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526 results about "Hydrolyzed protein" patented technology

Hydrolyzed protein is a protein that has been at least partially hydrolyzed or broken down into its component amino acids. While many means of achieving this exist, two of the most common methods are prolonged boiling in a strong acid (acid-HVP) or strong base, or using an enzyme such as pancreatic protease to simulate the naturally occurring hydrolytic process.

Chicken bone protein zymolyte and chicken essence substrate prepared by same

The invention provides a chicken bone protein zymolyte and a chicken essence substrate prepared by the chicken bone protein zymolyte, belonging to the technical field of poultry processing. The invention solves the problems of high cost for producing a chicken essence substrate, limited raw material sources, unavailable effective utilization generally by discarding leftovers, such as chicken bone, and the like, and the like in the prior art. In the invention, a novel chicken essence substrate is developed by adopting the cheap leftovers, namely chicken bone as a raw material and utilizing a biological enzymolysis technology and a hot reaction spice research technology; the chicken essence substrate is prepared by the following steps of: adopting the chicken bone zymolyte obtained after the chicken bone is subjected to double enzymolysis by pancreatic enzyme and Flavourzyme composite flavor protease as a main material, mixing the main material with hydrolyzed vegetable protein (HVP), a yeast extract, glucose, xylose, thiamine, chicken oil and propylene glycol according to a certain proportion; and carrying out Maillard reaction in a high-pressure reactor to prepare the chicken essence substrate with vivid chicken fragrance. The chicken essence substrate has vivid chicken fragrance, rich and strong chicken fragrance and long aftertaste.
Owner:FUZHOU UNIV

Plant nutrient liquid fertilizer

InactiveCN102701861AImprove stress resistanceSolve the problem of lack of nutrientsFertilizer mixturesSucrosePhosphate
The invention relates to a plant nutrient liquid fertilizer. In order to solve the problem of over fertilization, the plant nutrient liquid fertilizer is prepared from the following raw materials in proportion by weight: aqua brassin 12-36, gibberellin 1-4, indoleacetic acid 30-80, abscisic acid 10-20, naphthaleneacetic acid 50-90, salicylic acid 80-180, vitamin C 1-3, cane sugar 40-100, chitin 20-80, 0.05-0.2 percent triacontanol 400-1,000, hydrolyzed protein 2-5, potassium dihydrogen phosphate 300-400, thiourea 40-120, cobalt chloride 5-12, borax 50-100, sodium silicate 30-55, urea 300-500, ammonium molybdate 50-80, copper sulfate 30-65, zinc sulfate 120-200, magnesium sulfate 100-150, calcium chloride 50-120, manganese sulfate 40-80 and water in the amount of 3-8 times the total amount of all the raw materials or water in the amount capable of dissolving all the raw materials, wherein the water is de-ionized water or micro cluster water; and the preparation method is that all the materials are prepared into aqueous solution. The plant nutrient liquid fertilizer has the advantages of favorably solving the problems of over fertilization and shortage of nutrient elements in soil, obviously improving the plant adverse resistance, improving the photosynthesis and the accumulation efficiency of nutritive materials and improving the yield and the quality.
Owner:魏玉芳

Method and process for extracting animal micro-molecule polypeptides and amino acids by utilizing complex enzyme

The invention discloses a method and process for extracting animal micro-molecule polypeptides and amino acids by utilizing a complex enzyme. The method comprises the following steps: (1) crushing animal tissues so that the animal tissues can pass through a sieve of 80-200 meshes, and adding water to prepare a suspension with the concentration of 8-30 percent; (2) raising the temperature to be 35-40 DEG C, regulating the pH value to be 8.0-9.0 by using sodium carbonate, adding a complex enzyme I accounting for 0.5-2.0 percent of the animal tissues, performing ultrasonic enzymolysis at 14-16 kHz for 1-2 hours so that the proteins between cells are subjected to full enzymolysis, regulating the pH value to be 6.5-7.5, adding a complex enzyme II accounting for 0.5-3.0 percent of the animal tissues, fully and uniformly stirring, controlling the temperature of the water bath to be 37-45 DEG C, and performing ultrasonic enzymolysis at 15-17 kHz for 1-6 hours; (3) raising the temperature of the enzymolysis solution to be 90-100 DEG C to inactivate the enzyme for 20-30 minutes after the enzymolysis is finished; (4) filtering the solution subjected to enzymolysis through a 0.22mu m microfiltration membrane; and (5) concentrating the filtrate to the relative density of 1:1.0-1:1.2 to prepare the concentrated solution, wherein the complex enzyme II consists of Alcalase, Flavourzyme, Protamex, neutral protease and papain. According to the method, the enzymolysis efficiency can be improved, and the production cost can be reduced.
Owner:WEIHAI KANGBOER BIOLOGICAL PHARMA +1

Gynaecologic multi-item dry chemical united detection test paper strip and its measuring method

