Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Methyltransferase gene for glycoside compounds

A technology of methyltransferase and compound, applied in the direction of transferase, enzyme, biochemical equipment and method, etc., can solve problems such as activity reduction, and achieve the effects of enhancing stability, enhancing stability and improving transformation efficiency

Active Publication Date: 2018-10-09
THE INST OF BIOTECHNOLOGY OF THE CHINESE ACAD OF AGRI SCI
View PDF0 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] Various natural and unnatural glycosylated substances are easily affected by various factors from organisms and the outside world, resulting in self-degradation and reduced activity

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
  • Methyltransferase gene for glycoside compounds
  • Methyltransferase gene for glycoside compounds
  • Methyltransferase gene for glycoside compounds

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0089] Example 1 Synthesis of O-methyltransferase gene BbFkbM, and construction of yeast expression vectors to obtain yeast transformants

[0090] Sequencing the genome of a strain of Beauveria bassiana obtained, and obtained the genome sequence of the strain. During the process of analyzing glycosyltransferases through relevant bioinformatics software, an O-methyltransferase gene was found through comparison. We named it BbFkbM. The nucleotide sequence of BbFkbM was predicted and analyzed by various software to remove intron splicing to obtain the coding region sequence of BbFkbM. Extract the RNA of Beauveria bassiana and obtain cDNA by reverse transcription, use the designed primers to amplify the coding gene of BbFkbM, recover the target fragment and send it to the sequencing company for sequencing and comparison, and obtain the glycosyltransferase shown in SEQ ID NO.1 Gene BbFkbM.

[0091] Restriction sites are introduced during synthesis. An NdeI restriction site was a...

Embodiment 2

[0095] Example 2 Application of the O-methyltransferase recombinant vector PXW06F-BbFkbM to realize the modification of the glycosylated derivative of the polyketide compound Desmethyl-Lasiodiplodin (compound 1)

[0096] 1. Purpose of the experiment

[0097] The metabolites modified by glucosyltransferase and O-methyltransferase BbFkbM were separated by HPLC and their molecular structures were analyzed.

[0098] 2. Experimental method:

[0099] 1) Fermentation culture

[0100] Adopt the two-step fermentation technology, first inoculate the appropriate amount of yeast transformant cells into the corresponding 25-mL - Leu / - In Trp liquid deficient medium, culture at 30°C and 200r min-1 for about 16 hours, then add 25ml of YPD low-sugar medium, and add 5mg of pure Desmethyl-Lasiodiplodin at the same time to continue culturing for 48 hours; extract the fermentation product with ethyl acetate, ethyl acetate The ratio of ester to fermentation broth is 1:1, that is, 50ml of ethy...

Embodiment 3

[0115] Example 3 Modification of flavonoids and anthraquinones using O-methyltransferase recombinant vector PXW06F-BbFkbM

[0116] 1. Purpose of the experiment

[0117] The metabolites modified by glucosyltransferase and O-methyltransferase were separated by HPLC and their molecular structures were analyzed.

[0118] 2. Experimental method:

[0119] 1) Fermentation culture

[0120] Adopt two-step fermentation technology, first inoculate an appropriate amount of yeast transformant cells into the corresponding 25ml - Leu / - In Trp liquid deficient medium, culture at 30°C and 200r min-1 for about 16 hours, then add 25ml of YPD low-sugar medium, and at the same time add 5mg of pure product to continue culturing for 48 hours. A total of 20 flavonoid samples were used; extracted with ethyl acetate For the fermentation product, the ratio of ethyl acetate to fermentation broth is 1:1, that is, the fermentation product is extracted with 50ml of ethyl acetate; the dry extract of eth...

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 a methyltransferase gene for glycoside compounds. The methyltransferase gene can perform methylated modification on 4-position hydroxyls of glycosyls in the glycoside compounds; moreover, through a synergetic effect of the methyltransferase gene and glucosyltransferase, different active substances such as polyketones, flavonoids and anthraquinones can be converted throughcombined biosynthesis so as to obtain novel active compounds different from natural product structures, so that the oriented bioconversion of the compounds is achieved and the stability of the compounds is enhanced.

Description

Technical field: [0001] The invention relates to a gene capable of methylating the 4-hydroxyl group of glucose in glycosylated substances, and the glycosylated substances specifically include glycosylation of polyphenolic compounds such as polyketones, flavonoids, anthraquinones, etc. derivative. Background technique: [0002] Various natural and unnatural glycosylated substances are easily affected by various factors from the organism and the outside world, resulting in self-degradation and reduced activity. If the 4-hydroxyl of the sugar group in these substances is alkylated, it is beneficial to enhance their stability. [0003] Fungal biotransformation is the use of specific enzymes in cells to modify and transform the structure of exogenous compounds to obtain more valuable metabolic reactions. Invention content: [0004] The purpose of the present invention is to obtain the O-methyltransferase gene that can participate in the methylation of the 4-position hydroxy g...

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): C12N9/10
CPCC12N9/1007C12N15/81C12P19/62
Inventor 张礼文徐玉泉谢李楠王辰王晓婧
Owner THE INST OF BIOTECHNOLOGY OF THE 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
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