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212 results about "Ochratoxins" patented technology

Isocoumarins found in ASPERGILLUS OCHRACEUS and other FUNGI. Ochratoxin contaminated FOOD has been responsible for cases of FOODBORNE DISEASES.

Method for portably and rapidly detecting ochratoxin A

The invention discloses a method for portably and rapidly detecting ochratoxin A. The method comprises the following steps: first, preparing sucrose invertase-terminal alkyne modified DNA; subsequently, combining biotin-nitrine modified DNA with the surface of a magnetic bead, adding the ochratoxin A with different concentration, and mixing; adding the previously-prepared sucrose invertase-terminal alkyne modified DNA, a CuSO4 solution and an ascorbic acid solution, wherein the ascorbic acid solution can be used for reducing Cu(II) to obtain a Cu(I) compound so as to catalyze the biotin-nitrine modified DNA and the sucrose invertase-terminal alkyne modified DNA to have a click chemistry reaction; taking a supernatant liquor after the reaction is ended, then adding the supernatant liquor into a sucrose solution, wherein the sucrose invertase can effectively catalyze the sucrose in the solution to be transformed into glucose; and finally, measuring by adopting a glucometer. The method is used for organically combining the rapid reaction advantage of the click chemistry reaction with the high specificity characteristic of an aptamer, and adopting the simple and portable glucometer to acquire data, thus the operation complexity and detection cost are greatly reduced, and the sensitivity and selectivity are improved.
Owner:INST OF AGRI PROD QUALITY SAFETY & STANDARD JIANGXI ACAD OF AGRI SCI

Immunochromatography test strip for synchronously detecting mixed pollution of aflatoxin, ochratoxin A and zearalenone, and preparation method

The invention relates to an immunochromatography test strip for synchronously detecting the mixed pollution of aflatoxin, ochratoxin A and zearalenone, and a preparation method. The immunochromatography test strip comprises a paperboard, wherein a water-absorbing pad, a detection pad, a gold label pad and a sample pad are sequentially bonded on one surface of the paperboard from top to bottom, and the adjacent pads are connected at a junction in an overlapping manner; the detection pad takes a nitrocellulose membrane as a base pad, and a transversal quality control line and detection lines are arranged on the detection pad; three detection lines are located below the quality control line, distributed at intervals, and coated with OTA-BSA (ochratoxin A-bovine serum albumin), ZEA-BSA (zearalenone A-bovine serum albumin) and AFB1-BSA (aflatoxin B1-bovine serum albumin) respectively; and the quality control line is coated with a rabbit anti-mouse polyclonal antibody; the gold label pad is transversally spayed with a nanogold labelled anti-aflatoxin universal monoclonal antibody, a nanogold labelled anti-ochratoxin A monoclonal antibody and a nanogold labelled anti-zearalenone monoclonal antibody. The immunochromatography test strip can be used for synchronous detection for aflatoxin, ochratoxin A and zearalenone, as well as is simple and rapid to operate, and high in sensitivity.
Owner:INST OF OIL CROPS RES CHINESE ACAD OF AGRI SCI

Mycotoxin binding food and feed additives and processing aids, fungistatic and bacteriostatic plant protecting agents and methods of utilizing the same

Method is proposed useful to render harmless mycotoxins that contaminate food, animal feed and assist infection of plant hosts by microbial parasites, comprising binding mycotoxins by a novel adsorbent, consisting partially or in full of plant lignocellulosic biomass or isolated biomass components, e.g., acid hydrolysis lignin, enzymatic hydrolysis lignin, coniferous and deciduous wood, bark and needle particles, rice hulls, used coffee grounds, apricot stone shells, almond, walnut, sunflower hulls, cocoa and peanut shells. The materials may be further improved through genetic modification of plants and physicochemical treatment of lignocellulosic biomass, such as micronization. The resulting adsorbent can bind wide range of mycotoxins, including, mycotoxins difficult to bind (Ochratoxin, T-2, Deoxynivalenol, Nivalenol). Ability of porous materials containing lignin to thermally collapse at melting can be used to irreversibly entrap mycotoxins by adsorbing them in a wet system and then closing lignin pore structure under high-temperature treatment, such as drying.
Owner:CUBENA

