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36 results about "Capsaloides" patented technology

Method for synthesizing N-(3,4-dimethoxybenzyl)amide capsaicine homologous compounds

The invention relates to a method for synthesizing N-(3,4-dimethoxybenzyl)amide capsaicine homologous compounds the general structural formula of which are shown in formula (1), wherein R is alkyl group, naphthenic base or aromatic base the carbon atomic number of which is between 1 and 20. Compared with the existing synthetic method that reagent dimethyl sulfate with toxicity or iodomethane with toxicity and expensive price is used as a methylation regent in the process of synthesizing the compounds, the method of the invention has the maximal advantages that cheap and nontoxic dimethyl carbonate is used as the methylation regent, the reaction conditions are mild and the yield is high.
Owner:ZHEJIANG UNIV

PCR (Polymerase Chain Reaction) detection primer for phytophthora capsici leonian, kit containing primer and application thereof

The invention provides a PCR (Polymerase Chain Reaction) detection primer for phytophthora capsici leonian. The primer comprises Enl4s and Enl1a (as shown in Seq ID No.1 and 2). Four pairs of specific primers capable of quickly detecting phytophthora capsici leonian germs can be obtained based on the sequence difference between the Enl and Ypt genes of the phytophthora capsici leonian and other phytophthora nicotianaes: Enl2s / Enl3a, Enl4s / Enl1a, Ypt2s / Ypt3a and Ypt2s / Ypt5a, wherein the sensitivity of Enl4s / Enl1a is the highest. A PCR detection system is established on the basis, which is capable of quickly and accurately detecting the phytophthora capsici leonian from complex pathogenic bacteria environments in the tissues of plants having diseases and soil. A detection kit established according to the method is simple and convenient for operation, good in specificity and high in sensitivity; and the detection kit is capable of detecting the propagules in various forms of the phytophthora capsici leonian, such as hypha, oospore, zoospore and the like, thereby having great significance in the aspects of early warning on the epidemic situation of the phytophthora capsici leonian, pathogen supervision on the epidemic area and the like.
Owner:INST OF MICROBIOLOGY - CHINESE ACAD OF SCI

Primer for detecting pytophthora capsici developed on basis of plygalacturonase Pcipg8 gene and method therefor

InactiveCN102634585ABlock reproduction and spreadReduce disease control costsMicrobiological testing/measurementFluorescence/phosphorescencePentagalacturonic acidAgricultural science
The invention discloses a primer for detecting pytophthora capsici developed on the basis of plygalacturonase Pcipg8 gene and a method for detecting the pytophthora capsici. The primer for detecting the pytophthora capsici developed on the basis of the plygalacturonase Pcipg8 gene consists of single-strained DNA (deoxyribonucleic acid) shown by a sequence 1 in a sequence table and single-strained DNA shown by a sequence 2 in the sequence table. The primer can be used for carrying out qualitative and quantitative molecule detection on the phytophthora capsici leonian and different phytophthoracapsici leonian materials at different periods, and detecting and easily warning the primary infection source of the phytophthora capsici leonian and the dynamic status of the growth and decline of the germs at different periods in the process of infection, so that the optimum disease preventing and controlling period can be conveniently and timely confirmed, particularly the comprehensive prevention, control and treatment can be timely carried out in the early activity period of the germs, according to the existence and the quantity for detecting the oospore in the soil, the soil can be timely treated, the breeding and spreading of source germs can be cut off, and the disease preventing and controlling cost can be reduced.
Owner:SHANDONG AGRICULTURAL UNIVERSITY

Method for extracting capsaicin crystals from oleoresin capsicum

The invention discloses a method for extracting capsaicin crystals from oleoresin capsicum. The method comprises the following steps that chilli powder is extracted with an aqueous alkaline solution in a single-stage continuous countercurrent ultrasonic extraction machine, wherein the aqueous alkaline solution is prepared from sodium chloride, sodium acetate, sodium hydroxide and beta-cyclodextrin; filtrate obtained through filtering separation is processed through the steps of concentration, ethanol extraction, reduced pressure distillation, petroleum ether low-temperature recystalization and the like, and then the high-purity needle-shaped capsaicin crystals are obtained. According to the method, a continuous countercurrent and ultrasonic extraction technique, a micro-cutting interaction technique and the like are combined on the basis of a common solvent method, the extraction time is shortened, the solvent using amount is decreased, the recycle rate and the purity of the capsaicin crystals can be effectively increased, the whole operation process is easy and convenient, the requirements for the reaction condition and production equipment are low, and the method is a capsaicin crystal extraction technology which is suitable for industrialized popularization.
Owner:广西恒得润辣素有限公司

Method for rapid separation of phytophthora capsici and special culture medium thereof

