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56 results about "Multifunctional Enzymes" patented technology

Molecules that contain multiple active sites which are used to catalyze more than one enzymatic reaction. Proteins in this class generally contain multiple active sites within a single peptide chain and may also contain more than one enzymatically active subunit. They are distinguished from MULTIENZYME COMPLEXES in that their subunits are not found as distinct enzymes.

Multifunctional enzyme-supplemented colorful toothpaste and preparation method thereof

Disclosed is a multifunctional color bar enzymatic toothpaste and preparation method. The toothpaste is formed by one color regulation cream which containing chemical medicament additive and biologic enzyme activator, and multi-color cream containing biologic enzyme and biologic enzyme stabilizer. The preparation method is separately preparing regulation cream and enzyme cream and canning to color bar toothpaste. Functions of the toothpaste is to prevention and cure oral problem such as preventing and curing decayed tooth, diminishing inflammation, sterilization, desensitization, eliminating halitosis and whitening teeth. Simultaneously the toothpaste employing stabilizer and color bar to ensure the stability, and effectively exerting biology function of enzyme in release process by adding definite activator.
Owner:TSINGHUA UNIV +1

Multifunctional enzyme vinegar

The invention relates to the technical field of food, and particularly relates to multifunctional enzyme vinegar. The multifunctional enzyme vinegar comprises the following raw materials in parts by weight: 10-50 parts of starch raw material, 20-60 parts of fruits, 20-60 parts of vegetable, 1-3 parts of aspergillus niger, 1-2 parts of aspergillus oryzae, 10-20 parts of Daqu, 5-10 parts of Chinese koji, 5-10 parts of red yeast rice, 2-4 parts of yeast, 0.15-0.4 part of lactic acid bacteria, and 4-7 parts of acetic acid bacteria. In the enzyme vinegar, total acid is greater than 11g / 100 mL, citric acid is greater than 2g / 100 mL, malic acid is greater than g / 100 mL, and lactic acid is greater than 1 g / 100 mL. the invention further relates to a preparation method of the enzyme vinegar. The enzyme vinegar is rich in nutrients, and mellow in mounthfeeling, the proportion of total acid to non-volatile acid is proper, and the enzyme vinegar has multiple nutritional health-care efficacies of strengthening the stomach, moistening intestine, calming down and relieving thirsty, reducing blood pressure and blood lipid, being anti-oxidant and anti-aging, and the like.
Owner:TIANJIN TIDAI MEDICINE SCI & TECH

No-whey process for production of low fat hard cheese

InactiveUS20050238783A1Eliminates costly processing requirementSolve the real problemCheese manufactureMilk SerumWhey protein
The present invention provides a no-whey process for preparing a low-fat hard cheese product with completed capture of whey proteins using a modified milk protein concentrate. The modified milk protein concentrate comprises about 82 to about 96 percent milk protein concentrate and about 4 to about 18 percent multifunctional enzyme, wherein the multifunctional enzyme modifies the function of dairy proteins so that the completed capture of whey proteins into a cheese product will not interfere with the alignment of casein molecules into the fibers structure required for a good texture of hard cheeses such as mozzarella. The present invention solves problems associated with the whey generated from conventional making cheese plant and creates a new way of making low-fat hard cheese products.
Owner:HAN XIAO QING +1

Method for preparing ferulic acid by utilizing corn bran hydrolyzed by multifunctional enzyme

The invention provides a method for preparing ferulic acid by utilizing corn barn hydrolyzed by a multifunctional enzyme. The method comprises the following steps of: adding the corn bran into NaOH and soaking darkly, sterilizing at high pressure, adding the multifunctional enzyme with peptidase and esterase activities for hydrolyzing ester bonds and peptide bonds on the cell wall, centrifugallytaking supernatant, treating the supernatant by adopting a column chromatography and eluting, concentrating eluent, extracting by adopting ethyl acetate and rotatably evaporating to obtain the ferulic acid. The ferulic acid is produced by utilizing the corn bran as a by-product in the process of grain processing or fuel ethanol production and the hydrolysis of the multifunctional enzyme with peptidase and esterase activities, therefore, the invention has simple process, time and energy saving and increased additional value of the corn by-products.
Owner:JILIN UNIV

