333 results about "Kinetin" patented technology

Personal care composition comprising from about 0.05% to about 5% of at least one aquaporin-stimulating compound selected from the group consisting of xanthine, caffeine; 2-amino-6-methyl-mercaptopurine; 1-methyl xanthine; 2-aminopurine; theophylline; theobromine; adenine; adenosine; kinetin; p-chlorophenoxyacetic acid; 2,4-dichlorophenoxyacetic acid; indole-3-butyric acid; indole-3-acetic acid methyl ester; beta-naphthoxyacetic acid; 2,3,5-triiodobenzoic acid; adenine hemisulfate; n-benzyl-9-(2-tetrahydropyranyl)adenine; 1,3-diphenylurea; 1-phenyl-3-(1,2,3-thiadiazol-5-yl)urea; zeatin; indole-3-acetic acid; 6-benzylaminopurine; alpha-napthaleneacetic acid; 6-2-furoylaminopurine; green tea extract; white tea extract; menthol; tea tree oil; ginsenoside-RB1; ginsenoside-RB3; ginsenoside-RC; ginsenoside-RD; ginsenoside-RE; ginsenoside-RG1; ginseng root extract; ginseng flower extract; pomegranate extract, extracts from Ajuga turkestanica; extracts from viola tricolor and combinations thereof; an additional ingredient selected from the group consisting of niacinamide, glycerin and mixtures thereof, and a dermatologically-acceptable carrier.

The invention relates to a plant sprouting agent and a preparation method thereof. The materials of the sprouting agent are 6-benzyladenine, kinetin, gibberellin, dimethylsulfoxide, glycerol and lanolin; the dimethylsulfoxide solution and the glycerol are added into a glass beaker and dissolved, so that hormone solution is obtained; the lanolin is put into another big beaker, and is heated to 70 DEG C to be melted, and as the lanolin is stirred to be slowly melted, the hormone solution is slowly added into the lanolin and sufficiently and uniformly stirred; and after being cooled to the room temperature, the hormone mixture is coagulated into paste, which is the high-effective plant sprouting agent. Each component in the sprouting agent can rapidly penetrate the cell membranes of the dormant buds of plants and directionally enter cells, consequently, the efficacy is enhanced, and the acting time is shortened. The plant sprouting agent can increase the plant sprouting speed, shorten the growing time and accelerate seedling formation; bud dormancy is broken, so that the growth of plants is increased; the plant sprouting agent can change the hormonal balance in plant cells, promote sprouting and accelerate the elongation growth of the stems and leaves of plants; and the plant sprouting agent has a moisture-keeping effect, which can help to protect the new sprouts of plants.

The invention relates to a tender stem callus plant regeneration induction culture medium for lonicera caerulea and solves the problems of low plant differentiation rate and high culture medium cost problem of the auxiliary bud or stem tip culture, which is the main tissue culture of lonicera caerulea. The culture medium consists of a large amount of macroelements, microelements and hormone, wherein the hormone consists of 6-benzyl aminopurine at a concentration of 1.0 to 2.0mg/L and indolebutyric acid or naphthylacetic acid at a concentration of 0.05 to 0.2mg. When the LD1 culture medium of the invention is used, the tender stems of lonicera caerulea can be easily induced to form calla, and the induction rates of the calla are all over 90 percent; and the probability of the induction of the calla into plants is high, the plant differentiation rate is up to 50 to 82 percent which is 66.6 to 173.3 percent higher than that of the conventional Murashige-Skoog (MS) culture medium, and the cost is saved by 45.1 percent compared with the reference MS culture medium.

