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49results about How to "Improve the degree of enzymatic hydrolysis" patented technology

Comprehensive nutrition powder for reducing fat, lowering blood sugar, lowering blood pressure and lowering blood fat, and preparation method thereof

The invention discloses a comprehensive nutrition powder for reducing fat, lowering blood sugar, lowering blood pressure and lowering blood fat, and a preparation method thereof. The comprehensive nutrition powder comprises nutrients most easily deficient in modern people, auxiliary nutrients for promoting absorption of the nutrients, and effective components for reducing fat, lowering blood sugar, lowering blood pressure and lowering blood fat, and specifically comprises: broccoli powder or carrot powder, black fungus powder, pleurotus eryngii powder, oyster powder, vitamin C, vitamin B2, heme iron, hericium erinaceus cell wall-broken ultrafine powder, composite fermented powder of Chenopodium quinoa and chickpea, olive kernel peptide powder, and composite fermented powder of Sacha Inchikernel and linseed, wherein the pleurotus eryngii powder is dried in the sun. The comprehensive nutrition powder comprehensively considers interaction between various nutrients, eliminates interference of phytic acid on absorption of minerals, and can achieve effects of reducing fat, lowering blood sugar, lowering blood pressure and lowering blood fat from multiple sources and in various aspects.The preparation method can well retain nutrition of dietary ingredients in the comprehensive nutrition powder, and maximize functions of the effective ingredients in reducing fat, lowering blood sugar, lowering blood pressure and lowering blood fat.
Owner:重庆一家人生物科技有限公司

Method for producing edible and medicinal fungus peptides by performing enzymolysis thrice and fermentation once

The invention discloses a method for producing edible and medicinal fungus peptides by performing enzymolysis thrice and fermentation once. The method comprises the following steps: pulverizing edibleand medicinal fungi, and adding cellulase for performing enzymolysis; adding papain and neutral protease into the enzymolysis liquid for performing enzymolysis; after the enzymolysis is completed, inoculating bacillus subtilis for performing fermentation; and after the fermentation is completed, centrifuging the fermentation liquid, then taking supernatant liquid, performing filtration with an ultra-filtration membrane, and performing purification, sterilization, concentration and drying to obtain the edible and medicinal fungus peptides. The method disclosed by the invention has the advantages that fungi and enzymes are mutually matched to produce small peptides, respective advantages of enzymolysis and microorganisms are fully utilized, and synergistic effects of the microorganisms andproteases are exerted to ensure that the protein of the edible and medicinal fungi can be degraded more thoroughly and the degree of small peptides is higher; and during subsequent purification, an ultra-filtration membrane is utilized for performing filtration and ion exchange resin is utilized for performing purification so as to obtain high-content edible and medicinal fungus peptides.
Owner:安徽精准医疗产业研究院有限公司

Method for preparing pig cerebral protein antioxidative peptide

The invention discloses a method for preparing pig cerebral protein antioxidative peptide. The method comprises the following steps of 1, pretreatment, wherein fresh pig brain is taken to be prepared into degreased cerebral protein powder for use; 2, ultrasonic treatment of pig cerebral protein powder, wherein the degreased cerebral protein powder is added into deionized water according to the volume proportion of 1:200, the cerebral protein powder is completely dissolved; countercurrent pulse ultrasonic treatment is carried out, the cerebral protein powder cooled to room temperature is placed in a countercurrent pulse ultrasonic treating device to be treated, the ultrasonic frequency is 20 kHz, the power ranges from 60 W to 100 W, ultrasonic treatment is carried out for 4 min to 6 min, ultrasonic time is 2 s, and intermittent time is 2 s; 3, enzymolysis to extract crude pig brain polypeptide, wherein pig brain polypeptide crude extracting liquid is prepared; 4, separation, wherein an ultrafiltration membrane with the molecular cut off of 3-5 kDa is used for fractionation; 5, purifying, wherein a DEAE-52 fiber resin layer is utilized for carrying for secondary purification on the pig brain peptide prepared in the step 4, and the pig cerebral protein antioxidative peptide is prepared.
Owner:JIANGSU ACADEMY OF AGRICULTURAL SCIENCES

