New method for fast selecting engineering bacteria of leaven of efficient expression antimicrobial peptides

A high-efficiency expression and yeast engineering technology, which is applied in the field of expression products and yeast engineering bacteria, can solve the problem of no increase in the potency of antimicrobial peptides, and achieve the effects of saving initial screening time, saving time, and reducing manpower

Inactive Publication Date: 2010-02-10
HUBEI UNIV
View PDF0 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Yeast secretion vectors generally have genes encoding these antibiotics. Since yeast secretion vectors are integrated into chromosomes, in theory, if yeast can decompose high concentrations of antibiotics, then there will be multiple copies of secretion expression vectors on the chromosomes. , which may be high-yielding bacteria, but studies have shown that yeast that can grow on high-concentration antibiotics does not directly correspond to high-expressing yeast, that is to say, although the copy number is high, it can decompose high-concentration antibiotics. It must be a high-yielding bacterium of the target product; our research has also confirmed this conclusion. In the experiment, we screened a strain of yeast engineered bacteria whose resistance was increased by 10 times, but the potency of antimicrobial peptides did not increase

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
  • New method for fast selecting engineering bacteria of leaven of efficient expression antimicrobial peptides
  • New method for fast selecting engineering bacteria of leaven of efficient expression antimicrobial peptides
  • New method for fast selecting engineering bacteria of leaven of efficient expression antimicrobial peptides

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0019] A material

[0020] 1. Strains and plasmids

[0021] Pichia pastoris (Pichia pastoris) GS115 was purchased from Invitrogen, and plasmids pHBM905-man, pET23a-9elp-hal18, pHBM905-man-hal18 and pHBM306 were constructed experimentally.

[0022] 2. Reagents

[0023] Restriction enzymes, One-step ligation kit, LA Taq enzyme, four kinds of dNTPs were purchased from TaKaRa Company, YNB was purchased from Diffco Company, DNA gel extraction kit was purchased from AXYGEN Company, mannan, and Trinyl blue were purchased from sigma, Other conventional reagents were imported or domestically produced analytically pure.

[0024] B: Implement screening for engineering bacteria that express antimicrobial peptides efficiently

[0025] 1. Construction of yeast secretory expression vector pHBM306:

[0026] The antimicrobial peptide gene in 9elp-hal18 was cloned to the downstream of pHBM905-man to fuse with man, and the recombinant yeast secretion expression plasmid was named pHBM306

[...

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 provides a new method for fast selecting engineering bacteria of leaven of efficient expression antimicrobial peptides. The method comprises the following steps: 1. constructing plasmidsfor syncretizing antimicrobial peptide genes and chaperone protein genes; 2. carrying out enzyme restriction for linearizing the plasmids; 3. transforming the plasmids to pichia competent thalli through electroporation, utilizing auxotroph for selecting, and cultivating the plasmids for 36 to 48 hours at the temperature of 28 DEG C; 4. directly obtaining transformants from a prescreening plate, i.e. obtaining the engineering bacteria of the leaven of the efficient expression antimicrobial peptides primarily, and then the engineering bacteria of the leaven can be obtained from large number oftransformants through reselection. The invention has simple experiment process and easy operation, the entire screening process can be shortened by 5 to 6 days, and the expenses of labor, materials and finical resources are greatly reduced. The invention is suitable for the engineering bacteria expressed in the leaven for proteins of the antimicrobial peptides, enzyme, antibodies, polypeptide andthe like which is not easy to or can not adopt a functional approach for selection.

Description

technical field [0001] The present invention relates to high-efficiency expression and screening technology of bioengineering bacteria, and is especially suitable for expression products such as polypeptides and proteins that cannot be directly screened by function, or for expression products that are very complicated and require a lot of time to screen. It is especially suitable for large-scale, short-term, large-scale screening of yeast engineering bacteria that highly express antimicrobial peptides. Background technique [0002] Antimicrobial peptides are a kind of peptide substances produced by the host defense system to resist external pathogen infection, and are an important part of the host immune defense system. Antimicrobial peptides not only have a broad antibacterial spectrum, but also have the effect of inhibiting the growth of cancer cells and are not easy to produce drug resistance, which makes the development and utilization of antimicrobial peptides a recent ...

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): C12N15/81C12N15/64C12R1/84
Inventor 马向东胡凡
Owner HUBEI UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products