Descurainiasophia cold-resisting gene DsCOR gene, preparation method and application thereof
A technology of Artemisia annua and gene, applied in the field of cold resistance gene DsCOR of Artemisia annua and its preparation, can solve problems such as the research gap of cold resistance gene, and achieve the effects of improving cold resistance, cold resistance and cold resistance.
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Embodiment 1
[0033] Example 1 Preparation of Artemisia indica cold resistance gene DsCOR
[0034] 1. Cloning of cold resistance gene DsCOR of Artemisia indica
[0035] (1) The source of Artemisia persicae:
[0036] Seeds of Artemisia sophia (Descurania sophia L) were purchased from Chengdu Seed Company, Sichuan Province;
[0037] (2) Cultivation of materials:
[0038] After the seeds of Artemisia persicae were sterilized, they were sown in the 0 In the culture tank of the culture medium, culture at 25°C for 4 weeks, place the sterile seedlings at 4°C for low temperature stress, wherein the photoperiod is 16h light, 8h dark, and low temperature treatment for 3d;
[0039] (3) PolyA+RNA isolation (PolyA+RNAisolation):
[0040] Use Trizol reagent (Invitrogen) to extract cold-acclimated Artemisia annua total RNA, the extracted total RNA is subjected to 1% non-denaturing agarose gel electrophoresis, and then analyzed its quality by scanning ultraviolet light with a wavelength of 280nm;
[0...
Embodiment 2
[0078] Example 2 Containing the construction of Artemisia indica cold-resistant gene DsCOR recombinant plasmid
[0079] According to the coding sequence of Artemisia persicae cold resistance gene DsCOR of the present invention, design the primer that amplifies ORF, and introduce restriction enzyme site BamHI and SacI respectively on forward primer and reverse primer, also must have on the carrier The same restriction enzyme cutting site, and can make the target fragment inserted into the vector in the correct direction, so as to construct the recombinant plasmid containing the ORF of the cold-resistant gene DsCOR of Artemisia annua. Using the above-mentioned recombinant plasmid as a template, after PCR amplification, the cDNA of the cloned Artemisia persicae cold resistance gene DsCOR was inserted into the plant expression vector pBI121 or p2301G. The restriction sites of the two vectors are the same, both BamH1 and Sac1 , and then the recombinant expression vector was transfo...
Embodiment 3
[0080] Example 3 Preparation of Artemisia indica cold-resistant protein DsCOR
[0081] (1) Construct the prokaryotic expression vector pET32a-DsCOR, and transform Escherichia coli BL21:
[0082] The product amplified by the primers at both ends of the ORF was gel-recovered for the target fragment, that is, the ORF fragment of the COR gene of Artemisia indica, and double-digested with restriction endonucleases BamHI and SacI. The prokaryotic expression vector pET32a was also digested with BamHI and SacI. The carrier and DNA fragments were mixed at a molar ratio of 1:3, ligated with the DNA Ligase Kit Ver.2 kit, and left overnight at 16°C. The ligation product was transformed into BL21 competent cells, and positive clones were selected;
[0083] (2) Induced expression and SDS-PAGE detection of cold-resistant protein DsCOR of Artemisia indica:
[0084] Inoculate the verified Escherichia coli BL21 containing plasmid pET32a-COR into LB medium containing Amp with 1% inoculum amou...
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