Abstract: The present invention relates to the microbiological field, and particularly relates to a Leclercia adcarboxglata biocontrol strain efficiently inhibiting production of aflatoxins by Aspergillus flavus. The Leclercia adcarboxglata biocontrol strain Wt16 was deposited at China Center for Type Culture Collection (CCTCC) on Jun. 13, 2017, and the accession number of the strain is CCTCC No. M2017331. The Leclercia adcarboxglata strain Wt16 is isolated from peanut pods for the first time which can significantly inhibit aflatoxins production by Aspergillus flavus, and also has an extremely good effect on inhibiting aflatoxins production by Aspergillus flavus for peanuts from different sources.

Abstract: The present invention provides an antimicrobial peptide ID13 (with a sequence set forth in SEQ ID No. 1), a preparation method and use thereof. The antimicrobial peptide ID3 is successfully expressed in Pichia pastoris using genetic engineering technology. The antimicrobial peptide ID13 of the present invention has an excellent bactericidal activity against Gram-positive bacteria such as Staphylococcus aureus, Streptococcus pneumoniae, and Streptococcus suis, and has a low hemolytic activity against mouse red blood cells and a low murine macrophage cytotoxicity.

Abstract: A portable pesticide application equipment with accurate application, which includes a pesticide tank. Rollers are arranged at the bottom of the pesticide tank. An inclined pesticide guide plate is arranged below the filter. A side connector is arranged at one side of the pesticide tank. The side connector is connected with a long hose. The long hose is connected with a pesticide discharging device. The pesticide discharging device includes a pesticide control box, two sides of which are hinged with a first iron handle and a second iron handle. A first nozzle is connected with the bottom end of the first iron handle while a second nozzle is connected with the bottom end of the second iron handle. The upper end of the first iron handle is inserted into a first support rod while the upper end of the second iron handle is inserted into a second support rod.

Abstract: The disclosure discloses a solid material drying system, including a drying tower and a closed annular conveyor belt at the bottom of the drying tower. A solid material enters the drying tower through the conveyor belt, and a first airflow moves towards the top of the drying tower from the bottom of the drying tower through the conveyor belt. Side walls of the drying tower are provided with several openings, and a second airflow moves towards the outside of the drying tower from the inside of the drying tower. Blocking plates that can block the openings are disposed at positions close to and above the openings inside the drying tower, and the blocking plates are hinged with the side walls of the drying tower. The disclosure is suitable for drying solid materials, and can be efficiently and universally applied to the drying of various types of solid materials.

Abstract: The present invention discloses a system for site-specific modification of ALS gene by a CRISPR-Cas9 system to produce herbicide-resistant rice, and uses thereof. The system for site-specific modification in a plant genome of the present invention comprises a vector for site-specific modification in a plant genome and a donor DNA; wherein the vector for site-specific modification in a plant genome comprises a Cas9 protein expression cassette, gRNA expression cassettes and a donor DNA; the gRNA expression cassettes encode two gRNAs targeting two target sites of a target DNA of a plant of interest, respectively; the target DNA has a fragment to be site-specifically modified which is positioned between the two target site.

Abstract: The present invention provides use of a photoperiod-sensitive genic male sterility mutant of cotton in crossbreeding or hybrid seed production. The fertility of the photoperiod-sensitive genic male sterility mutant of cotton is influenced by the photoperiod. The photoperiod characteristic of the photoperiod-sensitive genic male sterility mutant of cotton is that, the photoperiod-sensitive genic male sterility mutant of cotton shows normal fertility when the illumination time is shorter than 11.5 h and shows genic male sterility when the illumination time is longer than 12 h; the photoperiod-sensitive genic male sterility mutant of cotton is in a fertility change period when the illumination time is in a range of 11.5-12 h and has less pollen. The photoperiod-sensitive genic male sterility mutant of cotton is PSM1, and/or a photoperiod-sensitive genic sterile line obtained through selective breeding of hybridized and/or backcrossed and/or self-bred offsprings of the PSM1.

Abstract: A temperature-sensitive attenuated FMDV strain, construction method and applications thereof. The construction method of the temperature-sensitive attenuated FMDV strain is as follows. Mutating a cytosine on K region loop of IRES domain 4 of an FMDV genome to a guanine or an adenine to obtain the temperature-sensitive attenuated FMDV strain, or replacing a K region of IRES domain 4 of an FMDV genome with a K region of IRES domain 4 of a bovine rhinovirus genome to obtain the temperature-sensitive attenuated FMDV strain.

