38 results about "Chlorophyll degradation" patented technology

The invention provides a key ethylene response factor CitERF6 (SEQ: NO. 1) for regulating the chlorophyll degradation of citrus peels. The key ethylene response factor comprises a conservative AP2/ERF structural domain and a Pat4(RKRK) nuclear localization signal. During the ethylene treatment of harvested citrus fruits, the expression of CitERF6 is enhanced under external ethylene induction. When the CitERF6 instantly overexpresses in the citrus peels, the chlorophyll degradation of the citrus peels can be promoted and accelerated. The key ethylene response factor has the advantages that by the PCR, real-time and quantitative PCR and citrus fruit instant expression technologies, the citrus ethylene response factor CitERF6 is cloned, and identification of the CitERF6 shows that the CitERF6 can participate in the chlorophyll degradation; the CitERF6 is applicable to genetic engineering breeding of plant color modification and especially to the regulation of the chlorophyll degradation of the citrus peels, and a theoretical basis is provided for the further researches of the peel coloring technology and the acting mechanism of the CitERF6.

The invention provides a critical ethylene response factor (ERF) CitERF13 for regulating and controlling orange peel chlorophyll removal. The gene contains a conservative AP2/ERF structural domain and a Pat4 (RKRK) core positioning signal. During the development of orange fruits, the expression peak of the CitERF13 is degraded in advance of peel chlorophyll, and is enhanced by exogenous ethylene. When the CitERF13 is excessively expressed instantaneously in orange peels, the degradation of chlorophyll can be promoted, and the peel chlorophyll removal is accelerated. A technology of PCR (polymerase chain reaction), real-time quantitative PCR and orange fruit instantaneous expression is utilized to clone and identify the critical ERF CitERF13 which can be used for regulating and controlling the chlorophyll degradation, and can be applied to plant color modified genetic engineering breeding especially to regulation and control of orange peel chlorophyll removal.

The invention uses fast neutron mutagenesis mode plant south-leaf mustard to filter to gain stay-green mutant. Separating crucial adjusting gene AtNYE1 would be gained by the method of image-location clone. And the stay-green feature would be created by RNA interrupt or other technology, and through NYE1 gene or the expression to restrain the gene, and lower the albumen activity of NYE1.

Strawberries are available year-around from production in the field or from controlled environments (e.g. high and low tunnel culture and greenhouse). Diversity of production conditions results in challenges in controlling diseases before, during, and after harvest. Fungicides, traditionally used to control diseases, have limitations. UV-C irradiation followed by a dark period was used to kill two major pathogens of strawberry, Botrytis cinerea and Colletotrichum acutatum. The UV-C irradiation and dark period was followed by repopulation with beneficial biocontrol microorganisms. The 4 hr dark period prevented activation of a light-dependent UV-C damage repair mechanism in the pathogens. This combination protocol makes it possible to use a lower dose of UV-C for reduction and/or elimination of pathogens. A mobile treatment apparatus was designed to provide the appropriately timed UV-C doses, dark period, and sprayable doses of biocontrol microorganisms. The UV-C dose and repeated exposure did not affect pollen germination or cause chlorophyll degradation in strawberry leaves.

The invention discloses a method for quickly preparing high-purity chlorophyll and chlorophyll degradation products. Satsuma mandarin peels and sweet potato leaves are used as raw materials for the first time to prepare the chlorophyll and derivatives thereof. The method disclosed by the invention is convenient and quick for taking materials, low in cost and easy to operate, and can complete the preparation of all the 8 products within three days. The purity of the obtained products can reach 90-95%, and the cost is much lower than the price of the same type of imported standard substance. The method can efficiently and quickly prepare the standard reference substances of the milligram-level chlorophyll and derivatives thereof required by the experiment, is suitable for popularization and application in commercial laboratories and enterprises, and has wide application prospects.

