86 results about "Alpha ketoglutarate" patented technology

The invention discloses a human adipose-derived stem cell serum-free basic medium. The medium uses a serum substitute, and is composed of a high glucose type DMEM basic medium, human serum albumin, transferrin, taurine, reduced glutathione, ceruloplasmin, L-ascorbic acid-2-sulfate, alpha-tocopherol succinate, linoleic acid, alpha-ketoglutarate and selenium. The serum-free basic medium can exempt potential threats caused by animal serum in conventional serum-containing mediums to human health, and the adipose-derived stem cells cultured by the medium is more suitable for clinical application.

Compounds and pharmaceutical compositions for use in the treatment and/or prophylaxis of cartilage and/or bone conditions and for methods of treating such condition. The compounds are salts of strontium that have a water-solubility of from about 1 g/l to about 100 g/l at room temperature, especially amino acid salts of strontium or dicarboxylic acid salts of strontium. Examples of novel water-soluble strontium salts are e.g. strontium glutamate and strontium alpha-ketoglutarate. The present invention also relates to an improved method for preparing the strontium salt of glutamic acid.

Belonging to the technical field of bioengineering, the invention relates to corynebacterium glutamicum and a production method of alpha-ketoglutarate through fermentation of corynebacterium glutamicum. The bacterial strain of the invention is corynebacterium glutamicum GKG-047, with a preservation number of CGMCC No. 5481. With a strain of glutamic acid producing strain GDK-9 as a parent, the bacterial strain of the invention is a mutant strain that is screened out through mutagenesis and sensitive to methotrexate. Under the circumstance of a limited nitrogen source supply, the bacterial strain can accumulate alpha-ketoglutarate. During fermentation, the bacterial strain is characterized by aerobic fermentation, fast bacterium growth, and rapid acid production rate. After fermentation of the bacterial strain for 32h in a fermentation tank of 10L, the maximum output of alpha-ketoglutarate can be 47.2g/L. The method provided in the invention has the advantages of simple and easily controllable fermentation process, and low production cost of alpha-ketoglutarate, thus being in favor of the popularization and application of industrial production.

The invention is a method of synthesizing alpha-ketoglutarate by fermenting microbes, promoting to produce a large amount of alpha-ketoglutarate in fermenting course by adding CaCO3 to the culture medium and increasing biotin concentration. in the course of fermenting candida glabrata CCTCC M202019 to producing pyruvic acid, the delay of time of adding CaCO3 will inhibit the generation of alpha-ketoglutarate and increase the carbon mole ratio of pyruvic acid to alpha-ketoglutarate (CPYR/CKG), and increase of CaCO3 concentration in the culture medium will promote accumulation of a large amount of alpha-ketoglutarate, when the CaCO3 concentration is 40g/L, it is most beneficial to alpha-ketoglutarate generation. Keeping the CaCO3 concentration in the culture medium but increasing biotin concentration in the culture medium so as to promote the continuous increase of the alpha-ketoglutarate concentration but continuous decrease of CPYR/ CKG value, and when biotin concentration is 60mum g/L, accumulated quantity of alpha- ketoglutarate is 23.5g/L. when Ca2+ exists, in-cell phosphoenolpyruvate carboxylase activity can be increased by 40%, and the activity of pyruvic acid dehydrogenase system does not change obviously. The increase of the Ca2+ and biotin concentration can remarkably the activity of enhance pyruvic acid dehydrogenase, thus making T.glabrata transfer from production of pyruvic acid by fermenting to synthesis of high-concentration alpha-ketoglutarate.

This invention relates to a test kit for diagnosing hepatic and biliary diseases. The test kit has such advantages as high stability, high accuracy and high sensitivity. The test kit comprises two reagents. Reagent 1 comprises oxidized thio coenzyme, buffer solution, preservative, and anti-interference agent. Reagent 2 comprises 3alpha-HSD, reduced coenzyme, buffer solution, preservative, complexing agent, polymer accelerator, stabilizer, and one of formate dehydrogenase-formic acid-NAD, glutamate dehydrogenase-glutamic acid-oxidized nicotinamide coenzyme, glucose-6-phosphate dehydrogenase-glucose-oxidized nicotinamide coenzyme, glucose dehydrogenase-xylose-oxidized nicotinamide coenzyme, lactate dehydrogenase-alpha-ketoglutarate-oxidized nicotinamide coenzyme, and glycerol dehydrogenase-ethylene glycol-oxidized nicotinamide coenzyme.

