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High-efficient expression of recombined swine IL 22 in escherichia coli and its application

A technology of porcine interleukin and Escherichia coli, which is applied in the field of biotechnology and genetic engineering, can solve problems such as unclear

Active Publication Date: 2018-05-25
NANJING AGRICULTURAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Whether porcine interleukin 22 can resist apoptosis by activating STAT3 signal and whether it can resist E. coli infection is still unclear

Method used

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  • High-efficient expression of recombined swine IL 22 in escherichia coli and its application
  • High-efficient expression of recombined swine IL 22 in escherichia coli and its application
  • High-efficient expression of recombined swine IL 22 in escherichia coli and its application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0048] Embodiment 1 Construction of recombinant plasmid pET-32a(+)-pIL-22

[0049] 1. Obtaining the recombinant porcine interleukin 22 gene fragment

[0050] OptimumGene was used with reference to the published gene sequence (GenBank accession number: KX588234.1) TM Gene design software, according to the preference of the host Escherichia coli E.coli BL21, remove the rare codons (AGA, GGA, CCC, CTA) of Escherichia coli, adjust the GC content of the sequence, optimize the codons, and design the recombinant porcine interleukin The 22 gene sequence is SEQ ID NO: 1, and then the homology arm CAGCCCAGATCTGG of the pET-32a(+) vector linearized by Kpn Ⅰ and Hind Ⅲ enzymes is added to the two ends of the SEQ ID NO: 1 gene sequence GTACC (SEQ ID NO:2) and CGAGTGCGGCCGCA AGCTT (SEQID NO: 3) (the underline is the enzyme cleavage site), the sequence was artificially synthesized (synthesized by Nanjing GenScript Biotechnology Co., Ltd.) to obtain the target fragment of the recombinant ...

Embodiment 2

[0053] Example 2 Verification of expressing porcine interleukin 22 recombinant Escherichia coli E.coli BL21 (DE3)

[0054] Take 1 μL (200ng / μL) of the recombinant plasmid pET-32a(+)-pIL-22 and add it to 50 μL of E. coli BL21(DE3) chemical transformation competent cells, flick it a few times, do not suck and blow, and put it on ice Leave it for 30min. Heat shock at 42°C for 90s in a water bath, incubate on ice for 5min, add 900μL of SOC medium, mix gently by inversion, put into a 37°C constant temperature incubator to recover for 10min, and place the recovered bacterial solution in a shaker at 37°C , 150rpm, cultivated for 40min, took out the bacterial solution, centrifuged at 5000rpm for 5min, discarded the supernatant, took 100μL of the bacterial solution and spread it on the ampicillin-resistant solid basal medium LB plate, and positive colonies could be seen in 12-16h. Pick colonies for verification, such as image 3 , 2-9 are colonies verified by PCR, the results show th...

Embodiment 3

[0058] Example 3 Extraction and Purification of Recombinant Porcine Interleukin 22 Expressed by Recombinant Escherichia coli E.coli BL21 (DE3)

[0059] The positive colony of the recombinant E. coli BL21 (DE3) obtained in Example 2 was picked and cultured overnight in LB medium containing ampicillin (50 μg / mL). Inoculate the overnight cultured bacterial solution in a new LB medium at a ratio of 1:100 for cultivation. When the OD value of the bacterial solution reaches 0.5, add IPTG to induce the expression of porcine interleukin-22 protein in recombinant E. coli, and induce at 15°C Two conditions were cultivated for 16h and induced for 4h at 37°C. 8000rpm, 10min, centrifuge to collect the bacteria. PBS was added to resuspend the bacteria collected by centrifugation, and the resuspension was ultrasonically disrupted. After crushing, centrifuge at 14000rpm for 30min. Collect the supernatant and precipitate for SDS-PAGE and Western blot verification. The results show that the ...

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Abstract

The invention discloses a gene for encoding recombined swine IL 22. The invention further discloses a recombined expression carrier containing a recombined gene, a transgene cell system, a transgene recombined bacterial and a host cell. The invention further discloses a recombined swine IL 22 and its extraction and purification method. The invention further discloses an application of recombined plasmid pET-32a(+)-PIL-22, recombined strain and recombined protein in anti-apoptosis and prevention of escherichia coli infection. The carrier pET-32a(+) of the expression recombined swine IL 22 structured in the invention contains His label, the recombined swine IL 22 protein extracted from escherichia coli is connected with the His label; through a His pillar, the highly purified recombined swine IL 22 protein is acquired; the expression output of the recombined swine IL 22 protein is counted through Quantity One software, the purity is up to 95.7%.

Description

technical field [0001] The invention relates to Escherichia coli expressing porcine interleukin 22, belonging to the field of biotechnology genetic engineering; specifically comprising: construction of a plasmid pET-32a(+)-pIL-22 expressing recombinant porcine interleukin 22, extraction and purification of recombinant porcine interleukin 22 expression , and the recombinantly expressed porcine interleukin 22 can be used in anti-apoptosis induced by deoxynivalenol (DON) and anti-Escherichia coli infection. Background technique [0002] 1. Research progress of porcine interleukin-22 [0003] Porcine interleukin 22 is a member of the interleukin 10 family, which is mainly produced by cell lines of the lymphatic system in innate and adaptive immunity, including αβT cells, γδT cells, natural killer cells and innate lymphocytes (ILCs), except lymphoid tissues In addition, macrophages and neutrophils can also produce interleukin-22. Studies have reported that IL-22 has a variety o...

Claims

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Application Information

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IPC IPC(8): C12N15/24C12N15/70C12N1/21C07K14/54C07K1/113A61K38/20A61P31/04A61P31/10C12R1/19
CPCA61K38/20C07K14/54C12N15/70C12N2800/22
Inventor 庾庆华栗云云杨倩
Owner NANJING AGRICULTURAL UNIVERSITY
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