The invention provides a method for rapid separation of phytophthora capsici and a special culture medium thereof, and belongs to the technical field of phytopathology research. The separation method comprises the steps of sick sample treatment, disinfection, culture medium preparation, and the like. The sick sample is selected from a freshly-picked sick stem, and a sick sample tissue of 9-11 cm is taken with a juncture of the sick part and the healthy part of the sick sample as a center; the tissue is cleaned with tap water, and is dried in the air to remove surface moisture; the dried tissue is uniformly sprayed with 75% alcohol, then soaked with a 1% sodium hypochlorite solution, and cleaned with sterile water; after drying in the air, the disinfected large block of the sick sample is cut into small blocks on an aseptic operating floor; and separation culture is performed with special culture medium. With the method of the invention, the separation rate of phytophthora capsici reaches 81.99% on average, which is increased by 32.6% when compared with the separation rate of a routine (small block disinfection treatment, small block separation) treatment method on average; the separation time is only 31.6 minutes on average; the separation time is shortened by 50.1% on average; and the operations are simple and practical.
Owner:INST OF AGRI ENVIRONMENT & RESOURCES YUNNAN ACAD OF AGRI SCI

A single spore isolation method of zoospores of Phytophthora capsici

The invention relates to a single spore isolation method of phytophthora capsici zoospores. The single spore isolation method comprises the steps that phytophthora capsici is inoculated to a V8 culture medium, sealing is performed with a sealing membrane, culture at the constant temperature of 25 DEG C is performed for 5 days, then the sealing membrane is removed, irradiation is performed for 24 hours, sterile water of 4 DEG C is added to perform induction and constant-temperature release respectively for 25 minutes so as to obtain a zoospore suspension, the suspension is diluted to reach the standard that 1-2 spores exist in each (10*) view, 1 mL of the suspension is taken and added to a V8 culture medium flat plate containing antibiotics in an evenly coated mode, constant-temperature standing is performed for 6 hours, a single germinated zoospore is found through an inverted microscope and is cut by using a scalpel to form a 0.5 cm square mark, it is confirmed that single spores are transferred to a flat antibiotic plate, and purified spores are single spore plants. The single spore isolation method is simple and convenient to operate, high in accuracy and good in rapid separating effect, adopts simple devices and can separate single spores of a large number of phytophthora capsici zoospores within a short time.
Owner:NORTHEAST AGRICULTURAL UNIVERSITY

Pectate lyase PCPEL16 from phytophthora capsici, and coding gene and application thereof

The invention discloses pectate lyase PCPEL16 from phytophthora capsici, and a coding gene and an application thereof. The pectate lyase PCPEL16 provided by the invention is protein of a) or b) or c), wherein a) protein consisting of amino acid sequences shown by 23-441 sites of a sequence 2 in a sequence table; b) protein consisting of amino acid sequences shown by the sequence 2 in the sequencetable; and c) protein which is obtained by carrying out substitution and / or deletion and / or addition of one or more amino acid residue on the amino acid sequences shown by the sequence 2 in the sequence table or the amino acid sequences shown by 23-441 sites of the sequence 2, has the activity of the pectate lyase and is derived from a). The pectate lyase PCPEL16 disclosed by the invention has higher enzymatic activity, and the specific activity reaches 28+ / -0.2U / mg protein, so that the pectate lyase PCPEL16 can be used for food processing, such as production of juice and wine.
Owner:SHANDONG AGRICULTURAL UNIVERSITY

Method for preparing high-purity natural capsaicin monomer

InactiveCN111187177AHigh yieldThe process is environmentally friendly, safe and simpleOrganic chemistry methodsCarboxylic acid amide separation/purificationAlcohol ethylAqueous ethanol
The invention discloses a method for preparing a high-purity natural capsaicin monomer. The method comprises the following steps: (1) grinding: taking a certain amount of a capsaicin crude product, and grinding the capsaicin crude product into powder; (2) alcohol dissolution: dissolving the powdery capsaicin-containing crude product obtained in the step (1) in an ethanol water solution, fully stirring for 20-30 minutes to obtain a capsaicin solution, and filtering the capsaicin solution for later use; (3) adsorption: pumping the capsaicin solution filtered in the step (2) into an adsorption resin column; (4) elution: eluting the resin column in the step (3) with an ethanol aqueous solution; and (5) crystallization: concentrating and crystallizing the capsaicin qualified eluent in the step(4) to obtain capsaicin crystals. According to the method for purifying capsaicin, the ethanol aqueous solution is adopted as an elution agent, the process is environmentally friendly, safe and simple, the separation efficiency is high, the finished product yield is high, the product quality is good, the equipment requirement is low, the production period is short, and the cost is effectively reduced.
Owner:海山都(上海)生物技术有限公司

Preparation method, application and use method of capsaicin molecularly imprinted magnetic beads

