Sturgeon disease-resistant immune protein and preparation method and application thereof
A sturgeon protein technology, applied in the field of sturgeon disease-resistant immune protein and its preparation, to achieve the effects of inhibiting microbial infection, promoting development, and improving immunity
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Embodiment 1
[0044] Example 1 Obtaining of Sturgeon Interleukin-6 Gene and Construction of Expression Vector
[0045] 1. Acquisition of interleukin-6 gene from sturgeon
[0046] In order to study whether conditional stress such as immunogen stimulation or high temperature affects the immune function of sturgeon, the inventor's team carried out liver transcriptome sequencing of sturgeon under different conditions. For the expressed gene, the nucleotide sequence of its cDNA is shown in SEQ ID NO.2, and the amino acid sequence of its encoded protein is shown in SEQ ID NO.1. According to the homologous sequence comparison and protein structure simulation analysis, the gene is speculated The encoded protein is interleukin-6.
[0047] Amplification primers F carrying NcoI and XhoI restriction sites were designed according to the mRNA sequence of the interleukin-6 gene of the above-mentioned targeted sturgeon: (SEQ ID NO.3:C CCATGG CTCCTATTGTAGAATTTTC) and R (SEQ ID NO.4: CCG CTCGAG TCATACAAAT...
Embodiment 2
[0055] Example 2 Induced Expression and Purification of Siberian Acipenser IL-6 Recombinant Protein
[0056] 1. Induced expression of Siberian sturgeon IL-6 recombinant protein
[0057] Inoculate pET30a(+)-AbIL6-BL21 in LB medium containing kanamycin (50 ng / μL), and shake culture at 37°C until OD 600 About 0.6, add 1mM isopropyl-β-D-thiogalactoside, continue to cultivate for 6h, and collect the bacteria by centrifugation. Suspend the cells with 1 / 10 volume of medium in PBS, and add PMSF to a final concentration of 1mM. Under ice bath conditions, lyse the cells by 100W ultrasonic disruption, centrifuge to collect the supernatant and precipitate of the lysate, and perform SDS-PAGE electrophoresis analysis , the results showed that the Siberian sturgeon Il6 recombinant protein existed in the inclusion body ( figure 1 ).
[0058] 2. Purification of Siberian sturgeon IL-6 recombinant protein
[0059] Resuspend the sonicated pET30a(+)-AbIL6-BL21 cell pellet collected in BufferA ...
Embodiment 3
[0070] Example 3 Expression analysis of AbIL6 gene in different tissues of Siberian sturgeon
[0071] The relative expression of IL-6 gene in different tissues of healthy Siberian sturgeon was detected by real-time fluorescent quantitative PCR method, and the tissue distribution of AbIL6 mRNA was studied.
[0072] Specific operation method: randomly select 10 tissues of healthy Siberian sturgeon (about 150 g in weight), which are: gills, eyes, head kidney, spleen, heart, muscle, skin, liver, brain and intestine. Total tissue RNA was extracted by Trizol method and reverse transcribed into cDNA by Takara reverse transcription kit.
[0073] Primers for fluorescent quantitative PCR were designed according to the cDNA sequence of AbIL6, and the primer sequences were as follows:
[0074] SEQ ID NO.5: Abil6F: 5'-CACTGTCAGCGTTGCTGGTTC-3';
[0075] SEQ ID NO.6: Abil6R: 5'-GCCACTCGGCTAAAGATTCCC-3';
[0076] The primer sequence of the internal reference gene 18S rRNA is as follows:
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