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34 results about "Xenorhabdus sp." patented technology

Serine protease inhibitor pp-pi polypeptide from chrysalis chrysalis chrysalis venom and its application

The invention discloses a Pteromalus puparum venom serine protease inhibitor Pp-PI polypeptide which has an amino acid sequence shown in SEQ ID NO: 2. At the same time, the invention also discloses a gene for encoding the Pteromalus puparum venom serine protease inhibitor Pp-PI polypeptide. The gene has a nucleotide sequence from the 126th nucleotide to the 290th nucleotide in SEQ ID NO: 1; or the gene has at least 70% homology with the nucleotide sequence from the 126th nucleotide to the 290th nucleotide in SEQ ID NO: 1; or the gene has a nucleotide sequence which can hybridize with the nucleotide sequence from the 126th nucleotide to the 290th nucleotide in SEQ ID NO: 1 at 40-55 DEG C. The Pteromalus puparum venom serine protease inhibitor Pp-PI polypeptide can be used to prepare a Pteromalus puparum venom serine protease inhibitor for genetically modifying crops or altering plant symbiotic bacteria.
Owner:ZHEJIANG UNIV

Symbiotic bacterium system for increasing biomasses of scenedesmus obliquus and improving quality of grease and application of symbiotic bacterium system

The invention relates to the field of micro-alga biotechnologies, in particular to a symbiotic bacterium system for increasing biomasses of scenedesmus obliquus and improving the quality of grease and the stability of culture systems and application of the symbiotic bacterium system. The symbiotic bacterium system comprises the scenedesmus obliquus and symbiotic bacteria. The symbiotic bacteria include one type or a plurality of types of brevunmdimonas sp., rhizobium sp., pseudomonas sp. and acidovorax sp. The symbiotic bacterium system and the application have the advantages that the symbiotic bacteria and mixed floras of the symbiotic bacteria are applied to scenedesmus obliquus culture procedures, extracellular substances and oxygen which are generated by the scenedesmus obliquus can be consumed by each single type of symbiotic bacteria and the mixed floras, carbon dioxides can be generated to be utilized by the scenedesmus obliquus, micro-environments favorable for growth of the scenedesmus obliquus can be created, and accordingly substance exchange and metabolism of the scenedesmus obliquus, the symbiotic bacteria and the mixed floras can be promoted.
Owner:INST OF PROCESS ENG CHINESE ACAD OF SCI

Gastrodia elata superoxide dismutase gene and application thereof

ActiveCN113528551AReduce incubation timeImprove resistance to low temperature stressFungiMicroorganism based processesDismutaseNucleotide
The invention discloses a gastrodia elata superoxide dismutase (SOD) gene. The nucleotide sequence of the gastrodia elata superoxide dismutase (SOD) gene is shown as SEQ ID NO: 1; 239 amino acid residues are encoded; a prokaryotic expression vector of the gastrodia elata SOD gene is constructed, prokaryotic expression analysis shows that the gastrodia elata SOD gene is soluble protein, and the molecular weight of the gastrodia elata SOD gene is about 47.4 kDa; an eukaryotic overexpression vector of the gastrodia elata SOD gene is constructed, gastrodia elata symbiotic bacteria armillaria mellea is transfected through an agrobacterium method to obtain gastrodia elata SOD transfected armillaria mellea, the SOD transfected gene engineering armillaria mellea is cultured at 13 DEG C, the growth vigor is better than that of wild armillaria mellea, and the growth speed is high; therefore, the gastrodia elata superoxide dismutase gene is beneficial to shortening the culture time of the armillaria mellea and improving the cold-resistant growth of the armillaria mellea, and an experimental basis for enhancing the cold resistance of the gastrodia elata, expanding the planting distribution range of the gastrodia elata and improving the yield of the gastrodia elata is provided. meanwhile, experiments also prove that the gastrodia elata superoxide dismutase gene can promote the growth of arabidopsis thaliana.
Owner:KUNMING UNIV OF SCI & TECH +1

