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30results about How to "Shorten the fruiting cycle" patented technology

Plantation method for oil tea trees

The invention discloses a plantation method for oil tea trees. The method comprises the steps of land selection and preparation, seedling selection and transplantation, topdressing at a seedling stage, branch trimming, fostering and weeding, topdressing at a fruit bearing stage, etc. A nutrient solution is sprayed and applied after the transplantation, at a seedling culture stage and at the fruit bearing stage respectively in combination with the topdressing. The nutrient solution is made through the steps that 3-5 parts by weight of selenium source, 6-7 parts by weight of humic acid, 9-12 parts by weight of protein powder, 2-4 parts by weight of EM bacteria, 12-14 parts by weight of amino acid, and 4-6 parts by weight of vitamins are mixed, water is added till the water content reaches 5-8wt%, and the mixture is treated by heat preservation for 12-15h under the temperature of 30-35 DEG C; and water with three to four multiples of weight added continuously, the mixture is mixed, heated to a boiling state and treated by heat preservation for 20-30min, filtering is conducted by a centrifuge, a filtering liquid is collected and evaporated till the organic selenium content in the filtering liquid is 7-8mg/L, and the nutrient solution can be obtained. Oil tea trees planted with the plantation method disclosed by the invention have a high survival rate, a short fruit bearing stage and significant economic benefits.
Owner:张运初

Pleurotus eryngii culture medium based on material particle granularity collocation and preparation method of pleurotus eryngii culture medium

The invention discloses a pleurotus eryngii culture medium based on material particle granularity collocation and a preparation method of the pleurotus eryngii culture medium. The culture medium comprises components in parts by weight as follows: 20-30 parts of sawdust, 15-25 parts of corncobs, 15-20 parts of bagasse, 5-15 parts of soybean meal, 10-20 parts of corn kernels, 10-20 parts of wheat kernels, 1 part of calcium carbonate and 1 part of lime powder, wherein the particle diameter of the sawdust is lower than 0.1 mm; the particle diameter of the corncobs is lower than 6 mm, and the corncobs lower than 40 meshes account for less than 15% of the total amount of the corncobs in mass ratio; the length of the bagasse is less than 5 mm; the granularity of the soybean meal is 5-40 meshes; the granularity of the corn kernels is 2-4 mm; the granularity of the wheat kernels is natural; the granularity of the calcium carbonate is lower than 60 meshes; and the granularity of the lime powder is lower than 60 meshes. According to the culture medium, compared with a conventional formula, the mycelium culture period is shortened by 18%, mycelia are denser and stronger, the fruiting period is shortened by 5%, and the output is increased by 5.5% stably.
Owner:成都中延菌菇业有限公司

Efficient disease-preventing auricularia polytricha culture medium and preparation method thereof

The invention belongs to the technical field of edible fungus cultivation and particularly relates to an efficient disease-preventing auricularia polytricha culture medium and a preparation method thereof. The culture medium comprises, by weight parts, 20-30 parts of broken wood shavings, 10-20 parts of trichoderma anti-mildew agent, 8-20 parts of soy sauce waste residue, 8-15 parts of hull of water chestnut, 8-15 parts of lotus seed hulls, 5-15 parts of banana stem, 1-10 parts of ambrosia trifida, 1-5 parts of rape flower straw and 1-5 parts of cottonseed hull and the like. The method comprises a step (1) of raw material processing, a step (2) of fermentation treatment, a step (3) of charging processing and a step (4) of sterilization processing. The formula design of the culture medium is more suitable for growth of auricularia polytricha, so that auricularia polytricha is bright red compared with fresh agaric, and the quality of the whole auricularia polytricha is improved. Part of raw materials of the culture medium are agricultural and industrial waste, the cost is low, so that the production cost is reduced, a novel handling way is provided for handling the agricultural and industrial waste, and the culture medium is economical and environmentally friendly. The preparation process is simple and easy to popularize.
Owner:博白县那林镇菌兴家庭农场

