer pairs
[0083] The coding sequence of the miR156 precursor is shown in Sequence 1 of the Sequence Listing, and a primer pair (composed of M156F and M156R) was designed at a position greater than 90 bp at both ends of the stem-loop structure sequence.
[0084] M156F: 5'-CCC AAGCTT TTGTACTCAGCCGACAGAA-3';
[0085] M156R: 5'-GG ACTAGT CCTCTAGCGGTAAATCTCAA-3'.
[0086] 2. Genomic DNA of Japanese larch was extracted as a template, and the composition of M156F and M156R was used for PCR amplification to obtain PCR amplification products.
[0087] 3. Digest the PCR amplification product obtained in step 2 with restriction endonucleases Hind III and Spe I, and recover the digested product.
[0088] 4. Digest the Super1300 vector with restriction endonucleases Hind...
Embodiment 2
[0092] Embodiment 2, genetic transformation of larch
[0093] For the flow chart of genetic transformation, see figure 1 .
[0094] 1. Preparation and pre-cultivation of receptor materials
[0095] 1. Inoculate Japanese larch embryogenic cells into S 0 On the culture medium, cultured statically at 23°C and in the dark for 15 days.
[0096] 2. After completing step 1, pick about 1g of embryogenic cells with vigorous growth on the surface, and add 92ml Y 0 In a 250ml Erlenmeyer flask with culture medium, shake culture at 100rpm under 23°C and dark conditions. Subculture once every 7 days (the method of each subculture is as follows: get about 1g of embryogenic cells, add 92ml Y 0 medium in a 250ml Erlenmeyer flask, 23°C, 100rpm shaking culture under dark conditions). On the 7th day of subculture, 1 mg of acetosyringone was added to each flask, and the timing was started from the addition of acetosyringone. After 12 hours, embryogenic cells were taken as the recipient mater...
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