51 results about "Coronatine" patented technology

The invention discloses a drought-resistant agent and application thereof. The plant drought-resistant agent comprises the active ingredients such as coronatine (COR) and S-abscisic acid (S-ABA). Compared with the present substance for improving the drought resistance of crops, the drought-resistant agent has the following characteristics: unexpected synergy can be obtained through COR, S-ABA and other plant growth adjusting substances which are added on the basis of the COR and S-ABA; an expected addition effect on the growth of crops and the adjustment of the activities can be exceeded, and on one hand, the crop application range can be enlarged, and on the other hand, the application concentration of coronatine, S-ABA and other plant growth adjusting agents can be reduced; and moreover, under the condition that the concentration of a single compound is lower than the effective concentration, a good adjusting degree on the growth of plants can be obtained through the plant growth adjusting agent.

The invention relates to a rooting agent formula for taxus chinensis branch cutting rooting. The rooting agent is prepared from, by mass, 200 mg-300 mg of indolebutyric acid, 200 mg-300 mg of naphthylacetic acid, 20 mg-30 mg of jasmonic acid methyl ester, 0.1 mg-0.5 mg of coronatine, 10 mg-20 mg of phenylalanine, 10 mg-20 mg of salicylic acid, 50 mg-100 mg of vitamin B2, 5 mg-10 mg of vitamin B6, 50 mg-100 mg of vitamin B12, 1 mg-5 mg of vitamin C, 1 mg-5 mg of vitamin H and 2 g-5 g of saccharose. According to the rooting agent formula for taxus chinensis branch cutting rooting, the content of chlorophyll in cutting branches and activity of enzymes in the branches can be improved, and growth of root systems and the survival rate of the cutting branches are effectively promoted. The invention further provides a preparation method of the rooting agent formula for taxus chinensis branch cutting rooting.

The present invention discloses a method for extracting coronatine, in which coronatine is generated through eluting and separating supernatant of microorganism fermentation liquids containing coronatine with adsorption column that takes macroporous adsorption resin as adsorbing agent. The method of present invention has the features of high extraction yield for coronatine, simple operation, low production cost and low environment pollution.

Stable genetically engineered bacterial strains that overproduce coronatine are provided. The stable strains can be successfully cultivated to overproduce coronatine at temperatures that are suitable for large scale, commercial preparations of coronatine. The overproducing strains are also non-pathogenic. An exemplary strain is Pseudomonas syringae APV1, which successfully overproduces coronatine at 26° C. Methods of optimizing culture conditions for coronatine production from the novel stable overproducing strains are provided, as are methods for using the overproducing strains to induce abscission and increase taxane production.

The present invention relates to a method of producing a taxane-type diterpene wherein a cell and / or a tissue of a plant which produces the taxane-type diterpene is cultured in the presence of at least one substance selected from the group consisting of coronatines, a bacterium which produces the coronatines, a culture solution or a culture extract of such bacterium, cyclic polysaccharides, fatty acids, and an imino or amino derivative of jasmonic acids, then the taxane-type diterpene is recovered from the resulting cultures.

The invention discloses a method for extracting coronatine from fermentation liquor by using a membrane separation technique, comprising micro-filtration and hyper-filtration steps: filtering a fermentation liquor containing coronatine by a micro filtering membrane with the aperture of 0.1-10 Mum so as to remove impurity particles and thalli; then filtering the liquor by a hyper-filtration membrane with the aperture of 0.001-0.1 Mum so as to remove macromolecule impurities of proteins, nucleic acids and colloid granules to obtain clear filtrate; and then carrying out common resin exchange or column chromatography, concentrating and crystallizing to obtain the coronatine. In order to improve the effect of separating purification, pre-treatment can be added before the micro-filtration, namely, the coronatine fermentation liquor is filtered though the filtration membrane with the aperture of 1-10 Mum; nano-filtration can be added after the hyper-filtration, namely, the effluence liquor is filtered by a nano-membrane system with cut-off molecular weight of 400-800. The method in the invention has simple operation and high yield which can be over 90%; in addition, the method has no influence on the structure and activity of the coronatine; and has low energy consumption and low pollution, thus completely satisfying the requirements of industrialized production.