Electrochemical sidestream immune quantitative test paper sensor based on microgap array electrode and method thereof for detecting biotoxin

The invention relates to an electrochemical lateral-flow immunity quantitative test paper sensor based on microclearance array electrode, and a method thereof used for detecting biological toxins such as ochratoxin A and fumonisin B1. The sensor includes two parts, namely, immune chromatographic analysis test paper strip and electrochemical detecting part. The fast detecting test paper sensor has strong specificity, can realize quantitative detection, can be used at the temperature between 4 and 40 DEG C, and the result can be observed after ten minutes, thus being suitable for units or individuals to quickly detect ochratoxin A and fumonisin B1 in animal derived food samples, and being expected to become an effective technical means for the field screening of ochratoxin A and fumonisin B1 in food and feed samples.
Owner:湖南省宜生科技有限公司 +1

Mycotoxin adsorbent and preparation method thereof

The invention belongs to the technical field of agriculture animal husbandry and food antitoxin and detoxication, and relates to mycotoxin adsorbent and a preparation method thereof. The mycotoxin adsorbent is composed of, by weight, 85-90% of montmorillonite, 5-7% of yeast cell walls, 1-3% of chitin, 1-2% of saccharomyces boulardii and 3-5% of natural plant extract in a mixing mode. The natural plant extract comprises tea tree oil, hesperidin, eugenol, citral, cinnamaldehyde and baicalein which are proportionally mixed. The mycotoxin adsorbent can be applied to fodder, aflatoxin B1 in the mycotoxin can be absorbed, other mold toxins such as zearalenone, ochratoxin, deoxynivalenol and fumitremorgin can also be effectively absorbed, the nutrient absorption rate of the fodder is low, meanwhile, breeding and balancing of probiotics in intestinal canals can be promoted, and the immunocompetence of animals is enhanced.
Owner:湖北回盛生物科技有限公司

Microorganism for biological detoxification of mycotoxins, namely ochratoxins and/or zearalenons, as well as method and use thereof

InactiveUS20090098244A1Stable and viableSimple and rapidly realizableMilk preparationFungiBacteroidesFungal toxin
A microorganism for the biological inactivation or detoxification of mycotoxins, in particular ochratoxins, which is selected from bacteria and / or yeasts, which cleaves the phenylalanine group of the mycotoxins, in particular ochratoxins, as well as a method for biologically inactivating or detoxifying mycotoxins, in particular ochratoxins, in food products and animal feeds by the aid of a microorganism, and the use of the microorganism(s).
Owner:ERBER AG

Biological degradation of ochratoxin a into ochratoxin alpha

ActiveUS20130209609A1Dough treatmentOrganic chemistryMicroorganismOchratoxin alpha
The invention relates to the use of a microorganism of the genus Brevibacterium for the biological degradation of ochratoxin A, in which the microorganism is preferably Brevibacterium casei, Brevibacterium linens, Brevibacterium iodinum or Brevibacterium epidermidis. In addition, the invention relates to a method for the production of ochratoxin α using said microorganism.
Owner:CENT DI RICERCA PER LENOLOGIA CRA ENO

One-step rapid detection method of ochratoxin A by using electrochemical aptamer sensor

The invention relates to a one-step rapid detection method of ochratoxin A by using an electrochemical aptamer sensor, comprising the following steps: (1)polishing the surface of a bare gold electrode; (2)modifying the electrochemical aptamer sensor; (3) detecting an ochratoxin A standard concentration solution, and establishing a standard curve; and (4) carrying out quantitative determination on an actual sample solution containing ochratoxin A. According to the invention, the sensitivity of detecting ochratoxin is raised, the minimum detectable amount of ochratoxin A is 0.01 pg / mL, the cost of detecting the target toxin is greatly reduced, the operation is simple and convenient, and the one-step detection of ochratoxin A can be realized in 5-10 min.
Owner:HEFEI UNIV OF TECH

Photoelectrochromic visualization biosensor based on ratio principle and preparation method and application thereof

