Natural antimicrobial peptides and application thereof
An antibacterial peptide, a natural technology, applied in the field of biomedicine, can solve the problem of high production cost of antibacterial peptides, and achieve the effect of significant bacteriostatic activity, broad application value and market prospect, and good bactericidal effect.
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Embodiment 1
[0037] Example 1 Discovery of natural antimicrobial peptides and Plectasin similar to fungal defensins
[0038] Through searching, two polypeptide sequences derived from Scedosperium apiospermum and Emmonsia parva UAMH 139 were found from the fungal proteome data of the UniProt database (http: / / www.uniprot.org / ) (A0A084GET2, A0A0H1BJF3). The group of polypeptide sequences and their functional regions are respectively shown in SEQ ID NO: 1-2 and SEQ ID NO: 3-4.
[0039]The group of polypeptide full-length gene sequences was compared with the blastX software (https: / / blast.ncbi.nlm.nih.gov / Blast.cgi?PROGRAM=blastx&PAGE_TYPE=BlastSearch&LINK_LOC=blasthome) of the NCBI website, and the results showed that the The encoded product of the gene may be the precursor of antimicrobial peptide of fungal defensin family. The polypeptide precursor sequences encoded by this group of genes were further compared with the protein blast software (https: / / blast.ncbi.nlm.nih.gov / Blast.cgi?PROGRA...
Embodiment 2
[0040] Embodiment 2 antimicrobial peptide P5, P6 gene synthesis
[0041] Antimicrobial peptide P5-P6 gene sequences (SEQ ID NO: 5-6) were designed according to the codon preference of Pichia pastoris. In order to ensure the integrity of the sequence during expression, an XhoI restriction site and a Kex2 restriction site were added to the 5' end of the mutant gene sequence, and a TAA, TAG terminator sequence and XbaI restriction site were added to the 3' end. The above sequence was completed by Shanghai Sangon Bioengineering Co., Ltd.
Embodiment 3
[0042] Example 3 Construction of Pichia pastoris inducible expression vector pPICP5-pPICP6
[0043] The synthetic gene fragment and vector pPICZαA were double-digested with restriction endonucleases XhoI and XbaI respectively, the vector fragment of pPICZαA and the antimicrobial peptide gene fragment were recovered, and ligated to obtain vectors pPICP5-pPICP6;
[0044] The detailed construction process of the vector pPICP5~pPICP6: use the restriction endonuclease XhoI and XbaI to carry out double enzyme digestion on the synthesized gene fragment and pPICZαA respectively, the enzyme digestion system and conditions are as follows:
[0045]
[0046] After adding the above enzyme digestion system, react at 37°C for 3 hours, and detect by 2% agarose gel electrophoresis, electrophoresis conditions: 130V, 30min. After electrophoresis, use a scalpel to cut the electrophoretic bands corresponding to the carrier fragment and the gene fragment under the ultraviolet light, and use the ...
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