Preparation method of peanut peptide with high immune activity

The invention discloses a preparation method of a peanut peptide with high immune activity. The preparation method comprises the following steps: (1) taking cold pressing peanut meal and hot pressingpeanut meal as raw materials, and preprocessing raw materials; (2) subjecting preprocessed raw materials to primary enzymatic hydrolysis (semidry method) to obtain enzymatic hydrolysate (A); (3) subjecting the enzymatic hydrolysate (A) to primary microbial fermentation; (4) after the primary microbial fermentation, evenly dividing the fermentation product into three parts, adding ficin, alkaline protease, and neutral protease into three parts respectively, carrying out synchronous secondary enzymatic hydrolysis to obtain enzymatic hydrolysate (B); (5) adding composite protease into the enzymatic hydrolysate (B), carrying out tertiary enzymatic hydrolysis, and after enzymatic hydrolysis, deactivating the enzymes to obtain enzymatic hydrolysate (C); and (6) subjecting enzymatic hydrolysate (C) to secondary microbial fermentation, and subjecting fermentation broth to ultrafiltration separation, discoloring, concentration, and drying to obtain the peanut peptide with high immune activity.The immune activity of the product is effectively improved, aflatoxin is removed effectively, and the preparation method has a high application value.
Owner:SHANDONG AGRICULTURAL UNIVERSITY

Method for preparing cornu cervi pantotrichum plate enzymatic hydrolysate and cornu cervi pantotrichum plate enzymatic hydrolysate tablet

The invention relates to the technical field of biological proteins, in particular to an enzymatic hydrolysis method for cornu cervi pantotrichum plates and a cornu cervi pantotrichum plate enzymatic hydrolysate tablet. The enzymatic hydrolysis method includes 1), crushing the cornu cervi pantotrichum plates, then adding the cornu cervi pantotrichum plates into water, decocting the cornu cervi pantotrichum plates, carrying out extraction to obtain extract liquid, centrifuging the extract liquid and discarding precipitates to obtain supernatant; 2), concentrating the supernatant, then carrying out cold storage and freezing, and carrying out sufficient drying and smashing to obtain cornu cervi pantotrichum plate gelatin powder; 3), adding the cornu cervi pantotrichum plate gelatin powder into water, dissolving the cornu cervi pantotrichum plate gelatin powder, adding trypsin into the water and carrying out enzymatic hydrolysis to obtain cornu cervi pantotrichum plate enzymatic hydrolysate. The enzymatic hydrolysis method and the cornu cervi pantotrichum plate enzymatic hydrolysate tablet have the advantages that the enzymatic hydrolysis method is high in cornu cervi pantotrichum protein hydrolysis degree, and the cornu cervi pantotrichum plate enzymatic hydrolysate prepared by the aid of the enzymatic hydrolysis method is excellent in anti-inflammation activity.
Owner:INST OF SPECIAL ANIMAL & PLANT SCI OF CAAS

Preparing method and application of gradient collagen and collagen polypeptide molecules

The invention discloses a preparing method of gradient collagen and collagen polypeptide molecules. The preparing method particularly comprises the steps of defatting, deodorizing, primary enzymolysis, secondary enzymolysis and the like. The invention further discloses application of the gradient collagen and collagen polypeptide molecules. The gradient collagen and collagen polypeptide moleculescan be applied to the fields of cosmetics, skin care products, nourishing and health products, food additives, feed and the like. According to the preparing method of the gradient collagen and collagen polypeptide molecules, animal skins are subjected to procedures such as defatting, deodorizing, primary enzymolosis and secondary enzymolysis to be prepared into the collagen and collagen polypeptide molecules with different molecular weights, the procedures are simple, the enzymatic hydrolysis degree of collagen is increased, and thus products are smaller in molecular weight and easy to absorbby the human body. The preparing method of the gradient collagen and collagen polypeptide molecules has good defatting, deodorizing and decolorizing effects and facilitates improvement of the qualityof the products; the whole technology process is simple and reasonable, the safety is high, the operability is high, and the products are high in yield and good in quality.
Owner:GUANGDONG OCEAN UNIVERSITY