The invention, which belongs to the field of photoelectrochemical visualization biosensor construction, relates to preparation of a photoelectrochromic visualization biosensor based on the ratio principle. A region 1 and a region 2 of two electrodes being a module A and a module B respectively are modified respectively by using Prussian blue and a Co-N-TiO2 / 3DGH nanocomposite material; the surfaceof region 2 is processed by using chitosan; the surface of region 2 of the module A is modified with an ochratoxin A adaptor solution, incubation is carried out, and washing is carried out by using aphosphate buffer solution; an active site that is not bonded is sealed by using bovine serum albumin; and then washing is carried out by using a phosphate buffer solution to obtain a photoelectrochromic visualization biosensor based on the ratio principle. The Co-N-TiO2 / 3DGH nanocomposite material represents the high photoelectric activity and stability; and with the constructed Co-N-TiO2 / 3DGH nanocomposite material, the interferences of various external and internal factors are reduced substantially and the detection accuracy is improved. Moreover, no complicated instrument is needed and naked-eye identification is used, so that the visual inspection is realized.
Owner:JIANGSU UNIV

Composite affinity column for purifying 3-acetyl deoxynivalenol, aflatoxin, ochratoxin A and zearalenone

The invention discloses a composite affinity column for purifying 3-acetyl deoxynivalenol, aflatoxin, ochratoxin A and zearalenone, a preparation method and an application thereof. According to the invention, by employing 4% of cylindrical agarose gel as a solid phase carrier, agarose gel and an antibody are coupled to form an immunoadsorbent, and filling in a column to prepare the immunization affinity column. When a sample containing 3-acetyl deoxynivalenol, aflatoxin, ochratoxin A and zearalenone passes through the immunization affinity column, 3-acetyl deoxynivalenol, aflatoxin, ochratoxin A and zearalenone can be specifically adsorbed by the immunoadsorbent, other impurities flows out of the immunization affinity column, then methanol is used for eluting 3-acetyl deoxynivalenol, aflatoxin, ochratoxin A and zearalenone from the column, so that the sample can be better purified.
Owner:INSPECTION & QUARANTINE TECH CENT OF CHONGQING ENTRY EXIT INSPECTION & QUARANTINE BUREAU +3

Ochratoxin degrading enzyme, coding gene, recombinant vector, cell, additive and application thereof

ActiveCN108251385AEfficient short-term degradationLow pH requirementAnimal feeding stuffAccessory food factorsBiotechnologyT2 toxin
The invention relates to the field of biotechnology, in particular to an ochratoxin degrading enzyme, a coding gene, a recombinant vector, a cell, an additive and application thereof. The invention more specifically relates to the ochratoxin degrading enzyme with a sequence shown as SEQ ID NO:2 or a mutant thereof, a coding gene of the enzyme, a vector and a cell containing the coding gene, and anadditive containing the enzyme and / or cell and / or a fermentation product thereof, application of the enzyme, the coding gene, the vector, the cell or additive in degradation of ochratoxin and / or other fungal toxins, as well as a method for degradation of ochratoxin / or other fungal toxins. The ochratoxin degrading enzyme provided by the invention is environment-friendly, can efficiently degrade ochratoxin in a short time, and does not generate any harmful by-product. The enzyme can tolerate high temperature catalysis up to 80DEG C, also has low pH value requirement, has good stability, and achieve degradation of fumonisins and T2 toxin to a certain degree.
Owner:COFCO NUTRITION & HEALTH RES INST +1

Compound enzyme, additive, application thereof and method for removal of fungal toxins

Relating to the field of removal of fungal toxins, the invention discloses a compound enzyme, an additive, application thereof and a method for removal of fungal toxins. Specifically, the invention relates to a compound enzyme, which contains amidase and esterase and can remove fungal toxins, especially fumonisins, ochratoxins and T2 toxin, additives containing the compound enzyme and applicationthereof in removal of fungal toxins, especially fumonisins, ochratoxins and T2 toxin, and a method for removal of fungal toxins. According to the technical scheme, combined use of the amidase and esterase can achieve simultaneous removal of ochratoxin A, fumonisins and T2 toxin, the removal efficiency is greatly improved than single use of one enzyme, and vomitoxins, aflatoxins and zearalenone toxin can be removed to certain degree.
Owner:COFCO NUTRITION & HEALTH RES INST +1

POSS (polyhedral oligomeric silsesquioxane)-based organic-inorganic hybrid silica gel monolithic column applied to ochratoxin specific recognition and preparation method thereof