Isolated culture method for nilaparvata lugens in-vivo yeast-like symbiotic bacteria and special culture medium

The invention discloses an isolated culture method for nilaparvata lugens in-vivo yeast-like symbiotic bacteria and a special culture medium, and belongs to the technical field of microculture. The special culture medium comprises 31 nutrient substances needed by nilaparvata lugens in-vivo yeast-like symbiotic bacteria, and the culture method comprises the following steps of: feeding adult nilaparvata lugen; treating ovaries of nilaparvata lugens; preparing culture solution, performing isolated culture and the like. By employing the culture method, two yeast-like strains are isolated from the nilaparvata lugens in vivo so as to provide basis for further researching genetic background of the yeast-like symbiotic bacteria and the interavailable nutrient relation between the yeast-like symbiotic bacteria and host nilaparvata lugens, and modifying the symbiotic bacteria to control the harm of the nilaparvata lugens. Meanwhile, the special culture medium is reasonable in components and provides necessary nutrition basis for isolated subculture of the nilaparvata lugens in-vivo yeast-like symbiotic bacteria. The method also provides technical support for isolated culture of other homoptera insect in-vivo yeast-like symbiotic bacteria.
Owner:ZHEJIANG ACADEMY OF AGRICULTURE SCIENCES

Large-scale entomopathogenic nematode production method and entomopathogenic nematode

The invention belongs to the production field of entomopathogenic nematodes and relates to a large-scale entomopathogenic nematode production method and entomopathogenic nematodes. The production method comprises the steps that the entomopathogenic nematodes in an infection period are inoculated onto greater wax moths for infection, and the entomopathogenic nematodes are collected to prepare an entomopathogenic nematode suspension after the greater wax moths die; separated entomopathogenic nematodes are utilized to infect greater wax moths, then the entomopathogenic nematodes are separated from died greater wax moth bodies for single bacterium culture, and the entomopathogenic nematodes cultured based single bacteria are separated for production and propagation; the entomopathogenic nematodes in the infection period are utilized to infect living greater wax moth bodies, then died greater wax moth hemolymphs are collected, and a symbiotic bacterium solution for production is obtained through culture, authentication, adaption, fermentation and symbiotic bacterium propagation; the obtained symbiotic bacterium solution is firstly inoculated to breeding bags of a shared culture medium,and then the obtained entomopathogenic nematodes are inoculated into the breeding bags of the shared culture medium for culture. The large-scale entomopathogenic nematode production method is convenient to operate, capable of making product quality good and higher in yield and efficiency and makes factory-like large-scale breeding easy to achieve.
Owner:吉林省怡科农业生物科技有限公司 +1

Gastrodia elata glutamine synthetase gene and application thereof

ActiveCN113564184AReduce incubation timeImprove resistance to low temperature stressFungiMicroorganism based processesNucleotideXenorhabdus sp.
The invention discloses a gastrodia elata Glutamine Synthetase (GS) gene. The nucleotide sequence of the gene is shown as SEQ ID NO: 1; and 342 amino acid residues are encoded; a prokaryotic expression vector of the gastrodia elata GS gene is constructed, and prokaryotic expression analysis shows that the gastrodia elata glutamine synthetase gene is soluble protein, and the molecular weight of the gene is about 59.94kDa. The eukaryotic overexpression vector of the gastrodia elata glutamine synthetase gene is constructed, gastrodia elata symbiotic bacteria armillaria mellea is transfected through an agrobacterium method, the armillaria mellea transfected with the gastrodia elata glutamine synthetase gene is obtained, the GS genetically engineered armillaria mellea is cultured at 13 DEG C and 28 DEG C, the growth vigor of the GS genetically engineered armillaria mellea is better than that of wild type armillaria mellea, and the growth speed is high. Therefore, the gastrodia elata glutamine synthetase gene is beneficial for shortening the culture time of the armillaria mellea and improving the cold resistance and high-temperature growth resistance of the armillaria mellea. The gastrodia elata glutamine synthetase gene provides an experimental basis for enhancing the cold resistance of gastrodia elata, expanding the planting distribution range of gastrodia elata, enhancing the nitrogen metabolism capacity of gastrodia elata and increasing the yield of gastrodia elata.
Owner:KUNMING UNIV OF SCI & TECH +1