The invention discloses an efficient tissue culture and rapid propagation technology for seedlings of bletilla striata. According to the technology, bletilla striata seeds are sown on a seed germination culture medium for sterile germination, the obtained seedlings are inoculated to a multiplication and subculture medium one by one for multiplication and subculture, clustering seedlings are obtained and inoculated to a rooting culture medium for rooting culture, the obtained tissue culture seedlings are planted on a prepared seedling hardening substrate, and the seedlings are transplanted to a large filed for plantation after seedling hardening, wherein the seed germination culture medium comprises MS (magnesium sulfate), 30g/L of sugar, 8g/L of agar and 10g/L-12g/L of potatoes; the multiplication and subculture medium comprises MS, 1.0 mg/L of KT (kinetin), 0.2 mg/L of NAA (naphthalene acetic acid), 30g/L of sugar and 9g/L of agar; the rooting culture medium comprises MS, 0.2 mg/L of NAA, 1.0mg/L of IAA (indole acetic acid), 30g/L of sugar, 9g/L of agar and 25-30 g/L of potatoes; the seedling hardening substrate comprises medium moor peat soil, perlite and wood dust in the volume ratio being 5:2:3. The technology is mature, a system is perfect, the problems of low natural germination rate of bletilla striata and difficulty in obtaining of seedlings can be effectively solved, and the technology has better popularization and application value and broad market prospect.

The invention discloses a peanut seed coating additive which consists of the following components in parts by weight: 15-20 parts of Tianda 2116, 3-6 parts of brassinolide, 4-7 parts of gibberellin, 2-5 parts of kinetin, 3-6 parts of 6-benayl aminopurine, 4-7 parts of naphthylacetic acid, 4-6 parts of indoleacetic acid, 3-5 parts of salicylic acid, 2-4 parts of triacontanol, 10-14 parts of amino-oligosaccharin and 2-3 parts of methyl cellulose. According to the optimum mixture ratio of plant growth regulators to physiological activators, the seed germination speed, the germination speed and the seedling growth speed are obviously increased, full, neat and strong seedlings are facilitated, a solid foundation is laid for the final yield of peanuts, the germination of mixed peanut seeds is ahead of time by 2.5-3.8 days, the emergence rate is increased by 4.1-5.4 percent, the content of dry matters in the seedling stage is increased by 13.3-25.0 percent, and the yield of peanut pods is increased by 12.7-21.4 percent.

The invention discloses a hybrid liriodendron somatic embryogenesis synchronization control method. In the method, 2,4-D concentration is reduced gradually by utilizing a growth hormone regulating mechanism; kinetin (KT) with the dose of 0.5 mg.L<-1> is added to induce uniform embryonic cell masses; the embryonic cell masses are subjected to fractional culture by a mechanically sieving method; and different subsequent synchronization control methods are adopted according to different cell mass sizes and somatic embryogenesis modes. After the synchronization control, the somatic growth synchronization ratio of hybrid liriodendron subjected to classified screening at the stage of globular embryo reaches about 90 percent; the synchronization ratio of fractional treatment at the stages of heart-shaped embryo and torpedo-shaped embryo is about 40 percent; after a proper period of refrigeration, the synchronization ratio is increased to some extent; and the conversion rate of a mature embryo, which develops from a material at the stage of globular embryo, to a regeneration plant can reach 70 to 80 percent.

The invention discloses a stem latent bud germination promoter and a method for promoting the germination of stem latent buds by using the stem latent bud germination promoter. The stem latent bud germination promoter comprises a water solution containing the following components with concentration: 10-30 mg/L of N6-kinetin (KT), 50-200 mg/L of 6-benzyladenine (6-BA), 300-1000 mg/L of gibberellin (GA3) and 200-400 mg/L of 2-chloroethyl phosphoric acids (ethephon). The stem latent bud germination promoter and the method for promoting the germination of the stem latent buds by using the stem latent bud germination promoter, which are disclosed by the invention, and can be used for overcoming the defects of the prior art and promoting the latent bud germination, realizing the latent bud germination on a designated position, ensuring the germination amount and cultivating the pot cultures with good tree crowns.