The invention discloses a POSS (polyhedral oligomeric silsesquioxane)-based organic-inorganic hybrid silica gel monolithic column applied to ochratoxin specific recognition and a preparation method thereof. The POSS-based organic-inorganic hybrid silica gel monolithic column is characterized in that the hybrid silica gel monolithic column prepared by nucleophilic reaction between a polyhedral oligomeric silsesquioxane (POSS) crosslinking agent and polyamine monomer is utilized as a matrix, the matrix has a high-crosslinking 3D skeleton, the surface of the matrix contains rich amino, the matrixcan load anti-ochratoxin aptamer surface modified gold nano particles in high density, and the monolithic column is prepared by nano gold amino bonding and self assembling. The prepared POSS-based monolithic column matrix disclosed by the invention has the characteristics of high-crosslinking structure and multiple acting sites and can efficiently load the nano gold particles; thus, the aptamer with specific recognition on ochratoxin A can be loaded and fixed to the POSS-based monolithic column in high density, and high-efficiency specific recognition separation on the ochratoxin A is achieved.
Owner:FUZHOU UNIV

Test paper card for synchronously detecting ochratoxin, vomitoxin and T-2 toxin, preparation method and detection method

The invention relates to a test paper card for synchronously detecting ochratoxin, vomitoxin and T-2 toxin, a preparation method and a detection method, and belongs to the field of immunological detection. The test paper card comprises a card shell and a test paper strip, wherein the test paper strip comprises a base plate, as well as an absorbent pad, a detection pad, a conjugate pad and a samplepad which are sequentially lapped and stuck to the base plate; the detection pad is an NC film provided with a quality control line, a detection line T1, a detection line T2 and a detection line T3;the quality control line coats a goat anti-mouse secondary antibody; the detection line T1 coats OTA-BSA; the detection line T2 coats DON-BSA; the detection line T3 coats T-2-BSA; the conjugate pad isa glass cellulose film, labeled by embedding time-resolved fluorescent microspheres, of an ochratoxin monoclonal antibody, a vomitoxin monoclonal antibody and a T-2 toxin monoclonal antibody; the sample pad is a dried glass cellulose film soaked by sample pad treating fluid. The invention provides a novel method for systematic, convenient and normalized quantitative synchronous detection of at least two fungaltoxins. The novel method has the advantages of good stability and high sensitivity.
Owner:洛阳现代生物技术研究院有限公司

Compositions and methods for mycotoxin decontamination of animal feed, food, soil and plants using biomass of filamentous fungi and its selected components

A method of rendering harmless mycotoxins contaminating food, animal feed and assisting infection of plant hosts by microbial parasites is proposed. The method comprises binding mycotoxins by a novel adsorbent, consisting partially or in full of the biomass of filamentous fungi or isolated fungal biomass components, such as chitin, chitozan and hyrdophobins, or fungal biomass enriched in its capacity to bind said mycotoxins using fungal species and strain selection, genetic engineering of fungi, modification of fungal fermentation conditions and downstream physical and chemical treatment of fungal biomass, such as milling or micronization in a dry state. The resulting adsorbent can bind a wide range of mycotoxins, including the ones difficult to bind (Ochratoxin, T-2, DON, NIV) using a current generation of mycotoxin adsorbents based on clay, resins, yeast and bacterial biomass. The adsorbent can be used as an animal feed additive, functional food additive and agricultural fungistatic / fungicide.
Owner:CUBENA

Electrochemical aptamer sensor for quantitatively detecting ochratoxin A and application thereof

The invention provides an electrochemical aptamer sensor for quantitatively detecting ochratoxin A and application thereof, and relates to the field of nano biosensors and electrochemical detection. The electrochemical aptamer sensor is a three-electrode system sensor, the working electrode is obtained by sequentially modifying the surface of a gold sheet electrode with a composite film of reducedgraphene oxide, molybdenum disulfide and nanogold, a capture probe 1, a capture probe 2 and an ochratoxin A aptamer, and every two of the capture probe 1, the capture probe 2 and the ochratoxin A aptamer are complementarily paired to form a Y-shaped structure. The electrochemical aptamer sensor disclosed by the invention is used for quantitatively detecting ochratoxin A and has the advantages ofsimplicity in operation, good stability, high sensitivity, strong specificity, good reproducibility and the like.
Owner:ANHUI SCI & TECH UNIV