Euphausia superba flavor peptide powder and preparation method thereof

The invention relates to the technical field of food processing, in particular to euphausia superba flavor peptide powder and a preparation method thereof. The preparation method includes the following steps: dissolving shrimp powder; adding flavourzyme and compound protease; adding papain after carrying out enzymolysis for four hours; carrying out secondary enzymolysis for six hours, adding flavourzyme and aminopeptidase, and continuously carrying out enzymolysis for two hours; after enzyme deactivation, filtering, taking supernate, and cooling to room temperature; adding 10% of calcium hydroxide for defluorination, then adjusting the PH to 7-8 by using phosphoric acid, centrifuging the mixture and collecting a supernatant; debitterizing the supernate by adopting an adsorption method, wherein the concentration of protein peptide during debitterizing is 20%, the dosage of an adsorbent is 15%, the adsorption temperature is 80 DEG C, and the adsorption time is 5-10 minutes; and carrying out spray drying on the debittered concentrated solution to obtain the euphausia superba flavor peptide powder. The euphausia superba flavor peptide powder with the highest enzymolysis degree and the weakest bitter taste is obtained by reasonably selecting the type of the compound protease and the enzymolysis time and optimizing the enzymolysis conditions.
Owner:OCEAN UNIV OF CHINA

Compound enzyme preparation, method for preparing feed from compound enzyme preparation and animal feed

InactiveCN107836573AShorten autolysis timeExcellent enzymatic hydrolysis processAccessory food factorsNeutral proteaseEthyl acetate
The invention provides a compound enzyme preparation, a method for preparing a feed from the compound enzyme preparation and an animal feed, and relates to the field of preparation of feeds. The compound enzyme preparation is compounded from alkali protease and flavored protease, wherein the mass ratio of the alkali protease to the flavored protease is (3 to 1) to (4 to 3), the alkali protease iscompounded from keratinase, papain and cellulase, and the flavored protease is compounded from neutral protease, aminopeptidase and maltodextrin. The method comprises the following steps of compounding beef waste yeast as a raw material into a yeast solution with a preset concentration, performing uniform dissolving, adding ethyl acetate, preheating the yeast solution, adding the compound enzyme preparation, performing an enzymolysis reaction to obtain enzymatic hydrolysate, and performing spray drying on the enzymatic hydrolysate. According to the compound enzyme preparation, the method for preparing the feed from the compound enzyme preparation and the animal feed disclosed by the invention, shortening of the self-dissolving time of yeast is facilitated, the enzymolysis degree is increased, the palatability of a yeast self-dissolving animal feed is improved, besides, the content of small-molecule nutrient components in the feed is increased, and the industrial production efficiency is improved.
Owner:WUHAN SUNHY BIOLOGICAL +1

Pearl shell whitening factor, and preparation method and application thereof

The invention discloses a preparation method for a pearl shell whitening factor. The preparation method comprises the following steps: 1) crushing clamshells, and conducting screening to obtain small-particle clamshell powder; 2) mixing the clamshell powder with an aqueous weak acid solution, conducting stirring and decomposing, and separating out a solid, namely crude protein; 3) cleaning the crude protein with deionized water, mixing the cleaned crude protein with a buffer solution having a pH value of 6.0-7.5, treating the mixed solution for 20-40 minutes at an ultrahigh pressure of 100-200Mpa and a temperature of 40-80 DEG C, and subjecting the mixed solution and protease to mixing and reacting for 2-7 hours at a temperature of 40-60 DEG C under ultrasonic conditions; 4) carrying outstirring for 20-50 minutes at 85-100 DEG C for enzyme deactivation, and performing filter pressing through a filter membrane to obtain a sterile filtrate; 5) mixing a freeze-drying protective agent with the filtrate, conducting pre-freezing, and then performing freeze-drying in a vacuum freeze-drying bin for 12-20 hours so as to finally obtain freeze-dried powder with a moisture content of 2-5%. The invention also discloses application of the pearl shell whitening factor obtained by the method in preparation of an endothelin antagonist. The preparation method is simple in process, and the obtained pearl shell whitening factor is obvious in whitening effect.
Owner:OSMUN BIOLOGICAL

Method for producing protein small peptide by utilizing north pacific squid

The invention relates to the technical field of aquatic product processing, and in particular relates to a method for producing a protein small peptide by utilizing north pacific squid. The method comprises the following steps: (1) slaughtering and cleaning fresh squids, and then rubbing; (2) adding purified water into the rubbed squids in a ratio of 2-3L purified water per kilogram squid meat, continuously rubbing and stirring uniformly, regulating pH to be 8-9, and carrying out ultrasonic treatment for 20-40 minutes at the action temperature of 50-55 DEG C and the power of 200-350W; (3) carrying out enzymolysis by adopting a compound protease; (4) carrying out ultrafiltration separation; (5) carrying out Sephadex G-25 gel column chromatography isolation, and screening out a product witha peak having the strongest antioxidation activity; and (6) carrying out reverse phase high performance liquid chromatography separation and purification, so that the protein small peptide of the north pacific squid is obtained. The method provided by the invention has the advantages that enzymolysis is improved, so that extraction rate and hydrolysis rate of proteins are improved, and further yield of the protein small peptide is improved.
Owner:舟山市常青海洋食品有限公司

