285 results about "Magnaporthe oryzae" patented technology

The invention relates to a Bacillus subtilis T-500. The Bacillus subtilis T-500 has been preserved in CGMCC (China General Microbiological Culture Collection), and the preservation number is CGMCC NO:6058. The Bacillus subtilis T-500 can be used as a biological pesticide for preventing and treating multiple plant diseases, and can also be used as a biological fertilizer for promoting the yield increase of crops. The Bacillus subtilis T-500 has higher antibacterial activity on Magnaporthe oryzae, Pellicularia sasakii, Xanthomonas oryzae, Ustilaginoidea virens, Xanthomonas oryzae pv. oryzicola, Fusarium graminearum, Aspergillus flavus, Aspergillus niger and other pathogenic bacteria, and has better prevention and control effects on diseases caused by the pathogenic bacteria. The Bacillus subtilis T-500 can prevent and treat rice leaf diseases when being diluted 200-500 times on the leaves of rice, can prevent and treat bakanae diseases of rice after seed soaking, and can prevent and treat soil-borne diseases of vegetables and the like after root irrigation.

The invention discloses an antibiotic Bacillus amyloliquefaciens with powerful bacteriostasis and wide bactericidal spectrum. The strain has been preserved in the China General Microbiological Culture Collection Center and the taxonomy name of the strain is: Bacillus amyloliquefaciens with preservation number CGMCCNo.4777. The antibiotic Bacillus amyloliquefaciens has powerful bacteriostasis, wide bactericidal spectrum, high inhibition rate up to above 93.5% on the rice blast fungus, the Botrytis cinerea and the Phytophthora parasitica; the Bacillus amyloliquefaciens also has very strong stress resistance, and very strong resistance to the acid and alkali, and is suitable to be used as microbial bactericide.

A method for identifying rice blast resistance of rice comprises the steps of scissoring three rice stems in a large bract period from a rice growing field, bringing the rice stems back to a laboratory, scissoring 2cm from the upper portion of each stem section and 5-6cm from the lower portion of each stem section to obtain one rice stem with the whole length of approximate 7-8cm, putting the three rice stems into culture dishes with two layers of filter paper, adding sterile water of 1mL into each culture dish, washing cultivated rice blast fungus spores with the sterile water, obtaining concentration of 106 pcs/ml, dropping spore suspending liquid of 8 muL to stem section sites of each rice stem through a liquid moving gun, putting the culture dishes into a illuminating incubator at the temperature of 26 DEG C, wrapping the culture dishes with transparent films to keep humidity in the culture dishes, cultivating for ten days in light and dark alternating modes to survey disease conditions, dividing survey disease levels into three levels, regarding the first level as disease-resistant cultivars, regarding the second level as susceptible cultivars, and regarding the third level as highly susceptible cultivars. The method optimizes the concentration and inoculation amount of inoculated rice blast fungus spores and establishes simple, convenient and accurate grading standards.

The invention discloses a method of researching the change of a proteome of rice responding rice blast bacterial infection through an iTRAQ technology and belongs to the field of plant biotechnology. The method includes following steps: A. extracting a plant materials and leaf protein; B. performing further FASP enzymolysis, peptide fragment marking, SCX classification and LC-MS analysis to the protein sample obtained in the step A; C. performing data query and quantitative analysis to the result after the LC-MS analysis to obtain the change situation of the whole proteome during an interaction process between rice and rice blast bacteria. The method can quickly and effectively screening a candidate gene relative to disease resistance of rice, can be used for researching the candidate gene relative to the disease resistance of the rice well with the proteomics researching method, iTRAQ, which is high-throughput and accurate, can be widely used for researching and developing the characters of plant disease resistance and breeding new plant varieties being strong in disease resistance with combination of the transgenic technology.

The invention discloses an anti-bacterial protein PBR1 as well as a preparation method and application thereof, and relates to the technical field of molecular biology and biological pesticides. The amino acid sequence of the anti-bacterial protein PBR1 is shown as SEQ ID NO.1. The anti-bacterial protein PBR1 has a superior effect on preventing and curing plant diseases such as cruciferous plasmodiophoromycetes, paddy rice magnaporthe oryzae, curvularia lunata, fusarium oxysporum f. sp. dianthi, fusarium oxysporum vasinfectum, konjac foot rot bacteria, panax notoginseng root rot pathogen, pomegranate wilt pathogen, gaeumannomyces gramini, cylindrosporium pomi brooks, alternaria alternata and/or botrytis cinerea. A pesticide taking the anti-bacterial protein PBR1 as an active ingredient is a novel environment-friendly biological pesticide, is safe to people and livestock, protects the environment, and has a favorable development prospect.

