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

Purification method and application of recombinant phytoplasma immune dominant membrane protein

A purification method and membrane protein technology, which is applied in the field of purification of recombinant phytoplasma immune-dominant membrane protein, can solve the problems of membrane protein hydrophobicity, solubility, difficulty in separating and purifying membrane protein, difficulty in expression, etc.

Inactive Publication Date: 2018-08-10
深圳市兰科植物保护研究中心
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to the specificity of different phytoplasma membrane proteins, some membrane proteins can be completely expressed in the E. coli system, while others are difficult to express and easily form inclusion bodies. On the other hand, even if the membrane proteins are expressed in the E. Due to the hydrophobicity, solubility and other properties of membrane proteins, it is difficult for subsequent downstream separation and purification of membrane proteins

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
  • Purification method and application of recombinant phytoplasma immune dominant membrane protein
  • Purification method and application of recombinant phytoplasma immune dominant membrane protein
  • Purification method and application of recombinant phytoplasma immune dominant membrane protein

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0067] For purification methods of recombinant phytoplasma immunodominant membrane proteins, see figure 1 shown, including the following steps:

[0068] S11, obtaining a recombinant bacterium expressing a phytoplasma immune-dominant membrane protein, the recombinant bacterium contains a phytoplasma immune-dominant membrane protein gene with a 6×His Tag sequence, and induces expression;

[0069] S12. Freeze and thaw 1 g of the recombinant bacteria in step S11 twice at -20°C, add 5ml of BugBusterMaster Mix extraction reagent, resuspend at 25°C, incubate with shaking for 30 minutes, and separate to obtain the supernatant liquid one and sediment one;

[0070] S13, weigh 1ml of 50% Ni-NTA-His.Bind resin suspension and mix with 4ml of 1×Ni-NTA binding buffer, the 1×Ni-NTA binding buffer does not contain imidazole, and then mix with 4ml of step S12 As soon as the supernatant was mixed, the pH value was 7, shaken at 4°C for 1 hour and then settled; then washed with 1×Ni-NTA washing ...

Embodiment 2

[0074] For purification methods of recombinant phytoplasma immunodominant membrane proteins, see figure 1 shown, including the following steps:

[0075] S21, obtaining a recombinant bacterium expressing a phytoplasma immune-dominant membrane protein, the recombinant bacterium contains a phytoplasma immune-dominant membrane protein gene with a 6×His Tag sequence, and induces expression;

[0076] S22, freeze and thaw 1 g of the recombinant bacteria in step S11 three times at -20°C, add 5ml of BugBusterMaster Mix extraction reagent, resuspend at 25°C, incubate with shaking for 30 minutes, and separate to obtain the supernatant liquid one and sediment one;

[0077] S23, weigh 1ml of 50% Ni-NTA-His.Bind resin suspension and mix with 4ml of 1×Ni-NTA binding buffer, the 1×Ni-NTA binding buffer does not contain imidazole, and then mix with 4ml of step S12 As soon as the supernatant was mixed, the pH value was 7, shaken at 4°C for 1 hour and then settled; then washed with 1×Ni-NTA wa...

Embodiment 3

[0081] For purification methods of recombinant phytoplasma immunodominant membrane proteins, see figure 1 shown, including the following steps:

[0082] S31, obtaining a recombinant bacterium expressing a phytoplasma immune-dominant membrane protein, the recombinant bacterium contains a phytoplasma immune-dominant membrane protein gene with a 6×His Tag sequence, and induces expression;

[0083] S32, freeze and thaw 1 g of the recombinant bacteria in step S11 twice at -20°C, add 5ml of BugBusterMaster Mix extraction reagent, resuspend at 25°C, incubate with shaking for 30 minutes, and separate to obtain the supernatant liquid one and sediment one;

[0084] S33, weigh 1ml of 50% Ni-NTA-His.Bind resin suspension and mix with 4ml of 1×Ni-NTA binding buffer, the 1×Ni-NTA binding buffer does not contain imidazole, and then mix with 4ml of step S12 As soon as the supernatant was mixed, the pH value was 7, shaken at 4°C for 1 hour and then settled; then washed with 1×Ni-NTA washing ...

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
Login to View More

Abstract

The invention provides a purification method of an immunodominant membrane protein of recombinant phytoplasma and an application thereof. According to the purification method of the immune leading membrane protein of recombinant phytoplasma provided by the invention, the soluble immunodominant membrane protein of recombinant phytoplasma expressed by recombinant bacteria is purified by using affinity chromatography, particularly an inclusion body is split, insoluble immunodominant membrane protein of recombinant phytoplasma in the inclusion body is purified by a dialysis method and affinity chromatography, and the purification conditions and process parameters are optimized, so that the purification effect of the immunodominant membrane protein of recombinant phytoplasma is greatly improved. The purification degree can reach 95% while the purification degree in the conventional method is 60%. The method is simple in process, easy to operate and high in yield, and the production cost is lowered.

Description

technical field [0001] The invention belongs to the field of biotechnology, and in particular relates to a method for purifying a recombinant phytoplasma immunodominant membrane protein and an application thereof. Background technique [0002] Phytoplasma (phytoplasma) is a kind of prokaryotic microorganism with relatively low GC content, no cell wall, and only three-layer unit membrane coating, obligately parasitic on plants and insects. The main symptoms of plant disease include arbuscules, yellowing, flower change and leaf degradation, etc. Due to the strong infectivity of phytoplasma and the extensive damage to hosts, it has caused a large number of economic crops and trees to die, causing serious economic losses. Because phytoplasmas are prokaryotic microorganisms without cell walls, they cannot be cultured in vitro on artificial medium, which brings many difficulties to the research of classification and identification, transmission mechanism and pathogenic mechanism. ...

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 Patents(China)
IPC IPC(8): C12P21/02C07K1/22C07K1/14C12R1/19
Inventor 刘仲健李利强肖新菊张丽君罗焕亮梁楠楠
Owner 深圳市兰科植物保护研究中心
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