Method for improving cellulase expression of trichoderma reesei by interfering phosphatase gene

A phosphatase gene, technology of Trichoderma reesei, applied in the field of genetic engineering, can solve the problems of decreased secretion of RutC-30 protein, decreased cellulase activity, etc.

Active Publication Date: 2022-03-01
INST OF ANIMAL SCI OF CHINESE ACAD OF AGRI SCI
View PDF10 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In the Trichoderma reesei Rut C-30 mutant, found by genome sequencing gls2α The gene has a frameshift mutation, while o...

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
  • Method for improving cellulase expression of trichoderma reesei by interfering phosphatase gene
  • Method for improving cellulase expression of trichoderma reesei by interfering phosphatase gene
  • Method for improving cellulase expression of trichoderma reesei by interfering phosphatase gene

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0016] Example 1 Construction of pPtef1-ymr1-Ppki plasmid

[0017] Construction of the pPtef1-ymr1-Ppki plasmid: tef1 Promoter, ymr1 Interference gene 413 bp, pki Promoter and ampr+ori sections. Using the APA-GOD plasmid as a template, amplify the ampr+ori part; using the Trichoderma reesei genome as a template, tef1 Promoter, ymr1 Interference gene 413 bp (ymr1iF: GACAATGACCAGCAGACCATCGAG

[0018] ;ymr1iR:CTTTTCGCTCTGATAATGGCCAGG) and pki Promoter, electrophoresis, and 4 recovered fragments were connected by homologous recombination. Transform Escherichia coli Trans1-T1 competent cells, perform colony PCR on the colonies grown on the plate, send the colonies identified as positive by PCR to sequencing, and name the plasmid with correct sequencing as pPtef1-ymr1-Ppki plasmid, such as figure 1 .

Embodiment 2

[0019] Example 2. Introduction of pPtef1-ymr1-Ppki plasmid

[0020] (1) Transform Trichoderma reesei SUS4-1 with pPtef1-ymr1-Ppki plasmid

[0021] Trichoderma reesei SUS4-1 was inoculated on a potato medium (PDA) plate, and cultured statically at 28 ºC for 7 days until it produced spores, and the spores were scraped off and inoculated in 100 mg / ml PDB medium containing uracil. Incubate overnight at 28ºC with shaking at 160 rpm. Collect the germinated mycelium by filtering through a 200-mesh sieve, add 10 mg / ml cellulase and digest at 30°C for 2-3 hours. After protoplasts were collected, the pPtef1-ymr1-Ppki plasmid was used Ssp I digestion, transformation of Trichoderma reesei host cells.

[0022] (2) PCR verification of the introduction of the pPtef1-ymr1-Ppki plasmid into the Trichoderma reesei genome

[0023] A single transformant was picked, inoculated on a 24-well plate containing MM-glucose medium, and cultured at 28°C for 5-7 days. Genomic DNA was extracted to ver...

Embodiment 3

[0024] Example 3. pPtef1-ymr1-Ppki Effect on protein expression

[0025] (1) interference ymr1 Shake flask induction of transformants

[0026] interference ymr1 Transformants and starting strains were inoculated with 2×10 7 The spores were cultured in 50 ml MM-glucose medium at 28°C and 160 rpm for 2 days. Transfer to 50 ml MM+2% Avicel medium with 10% inoculum size to induce the expression of cellulase. From the third day, samples were taken every 24 h, and the samples were taken continuously for 7 days.

[0027] (2) interference ymr1 Determination of the protein concentration and cellulase of the transformant of the gene

[0028] The protein was quantified by Coomassie Brilliant Blue method, after adding 250 µl 1 × dye reagent and 10 µl protein standard, reacted at room temperature for 10 minutes, then measured the absorbance at 595 nm, the results are shown in figure 2 . visible ymr1 The concentration of protein secreted extracellularly by the transformant a...

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 the field of gene engineering, in particular to a method for improving cellulase expression of trichoderma reesei by interfering a phosphatase gene. RNAi-mediated gene silencing is carried out on the phosphatase gene ymr1 related to the trichoderma reesei participating in intracellular protein degradation, and the operation improves the protein expression quantity of the trichoderma reesei and the enzyme activity of cellulase.

Description

technical field [0001] The invention relates to the field of genetic engineering, in particular to a method for improving the expression of Trichoderma reesei cellulase by interfering with the phosphatase gene. Background technique [0002] As an important industrial production strain, the filamentous fungus Trichoderma reesei is widely used in the production of industrial products such as feed enzymes, organic acids, antibiotics, etc. It has the characteristics of high expression and strong secretion ability. At the same time, it has a variety of post-translational processing methods similar to eukaryotes, such as glycosylation, protease cleavage and disulfide bond formation. In the mixed fermentation broth, the expression of cellobiohydrolase accounted for more than 50% of the total extracellular secreted protein. However, the high cost of cellulase is still one of the major bottlenecks in cellulose biorefinery, so it is necessary to continue to develop new methods to imp...

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
IPC IPC(8): C12N15/80C12N15/113C12N9/42C12R1/885
CPCC12N15/80C12N15/1137C12N9/2437C12N2310/14C12Y301/03
Inventor 苏小运孙先花姚斌罗会颖王晓璐秦星王苑涂涛张杰柏映国于会民黄火清张红莲王亚茹
Owner INST OF ANIMAL SCI OF CHINESE ACAD OF AGRI SCI
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap