406 results about "Signalling molecules" patented technology

The invention discloses a soil health and microbiological analysis intelligent environment monitoring device, and relates to the technical field of soil monitoring, the device comprises the following components: an outer shell, a sensor assembly, a microflora interaction monitoring sensor group, a data acquisition and transmission module, a power supply module, a microprocessor, a control unit and a data analysis module; signal molecule concentration change data and predatory relationship visual data are combined through the data analysis module, deep analysis is carried out by using bioinformatics and mathematical modeling means, and a multi-dimensional regulation network hidden in a microbial community can be comprehensively revealed; according to the soil health assessment device, the interaction relationship between the soil ecological system and the soil ecological system is analyzed accurately, the influence of the interaction relationship on key ecological functions such as material circulation and energy flow in the soil ecological system is analyzed accurately, the device can generate a detailed soil health assessment report based on the analysis results, agricultural scientific researchers, planting farmers and environmental protection monitoring departments can assess the soil health condition accurately, and the soil health assessment efficiency is improved. And targeted soil management measures are taken.

The invention discloses an all-optical three-dimensional scanning confocal fluorescent microscopic imaging device and an implementation method thereof. According to the invention, through a deep learning driven adaptive regulation and control method, CNN is adopted to process spatial distribution data and dynamically regulate and control a phase hologram and the light intensity and phase compensation of a laser, so that the focal point of exciting light is subjected to aberration-free axial displacement, a bidirectional parallel optical scanning track of a two-dimensional scanning system is optimized, and all-optical three-dimensional scanning is realized; lSTM and TCN are combined to obtain a time sequence dependency relationship, a laser light source, an adjustable diaphragm, an electric focus-adjustable lens and a photoelectric detector are integrally controlled, efficient synchronization and automatic operation and high-speed axial focusing adjustment are realized, errors and time sequence mismatch are eliminated, optical characteristics of different samples and environmental interference are automatically adapted, and high-quality imaging is kept. The robustness and the applicable scene range of the system are improved; the method is used for model biological embryo real-time tracking, intracellular signal molecule dynamic visualization, cell membrane protein migration and aggregation observation and intracellular organelle interaction tracking.

The invention discloses bacillus (Bacillus sp.) GB-1. The preservation number of the bacillus (Bacillus sp.) GB-1 in Guangdong Microbial Culture Collection Center is GDMCC NO: 65601. The bacillus (Bacillus sp. The strain GB-1 has a good effect of degrading quorum sensing signal molecules OHHL, the quorum quenching effect of the strain is stable and remarkable, a new way and method are provided for biological control of AHLs-mediated pathogenic bacteria, the strain has huge application potential, the use of chemical pesticides can be reduced, and the cost is reduced. A new way is provided for replacing chemical prevention and control with biological prevention and control, and the application prospect is good.

The invention belongs to the field of microbial preparations, and particularly relates to a complex microbial inoculant for promoting microbial quorum sensing and application of the complex microbial inoculant in compost. The composite microbial agent comprises pseudomonas A3 and paenibacillus polymyxa 21-2, and the preservation number of the pseudomonas A3 is CCTCC (China Center for Type Culture Collection) NO: M20251394. The pseudomonas A3 can express key genes such as rhlI and lasI of a gram-negative bacteria AHL quorum sensing system and signal molecules of the key genes, and the paenibacillus polymyxa 21-2 can express luxS genes of a gram-positive bacteria AI-2 signal system and signal molecules DPD of the luxS genes. In the pig manure compost, the complex microbial inoculant is added, so that the expression of AI-2 and AHLs system related genes in the compost and the content of signal molecules DPD are remarkably improved, the microbial population sensing process of the compost is promoted, finally, the compost temperature is increased by about 6 DEG C, the compost carbon-nitrogen ratio is reduced, and the compost maturity is promoted.

The invention discloses an SERS (Surface Enhanced Raman Scattering) sensor for detecting diabetic retinopathy serum biomarkers miR-21 and miR-152 as well as a preparation method and application of the SERS sensor, and belongs to the technical field of biomedicine. The preparation method comprises the following steps: self-assembling AuNHs through an oil-water interface to obtain an AuNHs array, and modifying an aptamer chain cDNA on the surface of the array to obtain an SERS (Surface Enhanced Raman Scattering) substrate; the method comprises the following steps: modifying a Raman signal molecule 4-MBA and a nucleic acid aptamer complementary chain H1 to the surface of AuNTs to obtain an SERS probe 1; a Raman signal molecule DTNB and a nucleic acid aptamer complementary chain H2 are modified to the surface of AuNTs, and an SERS probe 2 is obtained; and combining the prepared SERS probe with a complementary basic group in the nucleic acid aptamer chain cDNA on the SERS substrate, and fixing on the AuNHs array to construct the SERS sensor.

