Cordyceps militaris medium polysaccharide, method for separating and purifying same, and use thereof

Patent metadata

Field	Value
Publication number	US-11111317-B2
Application number	US-201816770983-A
Country	US
Kind code	B2
Filing date	Dec 12, 2018
Priority date	Apr 27, 2018
Publication date	Sep 7, 2021
Grant date	Sep 7, 2021

Abstract

A Cordyceps militaris medium polysaccharide, a method for separating and purifying same, and the use thereof, wherein the polysaccharide comprises the following monosaccharides in mole percentages: 0.11% ribose, 0.11% rhamnose, 0.45% arabinose, 0.13% xylose, 14.50% mannose, 83.96% glucose, and 0.73% galactose. The extraction method does not affect the biological activity of the Cordyceps militaris medium polysaccharide P1; the obtained purified polysaccharide P1 has high purity and stable properties, and has significant effects on resistance to oxidation, lowering uric acid and bacteriostasis, which are beneficial to human metabolism; due to the low cost, the purified polysaccharide P1 can be further used in the development of health products, drugs and cosmetics.

First claim

The invention claimed is:

1. A method for separation and purification of a Cordyceps militaris medium polysaccharide, comprising the following steps:
(1) extraction of the Cordyceps militaris medium polysaccharide: drying the Cordyceps militaris rice medium leftovers, pulverizing and sieving same to obtain a dry powder of the leftovers; weighing the dry powder and adding 15-16 times distilled water by mass into same, performing an ultrasonic treatment for at least 30 min, performing a reflux extraction at 70° C. for 1.5 h-2.0 h, pooling the extract solutions after several extractions, and filtering the pooled extract and concentrating same to obtain a polysaccharide concentrate; adding 3-4 times of 95% (V/V) ethanol by volume into the polysaccharide concentrate, stirring same, and allowing same to stand overnight at 4° C.; after centrifugation, drying the precipitate to obtain a Cordyceps militaris medium polysaccharide extract;
(2) decoloration of the Cordyceps militaris medium polysaccharide: dissolving the Cordyceps militaris medium polysaccharide extract by adding distilled water, adjusting the pH value to 8.0-8.5, adding H 2 O 2 solution dropwisely until colorless, and maintaining the temperature at 50° C.-55° C. for at least 2 h;
(3) deproteinization by an enzymatic method combined with Sevage method:
3-1: mixing a papain solution with the Cordyceps militaris medium polysaccharide extract solution, wherein the volume ratio of the two is 1.0:1.5-1.0:1.7, and performing an enzymolysis at 60° C.-70° C. for 2 h-3 h;
3-2: mixing a Sevage reagent with the solution obtained by the enzymolysis at a volume ratio of 1:5, culturing same with shaking for at least 30 min, then centrifuging for multiple times until no protein is precipitated out; and drying the supernatant to obtain a crude Cordyceps militaris medium polysaccharide;
(4) separation and purification of the Cordyceps militaris medium polysaccharide: dissolving the crude Cordyceps militaris medium polysaccharide with distilled water, then loading same to DEAE agarose gel FF ion exchange chromatography column, and eluting same with distilled water to obtain the polysaccharide.

2. The method for separation and purification according to claim 1 , characterized in that the concentration of step (1) is performed at 50° C.-55° C.

3. The method for separation and purification according to claim 1 , characterized in that the concentration of H 2 O 2 solution in step (2) is 30% (V/V).

4. The method for separation and purification according to claim 1 , characterized in that the papain solution of step (3) is prepared in PBS buffer with a pH value of 6.0, wherein the concentration of the papain is 250 U/ml.

5. The method for separation and purification according to claim 1 , characterized in that the Sevage reagent of step (3) is prepared from chloroform and n-butanol at a volume ratio of 5:1.

6. A method for scavenging free radicals, comprising:
adding Cordyceps militaris medium polysaccharide prepared by the method according to claim 1 into a ABTS or OH free radical containing solution.

7. A method for lowering uric acid in a subject, comprising:
administering Cordyceps militaris medium polysaccharide prepared by the method according to claim 1 to the subject.

8. The method for separation and purification according to claim 1 , wherein the Cordyceps militaris medium polysaccharide comprises the following monosaccharides in mole percentages: 0.11% ribose, 0.11% rhamnose, 0.45% arabinose, 0.13% xylose, 14.50% mannose, 83.96% glucose, and 0.73% galactose.

9. The method for separation and purification according to claim 1 , wherein the Cordyceps militaris medium polysaccharide has an average molecular weight of 2.18 k Da.

10. The method for separation and purification according to claim 1 , wherein the Cordyceps militaris medium polysaccharide comprises sulfate groups, pyranose rings and alpha-glucosidic bonds.

Assignees

• Univ South China Normal

Inventors

• Huang Ruqiang
• Zhang Jingwen
• Wang Jinghui
• Wang Qian
• Gao Linlin

Classifications

• A61K31/715 Primary

  Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters · CPC title

• A61P39/06

  Free radical scavengers or antioxidants · CPC title

• A61P19/06

  Antigout agents, e.g. antihyperuricemic or uricosuric agents · CPC title

• C08B37/006 Primary

  Heteroglycans, i.e. polysaccharides having more than one sugar residue in the main chain in either alternating or less regular sequence; Gellans; Succinoglycans; Arabinogalactans; Tragacanth or gum tragacanth or traganth from Astragalus; Gum Karaya from Sterculia urens; Gum Ghatti from Anogeissus latifolia; Derivatives thereof · CPC title

• C08B37/0003

  General processes for their isolation or fractionation, e.g. purification or extraction from biomass · CPC title