Abstract: Provided are acidic thermophilic polygalacturonase TePG28A, encoding gene and application thereof. The amino acid sequence thereof is as shown in SEQ ID NO. 1 or SEQ ID NO. 2. The expressed acidic thermophilic polygalacturonase by means of cloning has advantages such as high enzyme activity and high stability; can adapt to the high temperature environment in the industrial production; has better application prospect; and can effectively degrade pectic substances such as polygalacturonic acid and pectin; and can be effectively applied to the industrial field of feed, food, and textile, etc.

Abstract: Provided are a glucose oxidase CnGODA, an encoding gene thereof, a recombinant expression vector comprising the gene, and a recombinant strain; the amino acid sequence of the glucose oxidase CnGODA is as represented in SEQ ID NO:1 or SEQ ID NO:2. Further provided is a method for use in preparing glucose oxidase CnGODA, and application of glucose oxidase CnGODA.

Abstract: The invention provides an application of a nano RNAi preparation in PVY prevention and control, belongs to the field of genetic engineering and application thereof, and can solve the problem of the nano RNAi preparation in PVY virus prevention and control. The RNAi preparation is prepared from dsRNA and chitosan nano materials, wherein the dsRNA is prepared from three gene capsid proteins CP, auxiliary components-protease HC-Pro and genome connexin VPg, and the dsRNA plays a key role in replication, proliferation and movement of PVY virus in plants. The nano RNAi preparation provided by the invention is used for virus prevention and control of PVY, so that the stability of dsRNA is stronger, the effect is longer, a good virus prevention and control effect can be achieved, and the nano RNAi preparation has a good application prospect in the field of PVY virus prevention and control.

Abstract: The present invention relates to the field of agriculture biotechnology, specially relates to an amylase mutant having high specific activity and thermal stability, gene and use thereof. Said amylase mutant is obtained by performing substitution of S33A/S34E/V35H, and deletion of amino acids at the sites of 178 and 179 of the wild type amylase having amino acid sequence of SEQ ID NO:1, and having improved enzymatic activity and thermal stability than the wild type amylase.

Abstract: The present disclosure relates to a foot-and-mouth disease virus vaccine composition, especially a recombinant bivalent vaccine composition against type O and type A foot-and-mouth disease viruses. The present disclosure further relates to a method for preparing the foot-and-mouth disease virus vaccine composition, and a use of the foot-and-mouth disease virus vaccine composition in preparing medicines for preventing and/or controlling foot-and-mouth disease in animals.

Abstract: The present invention provides a soybean genetic transformation method using PMI as selectable gene, and relates to the technical field of genetic engineering. In the soybean genetic transformation method of the present invention, using the PMI gene as a selectable marker, soybean explants are infected by recombinant Agrobacterium with the PMI gene and a target gene, followed by co-culture; without recovery culture, the co-cultured explants are directly selected by a selective medium supplemented with mannose, where transformed explants with the PMI gene grow normally under selection pressure of mannose, while non-transformed explant growth is inhibited, thereby selecting successfully transformed positive plants; after shoot elongation and transplantation of the positive plants obtained, genetically transformed soybean plants are obtained successfully.

Abstract: A method for simultaneously extracting Lycopene and Citrulline from a watermelon includes: separating the rind and the pulp of the watermelon, preprocessing the rind, and using the preprocessed rind to extract the Citrulline; subjecting the pulp to biological enzymolysis and filtering, centrifuging a filtrate, using a precipitate and a filter residue obtained after the centrifuging to extract the Lycopene, and using a supernatant obtained after the centrifuging to extract the Citrulline. By using the method for synchronously extracting Lycopene and Citrulline from the watermelon of the present invention, about 0.5 kg of Lycopene (6% content) and more than 1.2 kg of Citrulline which are worthy of nearly ten thousand yuan can be extracted from each ton of imperfect watermelons, the economic benefit of each ton of watermelons can be increased by more than 5000 yuan after extraction costs are deducted, and the method is high in economic benefits.

