Brucella three-gene recombinant plasmid, construction method thereof and expression and application thereof in escherichia coli
A Brucella, gene recombination technology, applied in the field of genetic engineering, can solve the problems of infringement of the reproductive system and lymphatic system, economic loss of animal husbandry, threat to human health, etc., and achieve the effect of high expression efficiency, low cost and enhanced activity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0047] Three kinds of gene recombination plasmids of embodiment 1 Brucella
[0048] The embodiment of the present invention provides a kind of brucella three gene recombination plasmids, and described recombination plasmid is to take pET-28a (+) plasmid as carrier, in pET-28a (+) restriction site BamHI and xhoI Insert the full-length synthetic Omp10-Omp28-L7 / L12 gene between them, and construct the pET-28a(+) recombinant plasmid containing the Omp10-Omp28-L7 / L12 gene fragment and the kanamycin selection tag, namely pET-28a(+ )-Omp10-Omp28-L7 / L12 recombinant plasmid, the gene amplification sequence of the Omp10-Omp28-L7 / L12 gene fragment is shown in SEQ ID NO:5.
[0049] SEQ ID NO: Gene amplification sequence of 5Omp10-Omp28-L7 / L12 gene fragment
[0050]
Embodiment 2
[0051] The construction method of three kinds of gene recombination plasmids of embodiment 2 Brucella
[0052] The embodiment of the present invention provides a kind of construction method of three gene recombinant plasmids of Brucella, comprising the following steps:
[0053] 1) search Brucella standard strain (28M strain) Omp10, Omp28 and L7 / L12 (SEQ ID NO:1,2,3) nucleotide sequence from NCBI, and pET-28a (+) plasmid spectrogram By comparing the information, it is determined that the double restriction sites that need to be introduced during primer design are BamHI and Xhol I;
[0054] 2) Construction of recombinant plasmid pET-28a(+)-Omp10-Omp28-L7 / L12 recombinant plasmid
[0055] ①PCR amplification of Omp10-linker, linker-Omp28-linker and L7 / L12-linker genes
[0056] According to Brucella Omp10, Omp28 and L7 / L12 genes, the following primers were designed:
[0057] Primer1:5′-CGC GGATCC ATGAAACGCTTCCGCATCGTT-3′
[0058] Wherein, the underlined part is the restriction...
Embodiment 3
[0128] Expression of three kinds of gene recombinant plasmids of embodiment 3 Brucella in escherichia coli
[0129] The embodiment of the present invention provides the expression of three kinds of gene recombinant plasmids of Brucella in Escherichia coli, comprising the following steps:
[0130] 1) Transform the pET-28a(+)-Omp10-Omp28-L7 / L12 recombinant plasmid and pET-28a(+) constructed in Example 2 into Escherichia coli BL21(DE3) plysS competent cells, and coat with kana Mycin LB agar plate, identified after 8-12 hours of culture;
[0131] Among them, the steps of BL21(DE3)plysS competent cells are as follows:
[0132] a. Take 50 μL of competent cells melted on an ice bath, add 10 μL of target DNA, mix gently, and place in an ice bath for 30 minutes.
[0133] b. Heat shock in a water bath at 42°C for 45 seconds, then quickly transfer the tube to an ice bath for 2 minutes, and do not shake the centrifuge tube during this process.
[0134]c. Add 500 μL of sterile LB broth ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com