Patents
Literature
Patsnap Copilot is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Patsnap Copilot

37 results about "Ustilaginoidea" patented technology

Ustilaginoidea is a genus of anamorphic fungi whose teleomorphic states are in the Hypocreales order. The genus is widespread in subtropical regions, and contains six species. Ustilaginoidea was circumscribed by German botanist Julius Oscar Brefeld in 1895. Ustilaginoidea virens causes the disesase known alternatively as rice false smut, pseudosmut, or green smut.

Special rice fertilizer containing efficient silicon and preparation method of special rice fertilizer

InactiveCN104230533ARelieves symptoms of silicon deficiencyPromote growthFertilizer mixturesPhosphoric acidInsect pest
The invention discloses a special rice fertilizer containing efficient silicon and a preparation method of the special rice fertilizer, and belongs to the technical field of fertilizers in agricultural production. The fertilizer is prepared from the following raw materials in parts by weight: 40-55 parts of urea, 20-35 parts of calcium superphosphate, 10-25 parts of potassium chloride, 10-20 parts of potassium silicate, 1-5 parts of attapulgite powder, 0.2-1.2 parts of artemisia argyi extract, 0.2-0.8 part of radix peucedani extract and 0.5-1.5 parts of mint extract. The fertilizer disclosed by the invention is reasonable in nutrient matching, satisfies nutrient requirements and absorption characteristics of rice growth, and capable of promoting rice growth, increasing the rice yield, improving the lodging resistance and the insect resistance of the rice and lowering the lodging and insect pest risks. Besides, the traditional Chinese medicine extract in the fertilizer can be used for inhibiting the growth of rice sheath blight disease, rice blast and ustilaginoidea virens and lowering the rice disease harm. The fertilizer is applied once along with soil preparation before rice seedling transplanting, so that the utilization rate of the fertilizer is increased, and the fertilizer-application labor cost and fertilizer cost of the rice farmers are lowered.
Owner:CHINA NAT RICE RES INST

Penicillium capable of resisting false smut of rice and application thereof

The invention discloses penicillium capable of resisting false smut of rice and an application thereof. The penicillium is prepared through the following steps of: A, ustilaginoidea virens isolation, wherein a ustilaginoidea virens ear is collected, and the ustilaginoidea virens is isolated by adopting a chlamydospore suspension method; B, antibacterial isolation and culture of the ustilaginoideavirens, wherein a soil sample is ground, placed in an aseptic petri dish, and poured into a PDA (potato dextrose agar) culture medium to culture and isolate a single colony of fungus, the isolated fungus strain is inoculated into a PSA (prostate-specific antigen) culture solution for shaking culture, and the fermentation broth is filtered and degermed to obtain an aseptic supernatant sample; and C, antagonist screening of the ustilaginoidea virens, wherein a conidiophore suspension of the ustilaginoidea virens is coated on a PSA panel, an aseptic Oxford plate is placed in the panel, and the aseptic supernatant sample is added into the aseptic Oxford plate to culture penicillium. The invention also provides an application of the antagonist penicillium AF-25 in preparing a biological pesticide for controlling or preventing the false smut of rice. The penicillium has an antagonistic effect on ustilaginoidea virens, and can inhibit spore germination and mycelial growth of the ustilaginoidea virens. The fermentation broth of the penicillium has strong inhibition activity to the false smut.
Owner:WUHAN INST OF VIROLOGY CHINESE ACADEMY OF SCI

Drying and sealed preservation method of rice ustilaginoidea virens

The invention discloses a drying and sealed preservation method of rice ustilaginoidea virens. The method technologically utilizes the property that the ustilaginoidea virens can survive in completely dried rice endosperm for a long period; rice is used as a carrier and the ustilaginoidea virens is artificially inoculated onto sterile rice grains and hyphae fully cover endosperm tissues of the rice grains; after the rice grains are completely dried under the condition of 28 DEG C, a drying preservation manner is adopted. The method comprises the following technical steps: 1) obtaining purified ustilaginoidea virens strains by utilizing a chlamydospore single-spore isolation method; 2) immersing the rice grains until the endosperm is fully filled with water; loading the endosperm into a test tube and sterilizing; 3) inoculating the endosperm onto the sterile rice grains and culturing to enable the hyphae fully cover the inner parts of the endosperm tissues; drying until the rice grains are completely dried, preserving the test tube into a dryer filled with allochroic silica gel and preserving for a long period; smearing vaseline for sealing. The drying and sealed preservation method has the advantages that the preservation time of the ustilaginoidea virens exceeds 5 years; the survival rate is high; the pollution rate of the strains is low; the operation is convenient and a small space is occupied; the cost is low and energy sources are not consumed; the pollution to environment and residues are not caused.
Owner:贵州省植物保护研究所

