Dunaliella salina CPD photolyase, photolyase liposome prepared from the same and preparation method for the photolyase liposome
A technology of Dunaliella salina and photolytic enzyme lipid, applied in the field of biology, can solve problems such as production reduction, and achieve a good effect of repairing ultraviolet damage
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Embodiment 1
[0021] Cloning of the CPD photolyase gene from Dunaliella salina.
[0022] 1. Collection of Dunaliella salina
[0023] Dunaliella salina was purchased from the algae bank of Wuhan Institute of Hydrobiology, Chinese Academy of Sciences.
[0024] 2. Poly A+RNA isolation (Poly A+RNA isolation)
[0025] Total RNA of Dunaliella salina was extracted with Trizol reagent (Invitrogen, USA). The quality of total RNA was identified by formaldehyde denaturing gel electrophoresis.
[0026] 3. Synthesis of cDNA by RT-PCR
[0027] Using a reverse transcription kit (TaKaRa RNA PCR Kit (AMV) ver.2.1), follow the instructions to reverse transcribe RNA into cDNA.
[0028] 3. Full-length cloning of Dunaliella salina CPD photolyase gene (Cloning of Full-length cDNA)
[0029] According to the amino acid conserved sequence of CPD photolyase gene of known species (such as Chlamydomonas, Arabidopsis, cucumber, spinach, rice, etc.), degenerate primers were designed, and the principle of homologous...
Embodiment 2
[0042] Sequence Analysis of CPD Photolyase Protein from Dunaliella salina
[0043] The full-length sequence of Dunaliella salina CPD photolyase and its coding sequence were subjected to nucleotide and amino acid BLAST on NCBI, and it was found that there was no obvious sequence homology in the nucleic acid database. At the amino acid level, it has 52% identity with Chlamydomonas reinhardtii CPD photolyase, 48% identity with cucumber (Cucumissativus) CPD photolyase, and rice (Oryza sativa) CPD photolyase. 47% identity, and 49% identity with Arabidopsis thaliana CPD photolyase.
Embodiment 3
[0045] Construction of Expression Vector of CPD Photolyase Gene of Dunaliella salina
[0046] According to the full-length coding sequence of Dunaliella salina CPD photolyase gene, primers were designed to amplify the complete coding reading frame, and restriction enzymes BamHI and SalI restriction sites were introduced into the forward and reverse primers respectively. After PCR amplification, the Dunaliella salina CPD photolyase cDNA was connected to the vector pMD18-T, then digested with BamHI and XhoI, and further connected to the prokaryotic expression vector pGEX-4T-1. Then the constructed expression vector Transformed into Escherichia coli ultraviolet damage repair-deficient strain SY2 competent cells, picked a single clone, carried out enzyme digestion and PCR verification, the results proved that the Dunaliella salina CPD photolyase gene expression vector was successfully constructed.
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