The invention discloses a detoxification, tissue culture and rapid propagation method of common turmeric, which comprises the explant selection and treatment, induction culture, the virus identification of plant regeneration, proliferation culture, transplanting and other steps. In the invention, on the basis of the MS culture medium, the plant growth regulators such as 6-benzyladenine, kinetin, Alpha-banai acid, adenine sulphate are added for the induction culture of common turmeric apical meristem and the proliferation and rooting of multiple shoot two key stages. With the adoption of the packaged technology and method provided in the invention for the tissue culture and rapid propagation of common turmeric, the difficult problems of common turmeric such as virus accumulation, declining quality and yield reduction caused by propagation coefficient and technical stability are met. Therefore, the invention can provide a seedling-raising method with short cycle, high rate of reproduction, low-cost for the factory production of common turmeric.

The invention discloses a culture medium for in-vitro induced regeneration plants of double-haploid stems of potatoes, which belongs to the field of agricultural biotechnologies. The culture medium comprises the following compositions: potassium nitrate, ammonium nitrate, monopotassium phosphate, magnesium sulfate, calcium chloride, potassium iodide, boric acid, manganese sulfate, zinc sulfate, sodium molybdate, copper sulfate, cobalt chloride, ferrous sulfate, disodium ethylenediamine tetraacetic acid, nicotinic acid, pyridoxine hydrochloride, glycine, glutamine, casein hydrolysate, yeast extracts, sucrose, 6-benzylaminopurine, naphthalene acetic acid, kinetin, zeatin and heteroauxin beilining. The culture medium is applied to the induction and culturing of double-haploid stem regenerated seedlings of potatoes, the test effect is good, the initiating rate is increased by 76%, and the seedling rate is as high as 80.5%. The regeneration rate of double-haploid stems of potatoes is significantly increased, thereby laying a foundation for the establishment of a genetic transformation system; and the culturing mode adopts a one-step seedling method, so that the pollution probability is reduced.

The invention discloses a tangerine biological antistaling agent based on the activity of rhodosporidium and a fruit elicitor, which consists of rhodosporidium suspension, gibberellin/kinetin, salicylic acid, auxin and water, wherein each 1 liter of antistaling agent contains 1*1010 to 1*1012 rhodosporidium cells, 50 to 150 milligrams of gibberellin or kinetin, 8 to 100 milligrams of salicylic acid, 10 to 500 milligrams of auxin and the balance of water; and the rhodosporidium is rhodosporidium paludiagenum Fell and Tallman of which the collection number is IMI 394084. The biological antistaling agent can control post-harvest diseases of tangerine fruits effectively on the premise that chemical bactericides are not used.

The invention discloses a method for promoting sprouting of pitaya seeds. Before the pitaya seeds sprout and are cultivated, the pitaya seeds are soaked for 6-24 h with a seed soaking agent, and the seed soaking agent comprises gibberellins with the concentration being 50-250 mg/L, kinetin with the concentration being 5-30 mg/L, and DA-6 with the concentration being 5-15 mg/L. By the adoption of the method, the vitality of the pitaya seeds is improved, the sprouting uniformity is high, and the seedling quality is good.

The invention relates to a grafting and replanting method for a tea tree. The method comprises the following steps: sawing rootstocks; selecting scions, and carrying out combined scion treatment by using gibberellin with a concentration of 50mg/L and kinetin with a concentration of 50mg/L; splitting the rootstocks; peeling the scions; inserting the scions; carrying out bagging; and carrying out shading. With the grafting and replanting method provided by the invention, grafting survival rate reaches at least 90%; underground pest prevention and control effects are good; old tea garden can quickly put into production; after grafting, picking starts in the fifth month and is 10 to 15 days earlier than planting; and the method also has the advantages of low energy consumption, simple operation and easy popularization.