The invention provides an organ chip unit for simulating the pathogenesis of rheumatoid arthritis, and belongs to the technical field of cell culture. The chip comprises a top-layer chip, a bottom-layer chip and a middle microporous membrane, the top-layer chip and the bottom-layer chip are separated by the middle microporous membrane, and the middle microporous membrane is used for enabling cells in a cell culture space of the top-layer chip and cells in a cell culture space of the bottom-layer chip not to be in direct contact, but interaction of signal molecules and substance exchange can be carried out; synovial cells and cartilage cells are injected into the bottom-layer chip or the top-layer chip to be cultured. According to the invention, multi-cell three-dimensional co-culture can be realized. Through the additional stress stimulation co-culture part, the influence of pressure or tension on the cell environment can be judged, and the actual condition that rheumatoid arthritis joints receive pressure or tension for a long time can be simulated. The synovial cells and the cartilage cells are used, so that the structure of the inflammation joint in a living body can be truly reflected, and the interaction among various cell tissues can be reflected.

The invention discloses an SERS (Surface Enhanced Raman Scattering) detection platform for detecting gastric cancer biomarkers, and belongs to the technical field of materials. Comprising the following steps: (1) sequentially carrying out reactive ion etching and physical etching on a single-layer polystyrene microsphere (PS microsphere) colloid template to obtain a pure Si nano crown array SiNCA; (2) depositing gold nanoparticles on the surface of the SiNCA to obtain a gold-plated silicon nano crown array Au / SiNCA; and (3) adding a signal molecule 3-MPBA into the Au / SiNCA, and incubating, so as to obtain the SERS detection substrate material 3-MPBA (at) Au / SiNCA. The SERS microporous array chip prepared by the invention has the advantages of high sensitivity, strong specificity, simplicity in operation, high flux and the like.

The invention belongs to the field of membrane pollution control, and particularly relates to pseudomonas as well as a separation method and application thereof. The invention provides a pseudomonas, which is identified as Pseudomonas knackmussii HITSZ-Q1, is preserved in the Guangdong Microbiological Culture Collection Center, and has the preservation number of GDMCC (China General Microbiological Culture Collection Center) NO: 66162. The strain takes C6-HSL as the unique carbon source and nitrogen source, and the 16S rDNA sequence of the strain is as shown in SEQ ID NO. 1. The strain has a remarkable degradation capability on signal molecules such as C6-HSL, C8-HSL, 3-oxo-C12-HSL and the like, and the highest quenching rate can reach 98.9%. The strain and pseudomonas aeruginosa are co-cultured, so that the signal molecule concentration of the pseudomonas aeruginosa can be effectively reduced, and biofilm formation is inhibited. The strain is further prepared into a carrier in the form of immobilized pellets, the carrier is added into a membrane bioreactor, the operation cycle is prolonged from 6.5 days to 10.5 days, and the membrane pollution delay rate reaches up to 61.5%.

A viral particle. The surface of the viral particle comprises a T cell activation primary signaling molecule and a T cell activation secondary signaling molecule; the envelope glycoprotein of the viral particle is subjected to a first mutation, so that the receptor binding ability of the viral glycoprotein is weakened or lost with respect to its receptor binding ability before the first mutation; and the envelope glycoprotein of the viral particle can also be subjected to a second mutation, so that the viral particle has enhanced resistance to complement-mediated inactivation or is not subjected to complement-mediated inactivation. The viral particle has improved specificity for targeted activation, stimulation and transduction of non-activated T cells, and is thus more applicable for the preparation of CAR-T cells in subjects.

