Method for separating and purifying blue algae polysaccharide

A technology for the separation and purification of cyanobacteria polysaccharides, applied in the field of biochemical separation, can solve problems such as cumbersome process, high price, and increased production cost, and achieve the effects of simplifying steps, saving resources, and reducing usage

Active Publication Date: 2010-09-15
东台市赐百年营养科技有限公司
View PDF9 Cites 14 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The development and utilization of economical microalgae in my country is at the primary processing stage, and the extraction and separation and purification of seaweed polysaccharides mostly stay in the laboratory research stage. The reported patented technology of algae polysaccharides, such as Chinese patents CN1297948A, CN1397567A, CN101445565A, etc. Isoelectric point method, sevage method, trichloroacetic acid method, etc. to remove protein, and ion exchange column to purify polysaccharide, although the purity of polysaccharide is improved to a certain extent, but the production cost increases and the process is cumbersome; CN1392360A, CN101037483A use active amino and hydroxyl The cationic bioflocculant chitosan or modified starch, or the anionic flocculant that ionizes sulfonate groups when dissolved in water to extract seaweed polysaccharides, the addition amount is 50ppm ~ 500ppm, and the price is relatively inorganic macromolecule or polyacrylamide flocculation dose higher

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

[0017] (1) Preparation of cyanobacterial polysaccharide crude extract

[0018] Take the dry powder of Spirulina platensis produced in Dongtai, Jiangsu Province, use water as the extractant, and the solid-to-liquid mass ratio of algae powder to water is 1:20, stir evenly, soak for 1 hour, heat and stir at 80°C for 4 hours, and the cyanobacteria will break down. The wall fluid was centrifuged at 3800r / min for 15min to obtain a sugar content of 2.22mg / mL in the extract.

[0019] (2) Polyferric flocculant treatment of crude extract of cyanobacterial polysaccharide

[0020] Add the crude extract of spirulina polysaccharide (original pH=7.25) into the container, add the polyiron flocculant working solution, the content of the polyiron flocculant in the crude extract of spirulina polysaccharide is 50ppm, first stir rapidly for 1min (200r / min ), then stirred at a slow speed for 15min (50r / min), after standing at room temperature for 0.5h, centrifuged at 3800r / min for 15min, and the p...

Embodiment 2

[0025] (1) Preparation of cyanobacterial polysaccharide crude extract

[0026] Take fresh microalgae produced in Taihu Lake, Wuxi, Jiangsu Province, use water as the extractant, and the solid-to-liquid mass ratio of fresh algae to water is 1:30, heat and stir at 80°C for 4 hours, then centrifuge the cyanobacteria wall breaking solution at 6000r / min for 10min , the upper layer liquid was obtained, and the sugar content in the obtained extract was 1.80 mg / mL.

[0027] (2) Polyferric flocculant treatment of crude extract of cyanobacterial polysaccharide

[0028] Add the crude cyanobacterial polysaccharide extract (original pH=7.25) into the container, add the polyferric flocculant working solution, the content of the polyferric flocculant in the crude cyanobacterial polysaccharide extract is 50ppm, first stir rapidly for 1min (200r / min), Then stir slowly for 15min (50r / min), after standing at room temperature for 0.5h, centrifuge at 3800r / min for 15min, remove the precipitate, a...

Embodiment 3

[0033] (1) Preparation of cyanobacterial polysaccharide crude extract

[0034] Take the dry powder of Spirulina platensis produced in Dongtai, Jiangsu Province, use water as the extractant, and the solid-to-liquid mass ratio of algae powder to water is 1:20, stir evenly, soak for 1 hour, heat and stir at 80°C for 4 hours, and the cyanobacteria will break down. The wall fluid was centrifuged at 3800r / min for 15min to obtain a sugar content of 2.22mg / mL in the extract.

[0035] (2) Polyacrylamide-based anionic flocculants to treat crude extracts of cyanobacterial polysaccharides

[0036] Add crude cyanobacterial polysaccharide extract (original pH=7.25) into the container, add anionic polyacrylamide AN926SHu flocculant working solution, the content of flocculant in the crude extract of cyanobacterial polysaccharide is 10ppm, first stir rapidly for 1min (200r / min) , then stirred at a slow speed for 15min (50r / min), after standing at room temperature for 0.5h, centrifuged at 3800...

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

PropertyMeasurementUnit
purityaaaaaaaaaa
Login to view more

Abstract

The invention discloses a method for separating and purifying blue algae polysaccharide, which belongs to the technical field of biochemical separation. The method comprises the following steps of: preparing a crude extract of the blue algae polysaccharide; treating the crude extract of the blue algae polysaccharide by using a flocculating agent; performing vacuum concentration on the crude extract treated by using the flocculating agent; depositing the blue algae polysaccharide by using ethanol; and eluting a deposit and then performing vacuum drying on the deposit to obtain the blue algae polysaccharide with certain purity. The method relates uses the flocculating agent to flocculate impurities, but does not adopt the common isoelectric point, sevage method and the like to remove the impurities such as protein and the like. The method simplifies steps of the purification process, has simple operation, reduces the used amount of chemical reagents used in the preparation process, and saves resources, and the purity of the obtained polysaccharide can reach as high as 91.18 percent. Fresh or dried algae powder, even field Taihu Lake water bloom blue algae is used as a raw material, so a technical method for realizing scale utilization of algae resources is provided.

Description

technical field [0001] The invention provides a simple and fast method for extracting and separating blue-green algae polysaccharides from blue-green algae. It belongs to the technical field of biochemical separation. Background technique [0002] Studies by domestic and foreign personnel have shown that algae have various functions such as anti-fatigue, anti-radiation, anti-virus, anti-tumor, anti-allergy, and enhancing immunity, which determines that algae and its active ingredients have a wide range of functions in the research and development of functional foods. Application prospects. The biological activities of seaweed polysaccharides are mainly manifested in anticoagulant, antiviral, immune regulation and antitumor effects. The spatial structure of polysaccharides and the molecular weight of polysaccharides are related. [0003] There have been many research reports on polysaccharides and their biological activities of red algae, brown algae and green algae, but l...

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): C08B37/00
Inventor 王峰印小燕崔正刚韩成斌邹刚
Owner 东台市赐百年营养科技有限公司
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