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

Method for preparing rebaudioside M through fermentation catalysis of bacillus subtilis

A Bacillus subtilis, catalytic preparation technology, applied in the field of microbial fermentation enzyme preparations, can solve the problems of unsuitable industrial production, complex operation, high production cost, etc., and achieve the effects of being beneficial to industrial production, solving low enzyme activity and reducing operation steps

Pending Publication Date: 2022-03-22
ANHUI JINGHE IND
View PDF7 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The purpose of the present invention is to solve the problem that existing enzymatic method and fermentation method catalyze stevioside into rebaudioside M in the production of rebaudioside M, the production cost is high, the operation is complicated, and cannot be applied to industrial production, and to provide a method of using Bacillus subtilis Method for preparing rebaudioside M by fermentation and catalysis of bacillus

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] (1) Seed preparation: Link the synthesized glycosyltransferase UGT76G1 gene and glycosyltransferase UGT11 gene to the PBR322 plasmid vector, and the PBR322 plasmid vector carrying the glycosyltransferase UGT76G1 gene and glycosyltransferase UGT11 gene Introduced into the competent state of Bacillus subtilis, the Bacillus subtilis implanted with the glycosyltransferase UGT76G1 gene and the glycosyltransferase UGT11 gene was inserted into the LB medium, and the temperature of the LB medium was controlled at 35 ° C, and the rotation speed was 200 rpm. Culture time 20 h;

[0021] (2) Seed tank cultivation: The Bacillus subtilis obtained in step (1) was inserted into the seed tank containing LB medium according to the inoculation amount of 5% volume ratio, and the rotation speed of the seed tank was controlled at 300 rpm, and the ventilation ratio ( The aeration ratio is the volume ratio of air passing through a unit volume of culture solution per minute) is 0.5 V / V.min, cul...

Embodiment 2

[0028] (1) Seed preparation: Link the synthesized glycosyltransferase UGT76G1 gene and glycosyltransferase UGT11 gene to the PBR322 plasmid vector, and the PBR322 plasmid vector carrying the glycosyltransferase UGT76G1 gene and glycosyltransferase UGT11 gene Introduced into the competent state of Bacillus subtilis, the Bacillus subtilis implanted with the glycosyltransferase UGT76G1 gene and the glycosyltransferase UGT11 gene was inserted into the LB medium, and the temperature of the LB medium was controlled at 30°C, and the rotation speed was 220 rpm. Culture time 24 h;

[0029] (2) Seed tank cultivation: The Bacillus subtilis obtained in step (1) was inserted into the seed tank containing LB medium according to the inoculation amount of 8% volume ratio, and the rotation speed of the seed tank was controlled at 400 rpm, and the ventilation ratio ( The aeration ratio is the volume ratio of air passing through a unit volume of culture solution per minute) is 1 V / V.min, cultiva...

Embodiment 3

[0036] (1) Seed preparation: Link the synthesized glycosyltransferase UGT76G1 gene and glycosyltransferase UGT11 gene to the PBR322 plasmid vector, and the PBR322 plasmid vector carrying the glycosyltransferase UGT76G1 gene and glycosyltransferase UGT11 gene Introduced into the competent state of Bacillus subtilis, the Bacillus subtilis implanted with the glycosyltransferase UGT76G1 gene and the glycosyltransferase UGT11 gene was inserted into the LB medium, and the temperature of the LB medium was controlled at 30°C, and the rotation speed was 220 rpm. Culture time 24 h;

[0037](2) Seed tank cultivation: The Bacillus subtilis obtained in step (1) was inserted into the seed tank containing LB medium according to the inoculation amount of 8% volume ratio, and the rotation speed of the seed tank was controlled at 400 rpm, and the ventilation ratio ( The aeration ratio is the volume ratio of air passing through a unit volume of culture solution per minute) is 0.3 V / V.min, cultiv...

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 method for preparing rebaudioside M by fermentation catalysis of bacillus subtilis, which is characterized by comprising the following steps: (1) connecting glycosyl transferase UGT76G1 and UGT11 genes to a PBR322 plasmid vector, guiding into the bacillus subtilis, inoculating into an LB culture medium, and culturing for 20-24 hours at the temperature of 30-37 DEG C and the speed of 100-250 rpm; (2) inoculating into a seed tank according to the inoculum size of 1%-10%, and culturing for 20-24 hours at the temperature of 30-37 DEG C at the speed of 200-400 rpm and the ventilation ratio of 0.1-1 V / V.min; (3) inoculating into a fermentation tank according to the ratio of 1%-10%, and culturing for 48-72 hours at the temperature of 30-37 DEG C and the pH value of 6-8 at the speed of 200-1000 rpm and the ventilation ratio of 0.1-2 V / V.min; (4) carrying out ceramic membrane ultrafiltration on the fermentation liquor, carrying out resuspension and high-pressure homogenization on the thallus, and carrying out ceramic membrane ultrafiltration on the thallus crushing liquor to obtain crude enzyme liquor; and (5) mixing stevioside, uridine diphosphate glucose, a phosphate buffer and the crude enzyme according to a mass ratio of (5-10): (1-5): (40-60): (5-20), and reacting at 25-40 DEG C for 12-48 hours. The method has the advantages that two crude enzyme solutions are obtained through one-time fermentation, the operation is simple, the cost is low, and the conversion rate is 88.4% or above.

Description

technical field [0001] The invention belongs to the technical field of microbial fermentation enzyme preparations, and relates to a method for preparing rebaudioside M by fermenting and catalyzing Bacillus subtilis. Background technique [0002] Stevioside (steviol glycoside) is a natural sweetener extracted from the dried leaves of Stevia rebaudiana. Its sweetness is 200-300 times that of sucrose, and its energy is about 1 / 300 of that of sucrose. It is non-toxic, has no side effects, and has high stability. It is an ideal natural sweetener to replace sucrose, and it is known as the "third sugar source" internationally. Studies have reported that long-term consumption of stevia can prevent high blood pressure, diabetes, obesity, tooth decay and other diseases. Stevioside accounts for 60% to 70% of the total glycosides, and its taste is worse than that of rebaudioside M, with a certain after-bitterness. Rebaudioside M is a glycoside component in the steviol glycoside mixtur...

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): C12P19/56C12N1/20C12R1/125
CPCC12P19/56C12N1/20
Inventor 杨乐张敏祁飞戴永辉
Owner ANHUI JINGHE IND
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