The embodiment of the invention provides an organ chip, and relates to the technical field of organ chips, the organ chip comprises at least two function parts and a dielectric layer located between the two adjacent function parts, the at least two function parts are stacked, and each function part is provided with a cell culture chamber; the dielectric layer is used for isolating contact between cells of adjacent cell culture chambers and allowing interaction and substance exchange between signal molecules between the adjacent cell culture chambers, and through the stacked functional part and dielectric layer structure, interaction of the signal molecules is allowed while different cell culture chambers are physically isolated; the air guide part and the connector of the culture box are tightly pressed, the air pressure regulation and control precision and the culture environment stability are guaranteed, the air pressure stability in the culture box is effectively guaranteed, and external microorganisms, dust and other pollutants are effectively prevented from invading the culture environment.

The invention discloses a phycomycete symbiotic system and application of the phycomycete symbiotic system in treatment of aquaculture tail water, and belongs to the technical field of tail water treatment. The phycomycete symbiotic system comprises chlorella, scenedesmus and activated sludge, and the initial inoculation dry weight ratio of the chlorella to the scenedesmus to the activated sludge is 1: 1: 6. And exogenously adding octanoyl-L-homoserine lactone or tetradecanoyl-L-homoserine lactone into the phycomycetes symbiotic system, so as to construct the phycomycetes symbiotic system with enhanced functions. On the basis of a mixed algae-bacteria symbiotic system with an optimized ratio, directional enhancement of functions is realized by virtue of quorum sensing signal molecules, the stability and resistance gene interception capability of the quorum sensing signal molecules under the stress of antibiotics are verified, and finally efficient purification of the aquaculture tail water is realized. According to the invention, the blank of the prior art in the aspects of advanced regulation and control of a phycomycete synergistic mechanism and synergistic treatment of emerging pollutants is filled up.

The invention discloses an electrochemical biosensing system for detecting BVDV (bovine viral diarrhea virus) based on CRISPR-Cas13a (clustered regularly interspaced short palindromic repeats). The electrochemical biosensing system comprises an electrochemical biosensor and a CRISPR-Cas13a system, the electrochemical biosensor comprises a working electrode, and the surface of the working electrode is modified with an MB-RNA probe; one end of the MB-RNA probe is modified with sulfydryl, the other end of the MB-RNA probe is modified with signal molecules, and the MB-RNA probe is connected with the working electrode through an Au-S bond; the CRISPR-Cas13a system comprises a crRNA (Complementary Ribonucleic Acid) group and Cas13a; and the crRNA group comprises at least one of BVDV (bovine viral diarrhea virus)-crRNA 2, BVDV-crRNA 7, BVDV-crRNA 8, BVDV-crRNA 11, BVDV-crRNA 12 and BVDV-crRNA 14. The electrochemical biosensing system disclosed by the invention has extremely high clinical sensitivity and clinical specificity on the BVDV virus.

The invention discloses an engineered macrophage and a pharmaceutical composition and application thereof, and CCM3 expression in the engineered macrophage is inhibited, so that the engineered macrophage is polarized towards the M2 direction or the engineered macrophage is an M2 type macrophage. Besides, the invention further develops a temperature-sensitive cell-loaded hydrogel preparation which can promote polarization of macrophages in the M2 direction by inhibiting expression of signal molecules CCM3 on adhesion spots, and the temperature-sensitive cell-loaded hydrogel preparation can promote bone defect immune osteogenesis through local injection.

The invention relates to the technical field of fertilizers, and discloses an amino acid-containing water-soluble fertilizer and a preparation method thereof, and the method comprises the steps of raw material preparation, carrier system construction, signal molecule extraction and activation, stress-resistant amino acid compound preparation, multi-element synergistic system construction and the like. Through innovative combination of a soil penetrating carrier system and a plant source signal molecule technology, the technical problems of weak penetrating power, low bioavailability and the like of active components of a fertilizer in saline-alkali soil are solved, so that the effective penetrating depth of signal molecules in severe saline-alkali soil is effectively improved, the bioavailability is improved, and the application prospect is wide. The saline-alkali resistance of the plants is obviously enhanced, and the ecological restoration and sustainable utilization of the saline-alkali soil are promoted.

