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

High temperature resistant chaetomium polygalacturonase mutant and encoding gene and application thereof

A polygalactose and gene-encoding technology, applied in the field of genetic engineering, can solve problems such as increased production costs, limited application range, and easy inactivation

Active Publication Date: 2015-08-05
INST OF ANIMAL SCI OF CHINESE ACAD OF AGRI SCI
View PDF3 Cites 8 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Enzyme preparations for feed usually need to go through the processing of plasmids (transient high temperature), while polygalacturonase belongs to medium and low temperature enzymes (mostly used for clarification and extraction of fruit juice), and its poor thermal stability not only limits its application range, but also is easy to Inactivation, increasing production costs

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
  • High temperature resistant chaetomium polygalacturonase mutant and encoding gene and application thereof
  • High temperature resistant chaetomium polygalacturonase mutant and encoding gene and application thereof
  • High temperature resistant chaetomium polygalacturonase mutant and encoding gene and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0055] Example 1 Site-directed mutagenesis

[0056] Carry out homology modeling on polygalacturonase PG8fn (Tu et al., 2013), and design the mutation site as the 244th aspartic acid is mutated to alanine and the 299th aspartic acid Mutated to arginine. The primers used in the design are shown in Table 1:

[0057] Table 1. The mutant-specific primers

[0058]

Embodiment 2

[0059] Preparation of mutants described in Example 2.

[0060] The expression vector pPIC9r was subjected to double enzyme digestion (SnaB I+Not I), and simultaneously the gene ASA encoding the mutant was double enzyme digested (SnaB I+Not I), and the gene fragment encoding the mature mutant was cut ( Remove the signal peptide fragment) and connect with the expression vector pPIC9r to obtain the recombinant plasmid pPIC9r-ASA containing the mutant gene ASA and transform it into Pichia pastoris GS115 to obtain the recombinant yeast strain GS115 / ASA.

[0061] Take the GS115 strain containing the recombinant plasmid, inoculate it in a 1L Erlenmeyer flask with 300mL of BMGY medium, place it at 30°C, and culture it on a shaker at 220rpm for 48h; then centrifuge the culture solution at 3000g for 5min, discard the supernatant, and use 100mL of 0.5% methanol for precipitation. The BMMY medium was resuspended, and placed again at 30°C, 220rpm to induce culture. Add 0.5 mL of methanol ...

Embodiment 3

[0064] Activity analysis of embodiment 3 mutant and wild type

[0065] 1. DNS method: The specific method is as follows: under the given pH and temperature conditions, 1mL of the reaction system includes 100μL of appropriate diluted enzyme solution, 900μL of substrate, react for 10min, add 1.5mL of DNS to terminate the reaction, and boil for 5min. After cooling, the OD value was measured at 540 nm. One enzyme activity unit (U) is defined as the amount of enzyme required to decompose polygalacturonic acid to generate 1 μmol D-(+)-galacturonic acid per minute under given conditions.

[0066] 2. Determination of the properties of mutants and wild types

[0067] 1. The optimal pH determination method of mutant and wild type is as follows:

[0068] The mutant enzyme purified in Example 2 and the wild type were subjected to enzymatic reactions at different pHs to determine their optimum pH. The substrate polygalacturonic acid was tested for polygalacturonase activity in 0.1mol / L ...

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
Tm valueaaaaaaaaaa
Login to View More

Abstract

The invention relates to the field of genetic engineering, in particular to a high temperature resistant chaetomium polygalacturonase mutant and an encoding gene and an application thereof. Polygalacturonase from achaetomium sp.xz8 is used as a female parent, and the polygalacturonase mutant with improved heat stability is obtained through rational design and molecular biological technique. Related amino acid mutation is combined mutation (ASA, Asp244Ala / Asp299Arg) of two points Asp244Ala and Asp299Arg in each mutant sequence. Optimum temperature, T50 and T1 / 2 of the mutant are improved in comparison with those of wild type enzyme. The optimum temperature is increased from 45 DEG C to 55 DEG C, T50 is increased from 56 DEG C to 73 DEG C, half-life period T1 / 2 at 50 DEG C is increased from 1.5h to 10h, half-life period T1 / 2 at 55 DEG C is increased from 33min to 78min, and Tm value is increased from 43.8 DEG C to 54.1 DEG C. Besides, the mutant keeps enzyme catalytic activity which is equal to that of the wild type enzyme. Application demands in fields of feedstuff, foodstuff and the like can be met.

Description

technical field [0001] The invention relates to the field of genetic engineering, in particular to a high temperature-resistant chaetomium polygalacturonase mutant, its coding gene and its application. Background technique [0002] There are quite a lot of non-starch polysaccharides (Non-starch Polysaccharides, NSPs) in feed, which is a general term for all carbohydrates in plant tissues except starch, which are composed of four parts: cellulose, hemicellulose, pectin and resistant starch. NSPs not only have no nutritional value for monogastric animals, but also become anti-nutritional factors in the intestinal tract, which can bind a large amount of water in the intestinal tract of animals, increase the viscosity of chyme, affect the activity of digestive enzymes, and stimulate the compensatory function of the digestive tract. Increased, leading to excessive reproduction of intestinal harmful bacteria, reducing the intestinal absorption of nutrients. As a non-starch polysa...

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): C12N9/26C12N15/56C12N15/81C12N1/19A23K1/165C12R1/85
Inventor 姚斌罗会颖涂涛孟昆王亚茹石鹏君柏映国黄火清苏小运王苑马锐师霞
Owner INST OF ANIMAL SCI OF CHINESE ACAD OF AGRI SCI
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