Rose palmata, fruity mushroom and cultivation method thereof

ActiveCN113079945AIncrease contentPrevent and improve the three high effectsCultivating equipmentsMushroom cultivationBiotechnologyMicroorganism
The invention belongs to the technical field of microorganisms, and particularly relates to rose palmata, fruity mushroom and a cultivation method thereof. The rose palmata is preserved in the China General Microbiological Culture Collection Center, and the preservation number is CGMCC No.21941. The fruity mushroom cultivation method comprises the following steps: (1) culture of a test tube mother strain is conducted, specifically, a test tube filled with a mother strain culture medium is sterilized, a palmarosa palmosa tissue block is inoculated under an aseptic condition, and culturing is conducted at 20-22 DEG C for 20-25 days to obtain the test tube mother strain; (2) enlarged culture of the strain is conducted, specifically, the test tube mother strain obtained in the step (1) is subjected to enlarged culture to obtain an enlarged culture strain; and (3) fruiting culture is conducted, specifically, the enlarged culture strain in the step (2) is subjected to bag cultivation or bottle cultivation, and fruiting is conducted to obtain a finished product. The fruity mushroom obtained through the method is high in nutrient content and short in cultivation time, the biological conversion rate reaches up to 70% or above, and the method can be widely applied to industrial production.
Owner:河南果菇蓉生物科技有限公司

Root cutting method for promoting stable growth of sandy-area filbert

The invention discloses a root cutting method for promoting stable growth of sandy-area filbert. The root cutting method includes the steps that on May 20th about, primary root cutting treatment is carried out, when leaves of a tree body are expanded, an annular furrow with the depth of 40 cm is dug at the portion 40 cm to 50 cm away from the horizontal position of a main rod, a root system is stopped to grow in the horizontal direction, soil loosening and fertilizer applying are simultaneously carried out, and the root system is induced to extend towards the soil depth; on June 20th about, secondary root cutting treatment is carried out with the same method, the depth is 50 cm about, and soil loosening and fertilizer applying are simultaneously carried out; on July 20th about, tertiary root cutting treatment is carried out with the same method, and the depth is 60 cm about. Compared with the prior art, the innovative scientific principles are adopted, the resistance such as drought resistance and cold resistance of the filbert is greatly improved, the space range when the filbert absorbs soil moisture is widened, healthy growth when the filbert is cultivated in sandy areas is promoted, the fruiting period is shortened, economic benefits are improved, and the high-quality and high-yield aim is achieved.
Owner:陕西省治沙研究所

Method for shortening fruiting period of morchella

The invention discloses a method for shortening the fruiting period of morchella. The method comprises the following steps of (1), land preparation, wherein soil with the pH value being 6.5-7.5 is selected, a morchella strain is planted at the temperature lower than 20 DEGC, before planting, the soil is deeply turned one time, during planting, a sunshade net and plastic cloth are placed on a greenhouse body, and a plurality of ditches are dug; (2), planting, wherein the strain is broadcasted into the dug ditches, after planting, earthing is conducted, sufficient water is applied one time, andthe strain is covered with a black mulching film; (3), management, wherein the humidity of the morchella planting environmental is kept at 65-75%, after white spores emerge on the ground, the mulchingfilm is opened, nutrition bags are placed, and after placement, the mulching film is well put; after the mulching film is put, the sunshade net on the greenhouse body is removed, and only the plasticcloth remains; when the ground is dry, water is supplemented in time, after the morchella grows to 5 centimeters high, the mulching film is removed, and the sunshade net is placed on the greenhouse body. The method has the advantages that the fruiting period of the morchella is greatly shortened, the yield and quality of the morchella can be improved, and great improvement of the production benefit is facilitated.
Owner:江苏馨野生态农业科技有限公司