The invention provides an efficient induction medium of sorghum anther. The formula of the medium is composed of a certain content of KNO3, NH4NO3, KH2PO4, CaC12 2H2O, MgSO4, Na2-EDTA, FeSO4 7H2O, MnSO4 H2O, ZnSO4 7H2O, H3BO3, KI, CuSO4 5H2O, CoC1 6H2O, NaMoO4 2H2O, ethylmethane sulfonate, glycine, inositol, vitamin B1, vitamin B6, nicotinic acid, D-arabinose base-2-deoxidation hexose, cane sugar, Phytagel, 2,4-D, kinetin, compound phthalein nucleic acid, plant sulfuration kinetin PSK-alpha, insulin and protein hydrolysate. The medium has the advantages of being capable of remarkably improving the callus rate of the sorghum anther and substantially improving the cultivation efficiency of the sorghum anther.

The invention relates to a cut flower antistaling agent. In order to solve the technical problem, the invention adopts a technical scheme that the cut flower antistaling agent comprises the following main components in percentage by weight: 0.01-0.04% of 8- hydroxyquinoline, 0.02-0.09% of citric acid, 1-50% of glucose, 0.01-0.1% of sodium chloride or 0.01-0.02% silver nitrate, 0.01-0.03% kinetin KT, and others are water. The cut flower antistaling agent provided by the invention has the beneficial effects that the flower diameter is increased, the blossom rate of buds is increased, and the vast life of the cut flower is prolonged.

The invention provides a method for overcoming yellowing of leaves of tissue culture seedlings of Rosa damascena. The method comprises: taking rosa damascena stem segments with axillary buds as explants to be sterilized, inoculating the sterilized stem segments into an MS (Murashige and Skoog) culture medium to be subject to primary culture; and cutting the seedlings obtained after primary culture into segments and transferring the seedling segments to a multiplication culture medium to be subject to subculture at intervals, wherein 30g of cane sugar and 6g of agar are added to each litre of the MS culture medium; each seedling segment is provided with a leaf; the multiplication culture medium is the MS culture medium to each litre of which 0.5-4.0mg of 6-BA (6-benzylaminopurine), 0.5-2.0mg of KT (kinetin), 0.2mg of NAA (1-Naphthaleneacetic acid), 5-20mg of ABA (abscisic acid), 1-10mg of AgNO3, 30g of cane sugar and 6g of agar are added; and the primary culture and the subculture are carried out under the following conditions: the illumination intensity is 1500-2000Lx, the temperature is 23+/-2 DEG C, and the humidity is 75-80%.

The invention discloses a tissue medium for Lonicera macranthoides Hand. Mazz Yulei No.1 sprouts. The medium comprises at least one of the following mediums: a callus induction medium which comprises B5, 2mg/L of 6-BA (6-benzylaminopurine), 2mg/L of KT (kinetin), 0.1mg/L of NAA (naphthylacetic acid), 5.5-6.0g/L of carragheenan and 30g/L of sucrose and has a pH value of 5.6-5.8; an adventitious bud differentiation medium which comprises B5, 1mg/L of 6-BA, 2mg/L of KT, 0.1mg/L of NAA, 5.5-6.0g/L of carragheenan and 30g/L of sucrose and has a pH value of 5.6-5.8; an adventitious bud subculture medium which comprises MB, 1mg/L of 6-BA, 0.8mg/L of IAA (indoleacetic acid), 5.5-6.0g/L of carragheenan and 30g/L of sucrose and has a pH value of 5.6-5.8; and a rooting medium which comprises 1/3MB, 1.5mg/L of IBA (indolebutyric acid), 0.1mg/L of NAA, 5.5-6.0g/L of carragheenan and 20g/L of sucrose and has a pH value of 5.6-5.8. The medium of the invention, which has the advantages of high callusinductivity, high dventitious bud differentiation rate and propagation coefficient, high rooting rate, high transplanting survival rate of test tube sprouts, robust sprout growth, normal leaf shape and leaf color, rapid subcutaneous rooting and new leaf germination, and the like, can satisfy needs of the large-scale cultivation of Lonicera macranthoides Hand. Mazz Yulei No.1, and has a good application prospect.