Analyzing method for detecting activity of soil xylanase

The invention relates to an analyzing method for detecting activity of soil xylanase, which comprises the following steps: firstly, weighting n sieved air dry soil samples into n thick test tubes, adding acetic acid buffer solution into each test tube, oscillating by a vortex oscillator, getting soil suspension into 96 micropore plates under the oscillation condition, adding 4-MUB-7-Beta-D-xyloside substrate solution into n-1 holes, and adding water with equal quantity into the other one hole so as to be used as non-substrate contrast, adding substrate solution with equal quantity and water with equal quantity into the (n+1)th hole so as to be used as soli-free contrast, oscillating and culturing under constant temperature; secondly, adding NaOH into the micropore plates to terminate the reaction after the culture is finished; thirdly, performing the fluorimetric determination to resultant of reaction by a multifunctional microplate reader; and fourthly, calculating the activity of the xylanase. Compared with the traditional method, the invention shortens the culture time, omits the operation procedures of filtration, and the like, and simplifies the operation steps; meanwhile, the determination data of fluorescent materials in the micropore plate can be obtained within 15s through the multifunctional microplate reader, huge samples are allowed to be simultaneously determined; and moreover, the invention has high accuracy and easy operation, stable and reliable result and good reproduction quality.
Owner:SHENYANG INST OF APPL ECOLOGY CHINESE ACAD OF SCI

Fuel supply device for vehicle

The invention relates to a multifunctional enzyme that can be derived from crustaceans or fish. The enzyme has at least one of a chymotrypsin, trypsin, elastase, collagenase and exo peptidase activity, and a molecular weight between about 20 kd and about 40 kd as determined by SDS PAGE. Preferably, the multifunctional enzyme has substantial anti cell-cell adhesion activity. Preferably, the multifunctional enzyme has substantial homology with the krill multifunctional enzyme. These enzymes are useful for treating viral infections such as herpes outbreaks, fungal, bacterial or parasitic infections, including the primary and secondary infections of leprosy, colitis, ulcers, hemorrhoids, corneal scarring, dental plaque, acne, cystic fibrosis, blood clots, wounds, immune disorders including autoimmune disease and cancer. Additionally, the invention relates to a method of purifying the multifunctional enzyme, and to a preparation of essentially purified multifunctional enzyme.
Owner:MITSUBISHI ELECTRIC CORP

Method for high-sensitivity and low-background detection of fumonisin B1 through hydrogel silica photon crystal microsphere chemiluminescence method

InactiveCN105158459AIncreased chemiluminescent signal valueImprove throughputMaterial analysisMicrosphereMeasuring instrument
The present invention relates to a method for high-sensitivity detection of fumonisin B1 through a hydrogel silica photon crystal microsphere chemiluminescence method. According to the present invention, the gel is subjected to ultraviolet polymerization in the silica photon crystal microsphere gap so as to reduce the porous structure inside the microsphere, reduce the non-specific biological reaction background signal, and improve the detection sensitivity and the detection accuracy; and the fumonisin B1 probe carrier on the microsphere surface is used to construct the competitive fumonisin B1 chemiluminescent immunodetection system on the microsphere surface, the chemiluminescent signal is detected by using the multifunctional enzyme-labeling measuring instrument, the detection limit of the method on the fumonisin B1 is 0.0001 ng / mL, the linear detection range is 0.0001-1 ng / mL, and the method has advantages of high detection sensitivity and low background signal.
Owner:NANJING NORMAL UNIVERSITY

Method for rapidly and efficiently screening rhamnolipid producing bacteria nutrition system

The invention relates to a method for rapidly and efficiently screening a rhamnolipid producing bacteria nutrition system. The method comprises the following steps: synthesizing a primer of rhamnolipid producing gene rhlAB, performing gene amplification by using PCR, synthesizing rhlAB gene fragments, connecting the rhlAB gene fragment to the position in front of lux luminescence gene on pMS402 plasmid by utilizing gene engineering shearing and splicing technology, then transferring the recombinant plasmid into pseudomonas aeruginosa DN1, coating the recombinant strain onto an LB solid plate containing 200mg / L-300mg / LTmp, screening out positive clone, naming the strain as rhlAB-lux strain, picking out positive monoclonal colonies to be enriched on the solid LB culture medium, refrigeratingat at 4DEG C for later use; taking out the refrigerated rhlAB-lux strain, and enriching the thallus overnight; and screening a nutrient optimized system. According to the method, the luminescence value can be determined by a multifunctional microplate reader, and the method has the characteristics that the flux is high, and the screening process is simplified and rapid.
Owner:NORTHWEST UNIV(CN)