The invention relates to a test paper tape which can be used in the gynecological multiprogramming dry-chemistry joint detection. The test paper tape provided by the utility model comprises a dry-chemistry multiprogramming detection test paper tape which consists of a plastic substrate tape and various solidified regent blocks, and sample diluent. The dry regent blocks include combinations formed by increasing or decreasing at least three or more regent blocks of a Ph test regent block, a lactic acid regent block, a hydrogen peroxide concentration regent block, a leukocyte esterase concentration regent block, a neuraminidase activity regent block, an amine test regent block, a proline aminopeptidase substrate reagent block, an oxidase substrate reagent block, a N-acetylamine hexosidase substrate reagent block, a trichomonas specific protease substrate hydrolysis reagent block. the gynecological multiprogramming dry-chemistry joint detection test paper test provided by the utility model can detect Ph, lactic acid, hydrogen peroxide, leukocyte esterase, neuraminidase, amine test, proline aminopeptidase, oxidase, N-acetylamine hexosidase and trichomonas specific protease which are contained in leucorrhea sample at the same time, and can accurately reflect the microorganism environment of a women reproductive tract, the cleanness of leucorrhea secretion and the conditions of Candida albicans, trichomonas, gonococcus and the pathogens of bacterial vaginosis, thereby making the gynecological trichomonas detection more comprehensive; besides, the test paper tape provided by the utility model can be used easily and conveniently, and results can be obtained quickly. If the test paper tape is used together with a gynecological dry-chemistry analyzer, the operation can become easier and the result can be obtained more quickly.
Owner:杭州健宝医疗器械有限公司

Preparation method of fermented rice sticks

ActiveCN101623065APlay the effect of debranching and straighteningShorten fermentation timeFood preparationAmylaseProteinase activity
The invention relates to a preparation method of fermented rice sticks, which belongs to the field of food fermentation and comprises a pulp making procedure and a pulp steaming procedure. The preparation method of fermented rice sticks is characterized in that 1-1000ml of debranching amylase for per 100kg of rice is added into rice pulp with the weight percent of 5 to 50% before the pulp steaming procedure and after the pulp making procedure, the pH value is regulated to 4.0-5.0, and enzymolysis is carried out for 30-360 min under the temperature of 30-60 DEG C; 1-50 g of protease with proteolysis peptide bonds for per 100kg of rice is added into the rice pulp, and enzymolysis is carried out for 60-360 min under the temperature of 30-60DEG C and the pH value of 4.0-8.0; then, 0.2 ml/kg of zymophyte is added to the pulp and fermented for 360-3600 min under the temperature of 25-30DEG C and the pH value of 5.0-6.0. In the invention, the debranching amylase is utilized to hydrolyze Alpha-D-1, 6 glycoside bonds as the branched chains in starch and dextrine to generate straight-chain compound sugar containing Alpha-D-1, 4 glycoside bonds so as to obtain the effect on debranching and adding straight chains; the protease with proteolysis peptide bonds can be used for hydrolyzing molecular protein and amino acid to provide sufficient amino acid for following mixed fermentation, shorten fermentation time, and improve the quality and the taste of products.
Owner:江西蓓蕾食品有限公司

Method of breaking yeast cell wall and preparing yeast extract

The invention relates to a method of breaking yeast cell wall and preparing a yeast extract. Yeast emulsion is used as the raw material, sodium chloride is added into the yeast emulsion, the pH value of the yeast emulsion is regulated, so that the diluted yeast cell solution becomes basic or weakly basic, the yeast cell wall is broken through steam jet continuous sterilization, the wall-broken yeast cell solution is diluted with water to proper temperature and concentration, the pH value of the diluted yeast cell solution is regulated, so that the diluted yeast cell solution becomes basic or weakly basic, and alkaline protease is added into the yeast cell solution to perform autolysis and enzymolysis. The yeast cell solution is subjected to enzyme deactivation, centrifugal separation, evaporation and concentration and blending, so as to produce the yeast extract. The yeast emulsion is used as the raw material, the drying energy consumption of yeast cells is reduced, sodium chloride as the plasmolysis additive is added, in the basic or weakly basic condition, the common wall breaking action of the steam jet continuous sterilization is performed, so that the wall-breaking effect of the yeast cells is good, the dissolution rate of proteins is high, the protease easily acts, the alkaline protease is added, and thus the yield of the hydrolyzed protein and free amino nitrogen is high. The all-breaking rate of the yeast cells is obviously increased, and the content of total nitrogen and amino state nitrogen in the yeast extract is increased.
Owner:GUANGXI XIANGGUI BIOTECH CO LTD

Coordinated process extraction method of biological active substances in crayfish by-products