The invention discloses a method for separating alpha-ketoglutaric acid from a conversion solution, which comprises the following steps: sequentially carrying out ceramic filtration, ultrafiltration and reverse osmosis on the conversion solution to obtain an alpha-ketoglutaric acid concentrated solution; reacting the obtained concentrated solution with calcium superchloride, and filtering to obtain alpha-ketoglutarate; adding the alpha-ketoglutarate and ethanol into a reaction kettle, slowly and dropwisely adding sulfuric acid, stopping adding the acid when the pH value of the ethanol solution is 1.3-1.5, stirring to react to generate a calcium sulfate precipitate, filtering, and collecting the filtrate which is a ketoglutaric acid ethanol solution; eluting the residual alpha-ketoglutaric acid from the calcium sulfate with ethanol, and collecting the eluting solution; and mixing the filtrate and eluting solution, and heating and concentrating under reduced pressure to precipitate the alpha-ketoglutaric acid crystal. The membrane filtration technique is adopted to avoid abundant water evaporation; and thus, the method has the advantages of energy saving, high production yield, favorable crystal form, light color of the crystal grain, and stable product quality, and can easily implement industrialized large-scale production.

Purpose of the invention is to provide a reagent bar capable of half quantitative/ quantitative detecting whether content of glutamic-pyruvic transaminase (GPT) inside human body is normal or not rapidly, and relevant fabricating method. The reagent bar includes PVC hard strip for supporting reaction. The hard strip possesses carrier film of adsorbing L-alanine, pyruvate oxidase, and alpha-ketoglutarate. Belonging to fast test in micro scale, the disclosed product is one-off consumption material for testing. Range for detecting GPT is 0-1000U/L.

The invention belongs to the technical field of biopharmaceuticals and relates to a method for preparing L-arginine-alpha-ketoglutarate (AAKG) from raw materials comprising L-arginine and alpha-ketoglutarate obtained by fermentation. In the method, the L-arginine and alpha-ketoglutarate in the fermentation liquor are directly used as the raw materials for AAKG rather than being used for extracting the refined crystalline products. The process mainly comprises the following technical steps: fermentation liquor pretreatment, chelation, concentration, crystallization, dissolution for decolorization, recrystallization, drying and the like. The process is characterized by comprising the following steps: pretreating the fermentation liquor with L-arginine, adding a certain amount of fermentation filtrate with alpha-ketoglutarate to the pretreated fermentation liquor to be chelated, carrying out vacuum evaporation concentration and then cooling the crystal to obtain the coarse product; and recrystallizing the coarse product by utilizing an organic solvent to obtain the high-purity product. The process has the advantages of high product purity, short flow, obvious emission reduction effect and the like, and is easy for quality control. The AAKG is mainly used as a physique enhancer and has the functions of promoting the muscles to grow and recover rapidly, promoting liver cells to absorb the nutrients and energy, maintaining normal liver functions and the like.

The invention discloses a high-efficiency liquid-phase chromatography detection method of L-arginine-alpha-ketoglutarate, and relates to the technical field of column chromatography. According to chromatographic condition, a chromatographic column adopts a C18 chromatographic column; a mobile phase adopts a 0.02mol/L to 0.08mol/L phosphate buffer solution with pH value of 3.0 to 4.0; the flow rate of the mobile phase is 0.5 to 1.3 ml/min; the detection wavelength is 200nm to 210nm; the temperature of the chromatographic column is 15 to 30 DEG C, and the content of L-arginine and the content of alpha-ketoglutarate in L-arginine-alpha-ketoglutarate or preparations of the L-arginine-alpha-ketoglutarate are determined by carrying out the high-efficiency liquid-phase chromatographic analysis. The content of L-arginine and the content of alpha-ketoglutarate in L-arginine-alpha-ketoglutarate or preparations of the L-arginine-alpha-ketoglutarate can be accurately determined by virtue of one-step high-efficiency liquid-phase chromatographic detection, and the two components can be well separated; moreover, the balance time of the C18 chromatographic column is short and is about 30 to 40 minutes, and the working efficiency can be improved.

The present invention discloses a pig feed free of antibiotic addition. The pig feed comprises the following components in parts by weight: 10-30 parts of extruded soybeans, 5-35 parts of crushed rice, 1-20 parts of soybean meal, 30-80 parts of Northeast corn, 1-10 parts of Peruvian fishmeal, 0-5 parts of alpha-ketoglutarate, 0-5 parts of allicin, 1-15 parts of plasma protein powder, 1-8 parts of soybean oil, 1-8 parts of sucrose, 1-20 parts of whey powder lactose, 0-5 parts of glucoses, 0-5 parts of a sweetener, 1-5 parts of stone powder, 0-2 parts of calcium dihydrogen phosphates, 0-2 parts of edible salt, 0-2 parts of choline chloride, 0-2 parts of lysine, 0-2 parts of methionine, 0-2 parts of L-threonine, 0-2 parts of L-tryptophan, 0-5 parts of anhydrous citric acids, 0-2 parts of organic mineral essences, 0-2 parts of antioxidants, 0-2 parts of piglet multi-vitamins, 0-2 parts of zinc oxide, 0-2 parts of 5000U high-temperature resistant phytase, 0-2 parts of piglet enzymes, 0-2 parts of bacillus subtilis Calsporin and 1-15 parts of fermented soybean meal. The pig feed can improve meat quality, and is safe, pollution-free, green and antibiotic-free.