Pear tree high branch grafting method

InactiveCN108040649AReduce cultivation investmentShorten the fruiting cycleGraftingRootstockPear tree
The invention aims at providing a pear tree high branch grafting method through which the fruit bearing and cultivating time is short and pear flesh is excellent in mouthfeel. The method comprises thesteps of stock treatment, wherein old pear trees which do not bear fruits are selected, multiple branches are selected on trunks less than two meters above the ground at the leaf fall period in October and November of the previous year, and the branches are sawn off to form branch heads as stock heads for grafting next year; stock transplanting, wherein stocks are dug in ball shapes to new land in December; scion selection and collection, wherein after new tips of new pear trees grow over 10 cm, multiple new tips are cut off and wrapped with wet towels, and new tip grafting work should be completed the same day; from March 15 to March 25 when the moderate temperature is 15-18 DEG C in the same year, the selected and collected new tips are grafted to the stock heads; grafting sections at which the new tips are grafted are wrapped with 2-3 layers of preservative film to promote healing of grafting wounds. According to the pear tree high branch grafting method through which the fruit bearing and cultivating time is short and the pear flesh is excellent in mouthfeel, the cultivated pear branches can grow longer next year and bear fruits in the third year, the born fruits are numerous,and the purposes of increasing yield and overcome are achieved.
Owner:薛凤梧

Fixed-point fruiting chestnut mushroom cultivation method using large bacterium sticks without covering soil

The invention relates to a fixed-point fruiting chestnut mushroom cultivation method using large bacterium sticks without covering soil, and belongs to the technical field of chestnut mushroom cultivation. According to the technical scheme, the method comprises the steps of material preparation, bagging, sterilization, inoculation, spawn running management, fixed-point fruiting, harvesting and spawn culture. According to the method, fixed-point fruiting chestnut mushroom cultivation is conducted by using the large bacterium sticks without the covering soil, the limitation that the covering soil is needed in chestnut mushroom cultivation is made up, fruiting of cultivated chestnut mushrooms is in order, fruiting time can be manually controlled, the fruiting cycle is shortened, the yield in the first flush is high, the quality of the chestnut mushrooms is good, impurities do not exist, and diseases and pests are few; the chestnut mushrooms cultivated in bags are even in size, fresh and aesthetic, the shelf goods performance of the chestnut mushrooms is greatly improved, and the chestnut mushrooms are more likely to be welcomed by all customers; by means of the fruiting technology of the chestnut mushrooms cultivated in the bags without the covering soil, the sales volume and the sales value of the chestnut mushrooms can be directly improved, the production and operation costs of a mushroom grower are significantly lowered, economic income of the mushroom grower is increased, good economic values and social benefits are brought to people, and industrial bag cultivation year-round production with the covering soil can be achieved.
Owner:迁西县林中宝生物科技有限公司

Disease prevention medium for cultivating auricularia polytricha and method for preparing disease prevention medium

The invention belongs to the field of technologies for cultivating edible fungi, and particularly discloses a disease prevention medium for cultivating auricularia polytricha and a method for preparing the disease prevention medium. The disease prevention medium comprises, by weight, 10-20 parts of smashed wood shaving, 10-20 parts of spartina, 10-20 parts of trichoderma anti-mildew agents, 10-25 parts of soy sauce residues, 10-30 parts of water chestnut hulls, 10-20 parts of durian shells, 5-15 parts of apple pomace, 5-15 parts of garlic straw, 1-8 parts of sugarcane skins and the like. The method includes preparation steps of (1) raw material treatment, (2) fermentation treatment, (3) loading treatment and (4) sterilization treatment. The disease prevention medium and the method have the advantages that the disease prevention medium in a formula design is suitable for growth of the auricularia polytricha, the auricularia polytricha is bright red as compared with fresh auricularia polytricha on a year-on-year basis, and the integral quality of the auricularia polytricha can be improved; partial raw materials for the disease prevention medium are agricultural waste and industrial waste, accordingly, the disease prevention medium is low in cost, the production cost can be reduced, a novel treatment way can be provided for the agricultural waste and the industrial waste, and the disease prevention medium and the method are economical and environmentally friendly; the method is simple and is easy to popularize.
Owner:博白县那林镇菌兴家庭农场

Regulation and application of transcription factor lfc1 on fruiting body development of Flammulina velutipes