The invention relates to biocontrol Bacillus velezensis SF259 and application thereof. The Bacillus velezensis strain is collected in the China Center for Type Culture Collection (CCTCC) on September20, 2019, with the collection name of Bacillus velezensis SF259 and the collection number of CCTCCM 2019735. The Bacillus velezensis has a significant inhibition effect on xanthomonas oryzae pv. oryzae (Xoo), also shows broad-spectrum bacteriostatic activity for xanthomonas oryzae pv. oryzicola (Xoc), X. campestris pv. musacearum, X. axonopodis pv. vignicola, X. campestris pv. malvacearum, botrytis cinerea and magnaporthe oryzae, and has important biocontrol application prospects.

An object of the present invention is to search and identify novel antifungal proteins capable of inhibiting the growth of plant pathogenic microorganisms including Magnaporthe grisea and Rhizoctonia solani causing two major rice diseases at relatively low concentrations, and further to clone a gene for said protein. The present invention provides an antifungal protein which can be obtained from fraction(s) precipitated by ammonium sulfate precipitation using an aqueous extract from Pleurotus cornucopiae, wherein said protein has an antifungal activity against at least rice blast, and exhibits existence of a component having a molecular weight of about 15 kDa as determined by SDS-PAGE method; a gene encoding said protein and uses thereof.

The invention relates to Bacillus velezensis 229-15 and application thereof. The Bacillus velezensis is preserved in the Chinese Type Culture Collection on September 20, 2019, the sample name is Bacillus 229-15 Bacillus sp. 229-15, the preservation number is CCTCC No: CCTCC M 2019734, and the strain is isolated from a campus soil sample in Gansu Agricultural University, Anning District, Gansu Province in China. The Bacillus velezensis 229-15 has a bacteriostatic effect on Xanthomonas oryzae pv.oryzae, Xoo and Xanthomonas oryzae pv.oryzicola, Xoc, and also has bacteriostatic effects on X.campestris pv.musacearum, X.axonopodis pv.vignicola, X.campestris pv.phaseoli and Magnaporthe oryzae, Botrytis cinerea, Fusarium graminearum and other pathogenic fungi at the same time. It is shown throughresults that the strain has a broad-spectrum bacteriostatic ability, good biocontrol resources are provided for prevention and control of Xanthomonas oryzae pv.oryzae, Xoo and Xanthomonas oryzae pv.oryzicola, Xoc, and a foundation is laid for development of novel microbial agents.

The invention discloses a PCR detection and identification method capable of distinguishing pyricularia grise and magnaporthe oryzae and belongs to the technical field of plant fungus molecule biological detection. The PCR detection and identification method includes the steps of A, extracting DNA, to be specific, respectively extracting DNA of pyricularia grise and magnaporthe oryzae; B, designing primers, to be specific, designing a pair of specific primers Mol3-F/Mol3-F by inserting two ends of the retrotransposon of 849bp into a coding region of avirulence gene PWL3 of pyricularia grise; C, performing PCR, to be specific, performing PCR amplification by taking the extracted total DNA of pyricularia grise and magnaporthe oryzae as a template, so as to obtain an amplification product; D,determiningresults, to be specific, subjecting the amplification product to electrophoresis detection, if a target band of 1771bp is detected, then determining the product as pyricularia grise; if aband of 922bp is detected, then determining the product as magnaporthe oryzae. The PCR detection and identification method can rapidly accurately distinguish pyricularia grise and magnaporthe oryzae which are difficult to distinguish, and has a great significance in field spreading, breeding and evolving of Pyricularia on natural conditions.

The invention belongs to the technical field of plant biology, and particularly discloses a molecular marker for a rice blast resistance gene Pita and application thereof. The molecular marker consists of a pair of outer primers Pita-O-F and Pita-O-R and a pair of inner primers Pita-T-F and Pita-C-R, wherein the primer sequences are shown as SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3 and SEQ ID NO:4. The rice blast resistance gene Pita genotype is authenticated by utilizing the marker; rice blast resistance genes can be genotyped to distinguish a rice blast fungus resistant rice variety from a susceptible variety only through simple PCR without sequencing; auxiliary selection of the molecular marker of a rice blast can be realized; according to the molecular marker disclosed by the invention, the Pita gene detecting efficiency can be improved; the molecular marker is suitable for the molecular marker auxiliary selection of a rice improvement segregation population; the breeding efficiency is improved; the requirement on large-scale molecular breeding is met.

