Novel gene of virus original protease inhibitor as well as expression and application thereof
A protease inhibitor and protein technology, which is applied in the fields of genetic engineering and protein engineering, can solve the problem of few researches on protease inhibitors derived from microorganisms, and achieve the effect of strong poisonous killing and inhibition of protease activity
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example 1
[0024] Genomic DNA was extracted from overnight cultured bacterial liquid of Pathogenic Bacillus burgdorferi burgdorferi "BJFS" collected and screened in our laboratory, and PCR amplification was performed using the extracted genomic DNA as a template. Recover the PCR product and connect it with pMD18-Tvector to transform the competent cell DH5α, inoculate the transformed bacterial liquid on LB solid medium containing ampicillin, culture overnight at 37°C, pick positive colonies and inoculate them on LB liquid culture containing ampicillin solution, cultured at 200rpm / min for about 9h, extracted the plasmid, carried out double digestion and identification with restriction endonucleases BamHI and EcoRI, and sent the identified clones for sequencing. From the mass sequence sequencing results, protease inhibitor genes were obtained. The DNA sequence SEQ ID NO.1 of the gene (XbPI-1) of the present invention is the first report in the pathogenic bacteria of Nematophila burgdorferi,...
example 2
[0026] The DNA sequence SEQ ID NO.1 of Xenorhabdus bovienii protease inhibitor gene XbPI-1 obtained above, the encoded protein contains 119 amino acids, SEQ ID NO.2. After comparison in the database, the protein encoded by the protease inhibitor gene XbPI-1 has an amino acid sequence similarity of 77% and 60% to the protein encoded by the protease inhibitor gene Xenorhabdus nematophila and Photorhabdus sp.Az29 in the database. , Pectobacterium chrysanthemi amino acid sequence similarity is less than 60%.
example 3
[0028] According to the full-length sequence of the XbPI-1 gene obtained in Example 1, the pQE30UA expression vector was used to recover the PCR product obtained in Example 1 by electrophoresis, and the recovered gene fragment was ligated with the pQE30UA expression vector at 16°C for 2 hours to transform the large intestine Bacillus M15 competent cells were spread on LB solid medium (containing Amp and Kana antibiotics), and the obtained resistant colonies were picked and cultured in liquid LB medium for preliminary identification by PCR, extraction of plasmids for sequencing, and confirmation The reading frame of the constructed expression vector was correct.
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