Enzyme preparation method and product thereof

The invention relates to an enzyme preparation method and a product thereof, wherein natural fruits are used as raw materials, preferably 6-9 parts by mass of apple, 5-8 parts by mass of pear, 3-4 parts by mass of lemon, 4-7 parts by mass of grapefruit, 7-10 parts by mass of carrot, 3-4 parts by mass of orange, 2-3 parts by mass of hawthorn, and 2-3 parts by mass of ficus carica linn are mixed andcrushed to prepare a liquid fruit juice, 5-8 parts by mass of the liquid fruit juice, 3-5 parts by mass of rock candy, 0.01-0.07 part by mass of lactic acid bacteria and 0.01-0.09 part by mass of yeast are uniformly mixed, fermenting is performed for 3-6 months at a room temperature in a closed and dark environment, the supernatant is extracted, and filtering, disinfecting and filling are performed to obtain the enzyme finished product or the product thereof, wherein the filling is bottling or boxing. According to the present invention, the enzyme and the environmental protection multifunctional enzyme soap have advantages of no pigment addition during the manufacturing, mild property and no irritating, and are suitable for a variety of people; and the obtained product is the pure naturalenzyme beverage, and can further be used for washing, shampooing, face washing, bathing, tooth brushing and the like.
Owner:张艳

Enzyme biological organic fertilizer applicable to rice field eels and loaches and preparation method thereof

The invention discloses an enzyme biological organic fertilizer applicable to rice field eels and loaches and a preparation method thereof. The enzyme biological organic fertilizer comprises the following components by weight: 210 kg of albumen powder, 190 kg of oil cake, 370 kg of dried chicken manure, 10 kg of trace elements, 8 kg of enzyme bacterium, 100 kg of grass meal, 12 kg of dried earthworms, 3 kg of calcareous shale, 3 kg of brown sugar, 5 kg of rice bran and 100 kg of bentonite. In the invention, the multifunctional enzyme bacterium is used as a core, high quality organic matter isused as a carrier, and a right amount of inorganic nutrients and nutrient albumen is compounded to form an efficient biological organic-inorganic fertilizer for rice field eels and loaches. Various nutrients in the fertilizer for rice field eels and loaches are reasonably proportioned, the growth of unicellular algae, beneficial bacteria and beneficial algae can be rapidly promoted, and the waterbody environment is dually adjusted. Moreover, cultivated rice field eels and loaches have fresh and tender meat quality, toxic matter can be effectively degraded, the water quality is improved and becomes fertile, active, tender and cool, the immunity is increased, and the occurrence of bacterial diseases is inhibited.

Analyzing method for detecting activity of soil xylanase

The invention relates to an analyzing method for detecting activity of soil xylanase, which comprises the following steps: firstly, weighting n sieved air dry soil samples into n thick test tubes, adding acetic acid buffer solution into each test tube, oscillating by a vortex oscillator, getting soil suspension into 96 micropore plates (occupies n micropores) under the oscillation condition, adding 4-MUB-7-Beta-D-cellobioside substrate solution into n-1 holes, and adding water with equal quantity into the other one hole so as to be used as non-substrate contrast, adding substrate solution with equal quantity and water with equal quantity into the (n+1)th hole so as to be used as soli-free contrast, oscillating and culturing under constant temperature; secondly, adding NaOH into the micropore plates to terminate the reaction after the culture is finished; thirdly, performing the fluorimetric determination to resultant of reaction by a multifunctional microplate reader; and fourthly, calculating the activity of the xylanase. Compared with the traditional method, the invention shortens the culture time, omits the operation procedures of filtration, and the like and simplifies the operation step; meanwhile, the determination data of fluorescent materials in the micropore plate can be obtained within 15s through the multifunctional microplate reader, huge samples are allowed to be simultaneously determined; and moreover, the invention has high accuracy and easy operation, stable and reliable result and good reproduction quality.
Owner:SHENYANG INST OF APPLIED ECOLOGY - CHINESE ACAD OF SCI