The present invention belongs to the technical field of gene engineering, and particularly relates to a rice blast resistance gene RMg41 and applications thereof. According to the present invention, the nucleotide sequence and the amino acid polypeptide sequence encoded by the gene of the new rice blast resistance gene RMg41 are disclosed, and the gene belongs to the member of the NBS-LRR type resistance gene family; and the rice blast resistance gene RMg41 is cloned from the rice strain exhibiting high resistance on the rice blast bacteria, the rice blast resistance gene RMg41 is transformed into the rice blast bacterial susceptible variety, and the rice blast bacterial infection method is adopted to evaluate the disease resistance so as to finally determine the resistance of the gene on the rice blast.

The invention discloses bacillus velezensis LJBV19 separated from rhizosphere soil of grapes. The strain is collected in China General Microbiological Culture Collection Center of China Committee for Culture Collection of Microorganisms on April 2, 2021 and has an accession number of CGMCC No. 21804. The invention further discloses a broad-spectrum disease-preventing growth-promoting bacterium agent and application thereof in prevention and treatment of plant diseases caused by phytopathogens. The bacillus velezensis LJBV19 disclosed by the invention has broader-spectrum disease preventing and growth promoting effects and can be used for effectively controlling the plant diseases caused by paddy pathogens, grape pathogens, Solanaceae crop pathogens and wood pathogens, and the average inhibiting rate of the bacillus velezensis LJBV19 to Magnaporthe oryzae reaches up to 75.75%; and the bacillus velezensis LJBV19 can also be used for promoting growth of plants, improving crop yield, improving fruit quality, improving resistance of crops, developing agricultural economy and pushing agricultural development.

A rice blast bacterium innocuity gene Avr-Pib is obtained by separation and appraising in T-DNA insertion mutation. The out-knocking mutant of the gene can cause susceptibility of rice breed variety containing Pib disease-resistant gene. The out-knocking mutant and field susceptibility individual plant can recover non-toxicity by function complementation experiment and the breed variety is disease-resistant. The gene can be used as molecule target of newly pesticides and paddy rice disease-resistant genetic engineering.

The invention discloses a separation method of magnaporthe oryzae. According to the method, a special spore slippery filament is adopted, and a single conidium is directly separated from a rice blast standard sample and is cultured to form a rice blast bacteria strain with a single genetic composition. The implementation and operation steps of the isolated culture are as follows: 1) collecting a rice blast standard sample; (2) treating a magnaporthe oryzae standard sample; (3) preparing spore slippery filaments; (4) preparing a spore dispersing plate; (5) dispersing the conidia; (6) cutting the spore-carrying sliding scattering plate; and 7) culturing conidia and forming a monospore strain. The method has the following advantages: 1) a key appliance for separating spores is simple and easy to manufacture, and the separation operation is simple and easy; 2) single spore strains can be separated and obtained at one time; 3) the separation work consumes less time and labor; and 4) the working efficiency of separating the magnaporthe oryzae and the reliability of a separation result can be obviously improved.

The invention discloses a rice blast resistance gene Pikg, encoding protein and application thereof, and belongs to the field of rice disease resistance breeding. The rice blast resistance gene Pikg comprises Pikg<-1> and Pikg<-2>, and the nucleotide sequence of a coding region and the amino acid sequence of coding protein of the rice blast resistance gene Pikg are respectively shown in a sequencetable. The gene and the protein can be used for improving the resistance of rice plants to magnaporthe griseat.

The invention discloses a method for researching an oryza sativa and pathogen interaction mode, and belongs to the field of plant biotechnology. The method for researching the interaction mode of oryza sativa in response to pathogen infection through integrated application of a transtriptome, a proteome and a miRNA group comprises the concrete steps: A, respectively taking oryza sativa leaf blade total RNAs, Small RNAs and total proteins of a disease-resistant material and a susceptible material at different time points before and after pathogen inoculation; B, respectively carrying out differential-expression spectrum analysis, differential proteomics analysis and miRNA identification and target gene analysis; and C, integrating and associating differential genes, proteins and miRNA target genes identified by the three ways, to reveal disease-resistant and susceptible reaction paths activated or inhibited in the oryza sativa and pathogen interaction process, so as to relatively systematically illuminate an oryza sativa-magnaporthe oryzae interaction mechanism. The method can quickly and effectively screen candidate genes associated with oryza sativa disease resistance.

The invention relates to the technical field of microorganisms, in particular to a strain of pseudomonas having significant antagonistic action against Xanthomonas oryzae and magnaporthe oryzae and application of the pseudomonas. The strain is isolated from rice rhizosphere soil of Fengxian District, Shanghai; the pseudomonas provided by the invention was deposited in the China Center for Type Culture Collection on May 7, 2018, the preservation name is Pseudomonas mosselii 923, and the preservation number is CCTCC No:M 2018252. The pseudomonas provided by the invention has a significant inhibitory effect on Xanthomonas oryzae, has relatively strong inhibitory capacity against other plant pathogenic bacteria and magnaporthe oryzae of Xanthomonas, and has biological control application value.