Detoxifying agent for biologically degrading ochratoxin A in feeds and preparation technology of detoxifying agent

The invention relates to a detoxifying agent for biologically degrading ochratoxin A in feeds and a preparation technology of the detoxifying agent. The detoxifying agent comprises 40-60 parts of bentonite, 20 parts of immune polysaccharides, 10-20 parts of a free-radical scavenger and 20-30 parts of bacillus subtilis powder for degrading the ochratoxin A, wherein the bacillus subtilis powder is prepared through the following steps of (1) performing seed liquor activation on original strains, and performing mother seed culturing in a first-class fermentation tank loaded with culture mediums; (2) performing amplified culturing on mother seed culturing liquor in a second-class fermentation tank loaded with LB culture mediums; and (3) separating thalli from fermentation liquor, performing concentration, and performing drying so as to prepare the bacillus subtilis powder for biologically degrading the ochratoxin A. The bacillus subtilis powder, a first-time mixture and a second-time mixture in parts by weight are compounded so that a finished product of the detoxifying agent is obtained. According to the detoxifying agent disclosed by the invention, the degradation rate of the detoxifying agent for the ochratoxin A is as high as 92% or above, the degradation efficiency is high, and defects of an adsorbent are overcome; and besides, immune polysaccharide and free-radical removing ingredients are added to products, so that the functions of protecting the liver and enhancing the immunity of organisms can be achieved, and the effects are obvious.
Owner:北京科润生科技发展有限公司

AOZD multi-analyte affinity column

A multi-analyte column is disclosed. The column may contain at least one unit of resin having ochratoxin specific affinity and, for each unit of resin having ochratoxin specific affinity, the column further contains about 0.95 to 1.05 units of resin containing antibody having specificity for zearalenone, about 1.9 to 2.1 units of resin containing antibody having specificity for aflatoxin and about 4.7 to 5.3 units of resin containing antibody having specificity for DON. One unit of resin is the quantity of resin containing antibody that will bind 50 ng of aflatoxin, 500 ng of DON, 50 ng of ochratoxin or 1140 ng of zearalenone, respectively.
Owner:WATERS TECH CORP

Rapid detection method for ochratoxin A

The invention relates to a rapid detection method for ochratoxin A. The method comprises the following steps that A, an aptamer (Apt) of the ochratoxin A is hybridized with single-stranded signal probe DNA (ssDNA) to form a hybridized chain; B, the hybridized chain is made to make contact with a sample to be tested, and when the ochratoxin A exists in the sample to be tested, the hybridized chain and the ochratoxin A are subjected to a reaction to release the single-stranded signal probe DNA (ssDNA); C, DNA amplification is utilized for making the hybridized chain into a double-stranded DNA, then, an excision enzyme is used for selectively catalyzing the hydrolysis of the double-stranded DNA to form mononucleotide, and the single-stranded signal probe DNA (ssDNA) is not hydrolyzed and reserved; D, under the induction of the ssDNA, copper ions are reduced to generate near infrared fluorescence copper nanometer particles; the system fluorescence strength is detected, and therefore the content of the ochratoxin A in the sample to be tested is tested. The method has the advantages of being high in sensitivity, easy to operate, low in cost and the like.
Owner:HUNAN UNIV OF SCI & TECH

Preparation method of ratio electrochemical aptamer sensor for simultaneously detecting aflatoxin B1 and ochratoxin A

The invention belongs to the technical field of electrochemical sensing, and relates to a preparation method of a ratio electrochemical aptamer sensor for simultaneously detecting AFB1 and OTA. The sensor is prepared by assembling AQ-hDNA, Fc-Apt1 and MB-Apt2 on a gold electrode in sequence, the combination of a target object and an aptamer causes Fc-Apt1 and MB-Apt2 to be stripped from a surfaceof the electrode such that ratio signals IFc / IAQ and IMB / IAQ are reduced, and the purposes of respectively quantifying and detecting AFB1 and OTA are achieved; the linear detection range of the sensoron AFB1 is 10 pg / mL-3 ng / mL, and the detection limit is 3.3 pg / mL; the detection linear range on OTA is 30 pg / mL-10 ng / mL, and the detection limit is 10.0 pg / mL; two substances are detected at the same time, and the method has the characteristics of high sensitivity, good selectivity, high accuracy and the like.
Owner:JIANGSU UNIV

