38 results about "Lesser florican" patented technology

The invention discloses a strain bacillus methylotrophicus 4-L-16 for prevention and control of banana vascular wilt. The strain has a preservation name of bacillus methylotrophicus 4-L-16, and is classified and named as Bacillus methylotrophicus 4-L-16. The preservation organization is China Center for Type Culture Collection, the preservation date is June 26, 2012, and the preservation number is CCTCC NO:M2012248. The strain has a strong antagonistic effect on No.1 and No.4 physiological races of banana vascular wilt, and other banana common disease categories. The invention also discloses application of the strain in preparation of drugs with a banana vascular wilt prevention and control function, as well as a microbiological preparation containing the strain. The microbiological preparation not only has a better antagonistic effect on a variety of banana pathogenic bacteria, but also has a facilitating effect on plant growth.

The invention relates to a method for identifying tobacco black shank resistance in disease nursery. A continuous cropping tobacco field in a historical high occurrence area of the tobacco black shank disease is selected as a disease nursery; plants are inducted to develop the disease through the improvement of the field humidity, so that the complex operation of strain separated storage and culture is reduced; the strain is sourced from the field; the quantity and variety of the microspecies for inoculation are theoretically unlimited; and the method has better diversity and representativeness, and the inoculation conditions are under the control of nature, so the identification results reflect the local practical situation of the day more correctly. A one-off uprooting investigation method after the collection of the flue-cured tobacco is adopted so as to greatly reduce the workload, save the cost and bring about a correct and reliable result. The method is characterized by low cost and simple and feasible operation. The method is an economical and practical method and has bright market and application prospect.

A breeding method of saffron seed ball comprises the following steps: selection and disinfection of explants, induction of test tube ball, proliferation of test tube ball, and rooting and transplanting of test tube ball. Small saffron seed balls are taken as the explants. The pollution rate is reduced. The induction rate of test tube ball is increased. The callus phase is not needed, and multiple shoots can be induced out. Multiple shoots can be directly induced to obtain test tube seed balls. The induction time is shortened. The test tube seed balls can be applied to multiplication culture. After proliferation, the test tube balls are subjected to rooting. The saffron test tube ball is converted into saffron seed balls in one step, the time of tissue culture is saved, the operation steps are reduced, the excellent properties of original balls are preserved, and the breeding method can be applied to industrial efficient breeding of saffron. The breeding method provides technical support for the development of saffron industry.

The invention discloses SSR markers linked with resistance genes Bs_t of physiological races No. 0 and No. 1 of tobacco black shank and applications thereof. The SSR markers linked with resistance genes Bs_t of physiological races No. 0 and No. 1 of tobacco black shank are numbered as TM51207 and TM55805, and nucleotide sequences of amplified products of the SSR markers are shown as SEQ ID No. 1,SEQ ID No. 2, SEQ ID No. 3 and SEQ ID No. 4 respectively. The applications refer to applications of the SSR markers linked with resistance genes Bs_t of physiological races No. 0 and No. 1 of tobaccoblack shank in detecting whether resistance genes Bs_t of physiological races No. 0 and No. 1 of tobacco black shank exist in tobacco genomic DNA. The SSR markers disclosed by the invention have the characteristics of being stable, reliable, simple and convenient, rapid and low in cost, and therefore, the molecular markers can be applied as a molecular marker-assisted selection of Bs_t genes in breeding for disease resistance of tobacco black shank (physiological races No. 0 and No. 1).

The invention relates to the biological technical field and discloses a detection primer of plant pathogenic fungi and a detection method thereof. The invention adopts a special primer RF4 and optimizes action conditions to invent a PCR detection method for banana fusarium wilt physiological races (Race No. 4). The method can especially, sensitively and effectively detect banana fusarium wilt physiological races (Race No. 4) and mycelium even weighting 0.1 Mug can be detected and pathogen can even be detected from the root and the stem of bananas by adopting the method.

