Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Vector used for inserting exogenous gene in riemerella anatipestifer genome, and method

A technology for Riemer's duck disease and foreign genes, which can be applied to other methods of inserting foreign genetic materials, using vectors to introduce foreign genetic materials, and genetic engineering, etc., can solve problems such as adverse animal welfare, improvement, time-consuming and laborious problems, etc.

Inactive Publication Date: 2018-11-20
SICHUAN AGRI UNIV
View PDF5 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This method is time-consuming and laborious, and involves animal experiments, which is not conducive to the improvement of animal welfare

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Vector used for inserting exogenous gene in riemerella anatipestifer genome, and method
  • Vector used for inserting exogenous gene in riemerella anatipestifer genome, and method
  • Vector used for inserting exogenous gene in riemerella anatipestifer genome, and method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] The generation of embodiment 1.pheS mutant gene

[0034]Use primers pheS up p1: 5'-catgccatggcaatgttagaatacattgacgcatatc-3' (SEQ ID NO.1), pheS up p2: 5'-cccataccaaatccatagccg-3' (SEQ ID NO.2); pheS down p1: 5'-cggctatggatttggtatggg-3 ' (SEQ ID NO.3), pheS down p2:5'-ggactagtcccagacttgttgattttggacg-3' (SEQ ID NO.4) amplifies the pheSup part (914bp) and the pheSdown part (418bp), and the PCR amplification conditions are as follows: (1 ) 98°C pre-denaturation for 30s; (2) 98°C denaturation for 10s, (3) 55°C annealing for 30s, (4) 72°C extension for 30s, (2)-(4) cycle 30 times; (5) 72°C extension for 7min, (6) Store ∞ at 22°C; amplification results are as follows: figure 1 As shown, the two fragments are then fused using the method of fusion PCR, and the fusion result is as follows figure 2 As shown, the pheS mutant gene, namely pheS*, was obtained, the nucleotide sequence of which was shown in SEQ ID NO.5, wherein the 301st codon encoding amino acid was mutated from GC...

Embodiment 2

[0035] Example 2. Check whether the mutant gene can be used as a reverse screening marker

[0036] The fusion fragment was cloned into the shuttle plasmid pLMF03 (Genbank: KU997673) to obtain the recombinant plasmid pLMF03::pheS*, using the sequences shown in SEQ ID NO.1 and SEQ ID NO.4 for PCR amplification, and using NcoI and Sp e I Carry out enzyme digestion identification, the identification results are as follows image 3 shown. Then it was transformed into R. anatipestife ATCC by conjugative transfer, and the empty vector of the shuttle plasmid pLMF03 was used as a control to obtain strain R. anatipestife pLMF03::pheS* and strain R. anatipestife pLMF03 respectively. The strains R. anatipestife pLMF03 and R. anatipestife pLMF03::pheS* were cultured in GCB / cfx with different concentrations of p-cl-Phe (0mM, 10mM, 13mM) for 18h in an incubator at 37°C, and the results were as follows: Figure 4 shown. The results showed that when the concentration of p-cl-Phe was 13mM, t...

Embodiment 3

[0037] Example 3. Construction of suicide vector pOES for genomic tag insertion

[0038] Plasmid pLMF03::pheS* was used as a template, and primers were used: EXpheS*p1: 5'-acgcgtcgacatttcaaaaatttaacttaaaccactg-3' (SEQ ID NO. 6), EXpheS*p2: 5'-gctctagagccctttttttgttacttatagcg-3' (SEQ ID NO. 7) , the high-expression promoter of the plasmid and pheS* were amplified together, and its product was named EXpheS*, and the plasmid pMM47.A was cut with PstI restriction endonuclease to remove the origin of replication ( Figure 6 , A), making it a suicide plasmid and named it pMM47.B. Then clone the EXpheS* fragment into the restriction sites SalI and XbaI of pMM47.B. The plasmid is named pOES. The specific process is as follows: Figure 5 shown. The constructed plasmid was carried out with the sequence shown in SEQ ID NO.6 and SEQ ID NO.7 for PCR amplification detection and SalI and XbaI double enzyme digestion identification ( Figure 6 , B)

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention relates to a vector used for inserting an exogenous gene in a riemerella anatipestifer genome, and a method. The vector is connected by plasmid pMM47.A by using Pst I restriction enzymeto cut replication origin to obtain plasmid pMM47.B; a pheS mutant gene containing a high expression promoter can be cloned to the Sal I and Xba I restriction sites of the plasmid pMM47.B to obtain asuicide vector pOES; and the downstream of the suicide vector pOES can be connected to a recombinant gene sequence whose internal contains an exogenous gene coding sequence. The vector can simply insert an exogenous gene in a riemerella anatipestifer genome, so that technical reference can be provided for studies on the protein localization in bacteria.

Description

technical field [0001] The invention belongs to the field of biotechnology, and relates to a carrier for inserting a foreign gene into the Riemerella anatipestifer genome, and also relates to a method for inserting a foreign gene into the Riemerella anatipestifer genome using the vector. Background technique [0002] In bacteriological research, the localization of functional proteins is an important part of studying protein function. The currently used method is to heterologously express and purify the gene of the target protein in Escherichia coli by genetic engineering, and prepare polyclonal antibodies against the target protein by immunizing animals. Then, extract the components of the bacteria, such as outer membrane protein, cytoplasmic protein, etc., and detect the localization of the target protein by immunoblotting. This method is time-consuming and laborious, and involves animal experiments, which is not conducive to the improvement of animal welfare. Therefore,...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C12N15/74C12N15/90
CPCC12N15/74C12N15/902
Inventor 刘马峰黄月刘珈均程安春汪铭书朱德康
Owner SICHUAN AGRI UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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