The invention relates to a Raman probe for detecting hydrogen sulfide as well as a preparation method and application of the Raman probe. The gold and silver nanocage (AuAg NCs) is prepared, and after the gold and silver nanocage (AuAg NCs) is modified by a Raman signal molecule 4-ethynylaniline (4EA), it is found that the AuAg-4EANCs shows the strongest Raman enhancement effect at the position of 2010 cm <-1 > located in a cell silence zone. The SERS probe with the tumor targeting capability is developed through the functional modification of a mucoprotein 1 aptamer (MUin1aptamer, MUC1Apt) and polyethylene glycol (PEG), and the SERS probe with the tumor targeting capability is further developed through the functional modification of the mucoprotein 1 aptamer (MUin1aptamer, MUC1Apt) and the PEG (Polyethylene Glycol). In the presence of hydrogen sulfide (H2S) and oxygen, Ag in AuAg-4EANCs rapidly reacts with H2S to generate Ag2S with significantly reduced Raman enhancement performance, resulting in sharp attenuation of 4EA signal intensity. And along with the increase of the H2S concentration, the generation amount of Ag2S is increased, so that a quantitative detection model dependent on the H2S concentration is established.

The invention discloses a preparation method of cells with LTo-like functions, which is characterized in that adipose tissue-derived stem cells are treated by LTo differentiation induction signal molecules to obtain cells with LTo-like phenotypes, secretion of cytokines and chemotactic factors of the cells is up-regulated, and the cells have recruitment and support capabilities on lymphocytes in vivo and in vitro. The problems that LTo cells are rare and difficult to obtain are solved, and the adipose-derived stem cells are higher in efficacy, easy to obtain and culture in vitro, capable of being massively amplified, low in cost, efficient and safe.

The working electrode is characterized in that the working electrode is obtained by dispensing ferroferric oxide and lauric acid on the surface of a glassy carbon electrode. A working electrode for detecting the micro-plastic is a working electrode, an Ag / AgCl electrode is a reference electrode, and platinum is an auxiliary electrode; preparing a series of concentrations of micro-plastic standard sample solutions, preparing a ferrocene solution and an electrolyte, firstly putting a working electrode, a reference electrode and an auxiliary electrode into the standard sample solutions, incubating to reach adsorption equilibrium, then taking out the three electrodes, putting the three electrodes into the ferrocene solution, and incubating; and finally, taking out the three-electrode system, putting the three-electrode system into electrolyte, and carrying out DPV detection. A simple and low-cost electrochemical sensing detection method is established by utilizing the reaction of the micro-plastic reinforced ferrocene signal molecules. The method is rapid, simple and low in cost, and can effectively detect the micro-plastics in a wide range and maintain good sensitivity.

The invention relates to the technical field of biologic stimulant preparation, and discloses a biologic stimulant mixing preparation two-stage control method, which comprises: adopting dissolved oxygen gradient and carbon source pulse cooperative control, linearly reducing the concentration of dissolved oxygen in a fermentation tank from an initial value at a specific rate, and injecting a carbon source at regular time; when the flora density and the quorum sensing signal molecule concentration reach specific threshold values, triggering stage switching; starting pressure-metabolism coupling control, increasing the pressure of the fermentation tank at a specific rate, and adding coenzyme Q10; the quorum sensing inhibitory peptide containing a specific core structure is synchronously released in the boosting process; after the pressure is stable, a real-time mapping relation between a microbial metabolism state and physical parameters is constructed in a thallus proliferation stage through a coupling mechanism of dissolved oxygen gradient control and quorum sensing signal monitoring, and the industrial problem that a traditional static threshold value cannot respond to pressure fluctuation of a fermentation tank to cause signal attenuation is solved.

The invention relates to the technical field of sewage treatment, in particular to application of a signal molecule C8-HSL in strengthening sewage treatment of algal-bacterial symbiotic granular sludge. In-depth study finds that the signal molecule C8-HSL can improve the TN removal rate of the system; according to the present invention, with the application of the signal molecules, the flora composition is changed, the enrichment of denitrification functional bacteria such as Hydrogenphaga, Pseudoxanthobacteria and the like is promoted, and the abundance of the complex organic matter degrading bacteria Desulfomicrobe is enhanced; meanwhile, due to the increase of denitrifying bacteria such as Hydrogenphaga, Thauera and Zoogloea, the variety of species is optimized, and the nitrogen removal efficiency and the organic matter degradation efficiency are improved; based on PICRUSt2 analysis, the signal molecule C8-HSL can increase the abundance of the napAB gene and promote aerobic denitrification; expression of nirK and nirS genes is enhanced, and nitrite is promoted to be converted into nitrogen; meanwhile, the signal molecule C8-HSL effectively improves the denitrification performance of the system by optimizing a nitrogen metabolism pathway.

