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50 results about "Decarboxylase activity" patented technology

Fermentation agent for low ergamine salami sausage and method of use thereof

The invention discloses a fermentation agent and the application method for processing low histamine salami sausage, comprising the followings: 1. The selected strains of fermentation agent are CGMCCNo.1923-pediococcus pentosaceus and CGMCCNo.1572-staphylococcus xylosus both without decarboxylase activity; 2. The matching proportion between the CGMCCNo.1923-pediococcus pentosaceus and the CGMCCNo.1572-staphylococcus xylosus is 1:1; 3. The fermentation agent dosage of the pediococcus pentosaceus and the staphylococcus xylosus are 100kg respectively every 100g of mince when processing, the inoculated-pathogen quantity can be up to 1 x 10<7>cfu/g. The adding method is as follow: to make fermentation liquid by mixing the pediococcus pentosaceus fermentation agent and the staphylococcus xylosus fermentation agent with equal ratio and being dissolved in 500g water, spread the fermentation liquid uniformly on the mix mince surface, and mix the mince and the fermentation liquid thoroughly; 4. The preserved preparation used is as follow: the mass ratio to the material mince is salt 3.0%, glucose 1.5%, sodium nitrite 0.015%, and ascorbic acid 0.08%; 5. Using the fermentation agent, preserved preparation and processing technology, the histamine content of salami product is reduced by more than 40% and meets with the food histamine content limitation requirement of the European Union. The invention is tested according to the regulated hygienic standards of cured meat products in the GB2730-2005 hygienic standard for cured meat products, the hygienic state of products meets with the standard, the product flavor and the hygienic safety are better than the traditional technologic product evidently. The invention has the advantages of good application prospect in the aspects of quality improvement and new product development of salami products.
Owner:INST OF ANIMAL SCI OF CHINESE ACAD OF AGRI SCI

Method for biotransformation production of gamma-aminobutyric acid with aquatic products and processing leftovers thereof as raw materials

The invention specifically relates to a method for biotransformation production of gamma-aminobutyric acid by using aquatic products and processing leftovers thereof, which belongs to the technical field of bio-processing of aquatic products. The method comprises the following steps: inoculating 0.5 to 5% (V / V) of lactic acid bacteria with glutamic acid decarboxylase activity into a medium, carrying out fermentation culture at a fermentation temperature of 30 to 35 DEG C at a rotating speed of 100 to 500 r / min for 20 to 50 h so as to allow a viable count in fermentation broth to be as high as 10<6> to 10<7> cfu / ml and standing the fermented lactic acid bacteria for subsequent usage; carrying out centrifugation or filtering on transformation liquid, taking supernatant and subjecting the supernatant to reduced pressure concentration so as to prepare a GABA crude extract; and removing impurities in the crude extract with absolute ethyl alcohol by using a precipitation method, then carrying out separation and purification by successively using a macroporous resin, Sephadex gel and a cation exchange resin and subjecting a GABA product obtained after separation and purification to rotary evaporation and freeze drying so as to obtain a crystal. With the method, a novel application direction for aquatic products and processing leftovers thereof is opened up, and theoretical bases are provided for comprehensive and high-value utilization of aquatic products.
Owner:中科海洋生物研究院盘锦有限公司

Efficient production method of gamma-aminobutyric acid

ActiveCN104830745ASimplify separation and purification proceduresEfficient synthesisBacteriaMicroorganism based processesEscherichia coliGlutamate decarboxylase
The invention discloses an efficient production method of gamma-aminobutyric acid, and belongs to the field of fermentation engineering. In the provided method, a twin-arginine signal peptide gene (torA) and a glutamic acid decarboxylase gene (gadB) are fused and transferred to a escherichia coil BL21(DE3) host so as to obtain a recombinant bacterium pET20b(+)-torA-gadB / E.coli BL21(DE3) that can secret and express glutamic acid decarboxylase. The extracellular glutamic acid decarboxylase activity level of the recombinant bacterium in a shaking bottle can reach 5.11 U / mL, and 15.82 U / mL in a fermentation tank. By using the system and a substrate (sodium glutamate monohydrate), the output of gamma-aminobutyric acid can reach 203.7 g / L.
Owner:JIANGNAN UNIV

Method for the preparation of diols

The present invention concerns a new method for the biological preparation of a diol comprising culturing a microorganism genetically modified for the bioproduction of an aliphatic diol, wherein the microorganism comprises a metabolic pathway for the decarboxylation of a hydroxy-2-keto-aliphatic acid metabolite with an enzyme having a 2-keto acid decarboxylase activity, the product obtained from said decarboxylation step being further reduced into the corresponding aliphatic diol, and wherein the microorganism is genetically modified for the improved production of said hydroxy-2-keto-aliphatic acid metabolite. The invention also concerns a modified microorganism for the production of an aliphatic diol.
Owner:METABOLIC EXPLORER