The invention discloses a preparation method, an application and a use method of capsaicin molecularly imprinted magnetic beads, and belongs to the field of pretreatment of food analysis samples. Thepreparation method mainly comprises the following steps: by taking magnetic Fe3O4 microspheres as a carrier, carrying out surface modification on the magnetic Fe3O4 microspheres by utilizing a coupling agent containing double bonds; mixing and copolymerizing the double-bond modified magnetic microspheres with capsaicin template molecules, a functional monomer, a coupling agent, an initiator and adispersing agent; and eluting the synthesized magnetic microspheres with a methanol-acetic acid solution to remove template molecules, washing with water, and washing with alcohol for later use. The capsaicin molecularly imprinted magnetic bead prepared by the invention can selectively and efficiently extract and separate capsaicin in illegal cooking oil, and provides a sample pretreatment technology for subsequent detection by using HPLC, HPLC-MS, Raman and other instruments so as to identify illegal cooking oil.
Owner:JILIN INST OF CHEM TECH

Plant expression vector for targeting silence phytophthora capsici cellulose synthase 3 and application thereof

The invention discloses a plant expression vector capable of effectively interfering a phytophthora capsici cellulose synthase 3 gene through host-induced gene silencing and application thereof. The plant expression vector disclosed by the invention can be transcribed to form a double-stranded RNA with a reverse complementary structure, and the double-stranded RNA is formed by respectively inserting a nucleotide sequence shown as SEQ ID No.1 or SEQ ID No.2 into the vector twice in the forward direction and the reverse direction. The invention also discloses application of the expression vectors in preventing and treating plant diseases caused by phytophthora capsici. The plant expressing the vector provided by the invention has obviously enhanced disease resistance to phytophthora capsici, the expression of the cellulose synthase 3 gene of the phytophthora capsici infecting the plants is significantly inhibited, and the cellulose synthase 3 gene is necessary for the development and pathopoiesis of the phytophthora capsici, therefore, the plant expression vector disclosed by the invention can effectively inhibit plant infection caused by phytophthora capsici, and an effective way is provided for preventing and treating related diseases caused by phytophthora capsici.
Owner:CHINA AGRI UNIV

Double-stranded RNA molecule for targeted silence of phytophthora capsici cellulose synthase 3 and application of double-stranded RNA molecule

The invention discloses a double-stranded RNA (Ribonucleic Acid) molecule capable of efficiently inhibiting the expression of a phytophthora capsici cellulose synthase 3 gene, and belongs to the technical field of agricultural biology. The double-stranded RNA molecule disclosed by the invention consists of nucleic acid sequences as shown in SEQ ID No. 1 and SEQ ID No. 2. The invention also discloses application of the double-stranded RNA molecule in preventing and treating plant diseases caused by phytophthora capsici. The double-stranded RNA molecule disclosed by the invention can be used for inhibiting infection of phytophthora capsici by directly treating the phytophthora capsici or spraying the phytophthora capsici on plants. Meanwhile, the double-stranded RNA provided by the invention has strong specificity on essential genes for growth and development of the phytophthora capsici, does not have the problem of drug resistance, and can provide an effective way for preventing and treating related diseases caused by the phytophthora capsici when being used for preparing biopesticides.
Owner:CHINA AGRI UNIV

PCR (Polymerase Chain Reaction) detection primer for phytophthora capsici leonian, kit containing primer and application thereof

The invention provides a PCR (Polymerase Chain Reaction) detection primer for phytophthora capsici leonian. The primer comprises Enl4s and Enl1a (as shown in Seq ID No.1 and 2). Four pairs of specific primers capable of quickly detecting phytophthora capsici leonian germs can be obtained based on the sequence difference between the Enl and Ypt genes of the phytophthora capsici leonian and other phytophthora nicotianaes: Enl2s / Enl3a, Enl4s / Enl1a, Ypt2s / Ypt3a and Ypt2s / Ypt5a, wherein the sensitivity of Enl4s / Enl1a is the highest. A PCR detection system is established on the basis, which is capable of quickly and accurately detecting the phytophthora capsici leonian from complex pathogenic bacteria environments in the tissues of plants having diseases and soil. A detection kit established according to the method is simple and convenient for operation, good in specificity and high in sensitivity; and the detection kit is capable of detecting the propagules in various forms of the phytophthora capsici leonian, such as hypha, oospore, zoospore and the like, thereby having great significance in the aspects of early warning on the epidemic situation of the phytophthora capsici leonian, pathogen supervision on the epidemic area and the like.
Owner:INST OF MICROBIOLOGY - CHINESE ACAD OF SCI

Synthesis and application of capsaicin halogenated derivative

The invention relates to synthesis and application of a capsaicin halogenated derivative. The capsaicin halogenated derivative has a structural formula I as shown in the description; in the formula, Ris C1-9 alkyl, halogenated C1-9 alkyl, C1-9 alkenyl and halogenated C1-9 alkenyl. The invention further relates to an agricultural composition with the compound or an agricultural pharmacological acceptable salt. By adopting the compound and the agricultural composition provided by the invention, injurious insects can be effectively killed and / or prevented.
Owner:SHANGHAI NATURE STANDARD R&D & BIOTECH +1
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