Construction method and application of phenanthrene and pyrene combined aerobic degradation symbiotic flora

The invention relates to a construction method and application of a phenanthrene and pyrene combined aerobic degradation symbiotic flora, and the phenanthrene and pyrene combined aerobic degradation symbiotic flora uses four strains, namely Pseudomonas.sp,GenBank:GCA_000006765.1, Bacillus.sp,GenBank:AY881640.1, Sphingomonas.sp,GenBank:AB000106.1 and achromobacter.sp,GenBank:GCA_004296055.1. The construction method comprises an amplification culture method of each strain, an enhanced medium formula, culture conditions and operation methods, wherein the phenanthrene and pyrene combined aerobic degradation symbiotic flora is applied to biological extracellular polymers in a reactor device, the reactor device comprises a pipeline and a microbial inoculum ball group, and the biological extracellular polymers prepared from four strains are loaded in the microbial inoculum ball group. The method has the advantages that biodegradation of phenanthrene and pyrene in the chemical wastewater is achieved in an aerobic environment, secondary pollution is avoided in the treatment process, resources can be saved, the ecological environment can be protected, and finally, the purpose of treating degradation-resistant organic matter namely the phenanthrene and the pyrene is achieved.
Owner:JILIN INST OF CHEM TECH

Symbiotic bacterium composition, preparation method thereof and microalgae culture method

PendingCN113278557AMitigate the risk of pests and diseasesHarm reductionFungiBacteriaBiotechnologyRhodotorula
The invention relates to the technical field of microalgae culture, in particular to a symbiotic bacterium composition, a preparation method thereof and a microalgae culture method. The symbiotic bacterium composition consists of marine clostridium butyricum, marine rhodotorula benthica and marine purple non-sulfur bacteria. Through the symbiotic effect of the three probiotics including the marine clostridium butyricum, the marine rhodotorula benthica and the marine purple non-sulfur bacteria, the risk of diseases and pests in the seawater chlorella culture process is effectively inhibited, the harm of the diseases and pests is reduced, and the capacity and yield of chlorella factory culture are effectively improved.
Owner:HAINAN GREEN ALGAE WORLD BIOTECHNOLOGY CO LTD

Parasitic small-stem nematode preparation as well as preparation method and application thereof

The invention discloses a parasitic small-stem nematode preparation as well as a preparation method and application thereof, belongs to the technical field of biopesticides, and solves the problems oflow biocontrol quick-acting property and incapability of efficiently and quickly killing grassland spodoptera litura in the prior art. The parasitic small-stem nematode preparation comprises parasitic small-stem nematodes and RNA fragments interfering with polyphenol oxidase PO gene expression of the grassland spodoptera litura, the preparation also comprises an insect pest attractant matrix, a nematode humectant and nematode symbiotic bacteria nutrients. The invention creatively starts from the aspects of inducing, infecting, saprophytic, adding dsRNA to inhibit the immune response of pestsand the like, and the killing effect of the nematodes on the grassland spodoptera litura is effectively improved under the combined actions.
Owner:INST OF PLANT PROTECTION SICHUAN ACAD OF AGRI SCI

Biological seed coating agent based on trichoderma-bacillus sequential inoculation symbiotic culture fermentation liquor and preparation method thereof