Detection method for biological activity of liraglutide

According to the invention, the change of the level of 3',5'-cyclic adenosine monophosphate (cAMP) is taken as a detection index and a cAMP-depending type protein kinase A active analysis method is used for determining the biological activity of liraglutide. Rat insulinoma cells RIN-m5F are cultivated and a diluted liraglutide comparison product solution and a diluted test solution are added; a kit is used for detecting the change of the level of the cAMP in stimulated cells; a super-sensitive chemiluminiscence detection module of a multifunctional enzyme linked immunosorbent assay is used for reading a relative chemiluminiscence unit (RLU) and statistical software is used for fitting experimental data; the biological activity of a product to be detected is calculated by a formula. The method can be used for simply, conveniently, rapidly and accurately detecting the change of the biological activity of the liraglutide; the accuracy and the repeatability accord with the requirements of a biological activity determination method of biological products.
Owner:HANGZHOU JIUYUAN GENE ENG +1

Method for detection of P-gp mediated Rh123 transport in 3D type organ and application thereof

The invention relates to a method for detection of P-glycoprotein (P-gp) mediated rhodamine 123 (Rh123) transport in a 3D type organ and an application thereof in screening of P-gp inhibitors. The method comprises the steps: firstly, sorting small intestinal crypts of C57BL / 6 mice, inoculating a petri dish containing a matrix gel, culturing in an Advanced DMEM / F12 culture medium, and forming the 3D type organ; and then carrying out qualitative and quantitative detection of P-gp mediated Rh123 transport and influence of the P-gp inhibitor verapamil on Rh123 transport by using the 3D type organ model. The method particularly comprises the steps of respectively co-incubating the 3D type organ with (1) the P-gp substrate Rh123 and with (2) the Rh123 and the verapamil, releasing the Rh123 in the 3D type organ by using an ultrasonic crushing method, and finally detecting the concentration of the Rh123 on a multifunctional microplate reader. The method has the advantages of being simple, rapid, and high in sensitivity, can be combined with the 3D type organ model for carrying out research of the P-gp mediated drug transport, and also can perform research of in-vitro screening of the P-gp inhibitors.
Owner:EAST CHINA NORMAL UNIV

Avermectin aglycon synthase genes

The present invention relates to an isolated DNA which comprises a DNA sequence encoding avermectin aglycon synthase domains that corresponds to multifunctional enzyme proteins involved in the biosynthesis of a polyketide compound, or its mutants having avermectin aglycon synthase activity, particularly functional modules and submodules in the DNA sequence derived from Streptomyces avermitilis, a polypeptide or mutants thereof encoded by the DNA or the mutants, a vector containing the DNA or the mutants, a host cell transformed with the DNA, the mutants thereof, or the vector, and a method for producing avermectin.
Owner:THE KITASATO INST

Method for preparing dietary fiber by adopting corn bran hydrolyzed by multifunctional enzyme

The invention provides a preparation method of dietary fiber by adopting corn bran hydrolyzed by a multifunctional enzyme. The preparation method comprises the following steps of: adding the corn bran into NaOH and soaking darkly, sterilizing at high pressure, adding the multifunctional enzyme with peptidase and esterase activities for hydrolyzing ester bonds and peptide bonds on the cell wall, centrifugally taking precipitate, decoloring and rinsing, drying at the temperature below 60 DEG C, crushing and screening by adopting a 80-100 mesh sieve to obtain the dietary fiber. The dietary fiber which has the expansion force up to 10-15ml / g and the water-holding capacity of 9-11g / g and is superior to other methods is prepared by utilizing the corn bran as a by-product in the process of grain processing or fuel ethanol production and the hydrolysis of the multifunctional enzyme with peptidase and esterase activities. The invention utilizes the enzyme, has simple process, saves time and energy and increases the additional value of the corn by-products.
Owner:JILIN UNIV

Enzyme biological organic fertilizer applicable to rice field eels and loaches and preparation method thereof