InactiveCN103172763ACombined effectRetain astaxanthinCarboxylic acid salt preparationFermentationEvaporationAstaxanthin
The invention relates to a coordinated process extraction method of biological active substances in crayfish by-products, belonging to the field of a biological active substance extraction method. The coordinated process extraction method comprises the following steps of: sequentially carrying out enzymolysis treatment on crushed crayfish shells and crayfish heads which are obtained by boiling through water and removing crayfish meat, and taken as raw materials; spraying and drying a filtered solution to obtain hydrolyzed protein powder; carrying out organic acid leaching treatment on a filtered solid, and spraying and drying the filtered solution to obtain organic calcium; adding the filtered solid into ethanol to be treated; carrying out rotary evaporation on the filtered solution to obtain an astaxanthin rough product; and finally, carrying out hydrogen peroxide immersion de-coloring treatment on the filtered solid to obtain de-colored chitin. According to the coordinated process extraction method disclosed by the invention, the crushed crayfish shells and crayfish heads, which are obtained by boiling through the water and removing the crayfish meat, are taken as the raw materials, and a scientific and simple process route is utilized for sequentially obtaining the food-grade standard hydrolyzed protein powder, organic calcium, astaxanthin and chitin products; a production period is shortened, the production efficiency is improved and a product additional value is obviously improved; and a production process is clean production, wastewater emission is reduced and the coordinated process extraction method is good for environmental protection.
Owner:湖北省小龙虾产业技术研究院有限公司

Preparation method of small molecule peptides of vinasse and application of small molecule peptides of vinasse in skin care products

The invention provides a preparation method of small molecule peptides of vinasse and application of small molecule peptides of vinasse in skin care products. The preparation method comprises the following steps: S1, carrying out vacuum extrusion, cooling, crushing and sieving on vinasse, the water content of which is 11-22%; S2, carrying out alkali dissolution and acid settlement on the vinasse expanded powder obtained in the S1 to extract vinasse proteins so as to obtain vinasse protein extract; and S3, carrying out hydrolysis on the vinasse protein extract extracted in the S2 with proteolytic enzymes, and carrying out enzyme deactivation, filtration, concentration, freezing and drying to obtain the small molecule peptides of vinasse. By deeply processing the vinasse by adopting a special vacuum expansion technology, the extraction ratio of the vinasse proteins is increased effectively; meanwhile, by adopting the special proteolytic enzymes, the small molecule peptides of vinasse with relatively good moisturizing and repairing functions can be obtained. In addition, the small molecule peptides of vinasse are applied to skin care products, so that the moisturizing and repairing functions of the skin care products are improved while the additional value of the vinasse is increased.
Owner:GUANGDONG MARUBI BIOLOGICAL TECH CO LTD

Preparation meted for high-stability soybean protein emulsion

The invention discloses a preparation meted for high-stability soybean protein emulsion, and belongs to the field of soybean protein deep processing. The method includes the steps that soybean protein isolate is dissolved in distilled water to obtain a protein solution, the protein solution is preheated, the pH of the preheated protein solution is adjusted, alkaline protease is added for enzymolysis, and the protein solution is freeze-dried after enzymolysis to obtain hydrolyzed soybean protein powder; the hydrolyzed soybean protein powder is dissolved in a phosphoric acid buffer solution to obtain a hydrolyzed soybean protein solution; lecithin is added into the phosphoric acid buffer solution to obtain a lecithin solution; the hydrolyzed protein solution and the lecithin solution are mixed to obtain mixed liquor, sunflower seed oil is added into the mixed liquor, and then homogenization treatment is performed to obtain the high-stability soybean protein emulsion. The compound emulsion prepared through the method is high in emulsion activity and emulsion stability, safe, harmless and suitable for the food industry and other industries. Besides, the method has the advantages that the process is simple, reaction conditions are moderate, and operation is safe.
Owner:NORTHEAST AGRICULTURAL UNIVERSITY

Method for producing hydrolyzed wheat protein

The invention discloses a method for producing hydrolyzed wheat proteins. The method is characterized by comprising the following steps of: preparing enzymatic hydrolysate, namely adding 1,000 parts of vital gluten in mass for three times according to the weight ratio of the vital gluten to water being 1 to 5-3, after hydrolysis is performed, raising the temperature of the enzymatic hydrolysate to 75-100 DEG C, keeping the temperature of the enzymatic hydrolysate for 3-10 minutes, performing enzyme deactivation on the enzymatic hydrolysate, cooling the enzymatic hydrolysate subjected to enzyme deactivation to 30-35 DEG C, after fermentation is finished, filtering fermented liquid, and finally drying the filtrate by spraying. The method has the advantages that by a multi-enzymolysis and microorganism fermentation combination method, a novel hydrolyzed wheat protein product is developed by fully combining characteristics of a protein structure of wheat gluten proteins, the cleavage sites of protease, biological conversion of microorganisms, animal nutrition absorption and the like, so that the taste and the flavor of the product are greatly improved; the utilization of enzyme preparations can be greatly reduced; the production cost is reduced; the production technology is simple and novel; the period is short; three industrial wastes are not produced; and the hydrolyzed wheat proteins are environmentally-friendly.
Owner:江苏联海生物科技有限公司
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