The optimized gene of zebrafish defensin defbl3 and the preparation method of its recombinant protein
A defensin and zebrafish technology, applied in the field of genetic engineering, can solve the problems of troublesome post-processing of fermentation broth, no practical production application value, and high cost of culture medium, so as to facilitate later operations, save costs, and shorten the path of industrialization Effect
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Embodiment 1
[0039] Expression and purification of zebrafish recombinant defbl3 mature peptide in Pichia pastoris X-33
[0040] 1.1 Medium formula:
[0041] MGY (Minimal Glycerol Medium) medium: YNB 13.4g / L, biotin 4×10 -4 g / L, glycerol 10mL / L; MM (Minimal Methanol Medium) medium: YNB 13.4g / L, biotin 4×10 -4 g / L, methanol 10mL / L.
[0042] 1.2 Optimized synthesis of cDNA of mature peptide of zebrafish defbl3 and addition of enzyme cleavage sites
[0043] Referring to the cDNA sequence of zebrafish defensin defbl3 (GenBank: NM_001081555) published in GenBank, predict the cDNA sequence of its mature peptide (its nucleotide sequence is shown in SEQ ID NO: 1), according to the codon preference of Pichia pastoris Resistance to the original ACA, GTG, CAG, ACA, TGC, GGA, CGA, GGA, CTA, TGC, AGG, TGC, TAT, GCA, CGG, GAG, TAT, ATT, TAT, CGT, GGC, TGC, CCT, CGC, AGG, TGC, CGA, TTT and other codons have been optimized, and the optimized corresponding codons are ACT, GTT, CAA, ACT, TGT, GGT, AGA, G...
Embodiment 2
[0053] Antibacterial Activity of Recombinant Defensin defbl3 Mature Peptide by Agarose Diffusion Assay
[0054] The selected Gram-positive bacteria were Listeria monocytogenes (Listeria monocytogenes), Staphylococcus aureus (Staphylococcus aureus), and Bacillus cereus (Bacillus cereus), and the Gram-negative bacteria were Escherichia coli BL21 ( DE3), Escherichia coli DH5α, Escherichia coli ATCC25922, Vibrio parahaemolyticus, Salmonella, Pseudomonas aeruginosa. Cultivate the above-mentioned bacteria overnight in LB liquid medium, and then use fresh LB liquid medium to reduce the OD of the bacteria to 600Adjust it to 0.4, add it to the nutrient agar that has not yet solidified according to the dilution ratio of 1:1000, shake it well and pour it on the plate. After the plate solidifies, use a puncher to make a 6mm hole, add 50 μL of the expression supernatant, and use the pPICZαA empty plasmid The expression supernatant of the above-mentioned supernatant was used as a control, ...
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