The invention which belongs to the technical field of genetic engineering concretely relates to a rice blast resistant gene RMg1, RMg2 or RMg3, and its application. The invention discloses nucleotide sequences of the new rice blast resistant genes RMg1, RMg2 and RMg3, and amino acid polypeptide sequences coded by the nucleotide sequences. The three genes belong to an NBS-LRR (nucleotide-binding site and leucine-rich-repeat) type disease resistant gene family. The three rice blast resistant genes of the invention are cloned from a rice line highly resisting rice blast pathogens, and are converted to lines which can suffer from the rice blast pathogens, and the disease resistances of the lines are assessed through using a rice blast pathogen invasion method, so a case that the three genes have resistances to the rice blast is finally determined.

The invention relates to a novel wide-spectrum bacterial strain Bacillus sp. AH-E-1 inhibiting clinical and plant pathogenic fungi, and an application thereof. The main content comprises: (1) Bacillus sp. AH-E-1 is a newly-discovered bacillus strain or subspecies; (2) Bacillus sp. AH-E-1 can produce anti-fungus substances after fermentation under appropriate conditions; (3) Bacillus sp. AH-E-1 can significantly inhibit 20 clinical pathogenic fungi such as aspergillus flavus, aspergillus fumigates, trichophyton rubrum, trichophyton mentagrophyte, candida glabrata, cryptococcus neoformans, and the like; (4) Bacillus sp. AH-E-1 can significantly inhibit 13 plant pathogenic fungi such as staphylococcus, magnaporthe oryzae, rhizopusstolonife, and the like. The invention provides an excellent novel anti-fungus substance producing bacterial strain which has the advantages of wide fungus-inhibiting spectrum, obvious effect, and the like.

The invention provides a cultivating method of cross-year regrowing rice seeds. According to the cultivating method, wild rice containing cold-resisting and root-flourishing genes is adopted as a male parent, DS89-1 glutinous rice is adopted as a female parent, 3-5 times of recrossing is carried out, and then the cross-year regrowing rice seeds can be obtained. The invention further provides a seedling planting method of the cross-year regrowing rice seeds. Rice which is grown from the cross-year regrowing rice seeds obtained through the cultivating method and is planted according to the seedling planting method has the advantages of being high in yield and milled rice rate, good in rice quality, capable of regrowing in the next year and strong in cold resistance, drought resistance, lodging resistance and Magnaporthe oryzae resistance.

The invention discloses the function and the usage of a magnaporthe oryzae MoCHS1 gene and a coded protein thereof. The gene controls the conidium form, the conidium yield, the appressorium formation rate and the pathogenicity of magnaporthe oryzae. The gene as well as the cDNA and the coded protein thereof respectively comprise nucleotide or amino acid sequences SEQ ID No: 1, No: 2 and No: 3 in the sequence list. The knockout of the MoCHS1 gene causes the change of the form establishment of the magnaporthe oryzae conidium; the conidium is reduced and has no diaphragm or has only one diaphragm; the yield of the conidium is decreased to 2% of wild type bacterial strains; the formation rate of the appressorium is decreased to 60% of the wide type bacterial strains; and the infestation capability on rice vanes is obviously decreased. The protein coded by MoCHS1 or/and the expression or the modification of the homologous protein in other pathogenic fungi can be taken as important candidate targets and can be used for designing and screening novel antifungal drugs.

The invention relates to a biocontrol pseudomonas sp. and an application thereof, specifically to a biocontrol strain GZ9 with a preservation number of CCTCC M 20191037. The strain has a significant inhibition effect on botrytis cinerea, and shows a good inhibition effect on phytophthora capsici, magnaporthe grisea and gibberella zeae. The fermentation liquor of the strain has a good control effect on tomato gray mold, and can reach a control effect of 78.66%. Thus, the strain has good biocontrol application prospect.

The invention relates to a phenylimidazole derivative, a synthesis method of the phenylimidazole derivative and application of the phenylimidazole derivative to pesticide, particularly application tothe fungicide pesticide aspect, and belongs to the technical field of pesticide. In order to solve the technical problems, the invention provides a novel phenylimidazole derivative, a synthesis methodof the novel phenylimidazole derivative and application of the novel phenylimidazole derivative to the pesticide. The structure of the compound is shown as a formula I. The compound structure is simple and novel; the synthesis is easy; meanwhile, the fungicidal activity is realized; a better bacteriostasis or sterilization effect is achieved on important plant pathogenic fungi such as tomato early blight, tomato botrytis cinereal, cucumber fusarium oxysporum, magnaporthe grisea and rice rhizoctonia solani.