Abstract: The present invention provides a remediation method for degradation of cadmium in soil. The specific steps are as follows: step 1, determining the content of cadmium in the soil; step 2, crushing and sieving soil from a soil surface, and weighing; step 3, wetting the soil, and removing part of cadmium in the soil to obtain semi-remediated soil; step 4, mixing the semi-remediated soil with a remediation agent, and allowing to stand to obtain improved soil; and step 5, planting Bidens pilosa in the improved soil, and when a growing season is finished, uprooting, and ashing to obtain finished soil. The present invention utilizes anode and cathodes and a remediation agent to treat the cadmium contaminated soil, and plants Bidens pilosa in the soil to achieve a joint effect of electrodynamic remediation, chemical remediation, microbial remediation and phytoremediation to remediate the cadmium contaminated soil.

Abstract: The present invention relates to the technical field of natural substance extraction. Disclosed is a method for extracting Citrulline from a watermelon. The method for extracting Citrulline from a watermelon in the present invention comprises Raw material pretreatment, ultrasound-enzymatic hydrolysis assisted solvent leaching, and purification steps. The purification step comprises microbial fermentation, ion-exchange resin purification, macroporous adsorption resin discoloration, and crystallization and recrystallization. The method for extracting Citrulline in the present invention is simple, requires a mild condition, and has a good extraction effect on Citrulline. The purity of Citrulline after purification is more than 90%. In addition, the Citrulline extracted by the method in the present invention meets the related health requirements and product quality standards, can be applied to food and health food industries as a raw material, and has natural security advantages.

Abstract: A method for preparing serotype O foot-and-mouth disease virus-like particles, the method including: construction of small ubiquitin-like modifier fusion expression vector, construction of recombinant expression vectors, construction of recombinant co-expression vector, expression and purification of proteins, and in-vitro assembly of serotype O foot-and-mouth disease virus-like particles. The disclosure also provides a test strip for detecting serotype O foot-and-mouth disease including a bottom board, and a detection layer disposed on the top of the bottom board. A detection line and a control line are disposed on the detection layer. An absorbent layer is disposed at one end of the detection layer close to the control line, and an immuno-gold pad is disposed at the other side of the detection layer close to the detection line. A sample pad is disposed on the top of the immuno-gold pad.

Abstract: The present invention provides a remediation method for degradation of cadmium in soil. The specific steps are as follows: step 1, determining the content of cadmium in the soil; step 2, crushing and sieving soil from a soil surface, and weighing; step 3, wetting the soil, and removing part of cadmium in the soil to obtain semi-remediated soil; step 4, mixing the semi-remediated soil with a remediation agent, and allowing to stand to obtain improved soil; and step 5, planting Bidens pilosa in the improved soil, and when a growing season is finished, uprooting, and ashing to obtain finished soil. The present invention utilizes anode and cathodes and a remediation agent to treat the cadmium contaminated soil, and plants Bidens pilosa in the soil to achieve a joint effect of electrodynamic remediation, chemical remediation, microbial remediation and phytoremediation to remediate the cadmium contaminated soil.

Abstract: The invention belongs to the field of microbes and specifically relates to a myroides odoratimimus biocontrol strain for efficiently degrading aflatoxin and an application thereof. A myroides odoratimimus biocontrol strain 3J2MO is preserved at the China Center for Type Culture Collection (referred to as CCTCC) on Jun. 13, 2017 with preservation number CCTCC No. M 2017329. The myroides odoratimimus biocontrol strain of the invention can effectively degrade aflatoxin and may be configured to degrade aflatoxin and treat aflatoxin pollution of food crops.

Abstract: Match-paired monoclonal antibodies against major royal jelly protein 4 (MRJP4) are secreted by hybridoma cell lines having microbial deposit numbers of CGMCC No. 17294 and CGMCC No. 17295, which are used in an ELISA kit and a colloidal gold immunoassay strip for detecting the MRJP4. The positive and MRJP4-sepcific cell lines are obtained by cell fusion using an antigen of MRJP4 recombinant protein and a cross-reaction with other major royal jelly proteins. The MRJP4 recombinant protein is used as an antigen to obtain several positive and cell lines by cell fusion and twoMRJP4-specific fusion cell lines are obtained by a cross-reaction with other major royal jelly proteins. Primary screening of a matched antibody pair is performed according to antibody pairing for recognizing different epitopes.