The invention discloses a refrigerating preservation method of fresh lotus seedpods. The method includes the following steps of 1, low-temperature cleaning of fresh-picked lotus seedpods; 2, low-temperature soaking and ozone water sterilization; 3, composite color-protecting preservative film formation treatment; 4, polypropylene preservation bag packaging, and conduction of low-temperature refrigeration at the temperature of 0-2 DEG C to obtain finished products. According to the method, microorganisms on the surfaces of the lotus seedpods can be effectively restrained or killed, photosynthesis, respiration, rising, glycometabolism and other physiological metabolism activities of the fresh lotus seedpods are retarded, and ethylene release and chlorophyll degradation can be restrained; color browning of the fresh lotus seedpods in the storage period is retarded, the appearance quality of the fresh lotus seedpods is fully reserved, and the nutritional quality and flavor of lotus seeds are well kept; the effective length for preservation of the fresh lotus seedpods can be kept for as long as 50 days through the preservation method. The method is simple and easy to carry out, high in operability, low in energy consumption cost and free of excessive investment, the process is environment-friendly, safe and free of pollution, the obtained products are practical and convenient to eat, the shelf life of the fresh lotus seedpods is greatly prolonged, and a new way is developed for high-value utilization of the lotus seed products.

The invention discloses a compounded agent of a potassium fertilizer for rice as well as a preparation method and an application thereof. The compounded agent comprises the following components according to a certain ratio: potassium chloride, ibuprofen, Tween-20, and laurocapram. The method comprises the following steps: (1) potassium chloride is weighed, water is added for dissolving, and a solution A is obtained; (2) ibuprofen and laurocapram weighed and mixed uniformly, ethyl alcohol is added for dissolving, dissolving liquid is dropped into warm water with continuously stirring, and a mixed solution B is obtained; (3) at a normal temperature, the mixed solution B obtained in the step (2) is dropped into the solution A, uniform mixing is carried out, and a mixed solution C is obtained; (4) the Tween-20 is weighed and dropped into the mixed solution C, a mixed solution D is obtained, uniform mixing is carried out, volumetric flask preparation is carried out, and the compounded agent of the potassium fertilizer for rice is obtained. The method has the advantages of low cost, easy and simple operation; the compounded agent can substantially promote growth of rice root, inhibit chlorophyll degradation, and delay leaf aging; with the same application amount of the potassium fertilizer, compared with the common potassium fertilizer, the compounded agent of the potassium fertilizer has obvious yield increasing effects, and yield of rice is increased by 9.1-15.9%.

The invention belongs to the technical field of plant genetic engineering and particularly discloses a chlorophyll katabolism control associated protein of non-heading Chinese cabbage as well as an encoding gene and application thereof. The chlorophyll katabolism control associated protein provided by the invention is sourced from the non-heading Chinese cabbage with the variety of 'Xiadongqing',and has the name of BcNYE1 and the amino acid sequence shown as SEQIDNO:2. The encoding gene of the chlorophyll katabolism control associated protein of the non-heading Chinese cabbage has the nucleotide sequence shown as SEQIDNO:1 or the polynucleotide sequence of the amino acid sequence with the code of SEQIDNO:2. The gene disclosed by the invention can be applied to chlorophyll katabolism molecular mechanism research of the non-heading Chinese cabbage and improvement of plant stay-green property on the aspects of delaying blade chlorophyll degradation and blade senescence of plants.

The invention belongs to the technical field of plant gene engineering, and in particular relates to a Bambusa emeiensis 'viridiflavus' chlorophyll degradation pathway related protein and an encoding gene thereof as well as an application of the encoding gene. The chlorophyll degradation related protein provided by the invention is derived from Bambusa emeiensis 'viridiflavus'; and the name of the protein is BeCRN1, and the amino acid sequence of the protein is as shown in SEQIDNO: 2. The nucleotide sequence of the encoding gene of the Bambusa emeiensis 'viridiflavus' chlorophyll degradation pathway related protein BeCRN1 is as shown in SEQIDNO: 1, or a polynucleotide sequence for encoding the SEQIDNO: 2 amino acid sequence. The gene disclosed by the invention can be used for research on a Bambusa emeiensis 'viridiflavus' chlorophyll degradation mechanism and is used for color character improvement of ornamental bamboo plants, including improvement of green characters of ornamental bamboo plants and the like.

