Preparation and expression method of chicken beta-defensin 9 yeast engineered bacteria
An expression method and technology of engineering bacteria, which are applied in the fields of biotechnology and genetic engineering pharmaceuticals, can solve the problems of inconvenient operation and long production cycle of foreign proteins, and achieve the effects of simple operation, avoiding waste of host expression potential, and good stability
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Embodiment 1
[0048] In the present invention, the recipient bacterium is Pichia pastoris GS115, and the carrier plasmid is pGHKα; the target gene is a codon-optimized nucleotide fragment corresponding to 41 amino acids; The chicken AvBD9 target gene fragment was inserted between them; the recombinant plasmid was digested and linearized by SacⅠ and BglⅡ sequentially, and then electrotransformed into highly efficient Pichia pastoris GS115 competent cells; positive recombinants were screened out by MD plate primary screening and PCR identification, and G418 antibody High-copy recombinants were screened, and high-expression strains were selected by protein expression level, and then fermented and cultured, the expression product was directly secreted outside the cell, and the supernatant obtained by centrifugation contained the expressed target protein product - AvBD9.
Embodiment 2
[0050] The specific operation steps of the chicken β-defensin 9 yeast engineering bacteria preparation and expression method are as follows:
[0051] (1) Codon optimization and synthesis of the AvBD9 gene sequence, the optimized gene sequence is as follows figure 1 Shown, upper row: original sequence. Lower row: codon-optimized sequences. Bold font: modified bases. Underline: restriction endonuclease cleavage site. Italics: coding sequence of protease Kex2 restriction site. Inside the box: stop codon;
[0052] According to the AvBD9 gene sequence published by GenBank (accession number: AY534894.1), referring to the preferred codons of Pichia pastoris, the DNASTAR software was used to optimize the gene sequence without changing the amino acid sequence, and EcoRI restriction enzyme was added to the 5′ end of the gene site and Kex2 restriction site coding sequence AAAAGA, add TAA site and NotⅠ restriction site at the 3′ end of the gene, the optimized gene is 146bp in length,...
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