Preparation method of vegetable protein polypeptide liquid

The invention discloses a preparation method of vegetable protein polypeptide liquid. The preparation method comprises the following steps: (1) activating; (2) carrying out pre-enzymolysis; (3) carrying out secondary enzymolysis; and (4) filtering. According to the preparation method disclosed by the invention, soybean protein powder and peanut protein powder are used as raw materials, and are activated to improve the reaction activity of the protein powder; the pre-enzymolysis and the secondary enzymolysis are adopted, so that the content of soluble nitrogen in slurry is remarkably improved and the content of the nitrogen can reach 1.5%; the enzymolysis efficiency is high, the enzymolysis degree of protein is high and the recycling rate of the protein is up to 87.6%; the peptide yield is high and the balance of amino acids is good; abundant carbon and nitrogen sources, and growth factors can be provided for the growth of microorganisms; purified water is added for two times and time and energy sources are saved, so that the preparation method has remarkable economic and social benefits; vegetable protein polypeptide liquid prepared by the invention can be directly used for preparing a streptococcus fermentation culture medium, and does not need to be concentrated, and spray-dried, so that a lot of energy sources are saved and the production cost is reduced, and furthermore, the preparation method is suitable for industrial large-scale production.
Owner:SHANDONG TOPSCI BIO TECH

Extraction method of porcine blood antibacterial peptide

The invention discloses an extraction method of porcine blood antibacterial peptide. The method comprises the following specific steps: adding a sodium hexametaphosphate aqueous solution into fresh porcine blood, uniformly stirring, removing precipitate after centrifugalization, and adjusting the pH value of supernate, so as to obtain anti-freezing porcine blood; adding Alcalase enzyme and trypsininto the anti-freezing porcine blood, performing microwave enzymolysis, adjusting the pH value after enzymolysis is completed, heating the anti-freezing porcine blood to be boiled, and filtering, soas to obtain filtrate namely enzymatic hydrolysate; performing ultrafiltration and nanofiltration on the enzymatic hydrolysate, so as to obtain antibacterial peptide crude extract; performing gel chromatography on the antibacterial peptide crude extract, washing through double distilled water after loading, collecting components with high antibacterial activity, and performing freeze drying, so asto obtain the porcine blood antibacterial peptide. The method has the benefits that the method is simple and practical, the extraction efficiency, yield and purity are high, and the formed antibacterial peptide is high in activity, can rapidly kill bacteria and has broad-spectrum antibacterial property.
Owner:金华市铁骑士生物科技有限公司

Method for preparing collagen from deer sinew

The invention belongs to the technical field of collagen extraction and particularly relates to a method for preparing collagen from deer sinew by using the processes of extraction and purification through hydrochloric acid hydrolysis and trypsin enzymolysis. The method comprises the following steps: removing fat, skin and sinew membrane from the deer sinew; cutting the deer sinew into small pieces with the size being 0.5cm<3> to 1cm<3>; then, repeatedly washing the cut deer sinew with normal saline to remove sera and fat; further rinsing the washed deer sinew with distilled water; adding hydrochloric acid with the volume concentration thereof being 0.05% to 1.0% to the rinsed deer sinew by the solid-liquid ratio being 1g:5ml to 1g:15ml, and soaking the deer sinew in the hydrochloric acid for 12h to 60h; then, feeding the deer sinew in boiling water (100 DEG C) until the deer sinew is completely dissolved; centrifuging; neutralizing the supernatant with alkaline solution; adding trypsin for conducting the enzymolysis process with the ratio between the trypsin and the zymolyte being 1g:5,000g to 1g:50,000g; concentrating the supernatant and filtering with a 0.2mum-0.45mum filter membrane; and freeze-drying the filtrate in a vacuum to obtain the collagen powder. The method of the invention has the advantages of simple and easy-to-operate process and stable experimental result. Therefore, the method is suitable for large-scale industrialized production.
Owner:赵雨
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