New method for rapidly detecting ochratoxin A through molecular beacon probe

The present invention relates to a new method for rapidly detecting ochratoxin A through a molecular beacon probe. According to the present invention, based on the DNA key site for specifically recognizing OTA, a molecular beacon having the stem comprising sixes complementary bases and the ring having 8 bases is designed, wherein the sequence of the molecular beacon is 5'-FAM-CCGGGTCCACCCACACCCGG-DABCYL-3'; and the probe is stable and is easy to synthesize, is used for sample analysis, has the simple operation, can complete the detection within 20 min, further has advantages of good accuracy and high sensitivity, and can be used for the rapid screening of the ochratoxin A in malt, beer, and other samples.
Owner:INST OF MEDICINAL PLANT DEV CHINESE ACADEMY OF MEDICAL SCI

Kit for detecting ochratoxin A and detection method thereof

The invention belongs to the technical field of light initiated chemiluminescence immunoassay, and discloses a kit for detecting ochratoxin A and a detection method thereof, which are used for detecting content of the ochratoxin A (OTA) in grain, feeds and products thereof. The base of the kit is homogeneous label immunoreaction. Luminescent particles coated with OTA-BSA are added into a white opaque microtiter plate; an OTA standard sample or treated sample is added into micropores respectively, and then rabbit anti-OTA antibody and biotinylated goat anti-rabbit antibody are added into the micropores in sequence for label immunoreactions; and photosensitive particles coated with streptavidin are added into obscure corners for reaction to detect optical signals, under the excitation of light, photoluminescent particles generate fluorescent light through the generation and transmission of singlet ionized oxygen, the detection is performed by a light initiated chemiluminescence detector, the intensity of the optical signals is reciprocal to the concentration of the OTA, and the content of the OTA in the sample is calculated by referring to a standard curve. The kit has simple structure, simple and convenient operation, short detection time and high sensitivity.
Owner:JIANGSU INST OF NUCLEAR MEDICINE

Method of Mycotoxin Detection

The presence of mycotoxins in agricultural products necessitates large scale testing of a wide range of sample material to ensure the safety of food and feed. The mycotoxin ochratoxin A represents an enablement for all mycotoxins as the level of sensitivity necessary for regulatory requirements for this compound at the part per billion level are as low or lower than any other mycotoxin. This invention describes the identification of a set of DNA ligands with sufficiently high binding affinity and specificity for ochratoxin A to enable an improvement over existing methods for the separation, concentration and quantitative determination of ochratoxin A in sample material.
Owner:NEOVENTURES BIOTECH

Irradiation degradation treatment method for fumitremorgin and ochratoxin

The invention relates to an irradiation degradation treatment method for fumitremorgin and ochratoxin. The irradiation degradation treatment method comprises the following steps: (1) preparing standard solutions of standard products of the fumitremorgin FB1 and ochratoxin OTA; carrying out irradiation treatment on the standard solutions in an irradiation range of 0kGy-200kGy; determining the content of the FB1 and the OTA by adopting a liquid chromatogram-tandem mass spectrometry; (2) pre-treating a poisoned sample after irradiating in an irradiation range of 0kGy-9kGy; determining degradation effects on the FB1 and the OTA by adopting the liquid chromatogram-tandem mass spectrometry; and (3) selecting the FB1 and OTA standard solutions with the highest concentration as a sample and carrying out detection and analysis on a degraded product by using the liquid chromatogram-tandem mass spectrometry after irradiating in the irradiation range of 0kGy-200kGy. According to the irradiation degradation treatment method for the fumitremorgin and the ochratoxin, researches and applications of FB1 and OTA degraded products which are lack of irradiation degradation are solved; the degradation effect is good and the environment-friendly detoxification treatment of mildewed agricultural product wastes is realized.
Owner:JIANGSU ACADEMY OF AGRICULTURAL SCIENCES