The invention discloses a method for detecting miRNA-21 based on a paper base-friction power generation sensing chip of intelligent DNA hydrogel and application. The method comprises the following steps: preparing Pt-Ni NPs; the preparation method comprises the following steps: preparing hydrogel embedded with Pt-Ni NPs; designing a paper-based micro-fluidic chip; the miRNA-21 is recognized through a CRISPR-Cas12a system, the gel is cut, internal Pt-Ni NPs signal molecules are released, and a blue strip is displayed on the paper-based micro-fluidic chip; a nano generator is connected with the chip to prepare a paper base-friction power generation sensing chip; along with the change of the concentration of the miRNA-21, the gel releases Pt-Ni NPs with different concentrations to cause the voltage change on the paper-based friction power generation sensing chip, and the change value is in direct proportion to the concentration of the miRNA-21. The chip is used for detecting miRNA-21 and has the advantages of simplicity in operation, small size, portability, high sensitivity, good specificity and short detection period.

The invention provides a preparation method of a pump-free SERS (Surface Enhanced Raman Scattering) micro-fluidic chip for detecting mi RNA (Ribonucleic Acid) related to liver cancer and the pump-free SERS micro-fluidic chip. The method comprises the following steps: 1) preparing 20nm gold particles (AuNPs) by adopting a sodium citrate reduction method; 2) respectively modifying Raman signal molecules DTNB and 4-MBA and nucleic acid complementary chains H1 and H2 on AuNPs to prepare AuNPs (at) DTNB (at) H1 and AuNPs (at) 4-MBA (at) H2; (3) modifying the surface of the magnetic core Fe3O4 with nucleic acid aptamers cDNA (complementary deoxyribonucleic acid) 1 and cDNA 2 of the mi R-21 and the mi R-155 to obtain Fe3O4 (at) cDNA 1 and Fe3O4 (at) cDNA 2 (Fe3O4 (at) cDNA); (4) the AuNPs (at) DTNB (at) H1 and the AuNPs (at) 4-MBA (at) H2 prepared in the step (2) are coupled with the Fe3O4 (at) cDNA prepared in the step (3), and Fe3O4 (at) cDNA-AuNPs (at) Raman report (at) H is obtained; and 5) mixing polydimethylsiloxane (PDMS) with a curing agent, adding the mixture into the template to prepare a micro-fluidic chip, and carrying out hydrophilic treatment to construct the pump-free SERS micro-fluidic chip. The method has the advantages of high sensitivity, high specificity, high detection speed and the like.

The invention provides an immunological detection method for an object to be detected in a whole blood sample. The immunological detection method comprises the following steps: a) mixing a whole blood sample with a polyethylene glycol diluent to obtain a treating fluid; b) mixing the treating fluid and an immunodetection reagent, and incubating to obtain an incubated compound; wherein the immunodetection reagent comprises a signal molecule and a first affinity protein which is specifically combined with an object to be detected; and c) carrying out signal detection on the incubation compound, and obtaining the amount of the to-be-detected substance through the signal intensity. The problem of poor detection accuracy of the whole blood sample in the prior art can be solved, and the method is suitable for the field of whole blood sample detection.

The invention discloses a fluorescent array sensing system based on bionic taste sense, a construction method of the fluorescent array sensing system and application of the fluorescent array sensing system in food safety intelligent detection. According to the system, a functionalized ultrathin Ti3C2 MXene nanosheet serves as a bionic tongue carrier, multicolor silver nanoclusters synthesized by oligonucleotide chains are adsorbed on the surface of the functionalized ultrathin Ti3C2 MXene nanosheet to serve as bionic taste bud cells, different DNA chains can form different fluorescence emissions, the characteristic that fluorescence can be designed is achieved, and the preparation process of signal molecules can be greatly simplified. When a plurality of hazardous substances are added into the sensing array at the same time, the Ti3C2 MXene with strong binding capacity can preferentially capture a target object, and the silver nanoclusters with weak binding capacity can release or adsorb, so that fluorescence signals with different colors are changed, and a characteristic fingerprint spectrum is formed. And in combination with a machine learning algorithm, rapid, accurate, qualitative and quantitative intelligent identification of multiple food hazardous substances can be realized at the same time, and a new strategy is provided for simultaneous detection of multiple hazardous substances in food safety.