A method for dividing the bacterial blight strain of rice into microspecies by using the 6 subisopolar gene lines of known disease-resistant genes is disclosed. In the booting stage of rice, the bacterial suspension is inoculated to the leaf on the master stem of rice. The longth of disease spot and the length of whole leaf are respectively measured in 2 weeks and 3 weeks. If the length of disease spot is less than 0.25 times that of whole leaf, it is a disease-resistant plant (R). Otherwise, it is a disease-infectious plant(s). 6 varieties of rice are experimented in the interaction mode of 9 micropecies (R1-R9) to obtain the relative microspecies of bacterial blight strain.

The invention discloses a new wheat stripe rust resisting polygene-polymerized flower-nurture breeding method. Wheat-breeding parent materials with excellent agronomic characters are selected; 3 major micro-species of puccinia striiformis, which are recently popular, are used to evaluate stripe rust resistance of the wheat-breeding parent materials at seedling stage and adult stage; 3 wheat-breeding parent materials, which have high-resistance immunity to major popular individual micro-species of various puccinia striiformis, are sieved; the 3 wheat-breeding parent materials are hybridized and duplex hybridized to obtain duplex hybridized polygene-polymerized subsequent generation; the duplex hybridized subsequent generation is then cultured and wheat anther tissue is inoculated to one-step seeding culture medium of wheat anther, thereby obtaining complete pollen plant; chromosome doubling liquid with colchicines and dimethyl sulfoxide is injected to tillering node, thereby carrying out pollen plant chromosome doubling to obtain doubly purified individuals of doubled haploid which can be self-hybridized to form a stable doubled haploid system; and stripe rust resisting individual micro-species validation is carried out on the doubled haploid system, so as to obtain a new stripe rust resisting type or species system which is polymerized with 3 stripe rust resisting genes.

The invention relates to the technical field of soilless cultivation, and in particular to a cultivation method for breeding small seed potatoes of virus-free potatoes though areoponics. According tothe physiological basis of potato cultivation through aeroponic cultivation, the growth can be divided into six stages, and six formulas of suitable nutrient solutions are prepared according to the six growth stages; according to the method and technology involved in the invention, the requirements for external environment conditions of light, temperature, water, fertilizer and air at each growthstage of the potatoes obtained through the aeroponic cultivation are met, three latent traits of the potatoes of stem diversity, bud multiplicity and stem and leaf regeneration are sequentially induced into phenotypic fine traits, stolon promotion, tuber formation, potato pieces swelling and picking are continuous and ceaseless for 100 days or above for growth, 60 to 80 grains of qualified small seed potatoes with a yield of 10 g or above for a single plant are obtained, and the yield per mu of the aeroponic cultivation in a greenhouse is 450000 to 550000 grains; the production cost, storage resistance and preservation property of the potatoes obtained through the aeroponic cultivation are similar to or slightly lower than that of substrate potatoes, and the survival rate of seedlings andthe growth potential at a seedling stage are better than that of the substrate potatoes; the technological achievements of the invention achieve the purposes of the practical promotion and applicationof large-scale production.

The invention discloses a method for identifying phytophthora parasitica var nicotianae physiological strains, and belongs to the technical field of plant pathogen identification. According to the method, a tissue culture vessel method is used for identifying the phytophthora parasitica var nicotianae physiological strains; the environment conditions of culture and impregnation are more stable; the growth of tobacco pathogens is favorably accelerated; the seedling culture period and the dip dyeing period are greatly shortened; meanwhile, the interference of infectious microbes and other physiological strains on the identification result can also be avoided; the flux is high; labor and materials can be saved to the greatest degree; the high-flux, fast and accurate identification on the phytophthora parasitica var nicotianae physiological strains is realized. Compared with a land method and a greenhouse method, the method has the advantages that the identification is fast; the result is more accurate, stable and reliable; higher application values are realized; meanwhile, a thought can also be provided for the identification of physiological strains of other disease pathogenic bacteria of tobaccos.