The invention relates to yellow tea of new technology, and a production method thereof. The method particularly includes: with fresh tea tree leaves, with one bud and one leaf or one bud and two leaves, being a raw material, carrying out the steps of withering, deactivation of enzymes, rolling, heaping for yellowing, drying, and fragrance enhancing. The production method is used for producing high-quality yellow tea, which has the characters of sweet (fresh) corn-like fragrance or rice crust-like fragrance. In the method, withering time is prolonged, so that water content of the fresh leaves is reduced; the step of heaping for yellowing is carried out under sun to form a high-temperature and -humidity environmental conditions, thereby largely damaging chlorophyll; and yellow substances, such as theaflavin which is generated through non-enzymic auto-oxidization of polyphenols under the high-temperature and -humidity condition, are exposed, thereby improving the color quality of the yellow tea; the polyphenols are oxidized and the chlorophyll is degraded, and by means of ultraviolet ray in sunshine, generation of mildews and other adverse microorganisms in a tea base can be inhibited, so that the produced yellow tea have excellent quality and safety.

The invention discloses a method for improving the drought resistance of apples. <12>C<6+> ions with energy of 80Me V/u and LET of 33KeVmum<-1> are used for heavy carbon ion irradiation under an ion accelerator TR4 terminal in a modern physics research institution of Chinese Academy of Sciences, dosage rate is 50Gy/min, and dosage is 0.50Gy and 60Gy. By the aid of a heavy carbon ion irradiation induced mutation technology, the net photosynthetic rate of the apples under drought, the relative water content of leaves and biomasses can be remarkably increased, chlorophyll degradation is inhibited, and the steady state of cells under drought is maintained, so that the drought stress resistance of the apples is enhanced.

The invention relates to a cultivation method for making a ginkgo leaf color change in advance. The cultivation method comprises the specific steps that a matrix prepared by 25-30% of yellow sand, 20-30% of animal manure, 20-30% topsoil, 20-30% of composted straw and 0.03-0.05% of crosslinked polyacrylamide is used on the ground without planting hole digging, field planting is conducted on ginkgoes having the diameter at breast height of 8-15 cm by using tapered piled soil after even mixing, wherein the line spacings of plants are 3.5-4.5 m * 3.5-5.5 m; at the beginning of March in each year, 150-300g of urea is additionally applied to culture healthy leaves. The ginkgoes have poor resistance, if it rains in the middle ten days of September, protection is provided by using plastic cloth and other facilities sheltering from the rain, the moisture content of the matrix is reduced to 18-26%, drought stress is performed for 15 days, chlorophyll degradation can be accelerated, and a yellow leaf enjoying period of the ginkgoes can be advanced to the early of October.

The invention discloses cymbidium sinense chlorophyll catabolism regulatory protein as well as a coding gene and application thereof. The amino acid sequence of the cymbidium sinense chlorophyll catabolism regulatory protein disclosed by the invention comprises 307 amino acid residues and is shown in SEQ ID NO:2; the nucleotide sequence of a cymbidium sinense chlorophyll catabolism regulatory gene for coding the cymbidium sinense chlorophyll catabolism regulatory protein comprises 924 basic groups and is shown in SEQ ID NO:1. The cymbidium sinense chlorophyll catabolism regulatory protein disclosed by the invention has the activity of chlorophyll degrading enzyme; after the expression quantity of the cymbidium sinense chlorophyll catabolism regulatory protein is increased, the content of chlorophyll in arabidopsis thaliana leaf blades can be decreased; after the cymbidium sinense chlorophyll catabolism regulatory protein is highly expressed in cymbidium sinense, the contents of chlorophyll in leaf blades and flowering branches of cymbidium sinense are obviously decreased. The cymbidium sinense chlorophyll catabolism regulatory gene and the cymbidium sinense chlorophyll catabolism regulatory protein coded by the same can be used for research on a chlorophyll degradation molecular mechanism and character improvement of leaf color or flower color of plants.