The invention belongs to the technical field of genetic engineering. The invention discloses a transcription factor LFC1 involved in regulating the development of the sporocarp of Flammulina velutipes, its encoding gene and its application. The nucleotide sequence of the gene encoding the transcription factor LFC1 is shown in SEQ ID NO.1 in the sequence listing; the amino acid sequence of the transcription factor LFC1 is shown in SEQ ID NO.2 in the sequence listing. The present invention finds through overexpression and RNAi experiments on lfc1 in Flammulina velutipes that lfc1 is an important negative regulation factor for the development of fruiting bodies of Flammulina velutipes, and affects the generation of primordia, length of stipe and cap shape of Flammulina velutipes. Knockdown expression of lfc1 on the one hand promotes the growth of Flammulina velutipes stipe and increases the commodity value of Flammulina velutipes, on the other hand shortens the fruiting cycle, reduces energy consumption, and reduces production costs. However, the high expression of lfc1 leads to the deformity of the fruiting bodies of Flammulina velutipes. Therefore, the specific expression level of lfc1 in Flammulina velutipes strains is an important factor for the development of the fruiting bodies of Flammulina velutipes, and lfc1 can be used in the breeding of fine strains of Flammulina velutipes, which is convenient for screening Flammulina velutipes with long stipe and small canopy.
Owner:INST OF MICROBIOLOGY - CHINESE ACAD OF SCI

Pleurotus eryngii culture medium based on particle size matching of materials and preparation method thereof

The invention discloses a pleurotus eryngii culture medium based on material particle granularity collocation and a preparation method of the pleurotus eryngii culture medium. The culture medium comprises components in parts by weight as follows: 20-30 parts of sawdust, 15-25 parts of corncobs, 15-20 parts of bagasse, 5-15 parts of soybean meal, 10-20 parts of corn kernels, 10-20 parts of wheat kernels, 1 part of calcium carbonate and 1 part of lime powder, wherein the particle diameter of the sawdust is lower than 0.1 mm; the particle diameter of the corncobs is lower than 6 mm, and the corncobs lower than 40 meshes account for less than 15% of the total amount of the corncobs in mass ratio; the length of the bagasse is less than 5 mm; the granularity of the soybean meal is 5-40 meshes; the granularity of the corn kernels is 2-4 mm; the granularity of the wheat kernels is natural; the granularity of the calcium carbonate is lower than 60 meshes; and the granularity of the lime powder is lower than 60 meshes. According to the culture medium, compared with a conventional formula, the mycelium culture period is shortened by 18%, mycelia are denser and stronger, the fruiting period is shortened by 5%, and the output is increased by 5.5% stably.
Owner:成都中延菌菇业有限公司

Plastic biological particle strain preparation formula

The invention discloses a plastic biological particle strain preparation formula, relates to the technical field of strain cultivation, and aims to solve the problems that coriaria sinica cultured by an existing plastic biological particle strain preparation formula is poor in quality and low in strain survival rate, strain hyphae are easy to damage during inoculation, the hyphae of the strain grow slowly on a strain stick, the fruiting period is prolonged, and the production cost is reduced. In order to solve the problems that the cultivation cost is increased and the use effect is poor, the invention provides the following scheme. The culture medium is prepared from the following components in percentage by weight: 55-58% of coriaria sinifera wood flour, 6-8% of coriaria sinifera saw wood flour, 12-14% of high-quality wheat bran, 4-6% of high-quality cottonseed hull, 5-8% of peeled orange powder, 12-15% of high-quality corn flour, 0.5-1.5% of high-quality brown sugar, 0.02-0.04% of edible gypsum powder and 26-28% of mountain spring water. The method is reasonable in design, the quality of the cultivated coriaria sinica is good, the survival rate of the strains is high, hyphae cannot be damaged during inoculation, the hyphae of the strains on the fungus sticks grow faster, the fruiting period is shortened, the cultivation cost is reduced, the using effect is good, and the method is worthy of application and popularization.
Owner:贵州省马桑菌生物科技有限公司
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