Method for determining content of ochratoxin A in juice

The invention discloses a method for determining the content of ochratoxin A in juice. The method comprises the following steps: pretreating a sample by adopting a simple liquid-liquid extraction and purification step; scanning with parameters including optimized scanning wavelengths, scanning intervals and the like, and acquiring three-dimensional fluorescent data of a standard product and the sample; carrying out mathematic separation treatment on the obtained data by adopting a parallel factor analyzing method (PARAFAC); establishing a correction model by using the standard product with the known concentration and by combining mathematic separation with chemical and physical separation; and predicating a component to be detected under the conditions that unknown and uncorrected background interferences are included and spectrums are seriously overlapped. The method is simple and rapid, and has the high sensitivity; and the content of ochratoxin in the juice can be determined under the unknown background interferences. The method belongs to the field of food safety.
Owner:CHINA AGRI UNIV

Immunoadsorbent for purifying five kinds of mycotoxins including fumonisin b1 and aflatoxin b1, and complex affinity column

The invention relates to an immunoadsorbent for purifying five kinds of mycotoxins including fumonisin B1 and aflatoxin B1, and a complex affinity column. The immunoadsorbent comprises a solid-phase support, and an anti-fumonisin B1 monoclonal antibody, an anti-aflatoxin B1 monoclonal antibody, an anti-ochratoxin A monoclonal antibody, an anti-zearalenone monoclonal antibody and an anti-sterigmatocystin monoclonal antibody which are coupled to the solid-phase support, wherein the anti-fumonisin B1 monoclonal antibody is secreted by a hybridoma cell strain Fm7A11, and the hybridoma cell strain Fm7A11 has been preserved at China Center for Type Culture Collection, Wuhan University, Wuhan, China on Mar. 29, 2016 with the preservation number of CCTCC No. C201636. The complex affinity column can be used for purification and detection of a fumonisin B1 sample, an aflatoxin B1 sample, an ochratoxin A sample, a zearalenone sample and a sterigmatocystin sample at the same time.
Owner:INST OF OIL CROPS RES CHINESE ACAD OF AGRI SCI

Ochratoxin detoxification enzyme, encoding gene, recombinant vector and application thereof

The invention discloses an ochratoxin detoxification enzyme, an encoding gene, a recombinant vector and an application thereof, and belongs to the technical field of enzyme engineering. The inventionprovides the ochratoxin detoxification enzyme and the encoding gene thereof, and also provides the optimum pH of the ochratoxin detoxification enzyme and the application of the ochratoxin detoxification enzyme in degrading ochratoxin and ochratoxin biological detoxification in food. When ochratoxin A is processed by the ochratoxin detoxification enzyme at a temperature of 37 DEG C and at the pH of7.3 for 2min in a buffer system, the degradation rate of ochratoxin A reaches 100%, and the degradation efficiency is unprecedented in the field.
Owner:ANHUI AGRICULTURAL UNIVERSITY

Amidase and coding gene, recombinant carrier, recombinant strain and application thereof

The invention provides amidase and a coding gene, recombinant carrier, recombinant strain and application thereof, and belongs to the technical field of enzyme engineering. The invention provides theamidase and the coding gene thereof, and also provides appropriate pH of the amidase and an application of the amidase to hydrolysis of ochratoxin and detoxifying of ochratoxin of foods. Under the room temperature condition, the amidase is used for treating ochratoxin A in a buffer system of which the pH is 7.3 for 2 minutes, the degradation rate of the ochratoxin A achieves 100%, and the degradation efficiency is unprecedented in the field.
Owner:江苏奥迈生物科技有限公司

Method for quantitatively detecting ochratoxin A

The invention discloses an aptamer of ochratoxin A and a nucleotide sequence of complementary DNA of the aptamer, further discloses a method for quantitatively detecting ochratoxin A, and belongs to the field of quantitative detection of ochratoxin A. The method includes the following steps that 1, an aptamer biosensor is prepared; 2, ochratoxin A in a sample to be detected is extracted to obtain sample extraction liquor, the sample extraction liquor is added into the aptamer biosensor and evenly mixed, and incubation is performed; 3, supernatant liquor is separated, and an excessive sucrose solution is added for a reaction; 4, quantitative detection is performed through a glucometer. The method for quantitatively detecting ochratoxin A in food or feed by combining the aptamer biosensor with the glucometer is good in specificity and repeatability, high in sensitivity, fast to implement and low in cost and provides a new means for quantitatively detecting ochratoxin A.
Owner:INST OF ANIMAL SCI OF CHINESE ACAD OF AGRI SCI
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