Recombinant vector, host cell and application of ustilaginoidea virens effector protein

The invention discloses a recombinant vector, a host cell and an application of an ustilaginoidea virens effector protein, and belongs to the technical field of biology. The recombinant vector is usedfor expressing an ustilaginoidea virens effect protein, and is obtained by inserting a coding gene of the ustilaginoidea virens effect protein to a position between EcoR I and Xho I restriction enzyme cutting sites of a pET-32a vector. The amino acid sequence of the ustilaginoidea virens effect protein is shown in the formula of SEQ ID NO: 1 in a sequence table and the nucleotide sequence of thecoding gene of the ustilaginoidea virens effect protein is shown in the formula of SEQ ID NO: 2 in the sequence table. According to the invention, the ustilaginoidea virens effect protein obtained byin vitro expression is sprayed on arabidopsis thaliana leaves so that the contents of active oxygen and callose in the arabidopsis thaliana can be obviously improved and the disease resistance of thearabidopsis thaliana to pathogenic bacteria Pseudomonas syringae pv.tomato (Pst) DC3000 can be improved. A novel way is provided for improving the plant resistance and inducing the plant defense reaction, and the recombinant vector has a wide application prospect in agricultural production.
Owner:SHENYANG AGRI UNIV

Preparation and cultivation method for ustilaginoidea virens thin-wall conidia capable of preventing pollution

The invention discloses a preparation and cultivation method for ustilaginoidea virens thin-wall conidia capable of preventing pollution. A conical flask can be used for effectively obstructing the characteristics of common microorganisms, a common conical flask is adopted to manufacture a utensil for culturing spores, and a potato cane sugar culture medium is taken as a spore production culture medium to prepare and cultivate the high-quality ustilaginoidea virens thin-wall conidia. The preparation and cultivation method comprises the following steps: 1) cleaning the common conical flask for standby use; 2) taking the potato cane sugar culture medium as the spore production culture medium to prepare a conical flask type culture medium; 3) transplanting matrix thalluses; 4) carrying out spore production culture under a temperature condition of 28DEG C; 5) carrying out elution by bacteria free water to collect new-generation thin-wall conidia. The preparation and cultivation method has the following advantages: 1) shake cultivation equipment is not required, and obtained conidia liquid finished product contains few mycelia, culture media, thallus metabolism excretion products and the like; 2) after the conical flask is provided with a conventional bottle stopper, common microorganisms can be prevented from entering, the conical flask can be favorably prevented from being polluted by infectious microbes, so that pollution can be effectively prevented, and a high-quality spore finished product can be obtained; 3) an operation for collecting the spores in the conical flask is more convenient than the operation for collecting the spores in a culture dish. According to the protection of the conical flask, spore production bacterial colonies can be put for a period of time at will without pollution, and a spore production state is kept so as to be convenient to connect with a working procedure which needs spores.
Owner:GUANGXI UNIV

Pollution-reduction preparation and culture method of ustilaginoidea virens thin-wall conidia

The invention discloses a pollution-reduction preparation and culture method of ustilaginoidea virens thin-wall conidia. The method is characterized by adopting a triangular flask as a preparation and culture utensil, adopting a potato culture-medium as a sporulation medium, and preparing and culturing the high-quality ustilaginoidea virens thin-wall conidia. The preparation and culture method comprises the following steps of (1) cleaning the triangular flask for standby use; (2) preparing the bottle type sporulation medium of the potato culture-medium; (3) transplanting maternal ustilaginoidea virens; (4) sporulation culturing at the proper temperature; (5) eluting and collecting a new generation of thin-wall conidia. The pollution-reduction preparation and culture method of the ustilaginoidea virens thin-wall conidia provided by the invention has the advantages that (1) a shaking culture device has no need to be use; a conidia liquid finished product contains less impurities; the preparation process is fast, high in efficiency, and large in conidia quantity; (2) the pollution can be efficiently reduced during the preparation and culture process; (3) with the protection of the triangular flask, a sporulation bacterial colony can be placed at will for a period of time without being polluted, a sporulation state is kept, and a working procedure requiring the conidia can be linked conveniently.
Owner:GUANGXI UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products