The invention provides a regulation and control method for culturing saussurea involucrata cells in a scale manner for high-producing flavone. According to the technical scheme, first, an initial cell strain is quickly cultured in a liquid suspension way, passage is carried out once for every 7 to 10 days, and the increments of the fresh weights of cells are 3 to 5 times; subsequently, a two-stage culture method is adopted, the cells are enabled to quickly proliferate at a growth stage, the maximum cell concentration is obtained within 7 to 10 days, a precursor phenylalanine and an inducer coronatine are added into the cells in the condition of a certain high-density inoculum concentration of 150g / l to 400g / l (a fresh weight) at a production stage, the cells are harvested after being cultured for 3 to 5 days, and the flavone content is increased to 13 percent or above. The novel inducer coronatine is adopted for the process; the use level is few; the effect is obvious; no toxic or side effects exist; the flavone content of the saussurea involucrata cells can be quickly improved; the regulation and control method is applicable to a large-scale bioreactor of 20L or larger; the cells are already successfully cultured on scales of 20L, 100L, 200L and 1,000L by utilizing a bioreactor from the company of the inventor, furthermore, the cellular state is good, the yield is stable and the flavone content is 11 percent or above.

The invention discloses a cotton defoliating agent. The cotton defoliating agent is prepared by mixing the following components in parts by weight: 40-50 parts of magnesium chlorate, 6-8 parts of paclobutrazol, 20-40 parts of ethephon, 3-5 parts of thidiazuron, 2-4 parts of coronatine and 10-20 parts of a pesticide synergist. The product disclosed by the invention has the characteristics of small sizes, large active surface, strong permeability, no dust in a pesticide preparation process, low cost, high pesticide effect, cold prevention and frost resistance and the like.

The present invention provides a new bacterial strain capable of fermenting and producing high-component coronatin, that is, Pseudomonas syringae (Psendomonas syringae) Y-2018 bacterial strain, and the preservation number is CGMCC NO.1105. The weakness of the wild strain that must be low temperature to accumulate coronatin. The present invention also provides a method for industrialized production of coronatin, which comprises preparing the Pseudomonas syringae Y-2018 strain through slant strains, culturing the seeds in shaking flasks and aerated fermentation to obtain a fermented liquid containing coronatin. Concentrate, extract, crystallize and recrystallize to obtain crystal powder and non-crystallized mother liquor. This method can use organic nitrogen medium for fermentation, and the use of organic nitrogen not only increases the amount of bacteria, but also can synthesize more coronatine, thereby overcoming the defects that wild strains are not resistant to organic nitrogen, and organic nitrogen inhibits the accumulation of coronatin .

The invention discloses a plant growth regulator composition containing brassinolide, chlorine iron and coronatine and application thereof. The plant growth regulator composition is prepared from the following components in parts by weight: 0.001 to 1 part of brassinolide, 0.001 to 0.1 part of chlorine iron and 0.01 to 10 parts of coronatine. According to the invention, the activation performance of various enzymes can be improved, the metabolism of plants is accelerated, and the growth of crops is promoted; crops are induced to improve the resistance to cold injury and over-low-temperature cold injury period safely; the composition has significant effects in the aspects of synergism of nutrient balance in plants, increase of yield and improvement of quality.

The invention relates to a genetically engineered bacterium (Pseudomonas syringae soybean pathogenic variety CGMCC 1276), its construction method and its use. The engineering bacterium is obtained by inserting the Tn5 transposon S17-1 into the genome of the starting bacterium to inactivate its temperature control gene. The strain can be used for industrial fermentation to produce coronatine at the fermentation temperature of 26°C-28°C. The yield is similar to that of the starting bacteria (fermentation temperature is 18°C), and can reach 35mg / l-40mg / l.

The invention discloses a cotton defoliating agent. The cotton defoliating agent is prepared by mixing, by weight, 6-10 parts of paclobutrazol, 6-8 parts of ethephon, 1-3 parts of silky organic silicone surfactant, 15-25 parts of chlorate, 6-8 parts of coronatine, 6-10 parts of xanthan gum and 6-8 parts of thidiazuron. The cotton defoliating agent is harmless to plants, and boll opening is normal.