The invention discloses a spectrophotometric method for quickly detecting the content of ethyl carbamate, and belongs to the technical field of analytical chemistry and food safety inspection. Ethyl carbamate degrading enzyme and glutamate dehydrogenase construct a double-enzyme coupled system; the ethyl carbamate degrading enzyme hydrolyzes the ethyl carbamate to generate ethyl alcohol, water and ammonia, the ammonia reacts with a cosubstrate alpha-ketoglutarate under the catalysis of the glutamate dehydrogenase to generate glutamic acid, and reduced coenzyme namely NADH (Nicotinamide Adenine Dinucleotide Hydrogen) is oxidized concomitantly, so that the system changes the content of the ethyl carbamate into the content of the NADH, and the content of the ethyl carbamate in a liquid-state system can be detected by using the change of the light absorption value of the NADH at 340nm. By virtue of the method, the ethyl carbamate in a solution can be quickly detected, the ethyl carbamate in a yellow wine system can be simulated, the detection limit is as low as 0.1mu mol. L<-1>, and an effective way is provided for the detection of the ethyl carbamate in fermented food and beverages.

The invention discloses an aspartate transaminase mitochondrial isozyme detection kit, comprising: reagents 1: 0.02-0.5mol/L of buffer solution of which pH value is 6.5-8.0, 0.15-0.3mol/L of L-potassium aspartate, 0.3-5KU/L of malic dehydrogenase, 0.3-5KU/L of lactic dehydrogenase, 5-20mL/L of human cAST antibody, 0.01-3% of antibody stabilizer, 0.01-10% of enzyme stabilizer and 0.01-1% of preservative; and reagents 2: 0.02-0.5mol/L of buffer solution of which pH value is 7.0-9.0, 0.005-0.02mol/L of alpha-ketoglutarate, 0.1-0.5mmol/L of reduced coenzyme I, 0.01-1% of preservative and 0.01-10% of reduced coenzyme I stabilizer. The kit has the advantage of good stability.

The invention relates to an L-ornithine-L-aspartate preparation method. The preparation method comprises the following steps: dissolving anyone or a mixture of L-ornithine-alpha-ketoglutarate, L-ornithine citrate and L-ornithine malate in water, adding L-aspartic acid, adjusting the pH value of the obtained solution to 7.0-8.0, adding active carbon for decoloring, filtering, adding a proper amount of an organic solvent miscible with water to the obtained filtrate, carrying out stirring crystallization, filtering, and drying. The L-ornithine-L-aspartate preparation method has the advantages of high yield, good product quality (high content, low impurity contents and the like), low cost and the like.

The present invention relates to a method for lowering activity with respect to maltose in glucose measurement comprising a step of reacting modified pyrroloquinoline quinone dependent glucose dehydrogenase subjected to amino acid sequence modification, wherein pyrroloquinoline quinone dependent glucose dehydrogenase is reacted in the presence of at least one type of substance selected from the group comprising succinic acid, malonic acid, glutaric acid, malic acid, phthalic acid, 2-ketoglutaric acid, 3,3-dimethylglutaric acid, pimeric acid, suberic acid, adipic acid, maleic acid, potassium chloride, ammonium chloride, diammonium hydrogen citrate, L-lysine, taurine, calcium glycerate, amino-n-butyric acid, sodium glycolate, sodium alpha-ketoglutarate, fumaric acid, glycine, glutamic acid, serine and citric acid.

The present invention relates to a preparation method for L-ornithine-alpha-ketoglutarate. The L-ornithine-alpha-ketoglutarate is produced by arginase transformation. The preparation method comprises the following steps: (1) preparation of immobilized enzyme; (2) optimization of transformation conditions; (3) product extraction and refining process. Compared to the prior art, the preparation method of the present invention has the following advantages that: the preparation method of the present invention has characteristics of low production cost, mild production conditions, less impurities in the transformation system, simple process steps, safe production operation and high purity; qualified products meeting the light transmission requirements can be synthesized; each liter of the reaction solution contains 300-320 g of the L-ornithine-alpha-ketoglutarate, and the transformation efficiency of the alpha-ketoglutaric acid is more than 90%; the preparation method further has other advantages.

