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

Method for producing gentian oligosaccharides by immobilized beta-glucosidase

A technology of glucosidase and gentian oligosaccharide is applied in the field of immobilized beta-glucosidase to produce gentian oligosaccharide, and can solve the problems of unseen industrialized production and the like

Inactive Publication Date: 2019-03-29
JIANGNAN UNIV RUGAO FOOD BIOTECH RES INST +1
View PDF6 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Only Nippon Food and Chemical Industry Co., Ltd. has realized the industrial production of gentian oligosaccharides, and there is no report of industrial production in China

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 producing gentian oligosaccharides by immobilized beta-glucosidase
  • Method for producing gentian oligosaccharides by immobilized beta-glucosidase
  • Method for producing gentian oligosaccharides by immobilized beta-glucosidase

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] Example 1: Optimization of high-density fermentation conditions in a 3.6L tank of recombinant Pichia pastoris

[0032]The previously constructed recombinant strain P. pastoris KM71 / pPIC9K-bgl1 / pPICZ-A-pdi was used as the starting strain. For the strain construction method, see Preparation of Gentiooligosaccharides Using Trichoderma Virideβ-Glucosidase, F Wang, Food Chemistry, 2018, 248: 340- 345, carried out scale-up culture on a 3.6L tank, and optimized the fermentation process conditions from the three aspects of induction temperature, initial induction cell concentration and methanol concentration in the induction stage, so as to realize the expression of Trichoderma virideβ-glucosidase in recombinant Pichia pastoris efficient expression. The specific optimization process is as follows:

[0033] The seed culture solution is inserted into the fermentation medium at a ratio of 10%, cultivated to a certain extent under the conditions of a temperature of 30° C., a disso...

Embodiment 2

[0038] Embodiment 2: Preparation of immobilized β-glucosidase

[0039] The specific technical scheme is as follows:

[0040] (1) Using the recombinant Pichia pastoris (P.pastoris KM71 / pPIC9K-bgl1 / pPICZ-A-pdi) constructed in the laboratory as the starting strain, prepare the β-glucosidase enzyme solution;

[0041] (2) dissolving chitosan in 2.0% acetic acid solution, making the chitosan concentration reach 1.0-5.0%, making chitosan colloidal solution;

[0042] (3) drop the colloid solution obtained in 2) into 4mol / L sodium hydroxide solution at a speed of 40-60 drops / min with a syringe with a needle to form chitosan microspheres of uniform size, and then use deionized Wash to neutral;

[0043] (4) Add the chitosan microspheres that have been washed to neutrality into an aqueous glutaraldehyde solution with a volume concentration of 0.4%-1.2%, cross-link at 4°C for 2 hours, pour off the glutaraldehyde solution, and wash away with deionized water. excess glutaraldehyde.

[00...

Embodiment 3

[0046] Example 3: Conversion of immobilized β-glucosidase to produce gentiooligosaccharides

[0047] The immobilized enzyme was converted 6 times continuously, and the yield of gentiooligosaccharide was detected after each time. Specifically, the enzymatic conversion was carried out at pH 5.0, 60°C, with 20% glucose and 40% cellobiose as substrates, the amount of enzyme added was 400U / g cellobiose, and the reaction was terminated after 48 hours of reaction, and the immobilized enzyme Filter out of it. The content of gentiooligosaccharides in the reaction solution is detected, the yield of gentiooligosaccharides is calculated, and then the immobilized enzyme is put back into fresh substrates to catalyze the reaction. The results showed that with the increase of conversion times, the yield of gentiooligosaccharides (the ratio of actual yield to theoretical yield) gradually decreased, and the yield of gentiooligosaccharides at the sixth continuous conversion was still 15.2%. It...

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 discloses a method for producing gentian oligosaccharides by immobilized beta-glucosidase, and belongs to the technical field of bioengineering. The method obtains beta-glucosidase by fermentation, and uses chitosan as a carrier and glutaraldehyde as a crosslinking agent to immobilize the beta-glucosidase by an adsorption cross-linking method. The results show that enzyme recovery ofthe immobilized enzyme reaches a maximum of 65.4% under conditions of chitosan concentration of 3.0%, glutaraldehyde concentration of 0.8%, addition amount of a free enzyme of 400U / g microsphere carrier, and immobilized adsorption time of 20h. Continuous conversion is carried out 6 times under optimal transformation conditions, and the gentian oligosaccharide yield is still 15.2%. The immobilizedenzyme has good sustainable utilization and high production capacity of the gentian oligosaccharides.

Description

technical field [0001] The invention relates to a method for producing gentian oligosaccharides by immobilizing β-glucosidase, which belongs to the technical field of bioengineering. Background technique [0002] β-glucosidase (EC3.2.1.21) is also called β-D-glucoside hydrolase, also known as gentiobiase and cellobiase. It widely exists in plants, animals and microorganisms, and its microbial sources include prokaryotic microorganisms Flavobacter johnii, eukaryotic microorganisms Sake yeast, Aspergillus niger, etc. β-glucosidase can hydrolyze non-reducing β-D-glycosidic bonds, free β-D-glycosidic bonds and ligands. At the same time, β-glucosidase also has transglycosidic activity, which can transfer the ligand or glucosome released by the hydrolysis activity to other sugar substrates in the form of β-1,6 glycosidic bonds. [0003] Gentiooligosaccharides are functional oligosaccharides formed by connecting glucose with β-1,6 glycosidic bonds, including gentiobiose, a small ...

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): C12N9/42C12N11/10C12N11/04C12P19/14C12R1/84
CPCC12N9/2445C12N11/04C12N11/10C12P19/14C12Y302/01021
Inventor 吴敬陈晟杨国婷汪飞
Owner JIANGNAN UNIV RUGAO FOOD BIOTECH RES INST
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