The invention discloses a stem cell preparation for scalp hair follicle regeneration and a preparation method thereof, and relates to the technical field of biological agents, and the stem cell preparation comprises the following raw materials: exosome, normal saline, alpinetin extract and hydrogel. According to the stem cell preparation for scalp hair follicle regeneration and the preparation method of the stem cell preparation, mRNA, miRNA and protein carried by the exosome can act on hair follicle stem cells in a targeted mode, cell cycle related genes are activated, and cells are promoted to enter a proliferation period from a G0 period; meanwhile, by transmitting BMP, Notch and other signal molecules, hair follicle stem cells are inhibited from being differentiated into epidermal cells, the hair follicle stem cells are induced to be differentiated into hair follicle specific cells, and reconstruction of a hair follicle structure is promoted; anti-inflammatory factors in the exosome can inhibit excessive activation of fibroblasts around hair follicles, reduce collagenous fiber deposition and relieve inhibition of fibrosis on hair follicle regeneration; meanwhile, the levels of TNF-alpha, IL-6 and other proinflammatory factors are reduced, and a suitable growth environment is provided for hair follicle stem cells.

A surface-enhanced Raman scattering (SERS)-based test kit for Staphylococcus aureus includes a magnetic nanosphere, gold / silver core-shell nanoparticles (Au—Ag NPs), Au nanoparticles (Au NPs), a SERS signaling molecule, a rolling circle amplification (RCA) template, a target aptamer, a complementary deoxyribonucleic acid (cDNA) and a single-stranded deoxyribonucleic acid (ssDNA). A detection method for S. aureus using the SERS-based test kit is also provided.

The invention relates to the technical field of soil fertility management, in particular to a production quality control method of a special fertilizer for Yunnan cigar tobacco leaves, which comprises the following steps: step 1, preparing a waste-based functional carrier; step 2, signal response type fermentation control: based on a dynamic monitoring result of microbial population sensing signal molecules in a fermentation system, regulating and controlling the injection opportunity of an exogenous inducer and fermentation environment parameters, and directionally synthesizing a targeted antibacterial metabolite; step 3, adaptive packaging in a growing period; and 4, bionic verification and closed-loop optimization: verifying a nutrient release curve through a bionic root system simulation device, and feeding back and adjusting packaging parameters in combination with a field metabolite detection result to form a production-application self-optimization system. The production efficiency and fertilizer efficiency of the cigar tobacco leaf fertilizer are improved through accurate process control, it is ensured that nutrient supply and release of the fertilizer in all growth periods have excellent matching performance, and the effect of the fertilizer can be optimized in practical application.

The invention provides a Raman enhanced nano-label based on a polydopamine core-shell structure, a preparation method and application of the Raman enhanced nano-label in immunochromatography, and relates to the technical field of immunochromatography. The Raman enhanced nano-label based on the polydopamine core-shell structure sequentially comprises a PDA microsphere core, a PEI layer and a gold and silver nano-particle layer from inside to outside, the gold and silver nanoparticle layer is gold and silver nanoparticles with a core-shell structure; the gold and silver nanoparticle layer is connected with a Raman signal molecule DTNB, and a terminal carboxyl group of the Raman signal molecule DTNB is coupled with a capture antibody of an H1N1 virus or a capture antibody of an SARS-CoV-2 virus. The nano-label has colorimetric and SERS enhanced activity at the same time, has the advantages of rich hot spots, high stability, excellent optical performance and the like, is used for an immunochromatography sensor to detect two respiratory viruses at the same time, adopts qualitative and quantitative dual-mode detection, and improves the detection flexibility, sensitivity and accuracy.

The present invention relates to a control method for slowing down MBR membrane pollution by using microbial predation to inhibit quorum sensing, and belongs to the technical field of sewage biological treatment. The method comprises the following steps: 1. Cultivating obligate predatory bacteria with Gram-negative bacteria that can secrete signal molecules (N-acyl homoserine lactone) as the main host to obtain a quorum sensing inhibitor; 2. Directly putting the cultivated quorum sensing inhibitor into the MBR reaction pool, the quorum sensing inhibitor will carry out an obligate predation process in the MBR reaction pool; the quorum sensing inhibitor can prey on Gram-negative bacteria that secrete N-acyl homoserine lactone and inhibit quorum sensing. The present invention can effectively reduce the concentration of signal molecules in the MBR reaction pool, so that it cannot reach the threshold of triggering quorum sensing and thus avoid the production of extracellular polymers, so as to inhibit the formation of biofilm from the source, and has a significant control effect on MBR membrane pollution.