The invention discloses a multilayer-film dry chemical reagent strip for measuring glutamic-pyruvic transaminase by using enzyme coupled continuous monitoring assay. The reagent strip comprises four layers of film, namely diffusion film, blood filter film (in two layers) and bottom reaction film and is characterized in that corresponding enzyme reactants are adsorbed to the reaction film, pyruvic acid is generated from L-alanine and sodium Alpha-ketoglutarate under the catalysis of glutamic-pyruvic transaminase, the pyruvic acid acts with reduced coenzyme I(NADH) under the catalysis of lactic dehydrogenase (LDH) to generate NAD+, absorbance at 340 nm is decreased, and the amplitude of decrease is associated with the content of the glutamic-pyruvic transaminase. The reagent strip is applicable to the quick measurement of the activity of glutamic-pyruvic transaminase in human whole blood and serum or plasma, is simple and easy to operate, and is easy to clinically apply and popularize.

The invention discloses a method for alpha-ketoglutarate production by catalysis of L-glutamate dehydrogenase. Under conditions of existence of a hydrogen peroxide scavenging agent and in buffer solution, alpha-ketoglutarate is generated by oxidation reaction of L-glutamic acid or salts thereof under catalysis of L-glutamate dehydrogenase and cofactors. The L-glutamate dehydrogenase depending on the cofactors obtained by organic small-molecular catalytic regeneration is adopted for catalysis of L-glutamic acid or salts thereof to generate alpha-ketoglutarate through oxidation reaction, low cost of raw material and low production cost are realized, a production process is simple and easy to operate and free of environment pollution, resource recycling is realized, and a theoretical foundation is laid for industrial efficient production of alpha-ketoglutarate. The L-glutamic acid or salts thereof are directly used as raw materials to generate alpha-ketoglutarate through one-step reaction, and high reaction selectivity and high yield are realized.

The invention relates to the field of animal husbandry and animal reproduction and particularly discloses a method for improving the fertility including the litter size and the sexual period breeding rate of older animals. It is found for the first time that the sexual period breeding rate and the litter size of multiparous animals can be remarkably increased by enabling the older animals to orally take a proper dose (the daily dose ranges from 0.05 g/kg to 1.58 g/kg) of alpha-ketoglutarate for a long time. The multiparous animals take alpha-ketoglutarate by adding alpha-ketoglutarate to drinking water or feed of the animals, adding according to requirements can be conveniently achieved, the dose can be changed in time, and the method can be widely used under an automatic feeding and water feeding system. The method is applied to livestock breeding, the edible safety of meat can be guaranteed, and meanwhile development of the breeding industry is also promoted.

The invention provides a preparation method of calcium alpha-ketoglutarate, which comprises the following steps: a) adding sodium methoxide into methyl dichloroacetate, and dropwisely adding methyl acrylate to carry out reaction; b) washing the mixed solution in the step a) with water, separating the water phase from the organic phase, and carrying out vacuum distillation on the organic phase to obtain dimethyl 2,2-dichloroglutarate; c) adding NaOH into the dimethyl 2,2-dichloroglutarate, and reacting at 60 DEG C to generate sodium alpha-ketoglutarate; and d) adding calcium chloride into the product in the step c), and stirring to obtain the calcium alpha-ketoglutarate. By changing the addition mode of the catalyst, the catalyst is uniformly distributed in the reaction system; and as the other product is added gradually, the concentration of the catalyst becomes lower, thereby effectively controlling the reaction process between the methyl dichloroacetate and methyl acrylate and enhancing the product yield. The intermediate product can be prepared into the sodium alpha-ketoglutarate by hydrolysis once, thereby shortening the procedure and enhancing the yield.

The invention provides a recombinant vector for expressing L-glutamic oxidase and catalase, engineering bacteria, applications thereof and a method for producing Alpha-ketoglutarate and belongs to thefield of molecular biological technique and enzyme engineering. The recombinant vector for expressing L-glutamic oxidase and catalase provided by the invention is capable of promoting capacity of converted substrates of L-glutamic oxidase and catalase to generate Alpha-ketoglutarate by inserting a regulating sequence SD for regulating expressions of L-glutamic oxidase gene LGOX and catalase geneCAT into a vector and has a higher practical use value.

The invention relates to a feed additive and an addition method thereof, in particular to a feed additive for increasing a protein utilization rate of sturgeon feed and an addition method of the feed additive. The additive aims at solving the problems of low protein utilization rate, low conversion rate, poor use effect and high feed coefficient of the existing sturgeon feed. The feed additive is prepared by mixing alpha-ketoglutarate, arginine, N-carbamylglutamate and cellulose. The addition method comprises the step of mixing 2-4 parts of feed additive for increasing the protein utilization rate of the sturgeon feed with 96-98 parts of sturgeon feed. The invention provides a feed additive for increasing the protein utilization rate of the sturgeon feed and the addition method of the feed additive.