Antibacterial protein and preparation method and application thereof
An antibacterial protein and reaction technology, applied in the fields of biochemistry and molecular biology, can solve the problems of antibacterial protein’s killing effect on bacteria, low content of natural antibacterial protein, and inability to meet application needs, so as to prevent and treat infectious diseases, reduce Production costs, effects of overcoming adverse consequences
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Embodiment 1
[0026] Embodiment 1: Synthesis contains the DNA product of antibacterial protein gene
[0027] According to the amino acid sequence of the antibacterial protein, the gene sequence was designed (as shown in sequence 2 in the sequence listing), and four pairs of primers were synthesized with a DNA synthesizer: primer P1 shown in sequence 3 in the sequence listing and primer R1 shown in sequence 4 in the sequence listing , primer P2 shown in sequence 5 in the sequence listing and primer R2 shown in sequence 6 in the sequence listing, primer P3 shown in sequence 7 in the sequence listing and primer R3 shown in sequence 8 in the sequence listing, sequence 9 in the sequence listing The primer P4 shown and the primer R4 shown in sequence 10 in the sequence listing. Primer P4 introduces an EcoRI restriction site (GAATTC) and a methionine codon (ATG), and primer R4 introduces a stop codon and an EcoRI restriction site. Methionine was introduced to remove the increased N-terminal fusio...
Embodiment 2
[0032] Example 2: Construction of pPIC9K recombinant plasmid containing antibacterial protein gene. The specific process is:
[0033] (1) Digest the DNA product in step (4) of Example 1 with EcoRI.
[0034] (2) The pPIC9K plasmid was digested with EcoRI and dephosphorylated with CIAP alkaline phosphatase.
[0035] (3) Electrophoresis and recovery of the digested DNA product and pPIC9K, ligation with T4 DNA ligase at 16°C for 4 hours, transformation of the ligation product into Escherichia coli TOP10 strain, selection of single colony on LB medium containing ampicillin resistance, and expansion culture Plasmids were then extracted.
[0036] (4) The PCR method was used to screen the pPIC9K recombinant plasmid inserted into the antimicrobial protein gene. The PCR reaction conditions are: 1 μL of the plasmid to be detected, 1 μL each of primer α-Factor shown in sequence 12 in the sequence listing and primer R4 (10 μmol / L) shown in sequence 10 in the sequence listing, 10 μL of 2...
Embodiment 3
[0039] Example 3: Synthesis of the DNA product of the antimicrobial protein gene with histidine tag. The specific process is:
[0040] The steps are the same as in Example 1, except that primer R5 shown in sequence 13 in the sequence listing is used in step (4) to replace primer R4 shown in sequence 10 for PCR amplification to obtain the antimicrobial protein gene with histidine tag DNA product (see sequence 14 in the sequence listing), the process is as follows figure 1 shown. Primer R5 introduced a codon encoding six histidines (CATCACCATCACCATCAC), a stop codon (TAA) and an EcoRI restriction site (GAATTC).
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