The invention belongs to the technical field of crocus sativus cultivation and provides a crocus sativus production and processing method. The method is characterized by including steps: S1, selectinghealthy and plump crocus sativus bulbs lighter than 1g in weight, subjecting to cold treatment at 4-10 DEG C for 4-6 weeks, removing integuments, flushing with water for 1-5h, sterilizing, flushing for 3-5 times, and absorbing moisture to dry for standby application; S2, transplanting the crocus sativus bulbs outdoors in November in the last year, burying the bulbs underground by 8-10cm until thebulbs appear in May in the next year, digging out the crocus sativus bulbs, and placing in a shade place for 10 days; S3, from the early June to the late June, sequentially arranging the crocus sativus bulbs on a double-layer net rack according to two grades by a sorting device. The crocus sativus production and processing method has the advantage of high crocus sativus yield.

The invention provides a rapid breeding method of the seed of konjac, namely a method for sexual reproduction through apomixis, thus the seed of konjac is a small bulb. The reproduction rate of konjacseed bulbs is not more than 5-7 times in the way of digging big and staying small and large bulb-cutting propagation. According to the rapid breeding method of the seed of konjac, a seed bulb can breed 800-1500 seed bulbs, and the reproduction ratio is close to 1500 times, so that the problem of low breeding coefficient and degradation of seed source in konjac industry is solved. The rapid breeding method of the seed of konjac has the advantages of high breeding efficiency, keeping seed character, preventing and controlling seed source degeneration, fast breeding of konjac bulbs for farmers to grow, thereby producing more konjac bulbs to meet the market needs.

The invention relates to a Yunnan Oryza meyeriana Baill MeXB3 gene and application thereof to resistance to rice bacterial leaf blight and belongs to the technical field of molecular biology. A cDNA sequence of the Yunnan Oryza meyeriana Baill MeXB3 gene is a DNA sequence shown as SEQ ID NO.1, and the Yunnan Oryza meyeriana Baill MeXB3 gene is cloned and identified in Yunnan Oryza meyeriana Baill. An encoded Yunnan Oryza meyeriana Baill MeXB3 gene comprises an amino acid sequence shown as EQ ID NO.2. The Yunnan Oryza meyeriana Baill MeXB3 gene and application thereof have the advantages that the Yunnan Oryza meyeriana Baill MeXB3 gene is cloned and identified, and an MeXB3 transgene plant; the Yunnan Oryza meyeriana Baill MeXB3 gene belongs to inducible expression in the Oryza meyeriana Baill; after identification of obtained transgenic materials, it is discovered that the Yunnan Oryza meyeriana Baill MeXB3 gene is capable of improving resistance of rice to part of Xanthomonas oryzae pv.oryzae microspecies, so that resistance to rice bacterial leaf blight is enhanced, gene resources are provided for breeding for disease resistance, and the Yunnan Oryza meyeriana Baill MeXB3 gene is of great theoretical and practical significance to breeding of rice resistant to bacterial leaf blight.

The invention discloses an inoculation method of Ustilago scitaminea. The method includes the steps of inoculating Ustilago scitaminea spore suspension to the surface of sugarcane buds by spot inoculation and keeping in the wet place for 16-24h. The pore suspension is 106/ml in concentration. During moisture preservation, the inoculated sugarcane buds are wrapped with humid tissue and are then placed at a shade place after being covered with plastic paper. The inoculation method is convenient to use, incidence rate of susceptible varieties is increased effectively, up to more than 80%, sense resistance of the different sugarcane varieties to Ustilago scitaminea can be distinguished effectively, and accordingly good conditions are created for the intensive study on breeding for disease resistance to Ustilago scitaminea and the study on physiological race differentiation.

The invention provides actinomycetes which is streptomyces manipurensis S-1 and is assigned the accession number CCTCC No: M2017261. The streptomyces manipurensis S-1 is 5.0-10.0 in growth pH range, preferably 7.0, and has optimum growth temperature of 28-32 DEG C and cannot grow on a culture medium being more than 3% in content of NaCl. The streptomyces manipurensis S-1 has an antagonism effect against Fusarium oxysporum f. sp. cubense (FOC) race 1 and 4, and especially has significant antagonism effect against Fusarium oxysporum f. sp. cubense (FOC) race 4. The streptomyces manipurensis S-1has extensive development space and has great development and application prospects.

