Preparation method of phosphorylated peptidoglycan

A technology of phosphorylated peptidoglycan and peptidoglycan, applied in biochemical equipment and methods, methods based on microorganisms, microorganisms, etc., can solve problems that have not been reported before, and achieve improved enzyme digestion range, mild reaction conditions, Significant effect of immune effect

Active Publication Date: 2013-11-20
NINGBO UNIV
View PDF2 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, at present, the phosphorylation modification is mainly concentrated on starch, chitosan and cellulose, etc., and the research on the phosphorylation modification of peptidoglycan has not been reported so far.

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
  • Preparation method of phosphorylated peptidoglycan
  • Preparation method of phosphorylated peptidoglycan
  • Preparation method of phosphorylated peptidoglycan

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] The invention uses common commercially available Lactobacillus acidophilus bacteria powder as a raw material to extract the peptidoglycan. First, inoculate 2mg of bacterial powder into 200mL of MRS liquid medium, and culture it statically at 37°C for 24 hours to activate the strain. A method for preparing phosphorylated peptidoglycan of the present invention specifically includes the following steps:

[0037] (1) Preparation of peptidoglycan

[0038] a. Bacteria collection: Inoculate the activated Lactobacillus acidophilus into the MRS liquid medium with an inoculum volume of 4% by volume, culture it in a constant temperature incubator at 38.5°C for 20 hours, centrifuge at 6500r / min for 15min to collect the bacteria, and use distilled water repeatedly Wash until the cells are milky white; the preparation method of the MRS liquid medium is as follows: 10g of peptone, 10g of beef extract, 5g of yeast extract, 10g of glucose, 2g of triamine citrate, 2g of dipotassium hydro...

Embodiment 2

[0047] With embodiment 1, its difference is:

[0048] (1) Preparation of peptidoglycan

[0049] Inoculate the activated Lactobacillus acidophilus into the MRS liquid medium with an inoculation amount of 3% by volume, and culture it in a constant temperature incubator at 37°C for 16 hours, then centrifuge at 5000r / min for 20 minutes to collect the bacteria, and wash them repeatedly with distilled water until the bacteria are milky white Suspend the bacterium in a 40% hydrofluoric acid solution at a solid-to-liquid ratio of 1g:9ml, place it overnight at 4°C, and centrifuge at 7000r / min for 20min to collect the cell wall precipitate that does not contain teichoic acid, and wash the precipitate with distilled water until Neutral; dissolve the precipitate in chymotrypsin phosphate buffer at a solid-to-liquid ratio of 2g:5ml, shake on a shaker at 110r / min at 37°C for 17h, inactivate in a boiling water bath for 4min, centrifuge at 1500r / min for 6min, discard Remove the undissolved p...

Embodiment 3

[0055] With embodiment 1, its difference is:

[0056] (1) Preparation of peptidoglycan

[0057] Inoculate the activated Lactobacillus acidophilus into the MRS liquid medium with an inoculation amount of 5% by volume, and culture it in a constant temperature incubator at 40°C for 24 hours, then centrifuge at 8000r / min for 10 minutes to collect the bacteria, and wash them repeatedly with distilled water until the bacteria are milky white Suspend the bacterium in a 50% hydrofluoric acid solution at a solid-to-liquid ratio of 1g:9ml, place it overnight at 4°C, centrifuge at 9000r / min for 10min to collect the cell wall precipitate, and wash the precipitate with distilled water to neutrality; The solid-liquid ratio of 2g:5ml was dissolved in chymotrypsin phosphate buffer, shaken at 130r / min at 40°C for 15h, inactivated in a boiling water bath for 6min, centrifuged at 2500r / min for 4min, and the supernatant was placed at 12000r / min Centrifuge for 10 min, and wash the obtained precip...

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 preparation method of phosphorylated peptidoglycan. The method is characterized by comprising the following steps of: inoculating Lactobacillus acidophilus on a culture medium for cultivation, centrifuging to collect thallus, repeatedly washing the thallus, suspending the thallus in hydrofluoric acid solution for one night at 4 DEG C, centrifugally collecting cell wall sediment, and washing the sediment to become neutral; dissolving the sediment into Trypsin chymotrypsin phosphate buffer solution, inactivating in boiling water, centrifuging the liquid supernatant, washing the sediment; dissolving the sediment in diethyl ether, stirring and centrifuging to collect sediment, and washing the sediment with water until completely removing the smell of diethyl ether, then obtaining the peptidoglycan; dissolving the peptidoglycan in Lysostaphin phosphate buffer solution for performing enzymolysis and centrifuging, taking the liquid supernatant, centrifuging the liquid supernatant, and centrifugally washing the sediment with water to get micromolecule peptidoglycan; and finally, dissolving the micromolecule peptidoglycan in mixed phosphate solution, precipitating with alcohol after reaction, treating the alcohol precipitated peptidoglycan by freeze drying and redissolving, and adding the redissolved solution in a dialysis bag, performing dialysis concentration, and then, performing freeze drying to get the phosphorylated peptidoglycan. The method has the advantages of increasing the solubility remarkably and improving the immunological effect to a certain extent.

Description

technical field [0001] The invention relates to a method for preparing peptidoglycan, in particular to a method for preparing phosphorylated peptidoglycan. Background technique [0002] As an important intestinal probiotic, lactic acid bacteria play an important role in regulating the intestinal microbial flora, enhancing the body's immunity and preventing diseases such as tumors. In recent years, in addition to paying attention to the long-term research of Bifidobacterium and Bacillus subtilis at home and abroad, they have begun to focus on another important member-Lactobacillus acidophilus. These bacteria use their unique peptidoglycan components to induce the release of various cytokines to regulate the immune function of the host. [0003] Peptidoglycan is one of the main components of bacterial cell walls. Its monomer is composed of a tetrapeptide tail and a disaccharide unit. This microbial polysaccharide has different immune effects due to the particularity of its ...

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): C12P19/14C12P19/04C12R1/23
Inventor 潘道东王琳珺曾小群孙扬赢曹锦轩
Owner NINGBO UNIV
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap