Patents
Literature
Patsnap Copilot is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Patsnap Copilot

199results about How to "Reduce abundance" patented technology

Non-woven base composite membrane for lithium isotope separation, and preparation method thereof, as well as lithium isotope separation method by using membrane chromatography

The invention provides a non-woven base composite membrane for lithium isotope separation and a preparation method thereof, as well as a lithium isotope separation method by using a membrane chromatography. The non-woven base composite membrane takes a non-woven fabric as a porous support body or a micropore membrane, a coating is prepared on the non-woven fabric by taking a crown ether graft polymer or a Kryptofix graft polymer with a lithium isotope separation effect as a film forming matter, or a coating can be prepared on the non-woven fabric by blending crown ether or Kryptofix and derivates of the crown ether or the Kryptofix into a film-formation polymer solution, and the coating and a base membrane are combined to form a composite separated membrane; the composite separated membrane is taken as a membrane chromatography medium stationary phase, so as to separate lithium isotopes by using the membrane chromatography. The non-woven base composite membrane or the lithium isotope separation method by using the membrane chromatography can effectively improve the contact and coupling efficiency of crown ether molecules and Lithium Ions in the separation process for solid-liquid extraction lithium isotopes, and realize the greenization, serialization and high efficient of the process of lithium isotope separation.
Owner:TIANJIN POLYTECHNIC UNIV

Sargassum pallidum polysaccharide with effects of resisting oxidation and regulating intestinal flora as well as preparation method and application of sargassum pallidum polysaccharide

The invention discloses sargassum pallidum polysaccharide with effects of resisting oxidation and regulating intestinal flora as well as a preparation method and application of the sargassum pallidumpolysaccharide. The preparation method comprises the steps of hot water extraction, deproteinization, decoloration, alcohol precipitation, dialysis and degradation, wherein the degradation process comprises the steps: adding a sargassum pallidum crude polysaccharide solution with the concentration of 5-8 mg / mL into an H2O2 solution until the volume concentration is 1-5%, placing the mixture in anultrasonic field, carrying out radiation treatment at the ultrasonic frequency of 20-25 kHz and the power of 450-550 W, and performing freeze drying to obtain sargassum pallidum polysaccharide. Compared with sargassum pallidum crude polysaccharide, the sargassum pallidum polysaccharide has the average molecular weight of 130-510 kDa, the particle size of 400-500 nm and low viscosity, can significantly improve the abundance of beneficial bacteria in human intestinal tracts and reduce the abundance of harmful bacteria, has an intestinal microorganism utilization rate improved by about 7%, and can be used as a food additive in functional food for regulating intestinal health.
Owner:SOUTH CHINA UNIV OF TECH

Polypeptide probe and application of polypeptide probe to identification of post-translational modification binding protein

The invention provides a polypeptide probe based on photo-crosslinking and nano-metal particle self-assembly technologies. The polypeptide probe is modified with protein-post-translational modified polypeptide. According to the polypeptide probe, affinity recognition and enrichment capture processes are integrated, so that the convenient and efficient recognition and identification of a protein-post-translational modified binding protein or a compound of the binding protein. According to the polypeptide probe of the invention, a photo-crosslinking group is introduced into nano metal particles,so that a weak acting force between the polypeptide and the binding protein is converted into a strong covalent bond effect formed by the photo-crosslinking group, and therefore, the polypeptide probe can bear strong elution conditions and can capture proteins with low abundance and transient interaction; the influence of the modification of the photo-crosslinking group on a polypeptide frameworkis avoided, and therefore, the original structure and recognition characteristic of the polypeptide framework are well maintained, and influence on the binding specificity of the corresponding binding protein is greatly reduced. The invention further provides a preparation method of the polypeptide probe, and the application of the polypeptide probe to the identification of post-translational-modified binding proteins, the identification of interaction between protein modifications and the discovery of new protein-modified binding proteins.
Owner:TIANJIN MEDICAL UNIV

Cordyceps militaris intracellular polysaccharide and preparation method thereof, and applications in regulation of intestinal flora

The invention discloses cordyceps militaris intracellular polysaccharide and a preparation method thereof, and applications of the cordyceps militaris intracellular polysaccharide in regulation of intestinal flora. The method comprises the following steps: carrying out fermentation culture on cordyceps militaris strains, and separating to obtain cordyceps militaris mycelia; degreasing the cordyceps militaris mycelia, and performing hot water leaching to obtain a cordyceps militaris leaching liquid; and removing protein by adopting trypsin and a Sevage method, carrying out ethanol precipitation, and carrying out DEAE-Sepharose Fast Flow column chromatography purification to obtain the cordyceps militaris intracellular polysaccharide. The cordyceps militaris intracellular polysaccharide prepared by the invention can regulate the intestinal bacterial flora structure of a high-fat diet mouse, promote the growth of intestinal probiotics of high-fat diet mice, improve the proportion of phylum firmicutes / bacteroides, adjust the structure of fungal flora, promote the synthetic route of intestinal butyrate, induce activation of short-chain fatty acid receptors, promote fat metabolism and inhibit fat accumulation so as to achieve the effects of reducing blood fat and protecting the liver.
Owner:SOUTH CHINA NORMAL UNIVERSITY

Modified apple pectin with excellent colon fermentation property and preparation method thereof

ActiveCN110801028AFast colonic fermentationSimple structureFood ingredient functionsBiotechnologyAmylase
The invention discloses a modified apple pectin which has a purity of higher than 90%, a methyl esterification degree of lower than 6%, an acetylation degree of less than 2%, a molecular linearity ofgreater than 12, and an average molecular weight of 8.0-15 kDa, and a degradation rate of higher than 90% after 12 h in the intestinal tract. The invention further discloses a preparation method of the pectin, which comprises the following steps: uniformly mixing water and apple powder; sequentially carrying out enzymolysis by using alpha-amylase and the like to obtain an apple powder enzymatic hydrolysate, carrying out concentration and suction filtration, and performing hot leaching on the filter residue with acid water to obtain a crude pectin extract; firstly adding pectin methylesterase and pectin acetylesterase to the crude pectin extract for enzymolysis, and then adding rhamnogalacturonase and the like thereto for enzymolysis to obtain a pectinase enzymatic hydrolysate; subjecting the pectinase enzymatic hydrolysate to high-pressure dynamic micro-jet treatment before concentration, adding ethanol to precipitate, re-dissolving the precipitate for ultrafiltration and dialyzing, and carrying out concentration and drying to obtain the modified apple pectin. According to the invention, the modified apple pectin has an increased intestinal fermentation speed and a higher degradation rate than commodity apple pectin.
Owner:INST OF AGRO FOOD SCI & TECH CHINESE ACADEMY OF AGRI SCI
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