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

Structure of recombined T4 bacteriophage of expression infectious cysticercosis virus VP2 protein and its use

A phage, infectious technology, applied in the field of recombinant T4 phage, to achieve the effect of strong immunogenicity, high copy number and easy purification

Inactive Publication Date: 2004-12-15
SOUTH CHINA AGRI UNIV
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there is no report on the expression of IBDV structural proteins by phage

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
  • Structure of recombined T4 bacteriophage of expression infectious cysticercosis virus VP2 protein and its use
  • Structure of recombined T4 bacteriophage of expression infectious cysticercosis virus VP2 protein and its use
  • Structure of recombined T4 bacteriophage of expression infectious cysticercosis virus VP2 protein and its use

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0031] 1. Construction of integrated plasmid pR-VP2

[0032] The pR plasmid (Ren et al, 1996) was used to construct the recombinant integration plasmid pR-VP2. The PCR product of the vp2 gene and the plasmid pR were respectively digested with EcoRI at 37° C., and then the digested PCR product of vp2 and the plasmid pR were ligated under the action of T4 ligase. Escherichia coli DH5α was transformed with the ligation product. Conversion method to CaCl 2 Law. via Amp r Resistance screening was performed to obtain recombinants inserted with the vp2 gene. Then use a pair of specific primers SOC-S / VP2-A for PCR screening. For the positive bacteria screened by PCR, pick a single colony and inoculate it in 3mL LA medium, and culture it at 37°C with shaking at 200r / m for 16-20 hours. The plasmid was extracted with E.Z.N.A.®Plasmid Minipreps Kit, and then digested with restriction endonucleases and sequenced to obtain the recombinant integrated plasmid pR-VP2.

[0033] 2. Acquis...

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

PropertyMeasurementUnit
molecular weightaaaaaaaaaa
molecular weightaaaaaaaaaa
diameteraaaaaaaaaa
Login to View More

Abstract

The present invention provides recombinant T4 bacteriophage expressing infectious chicken bursal disease virus structure protein VP2. The recombinant T4 bacteriophage has the nucleotide sequence of infectious bursal disease virus VP2 gene and the amino acid residue sequence of VP2 protein. The present invention also relates to the application of the recombinant T4 bacteriophage in the immunity with infectious bursal disease vaccine and the detection of infectious bursal disease virus.

Description

technical field [0001] The invention relates to the construction and application of a recombinant T4 phage expressing chicken infectious bursal disease virus structural protein. The present invention further relates to the application of the recombinant T4 phage in the detection of infectious bursal disease vaccine and infectious bursal disease virus antibody. Background technique [0002] Infectious bursal disease virus (IBDV) belongs to the family Birnaviridae (Birnaviridae) of the genus Avibirnavirus, and it is the pathogen of chicken infectious bursal disease. It is generally believed that IBDV has four mature proteins: VP1, VP2, VP3 and VP4, with molecular weights of 90kDa, 37-40kDa, 32-35kDa and 24-30kDa, respectively. Among them, VP2 and VP3 are the main structural proteins, accounting for 51% and 40% of the total viral proteins, respectively. The molecular weight of VP2 is about 40kDa. It contains serotype-specific antigenic determinants tha...

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): A61K39/12C12N7/01C12N15/40C12N15/73
Inventor 曹永长毕英佐史泉城马静云
Owner SOUTH CHINA 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