An immunoprotective Photobacterium mermaid hemolysin hly ch protein
A photobacillus, immune protection technology, applied in the biological field, can solve the problems of economic loss, rapid morbidity and high mortality
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Embodiment 1
[0051] Bacterial hemolytic activity observation
[0052] Prepare sheep blood and rabbit blood plates respectively, pick a single colony of Photobacterium mermaidus MCCC 1K03226, streak on the sheep blood and rabbit blood plates, incubate at 30°C for 24 hours, and observe the hemolytic activity. The results are as follows: figure 1 and figure 2 As shown, in which Figure 1 is sheep blood, figure 2 For rabbit blood. Depend on figure 1 and figure 2 It can be seen that the bacterium exhibits β-type hemolysis on the sheep blood and rabbit blood plates, showing that the bacterium has very strong hemolytic activity.
Embodiment 2
[0053] Example 2 Recombinant vector pMD18T-hly ch build
[0054] Download the whole genome sequence of Photobacterium damselae subsp.Damselae CIP 102761 (PhddCIP102761, gene accession number: NZ_ADBS00000000) from NCBI, find dly, hlyA pl and hlyA ch Gene sequence, designed primers, the primer sequence is shown in Table 1; wherein the dly gene sequence is SEQ ID NO: 1; hlyA pl The gene sequence is SEQ ID NO: 2; hlyA ch The gene sequence is SEQ ID NO:3. Use the bacterial genome extraction kit to extract the genomic DNA of the strain MCCC 1K03226 DNA, use the genomic DNA as a template, and use the primers in Table 1 to amplify by touchdown PCR. After the reaction, use 1% agarose gel electrophoresis. The results are as follows: image 3 , wherein primer Dly-f checks, Dly-r checks and amplifies the length of Dly gene part, is used for detecting hemolysin Dly protein; Primer Hly pl -f check, Hly pl -r detection amplification Hly pl Gene portion length for detection of plasmid...
Embodiment 3
[0061] Example 3 Recombinant expression vector pET32a-hly ch Construction and prokaryotic expression
[0062] Use restriction endonuclease BamH I and Sal I to pMD18T-hly ch Carry out double digestion with the expression vector pET32a(+), recover the digested products by gel electrophoresis and mix them at a ratio of 3:1, connect at 22°C for 2 hours, transform the conjugate into E. coli competent DH5α, and spread it on the Incubate overnight at 37°C on LB plates. Pick a single colony and shake it, and use the vector universal primers for PCR identification. Pick positive colonies to expand culture, save the strain and extract the plasmid, the recombinant plasmid is marked as pET32a-hly ch .
[0063] The extracted recombinant plasmid was transformed into the expression strain BL21, spread on the LB solid plate containing Amp, and cultured overnight at 37°C. Pick a single colony on the Amp plate and shake overnight, inoculate 1mL of the bacterial solution into 100mL liquid L...
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