PendingCN113444649AOvercome antagonismOvercoming is a competitive effectBiocideFungiBiotechnologyTrichoderma sp.
The invention discloses a biological seed coating agent based on trichoderma-bacillus sequential inoculation symbiotic culture fermentation liquor and a preparation method of the biological seed coating agent. According to a synthetic biology principle, a symbiotic bacterium solution is prepared from trichoderma having the characteristics of inducing disease resistance, stress resistance and the like, bacillus having the characteristics of antagonizing pathogenic bacteria, promoting crop growth and the like through a staged inoculation co-fermentation technology; and meanwhile, the symbiotic bacterium solution not only meets the balance of the contents of two types of spores, but also contains components for mutual action and specific induction of two types of microorganisms. The symbiotic bacterium liquid is mixed with diatomite and brassinolide in proportion to prepare the powder type biological seed coating agent, the biological seed coating agent contains high-content spores, antagonistic substances, growth promoting substances and the like, the growth, disease resistance and stress resistance of crops such as corn, wheat, rice and the like are obviously improved, and the technology is a new technology for beneficial bacteria treatment of food crop seeds.
Owner:SHANGHAI JIAO TONG UNIV

A kind of Phalaenopsis single bud propagation method using symbiotic bacterial agent

The invention provides a single bud propagation method of Phalaenopsis phalaenopsis, comprising the following steps: S1, taking a pedicel stem section that grows robustly in spring and full with axillary buds as explants and carries out disinfection treatment; S2, cutting the explants with axillary buds into pieces Grow 1.5cm and receive it into the bud induction medium for axillary bud induction; S3, when the axillary bud grows to 2cm in step S2, cut the sprouts and transfer them to the proliferation medium for proliferation culture; S4, when the proliferation culture sprouts > 2cm , when it grows to 3-4 leaves, remove weak seedlings and ineffective seedlings less than 2 cm, select seedlings > 2 cm to carry out rooting culture of strong seedlings; S5, move the culture bottle seedlings to 25-30 ℃ temperature conditions to strengthen seedlings for 10- After 15 days, the rooted seedlings can be taken out of the culture bottle, the residual medium attached to the roots is washed with running tap water and dried until no water drips, and then transplanted into the pre-prepared mixed matrix and pressed. If it is planted, it should be watered for the first time after planting, and then every 4-6 days after that. The method has the advantages of short reproductive cycle, strong seedlings, strong adaptability and good quality.
Owner:FUJIAN AGRI & FORESTRY UNIV

Extraction and purification method of anoectochilus roxburghii symbiotic bacteria

The invention discloses an extraction and purification method of anoectochilus roxburghii symbiotic bacteria. The extraction and purification method comprises the following steps: S1, removing mixed bacteria of anoectochilus roxburghii; S2, separating mother strains of the symbiotic bacteria; S3, purifying and culturing the symbiotic bacteria; and S4, expanding culture of the symbiotic bacteria. The method is used for producing the symbiotic bacteria in the anoectochilus roxburghii tissue culture and planting industry, the growth period of the anoectochilus roxburghii can be obviously shortened by adding the symbiotic bacteria into an anoectochilus roxburghii tissue culture sterile culture medium or an anoectochilus roxburghii planting culture medium, leaves of plants are more stretched, golden lines of the leaves are more obvious, stem nodes are shortened, and single plant quality is improved by 20% in average; in addition, the pollution rate of the culture medium added with the symbiotic bacteria is reduced by 30%, and the requirement of the anoectochilus roxburghii tissue culture industry for symbiotic bacteria additive products can be met; meanwhile, the preparation process issimple, operation is easy, the symbiotic bacteria can be added for co-culture in tissue culture seedlings of anoectochilus roxburghii produced in factories, the quality and yield of anoectochilus roxburghii seedlings are improved, and the survival rate and environmental adaptability of later underground cultivation of the anoectochilus roxburghii are facilitated.
Owner:厦门乐莲乐生物科技有限公司

Method for direct seeding and seedling raising of pleione bulbocodioides by using symbiotic bacteria