The invention provides a method for improving cold resistance of red bract pineapples, and belongs to the field of plant cultivation. The method for improving cold resistance of the red bract pineapples comprises the following steps that S1, tissue culture seedlings of the red bract pineapples are inoculated into an MS culture medium containing a low-temperature treating agent for culture; and S2, low-temperature exercise treatment is conducted after culture is completed. According to the method for improving cold resistance of the red bract pineapples, the activity of protective enzyme systems (SOD, POD and CAT in bodies of the red bract pineapples can be improved, so that the damage of low-temperature stress to the red bract pineapples is reduced, the integrity of leaf structures is kept, chlorophyll degradation is relieved, photosynthesis is promoted, and the overall cold resistance of the red bract pineapples is improved.

The invention relates to a greenness-protecting and brittleness-keeping compound agent for heracleum moellendorffii hance and belongs to the technical field of processing of agricultural products. A method comprises the concrete steps: after grading and cleaning fresh heracleum moellendorffii hance, soaking the heracleum moellendorffii hance into a greenness-protecting and brittleness-keeping water solution composed of 0.03%-0.30%(w/v) of tea polyphenol, 0.02%-0.25%(w/v) of ascorbic acid, 0.06%-0.50%(w/v) of nobiletin, 0.01%-0.30%(w/v) of calcium lactate and 0.01%-0.30%(w/v) of zinc chloride;and performing treatment with an ultrasonic wave device for 10-15min, rinsing, dewatering, cooling, vacuum packaging and low-temperature storage. After the heracleum moellendorffii hance is treated bythe above steps, degradation of chlorophyll and decomposition and browning of pectin can be obviously postponed and the respiratory intensity and peroxidase activity of the heracleum moellendorffii hance can be obviously reduced. The method is a green, environment-friendly, safe, economic and high-efficiency greenness-protecting and brittleness-keeping method and provides a research basis for theresearch and development of the related products of the heracleum moellendorffii hance in the future.

The invention discloses a strain and method for degrading chlorophyll. The name of the strain determined by China Center for Type Culture Collection is Aspergillus GLHZB319, and the collection number is CCTCC NO:M2011101. The residual chlorophyll on the plant is degraded by a microbial fermentation method. When the strain ferments and degrades chlorophyll, no additional carbon source, nitrogen source or inorganic sodium salt is needed; and in the strain growth and development process, the chlorophyll can be used as a substrate for degrading chlorophyll. The strain has the characteristics of high degradation speed, high degradation rate, low cost, no residue, no pollution, high safety and environmental protection for chlorophyll, and can partially substitute decolorizing resin in the existing natural product extraction process.

The invention discloses an apple fertilizer nutrient synergist. The synergist is composed of the following raw materials by weight: 13-30 parts of effective active ingredient, 12-18 parts of traditional Chinese medicine preparation, 25-40 parts of super absorbent resin, 4-7 parts of alkanol milk powder, 8-20 parts of diphenhydramine, 4-10 parts of humic acid chelated magnesium, 6-12 parts of seaweed fermentation residue, 2-4 parts of synergist, 0.5-1. 3 parts of nitrogen-fixing bacteria, 3-8 parts of phosphorylated chitosan, 5-10 parts of camellia seed meal, 13-20 parts of polyacrylamide and 2-6 parts of surfactant. Compared with the prior art, the synergist has the advantages of affecting the development of plant buds, accelerating cell mitosis, promoting cell enlargement and differentiation and preventing fruit and flower dropping, thereby promoting plant growth, premature ripening, delaying aging of crop leaves in the later period and increasing yield. Further, the synergist can promote the growth of apple trees, improve the disease resistance, achieve an insect repellent effect, reduce disease and insect pests, promote plant cell growth, and inhibit plant chlorophyll degradation.

The invention discloses a method for culturing a root-growth-enhanced leaf-ageing-delayed transgenic plant. The gene shown as SEQ ID NO:1 is introduced into a target plant and is stably expressed and inherited, so that the anti-ageing transgenic plant with growth-enhanced root is obtained compared with a non-transgenic contrast plant. Growth of root of the transgenic plant is obviously promoted, also the functional leaf photosynthesis is obviously enhanced at the late growth stage, leaf chlorophyll degradation is delayed, ageing of the transgenic plant is delayed, and therefore crop output is improved.