The invention discloses an enzyme biological organic fertilizer applicable to rice field eels and loaches and a preparation method thereof. The enzyme biological organic fertilizer comprises the following components by weight: 210 kg of albumen powder, 190 kg of oil cake, 370 kg of dried chicken manure, 10 kg of trace elements, 8 kg of enzyme bacterium, 100 kg of grass meal, 12 kg of dried earthworms, 3 kg of calcareous shale, 3 kg of brown sugar, 5 kg of rice bran and 100 kg of bentonite. In the invention, the multifunctional enzyme bacterium is used as a core, high quality organic matter isused as a carrier, and a right amount of inorganic nutrients and nutrient albumen is compounded to form an efficient biological organic-inorganic fertilizer for rice field eels and loaches. Various nutrients in the fertilizer for rice field eels and loaches are reasonably proportioned, the growth of unicellular algae, beneficial bacteria and beneficial algae can be rapidly promoted, and the waterbody environment is dually adjusted. Moreover, cultivated rice field eels and loaches have fresh and tender meat quality, toxic matter can be effectively degraded, the water quality is improved and becomes fertile, active, tender and cool, the immunity is increased, and the occurrence of bacterial diseases is inhibited.

Device for automatically and synchronously replacing optical filter and optical fiber

The invention relates to a device for automatically and synchronously replacing an optical filter and an optical fiber. The device is mainly applied to multifunctional enzyme marking instrument and like optical detection instruments; the replacing device is composed of an optical filter replacing mechanism and an optical fiber path replacing mechanism; the device can automatically and synchronously replace the optical fiber and optical fiber path on the light path through an integrated driving design of an optical filter fixing wheel and an optical fiber fixing wheel, and then the quick, convenient and accurate switching of different detection modes can be realized.
Owner:吉林亚泰中科医疗器械工程技术研究院股份有限公司

Novel multifunctional enzyme gene HG32 and application

The invention discloses a novel multifunctional enzyme gene HG32 and application, the enzyme is derived from Chinese rhizomyidae enteric microorganisms, can be compatible with an eukaryotic cell expression system, expresses cellulase with high biological activity, and can be applied to the fields of livestock and poultry feed enzyme preparations, transgenic animal preparation, food and medicine industries and the like; the invention solves the problems that plant cellulose is difficult to degrade, the feed nutrition utilization rate is low and the like are solved, and pollution of nitrogen, organic matter and the like in animal excrement. According to the invention, the application comprises the following steps: sequencing a bamboo rat intestinal microbe macro transcriptome, and splicing the sequences; performing homology comparison with the existing glycoside hydrolase family on NCBI, and screening high-expression suspected cellulase genes with homology higher than 50%; predicting the signal peptide, and replacing the original signal peptide with the pig parotid gland secreted protein signal peptide; optimizing according to pig codon preference, and cloning to an eukaryotic expression vector; transfecting into pig kidney epithelial cells through lipidosome for expression; collecting a cell culture supernatant; and carrying out enzyme activity analysis and comparison.
Owner:WENS FOOD GRP CO LTD +1

Rotary multifunctional enzymolysis fermentation machine and fermentation process thereof

The invention discloses a rotary multifunctional enzymolysis fermentation machine, which comprises a tank body, wherein the tank body is arranged in an inclined rotation manner and adopts a stirring tank structure provided with a sealed wind supply device, the top end of the tank body is sealedly connected to the wind supply device, and the temperature, the ventilation, the humidity and the drying process are automatically set through the wind supply device so as to perform assisted fermentation. According to the present invention, the rotary multifunctional enzymolysis fermentation machine adopts the inclined rotation design, has characteristics of rotary function, time saving, labor saving and energy consumption reducing, and provides good mixing homogenization functions for various kinds of dry powder materials, half-wet materials and block material; the inside-tank material plane is wide, the ventilation contact surface is large, the fermentation is easily achieved, the whole machine does not have the easily-wearing part, and the continuous use after the machine starting can be met; and the rotary function is used, such that the power consumption is less, the maintenance is not required, the maintenance work does not contain the inside-tank operation projects, a large number of the subsequent manual maintenance cost of the equipment are reduced, the replacement cost of a large number of the easily-wearing parts are reduced, and the prices is substantially reduced.
Owner:WEIFANG FUXIN AUTO PARTS