The invention provides a method for direct sowing and seedling raising of pleione bulbocodioides by utilizing symbiotic bacteria, which comprises the following steps: mixing piriformospora indica into a culture medium, sowing pleione bulbocodioides seeds, and performing symbiotic culture to obtain symbiotic pleione bulbocodioides seedlings. The method is simple and convenient to operate, the symbiotic bacteria and pleione bulbocodioides seeds are directly sown for seedling raising for the first time, after 10-15 days, most of the seeds appear green, after 30 days, a large number of protocorms appear native meristem, after 45 days, the protocorms grow first leaves, after 2 months, seedlings form 2-3 leaves and grow roots, and the seedlings can be transplanted to a nursery garden.
Owner:KUNMING INST OF BOTANY - CHINESE ACAD OF SCI +1

Portable biological crust seed source and preparation method thereof

The invention discloses a portable biological crust seed source and a preparation method of the portable biological crust seed source, and the portable biological crust seed source comprises a biological crust seed source small ball prepared from a stone coat symbiotic bacterium (Endocarpon bacillus) F07020, a stone coat symbiotic alga (Diplosphaera chodatii) A07020 and a forming culture medium. The method is favorable for forming a seed source of the lichens which are collected in a state closer to a natural state, can be applied to desertification land control engineering on a large scale, and is favorable for promoting the formation of artificial biological crust.
Owner:INST OF MICROBIOLOGY - CHINESE ACAD OF SCI

Method for extracting symbiotic microorganisms in coleopteran insects

The invention relates to a method for extracting symbiotic microorganisms in coleopteran insects, which comprises the following steps of: selecting a plurality of sexually mature female coleopteran insects, enabling the bellies of the female coleopteran insects to face upwards, and extruding the middle and rear sections of the bellies to extend out of symbiotic bacterium sacs (one ellipse has a small cyst type structure, and the interiors of the symbiotic bacterium sacs are mostly yellow or white tissues); the method comprises the following steps: completely picking off the tissue with tweezers under a microscope, immersing the tissue into a vessel containing a PBS (Phosphate Buffer Solution) with a certain concentration, grinding the tissue with a grinding rod to fully dissolve the content in the solution, carrying out concentration dilution, transferring the tissue into a culture dish containing YNB, placing the culture dish in a constant temperature box with a proper temperature (25 DEG C), culturing for 2-3 days, and if white dot-shaped or strip-shaped tissue appears, taking out the tissue. And comparing with the known symbiotic bacteria gene sequence, and if the symbiotic bacteria belong to the same clade, indicating that the symbiotic microorganisms in the coleopteran insects are successfully extracted.
Owner:SOUTH CHINA AGRI UNIV

Bletilla striata direct seeding and seedling raising method using symbiotic bacteria

PendingCN113207590AImprove the germination rate of natural live broadcastFast growthMicroorganismsGrowth substratesBiotechnologyBletilla striata
The invention discloses a bletilla striata direct seeding and seedling raising method using symbiotic bacteria. The method specifically comprises the following steps: S1, acquiring of the symbiotic bacteria of bletilla striata: culturing a bletilla striata explant to obtain a strain of the symbiotic bacteria of bletilla striata for later use; S2, direct sowing and seedling raising of bletilla striata: mixing pretreated bletilla striata seeds and the symbiotic bacteria of bletilla striata in the step S1, and then sowing the seeds in a seedbed; S3, sowing later-period management: after the sown seeds germinate and emerge, carrying out fertilization and seedling hardening treatment, and then transplanting. The symbiotic bacteria of bletilla striata and bletilla striata seeds are uniformly mixed, direct seeding is performed, then seedling hardening treatment is performed, due to the fact that the symbiotic bacteria of bletilla striata are added in the germination process of the bletilla striata seeds, the direct seeding germination rate of the bletilla striata seeds is as high as 86%, a Huabao leaf fertilizer is sprayed in the later-period management process, and the seedling growth speed is high. Compared with a tissue culture seedling raising method, the method has the advantages that the production cost and labor consumption are greatly reduced, the cultured bletilla striata seedlings are vigorous and uniform in growth vigor, and the transplanting survival rate reaches up to 99%.
Owner:INST OF DAFENG MARINE IND NANJING UNIV OF TECH
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