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

A preparation method and application of immobilized cells for mannose production

A technology for immobilizing cells and mannose is applied in the production and preparation of mannose and in the fields of bioengineering, and can solve the problems of high production cost of mannose, low enzyme recovery rate, cumbersome production steps, etc. Conducive to the effect of separation and purification, simplifying the production and preparation process

Active Publication Date: 2021-10-08
天津怡和生物科技有限责任公司
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] Aiming at the problems existing in the existing multi-enzyme catalyzed method for preparing mannose, such as cumbersome production steps of the enzyme, complicated separation and purification, low enzyme recovery utilization rate, difficulty in recycling and high production cost of mannose, the purpose of the present invention It aims to provide a method for immobilized cells to produce mannose, simplify the production steps of enzymes in the mannose production process, simplify the separation and purification of products and enzymes in the mannose preparation process, and realize the synthesis of multiple enzymes in the new multi-enzyme synthesis route of mannose Recycling, reducing the production cost of mannose, and realizing the industrial production of mannose

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
  • A preparation method and application of immobilized cells for mannose production
  • A preparation method and application of immobilized cells for mannose production
  • A preparation method and application of immobilized cells for mannose production

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] Embodiment 1: the preparation of the Bacillus subtilis fermented liquid expressing enzyme

[0040] (1) Construction of pMA5-Pylb-aGP

[0041] In this example, the agp sequence (NCBI-ProteinID: BAD85595), the gene encoding thermostable a-glucan phosphorylase, was synthesized by Suzhou Jinweizhi Biotechnology Co., Ltd. and spliced ​​into a common plasmid. The thermostable α-glucan phosphorylase gene agp gene was obtained by PCR using a pair of primers (1-IF and 1-IR). The linear backbone of pMA5‐Pylb was obtained by PCR using a pair of primers (1-VF and 1-VR). The thermostable α-glucan phosphorylase gene fragment and the pMA5-Pylb vector backbone were then assembled using POE-PCR. The ligation product was transferred into competent SCK6 by the calcium chloride method, and the transformant was selected for colony PCR, double enzyme digestion identification and sequencing verification to obtain an expression vector, which was named pMA5-Pylb-aGP.

[0042] 1-IF: AGAAACAAC...

Embodiment 2

[0072] Embodiment 2: Production of mannose by immobilized Bacillus subtilis

[0073] According to the OD600 ratio of 1:1:1:1:1, the Bacillus subtilis fermentation broth expressing thermostable α-glucan phosphorylase prepared in Example 1 and the Bacillus subtilis expressing thermostable glucose phosphomutase were fermented subtilis fermentation broth expressing thermostable glucose phosphoisomerase, Bacillus subtilis fermentation broth expressing thermostable mannose 6-phosphate isomerase, fermentation broth of Bacillus subtilis expressing thermostable mannose 6-phosphate phosphatase The solution was mixed so that OD 600 = 100, and 2% w / v montmorillonite was added to the bacterial suspension, and stirred evenly. Subsequently, 1% w / v polyethyleneimine aqueous solution with a molecular weight of 600 was added to flocculate at room temperature. Then, 0.5% v / v glutaraldehyde aqueous solution was added to crosslink for 2 h at room temperature. The filter cake is obtained after va...

Embodiment 3

[0075] Embodiment 3: Production of mannose by immobilized Bacillus subtilis

[0076] According to the OD600 ratio of 1:1:1:1:1, the Bacillus subtilis fermentation broth expressing thermostable α-glucan phosphorylase prepared in Example 1 and the Bacillus subtilis expressing thermostable glucose phosphomutase were fermented subtilis fermentation broth expressing thermostable glucose phosphoisomerase, Bacillus subtilis fermentation broth expressing thermostable mannose 6-phosphate isomerase, fermentation broth of Bacillus subtilis expressing thermostable mannose 6-phosphate phosphatase The solution was mixed so that OD 600 = 100, and 5% w / v diatomaceous earth was added to the bacterial suspension, and stirred evenly. Subsequently, 0.5% w / v polyethyleneimine aqueous solution with a molecular weight of 70000 was added to flocculate at room temperature. Then, 0.5% v / v glutaraldehyde aqueous solution was added to crosslink for 2 h at room temperature. The filter cake was obtained ...

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 preparing immobilized cells for producing mannose and a method for producing mannose. Wherein, when the immobilized Bacillus subtilis of the present invention continuously catalyzes the reaction, the initial product yield can reach up to 65%, and after 25 batches of continuous catalysis, the product yield can still maintain 45%. When the immobilized Escherichia coli of the present invention continuously catalyzes the reaction, the initial product yield can reach up to 65%, and after 25 batches of continuous catalysis, the product yield can still maintain 44%. The invention simplifies the separation and purification steps of the enzyme, improves the recycling rate of the enzyme, and realizes the recycling of the enzyme. The method of the invention has the advantages of easy product separation, simple production process, low cost, etc., and provides reference for industrial application.

Description

technical field [0001] The invention relates to the technical field of bioengineering, in particular to the field of production and preparation of mannose. Background technique [0002] Mannose is a six-carbon sugar that is an isomer of glucose. Mannose has the functions of regulating immunity, resisting bacterial and viral infection, promoting glycoprotein synthesis in the body, and anticancer. Therefore, mannose is widely used in the fields of biology and medicine. Mannose can not only be used as a raw material for the synthesis of some pharmaceutical chemical raw materials and important sugar drug precursors, but also can be used as a sweetener for food and beverages. In recent years, the demand for mannose in the fields of functional food, feed additive and medicine has increased significantly, and it has huge economic development value. [0003] The main methods of industrial production of mannose are extraction and isomerization. The extraction method mainly uses c...

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): C12N11/14C12N11/10C12N11/089C12N11/087C12N11/082C12P19/02C12R1/19C12R1/125
CPCC12N11/14C12N11/10C12N11/089C12N11/087C12N11/082C12P19/02
Inventor 马延和石婷韩平平
Owner 天津怡和生物科技有限责任公司
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