Method for expressing salmon calcitonin and special expression cassette for method
A salmon calcitonin and expression cassette technology, which is applied in the fields of calcitonin, chemical instruments and methods, botanical equipment and methods, etc., can solve the problems of chemical synthesis with many steps, low yield and high price, and achieve important The effect of applying value
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Embodiment 1
[0064] Example 1. Expression of salmon calcitonin by transgenic rapeseed expression system
[0065] 1. Construction of recombinant plasmid pPha(p / gc / t)2300
[0066] 1. Artificially synthesize the double-stranded DNA molecule shown in sequence 1 in the sequence listing. In Sequence 1 in the sequence listing, the 1st to 6th positions from the 5' end are the recognition sequence of the restriction endonuclease SacI, the 7th to 1625th are the nucleotide sequence of the promoter of phaseolin storage protein, and the 1626th to 1631st The bit is the recognition sequence of the restriction endonuclease KpnI.
[0067] 2. Digest the double-stranded DNA molecule synthesized in step 1 with restriction endonuclease SacI and KpnI, and recover 1631bp DNA fragment A.
[0068] 3. Digest the vector pCAMBIA2301 with restriction endonucleases SacI and KpnI to recover the vector skeleton A of about 11.6bp.
[0069] 4. Linking the DNA fragment A and the vector skeleton A to obtain the intermedia...
Embodiment 2
[0189] Example 2. Expression of salmon calcitonin by transgenic rapeseed expression system
[0190] According to the method of step 1 to step 3 of Example 1, the recombinant plasmid pPha(p / gc / t)2300 in step 1 was replaced with recombinant plasmid pPha(p / gc / t)2300-DZ, and other steps were all unchanged, and obtained Salmon calcitonin solution; yields 0.15 mg salmon calcitonin (at 100% purity) per 10 g rapeseed.
[0191] The construction method of the recombinant plasmid pPha(p / gc / t)2300-DZ is as follows: according to the method of step 1 of Example 1, in step 13, "artificially synthesized double-stranded DNA molecule shown in sequence 4 in the sequence listing" is replaced with " Artificially synthesize the double-stranded DNA molecule shown in Sequence 8 in the Sequence Listing", and keep other steps unchanged to obtain the recombinant plasmid pPha(p / gc / t)2300-DZ. The recombinant plasmid pPha(p / gc / t)2300-DZ also expresses the fusion protein A shown in sequence 6 in the sequen...
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