Therapeutical effect of atabrine and substitutes thereof on hepatitis B

By adopting methods of fluorescent quantitation PCR, fluorescent quantitation RT-PCR, HBV DNA quantitation, HBsAg quantitation, HBeAg quantitation, cccDNA quantitation, Northern blot, Southern blot, Western blot, immunohistochemistry, and the like in the research and using the maintenance dose within the treating dose range for a long time (30-60 days), supernatant HBV DNA HBsAg HBeAg cultured by HepG-2.2.15 cells can completely disappear, HBsAg, HBeAg, HBcAg, and the like in the cells are completely turned to be negative, HBV DNA is in a high inhibited state, HBV cccDNA is completely negative, fluorescent quantitation RT-PCR detection finds that the mRNA for expressing HBsAg and HBcAg antigens in the cells is completely negative, and in addition, the curative effect of the atabrine is 30 times that of lamivudine as a first-line drug for resisting HBV in current clinic. In order to illustrate the action mechanism of the atabrine and the pyronaridine as a drug belonging to the same kind with the atabrine, an HBV genome is divided into 3 segments which are respectively inserted into an Xb1 position on a luciferase report carrier PGL3, a multifunctional microplate reader detects and finds that the light production value of the luciferase is remarkably reduced, which shows that the molecules of the atabrine and the pyronaridine as a drug belonging to the same kind with the atabrine can be nonspecifically combined with the HBV DNA in the cells, thereby inhibiting the copying of the virus and ensuring that the HBV DNA content of the virus in cells copied by the filial generation is reduced till to disappear. The patent requires protecting the application of 3 linked benzyl structures (named as ethyleneimine) and radicals such as CH3O-,-NH-, CL-, and the like for resisting HBV virus in clinic.
Owner:蔡荣 +3

Method for accurately and quantitatively detecting autophagy flux

The invention discloses a method for accurately and quantitatively detecting an autophagy flux. The method comprises the following steps: (1) constructing an EGFP / LC3HIBIT co-expression vector, and respectively applying EGFP and LC3HIBIT to independent promoters without mutual influence; (2) obtaining co-expressed cells of EGFP and LC3-HIBIT proteins by a transient transfection or monoclonal screening method; (3) after screening the monoclonal stably transfected cells, carrying out various genetic operations related to autophagy on the basis of the cells, and screening autophagy related drugsand the like; and (4) setting programs on a multifunctional microplate reader to respectively measure luminescence and fluorescence readings, and calibrating a HIBIT reading caused by cell differencesby taking the EGFP as an internal reference in the experiment so as to accurately reflect the autophagy degree of the cells.
Owner:SHENZHEN UNIV

Continuous endo-cellulase as well as coding gene and application thereof

ActiveCN113430217AImprove hydrolysis activityLow hydrolytic activityBacteriaMicroorganism based processesHeterologousNucleotide
The invention discloses a continuous endo-cellulase as well as a coding gene and application thereof, and belongs to the technical field of bioengineering. The nucleotide sequence of the gene is shown as SEQ ID NO.3. The amino acid sequence of the continuous endo-cellulase coded by the gene is shown as SEQ ID NO.4. The continuous endo-cellulase SmCel5A is a multifunctional enzyme of a single structural domain, the molecular weight of the continuous endo-cellulase SmCel5A is less than 40 kD, heterologous expression is easy to conduct, active protein with the activity of endo-cellulase and excision-cellulase enzyme is obtained, and the problems that the growth cycle of sporocytophaga is long, enzyme components are complex, and the cellulase is not easy to directly separate and purify are effectively solved. The enzyme has wide application potential in the industries of biological energy, feed and the like.
Owner:DALIAN POLYTECHNIC UNIVERSITY

Method for measuring activity of cellobiohydrolase I in subtropical forest soil

InactiveCN104988209ASolve the problem of difficult activity determinationImprove accuracyMicrobiological testing/measurementSoil scienceAssay
The invention relates to a method for measuring the activity of cellobiohydrolase I in the subtropical forest soil, and especially relates to a method utilizing a multifunctional enzyme-linked immunosorbent assay (ELISA) instrument to measure the activity of cellobiohydrolase I in the subtropical forest soil. According to the provided method, nitrobenzene cellobioside is taken as the substrate, then the substrate is mixed with a soil sample for reactions in a water bath, and after the reactions, a multifunctional ELISA instrument is used to measure the reaction products. The provided measuring method has the advantages of simpleness, efficiency, and accuracy.
Owner:WEIFANG MEDICAL UNIV

Method and screening model for screening small-molecule inhibitor of main protease of new coronavirus