The invention provides a method for separation and identification of kenaf root knot nematode and belongs to the technical field of microorganisms. The technical scheme is that (1) classical morphological identification; (2) isozyme analysis and identification; (3) molecular biological identification: the PCR identification is performed through primers 5-GGTCAATGTTCAGAAATTTGTGG-3 and 5-TACCTTTGACCAATCACGCT-3, COll genes and lrRNA genes thereof located in mitochondrion DNAs are amplified, and sequences are subjected to comparative analysis and identification. The physiological race of the root knot nematode is made clear. The method integrates separation, purification and identification, a method of combining morphology, isozyme and molecular biology is adopted for identification and verification, the result shows that the molecular biological identification is high in efficiency and accuracy and suitable for field sampling fast separation, and the biological characteristics of insect body wild type population or the physiological race are identified.

The invention provides a method for identifying soybean aphid physiological races. The method for combining identification of the number of bred aphids with a differential host under a greenhouse condition and representation of plant diseases is adopted, the soybean aphid physiological races from different sources can be identified fast, targeted soybean aphid race resisting resource screening, new variety breeding and other studies are carried out, bases are provided for determining the target of comprehensive preventing and treating of the soybean aphids and aphid resisting breeding, and the identification method is fast and high in operability, and has good application prospects.

The invention relates to a method for breeding an intermediate material with rice blast resistance. The method belongs to the technical field of rice genetic breeding design, and is characterized by including the following steps: (1) screening a plurality of different physiological races of rice blast in the same region; and (2) preforming gradient selection of rice blast resistance on the same material in different regions. Under the selection pressure of multiple physiological races of Magnaporthe grisea, the breeding intermediate material can obtain broad-spectrum high-resistance breeding material. The tested materials are planted in different regions, and local meteorological data are observed and recorded to screen out rice breeding material that can adapt to different disease pressures. Rice blast resistance screening is carried out by utilizing physiological races of rice blast in different regions and disease pressures in different regions, the efficiency of breeding intermediate material with rice blast resistance by breeders is improved, and the method has the advantages of rapidness, simplicity and economy.

The invention discloses a method for microbe gene clone. The method comprises the steps of constructing segregation populations by hybridizing parents having target character differences; automatically screening the segregation populations by setting a selection pressure to obtain screened populations; high-throughput genome sequencing of the two parents, populations before screening and populations after screening; obtaining specific loci of the parents by preliminary direct assembly and comparison; comparing the specific loci of the parents with the genomes of the populations before screening and the populations after screening in a completely matching mode; looking for loci which exists in the parents and the populations before screening but disappears in the populations after screening, wherein the loci are candidate gene loci for controlling target characters; obtain full-length sequence of the genes by comparing with the genomes of the parents; cloning target genes via PCR amplification; and verifying functions of the cloned target genes via genetic complementary experiments. The method directly clones genes themselves, and reduces a lot of microspecies isolation and identification work of the microbes. The method has little workload, fast speed and low risk.

The present invention aims at provides one kind of physiological microspecies monogenically identifying system for rice blast germ with high identification capacity and wide applicable range and its culture method. The system is one monogenic near isogenic line cross bred with LTH as one local japonica rice variety without major disease resistant gene as recurrent parent and through cross breeding and backcross to introduce known disease resistant gene into LTH. The system constituting process includes cross breeding and backcross with LTH as recurrent parent to introduce known disease resistant gene into LTH and to obtain the near isogenic line; identifying and confirming the monogenic characteristic of the near isogenic line; and deciding the physiological microspecies discriminability of the near isogenic line and constituting new discrimination system. The monogenic near isogenic line is suitable for various rice producing areas in the world.