A method for detecting amino acid decarboxylase activity of spoilage bacteria in food

A method for detecting amino acid decarboxylase activity of spoilage bacteria in food belongs to the technical field of agricultural products. First, spoilage bacteria are isolated from food, fermented to obtain strain fermentation liquid, and then inoculated into a liquid medium containing amino acids to obtain biogenic amine detection. Use the spoilage bacteria fermentation liquid, and then obtain the supernatant of the sterile body by centrifugation, add Na2HPO4, NaOH and dansyl chloride to the supernatant and the mixed standard solution of biogenic amines, and obtain the derivatives of spoilage bacteria biogenic amines in a water bath under dark conditions. Derivative samples of samples and standard biogenic amines; after pointing and drying, put them into the development tank, wait for the developer to expand to 17cm from the sample point, take them out and dry them, then use automatic gel imaging analysis under ultraviolet light to take pictures respectively, and compare them Yes, determine the type of biogenic amine in the sample according to the Rf value, and judge the amino acid decarboxylase activity of the strain. The invention is convenient and quick, has low cost and can accurately realize the qualitative detection of biogenic amine.
Owner:JIANGSU ACADEMY OF AGRICULTURAL SCIENCES

Coryneform bacterium transformant and process for producing phenol using the same

Provided is a phenol-producing transformant constructed by transferring a gene which encodes an enzyme having chorismate-pyruvate lyase activity and a gene which encodes an enzyme having 4-hydroxybenzoate decarboxylase activity into a coryneform bacterium as a host. Also provided is a process for producing phenol, which comprises a step of allowing the transformant to react in a reaction mixture containing a saccharide under reducing conditions, and a step of collecting phenol from the reaction mixture.
Owner:GREEN CHEM

Method for increasing activity of GAD (Glutamate Decarboxylase) by using D101 macroporous adsorption resin

ActiveCN107326052AAvoid inactivationAccelerate the speed of leaving the active center of glutamic acid decarboxylaseMicroorganism based processesFermentationWater bathsGlutamate decarboxylase
The invention relates to a method for increasing the activity of enterococcus faecium Glutamate Decarboxylase by using D101 macroporous adsorption resin, and belongs to the technical field of biology. According to the method disclosed by the invention, the D101 microporous adsorption resin is used as an enzyme activity accelerator of enterococcus faecium GAD, and a D101 microporous adsorption resin-GAD composite catalytic system is constructed according to a proportion that the mass of the D101 macroporous adsorption resin to the volume of a substrate solution to the volume of an enterococcus faecium bacterial suspension solution or a GAD free enzyme solution is 1 to 1 to 1; when the D101 microporous adsorption resin-GAD composite catalytic system is subjected to reaction in a water bath oscillator of which the temperature is 37 to 43 DEG C at 80r / min or stirring reaction in a stirring tank at a low speed for 24 to 36 hours, the yield of GABA (Gamma-Aminobutyric Acid) can be increased by 18.54 to 149.11 percent; the D101 macroporous adsorption resin is capable of remarkably increasing the activity of the GAD, an exchange adsorption function of the D101 microporous adsorption resin on the GABA is also a purifying process of the GABA, a downstream extracting and purifying technology is simplified, and the production cost is reduced; the method is simple, green and environment-friendly.
Owner:LINGNAN NORMAL UNIV

Method for preparing beta-alanine from maleic acid through multi-enzyme coupling

The invention specifically relates to a method for preparing beta-alanine from maleic acid through multi-enzyme coupling, belonging to the field of biotechnology. The method comprises the following steps: adjusting the pH value of an aqueous maleic acid solution with a certain concentration to 6 to 9 by using ammonia water; then separately adding bacterial cells respectively with maleate isomerase activity, aspartase activity and aspartate-alpha-decarboxylase activity or crude liquid of the three enzymes; carrying out enzymatic reaction at 30 to 50 DEG C; and separating and converting products by using isoelectric-point crystallization or a combination of isoelectric-point crystallization and ion exchange resin so as to obtain high-purity beta-alanine. The method provided by the invention uses maleic acid as a substrate for preparation of beta-alanine via multi-enzyme coupling and has the advantages of wide sources of raw materials, low price, simple operation, low production cost, suitability for large-scale industrial production, etc.
Owner:NANJING UNIV
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