PendingCN113699212AHigh mP valueLow mP valueHydrolasesMicrobiological testing/measurementFluoProbesHydrolysis
The invention relates to a method and a screening model for screening a small-molecule inhibitor of main protease (Mpro) of a new coronavirus. The method and the screening model are based on the basis of a fluorescence polarization principle, a fluorescent probe FITC-Substrate-Biotin is used as a hydrolysis substrate of the new coronavirus Mpro, avidin is used for terminating the hydrolysis reaction of the new coronavirus Mpro, and a multifunctional microplate reader is used for detecting the millipolarization units (mP) of an experimental system. The active compound shows a high mP value in the screening model, and the inactive compound shows a low mP value.
Owner:MEDICINE & BIOENG INST OF CHINESE ACAD OF MEDICAL SCI

Multifunctional enzyme gene HG27 and application

ActiveCN112899294AStrong toleranceHigh cellulase activityBacteriaHydrolasesCellulosePorcine kidney
The invention discloses multifunctional enzyme gene HG27 and application. The multifunctional enzyme gene HG27 comprises the following steps of comparing a nucleic acid sequence spliced by rhizomys sinensis intestinal microbe macro transcriptome with a glucoside hydrolase family, screening a sequence with relatively high homology, removing original signal peptide, adding pig parotid gland secretory protein signal peptide, optimizing a pig codon, and connecting to a pcd3.1 vector; transfecting to porcine kidney epithelial cells for expression verification, collecting a cell culture solution for enzyme activity analysis, comparing the enzyme activity, selecting the optimal HG27 gene, and detecting the optimal pH value, protein tolerance and enzymatic reaction of different substrates of the HG27 gene, thereby obtaining the multifunctional enzyme gene HG27 which can be applied to the fields of livestock and poultry feed enzyme preparations, transgenic animal preparation, food and medicine industries and the like, and the problems that cellulose is difficult to degrade and absorb and excrement pollutes the environment are solved.
Owner:WENS FOODSTUFF GRP CO LTD +1

SOD (superoxide dismutase) multifunctional enzyme extracted from pine needles and pine gum and preparation method of SOD multifunctional enzyme

The invention relates to an SOD (superoxide dismutase) multifunctional enzyme extracted from pine needles and pine gum and a preparation method of the SOD multifunctional enzyme. In an SOD multifunctional enzyme preparation process, the SOD multifunctional enzyme is extracted from eukaryocyte mitochondria in the pine needles and pine gum of a pine tree which is an evergreen plant tree even after millions of years; during the preparation, a chemical raw material harmful to a human body is not used, no residues are caused, and thus, the SOD multifunctional enzyme is an enzyme with comprehensive healthcare functions. The SOD multifunctional enzyme not only is used for solving complexity in production, but also is safe and non-toxic, has various functions and effects which are much higher than those of the existing commercially available SOD, and is suitable for large-scale production and popularization.
Owner:中志浩(海南)科技有限公司

Application of FBA8 gene or FBA8 protein in preparation of reagent with phosphate transfer activity and/or proteolytic activity

ActiveCN113528497AIncreased aldolase activityMaximized aldolase activityHydrolasesTransferasesKinase activityProteinase activity
The invention relates to application of an FBA8 gene or FBA8 protein in preparation of a reagent with phosphate transfer activity and / or proteolytic activity, and belongs to the technical field of multifunctional enzymes. The FBA8 gene or the FBA8 protein can be used for preparing a reagent with phosphate transfer activity and / or proteolytic activity, and the aldolase activity of the FBA8 can be remarkably improved, the kinase activity of the FBA8 can be maximized, and all activities of the FBA8 can be closed; besides, the protease activity of the FBA8 can be maximized.
Owner:INST OF FORESTRY CHINESE ACAD OF FORESTRY

Protein for catalytic synthesis of amyrin, and preparation method and application for protein

The invention discloses a protein for catalytic synthesis of amyrin, and a preparation method and an application for the protein, and relates to the technical field of biomolecules. The protein has anamino acid sequence as shown in SEQ ID No. 2, or has a sequence which has 90% or above of sequence homology with the sequence as shown in the SEQ ID No. 2 and has the same protein function as the sequence as shown in the SEQ ID No. 2. According to the protein, 2,3-squalene oxide is used as a substrate; alpha-amyrin, beta-amyrin and delta-amyrin can be catalytically synthesized simultaneously; thealpha-amyrin is mainly synthesized; and a new direction is provided for research of multifunctional OSC enzymes.
Owner:GUANGZHOU UNIVERSITY OF CHINESE MEDICINE
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