Novel method for fermentation production of erythrocin by utilizing saccharopolyspora erythraea

A technology of erythromycin and fermentation liquid, applied in the field of bioengineering, can solve the problems of low industrial application value, unfavorable erythromycin research, low erythromycin yield, etc.

Active Publication Date: 2019-11-15
EAST CHINA UNIV OF SCI & TECH
View PDF6 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] In summary, the erythromycin yield of the synthetic medium of Saccharopolyspora rubrum is very low at present, which is

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
  • Novel method for fermentation production of erythrocin by utilizing saccharopolyspora erythraea
  • Novel method for fermentation production of erythrocin by utilizing saccharopolyspora erythraea
  • Novel method for fermentation production of erythrocin by utilizing saccharopolyspora erythraea

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0069] Embodiment 1, fermentation culture

[0070] In this example, a 5L fermenter was used for fermentation, and the optimized synthetic medium of the present invention was used as the fermentation medium.

[0071] 1. Cleaning, inoculation and cultivation

[0072] Before inoculation, the strains were washed. For the rapid germination of spores and the growth of hyphae, the seed medium is a compound medium, and the bacteria are cleaned with physiological saline. First, after sterilizing the normal saline, empty 500mL shaker flasks and enough empty 50mL centrifuge tubes, put them into the ultra-clean workbench. Wipe the seed shake flask cultivated for 48 hours with alcohol cotton, and put it into the ultra-clean workbench. Then, pour the culture medium in the seed shake flask into an empty centrifuge tube, close the lid tightly, and centrifuge at 3000rpm for 10min. After taking out the centrifuge tube, wipe the tube wall with alcohol cotton, put it into the ultra-clean work...

Embodiment 2

[0117] Embodiment 2, the research of erythromycin yield and cell dry weight in fermentation process

[0118] Use 0.5L shake flasks as seed shake flasks, the initial group is to apply the original medium (M1); the strategy of the strategy group for supplementing ammonia water is to reduce the total amount of amino acids in the original medium by 20% (M2), and add ammonia water in the process. Nitrogen source: Ammonium sulfate supplementation strategy The strategy of the group is to use medium M2 and supplement ammonium sulfate as a nitrogen source during the process.

[0119] See figure 1 In the left picture, in terms of dry cell weight, due to the high amino acid content in the basal medium of the initial group, the dry cell weight at 30-60h is higher. However, the inventors also noticed that although the dry weight of the cells increased rapidly, the bacterial cells autolyzed rapidly after the nitrogen source was consumed. That is to say, there is a rapid decrease in dry ce...

Embodiment 3

[0121] Embodiment 3, the utilization of glucose, phosphorus, nitrogen source in fermentation process

[0122] Glucose is utilized during fermentation as figure 2 (a), from the perspective of residual sugar in the first 40 hours, the sugar consumption rate of the initial group was the fastest, and the sugar consumption rate of the ammonia supplementation strategy group and the ammonium sulfate supplementation strategy group were basically the same, but after 40 hours, the residual sugar of the ammonium sulfate supplementation strategy group The overall value was higher than that of the ammonia supplementation strategy group, which may be related to the lower supplementation of ammonium sulfate. The residual sugar in the ammonia water supplementation strategy group was zero at 118 hours due to more ammonia water supplementation and glucose depletion.

[0123] The utilization of amino nitrogen in the fermentation process is as follows: figure 2 (b), before 100h, the change tr...

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 novel method for fermentation production of erythrocin by utilizing saccharopolyspora erythraea. According to the method, glucose is taken as a carbon source, amino acid istaken as a nitrogen source, the saccharopolyspora erythraea is subjected to fermentation culture, at a proper fermentation stage, the carbon source and ammonium sulfate are replenished, and efficientproduction of the erythrocin is achieved. In addition, the method is environmentally friendly and low in culture cost.

Description

technical field [0001] The invention belongs to the field of bioengineering, and more specifically relates to a novel method for producing erythromycin by fermentation of Saccharopolyspora rubrum. Background technique [0002] At present, the industrial production of erythromycin uses compound culture medium. Although the compound culture medium has carbon and nitrogen sources such as soybean cake powder and starch, which can be absorbed and utilized by the bacteria, these solid particles also cause a high degree of fermentation liquid, and due to the red Saccharopolyspora is a highly aerobic bacterium, so high tank pressure and ventilation during the fermentation of erythromycin can ensure the oxygen supply of the bacteria, which requires higher equipment for fermentation tanks and air compressors, which increases the cost. At the present stage, the national government has more requirements on the environmental protection of enterprises, and the penalties have been increase...

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
IPC IPC(8): C12P19/62C12R1/01
CPCC12P19/62
Inventor 储炬杨含廖建国洪铭杭海峰庄英萍
Owner EAST CHINA UNIV OF SCI & TECH
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
Try Eureka
PatSnap group products