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

Polyamine-polyphenol modified graphene oxide carrier, and preparation method and application thereof

A polyphenol oxidation, graphene technology, applied in biochemical equipment and methods, chemical instruments and methods, immobilized on or in inorganic carriers, etc., can solve problems such as poor stability and reusability of immobilized enzymes

Active Publication Date: 2020-11-20
NANJING TECH UNIV
View PDF3 Cites 11 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] Purpose of the invention: the technical problem to be solved by the present invention is to provide a polyamine-polyphenol modified graphene oxide carrier to solve the problems of poor stability and reusability of immobilized enzymes in the prior art

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
  • Polyamine-polyphenol modified graphene oxide carrier, and preparation method and application thereof
  • Polyamine-polyphenol modified graphene oxide carrier, and preparation method and application thereof
  • Polyamine-polyphenol modified graphene oxide carrier, and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] Example 1: Preparation of dopamine-polyethyleneimine co-modified graphene oxide (GO) as a carrier of adenylyl cyclase (AC) cross-linked enzyme polymer

[0039] 1. Preparation of dopamine-polyethyleneimine co-modified GO

[0040] Dissolve 100 mg of GO in 100 ml of Tris-HCL buffer (pH 8.5), and disperse it uniformly by ultrasound to prepare a 1 mg / mL GO dispersion. Prepare a 2 mg / ml PEI solution with Tris-HCL buffer, add 50 mg of DA into the PEI solution, and adjust the volume to 50 ml with a volumetric flask to obtain a DA / PEI mixed solution. Take 5ml graphene oxide dispersion (1mg / mL), add 2ml Tris-HCL buffer solution and 3ml DA / PEI mixed solution. The final system is 10ml, the concentration of dopamine is 0.3mg / ml, and DA:PEI=1:2. The mixture was reacted in a shaker at 25° C. for 16 h, and then centrifuged, washed and dried to obtain the modified carrier GO-PEI / PDA. Take the same amount of graphene oxide and GO-PEI / PDA solids and grind them into powder. According to...

Embodiment 2

[0057] Example 2: Dopamine-polylysine co-modified GO as carrier to prepare AC cross-linked enzyme polymer

[0058] Use Tris-HCL buffer solution with a pH of 8.5 to prepare a 5 mg / mL polylysine (EPL) solution, dissolve DA in the EPL solution so that the ratio of DA to EPL in the solution is 1:1, take 5 mL of the mixed solution and add 5ml of graphene oxide dispersion (20mg / mL) was reacted in a shaker at 30°C for 24h, then centrifuged, washed, and dried to obtain dopamine-polylysine co-modified GO.

[0059] The prepared dopamine-polylysine co-modified GO was processed according to the preparation method of the cross-linked enzyme polymer in Example 1, and finally the AC cross-linked enzyme polymer immobilized on the dopamine-polylysine graphene oxide was obtained. body.

[0060] Referring to the adenylyl cyclase enzyme activity assay method in Example 1 above, the assay results show that the relative enzyme activity of the cross-linked enzyme polymer with dopamine-polylysine co...

Embodiment 3

[0063] Example 3: Tannic acid-polyetheramine co-modified GO as carrier to prepare AC cross-linked enzyme polymer

[0064] Use Tris-HCL buffer (pH7.5) to prepare 2 mg / mL polyetheramine solution, dissolve tannic acid in the polyetheramine solution, so that the ratio of tannic acid and polyetheramine in the solution is 1:1, Take 5mL of the mixed solution and add 5ml of graphene oxide dispersion (1mg / mL), react in a shaker at 10°C for 16h, then centrifuge, wash, and dry to finally obtain tannic acid-polyetheramine co-modified graphene oxide .

[0065] Referring to the above method, tannic acid and polyetheramine were added separately to the system to prepare GO modified with tannic acid and GO modified with polyetheramine, respectively.

[0066] 1 mL of tris(carboxymethyl)ethylenediamine solution with a concentration of 100 mM and 1 mL of NiCl with a concentration of 100 mM 2 React for 1h, then react with 5mL AC enzyme solution for 1h, the protein concentration in the AC enzyme ...

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
concentrationaaaaaaaaaa
Login to View More

Abstract

The invention discloses a crosslinking enzyme polymer based on polyamine-polyphenol codeposition, and a preparation method and application thereof, and belongs to the technical field of immobilized enzyme application. Graphene oxide is dispersed in a buffer solution, and then, polyphenol solution and multi-amido polymer solution are added into the buffer solution so as to react to obtain the polyamine-polyphenol modified graphene oxide. The polyamine-polyphenol modified graphene oxide carrier obtained by the method is used for the immobilized enzyme so as to obtain the crosslinking enzyme polymer. The polyamine-polyphenol modified graphene oxide carrier has the advantages of universality, high activity, simpleness in operation and the like.

Description

technical field [0001] The invention belongs to the technical field of immobilized enzyme application, and in particular relates to a polyamine-polyphenol modified graphene oxide carrier and a preparation method and application thereof. Background technique [0002] At present, the application of biocatalysis technology has become more and more extensive. Enzymes, as a common biocatalyst, have many advantages compared with chemical catalysts: the catalytic conditions are mild, generally at room temperature, normal pressure and pH close to neutral conditions Catalytic reaction; Compared with chemical catalysis, it has higher catalytic efficiency and faster reaction speed; less environmental pollution, which is in line with the development concept of green chemistry. However, the shortcomings of enzymes as catalysts are also obvious, such as poor stability, easy inactivation under high temperature, high pressure, and strong acid and strong alkali conditions, and harsh reaction...

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): C12N11/10C12N11/096C12N11/089C12N11/082C12N11/087C12N11/02C12N11/14C12N11/18C12N9/22C12N9/88C12N9/20C12N9/42C12N9/08C12N9/04C01B32/198
CPCC12N11/10C12N11/096C12N11/089C12N11/082C12N11/087C12N11/02C12N11/14C12N11/18C12N9/22C12N9/88C12N9/20C12N9/2437C12N9/0006C12N9/0065C12Y406/01001C12Y101/03004C12Y111/01006C12Y301/01003C12Y302/01004C01B32/198
Inventor 庄伟刘彤乐朱晨杰应汉杰饶远李明陈勇吴菁岚杨朋朋柳东牛欢青
Owner NANJING TECH UNIV
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