The invention relates to the fields of agricultural planting and vegetable cultivation, in particular to a grafting activator and a method for increasing grafting survival rate. The grafting activator is prepared from 6-benzylamine adenine, kinetin, indolebutyric acid and cane sugar. A grafting cultivation test proves that by the grafting activator and the grafting method, the grafting survival rate of potatoes and cherry tomatoes is increased from 18.6 percent to 96.0 percent, the cost of the cherry tomato seeds is reduced by 75 percent or above, the yield profit of overground and underground vegetable three-dimensional cultivation is doubled. In addition, the grafting activator is simple in constitution and safe to use, the formula contains no antibiotic or chemical preservative component, and any adverse influence on the growth and development of the grafted plants and the quality of the plant fruit is avoided.

A method for inducing the adventitious root of notoginseng and its tissue culture includes such steps as taking the callus and explant of notoginseng, putting them on the fixing culture medium MS containing one or more of indole-butanoic acid, naphthylacetic acid and kinetin, inducing adventitious root in aseptic and dark condition, transferring the induced adventitious root and its mother tissue the liquid MS culture medium, culturing, separating the adventitious root from its mother tissue, and culturing the adventitious root in liquid MS culture medium containing indole-butanoic acid and/or naphthylacetic acid.

The invention discloses efficient apple tree wound consolidant. The efficient apple tree wound consolidant is prepared from, by weight, 11-13 parts of Arabic gum, 14-16 parts of tara gum, 18-20 parts of salicylic acid, 24-26 parts of potassium citrate, 18-20 parts of fatty alcohol-polyoxyethylene ether, 23-25 parts of octaphenyl polyoxyethyiene, 12-14 parts of coumarone resin, 13-15 parts of petroleum resin, 9-11 parts of aldehyde ketone resin, 29-31 parts of alpha-pimacol, 36-38 parts of brassinolide, 34-36 parts of kinetin and 43-45 parts of insecticidal pulp. The efficient apple tree wound consolidant can promote apple tree wounds to heal effectively and fast, injurious insects on the wounds are effectively dispelled and killed, it is avoided that malignant bacteria and pathogenic mildew infect trees through the wounds, nutritional ingredients can be provided for growth of the trees, the biological activity of cells of the trees is improved, robust growth of the trees is promoted, therefore, the yield of apples is increased, and the quality of the apples is improved.

The present invention discloses the process of culturing adventitious root tissue of astragalus, and belongs to the tissue culture of astragalus as one kind of Chinese medicinal materials. The process of the present invention includes soaking astragalus seed in solution with ethanol in 70-75 vol% and sodium hypochlorite in 2 vol% to sterilize and planting in MS culture medium to induce bacteria-free bud; inoculating the cut cotyledon and bud in MS culture medium containing different plant growth regulator to induce callus; transferring the callus in MS culture medium with indolebutyric acid and kinin to induce adventitious root; and finally transferring the adventitious root to liquid culture medium containing the same plant growth regulator for fast growth. The present invention has simple process, high inducing rate, fast adventitious root proliferating speed and other features.

The invention discloses a bean growth healthy agent and an application method thereof, which is composed of 6-furfuryl adenine (kinetin KT), gibberellic acid (GA3), 2-vinyl phosphate (ethephon CEPA) and water; according to the change of environment and temperature of different seasons, kinetin and gibberellic are respectively dissolved by solvent, and are prepared into mother solution with water, and are added with ethephon to be prepared into 100 percent working liquid. Bean seeds and the working liquid are weighed, and the bean seeds are dipped for 4 hours to 6 hours to cause the liquid medicine to be fully absorbed, and the swelled bean seeds are placed in a condition with temperature between 20 DEG C to 30 DEG C, and are rinsed regularly for cultivation. The bean sprouts produced by the invention has regular size, pure white sprout bodies and high commodity rate, which are particularly applicable to the supply of upscale guest houses, hotels and unit canteens and being used as the material of bean sprout cans.

The invention discloses a method for promoting germination of ardisia maclurei seeds. The method comprises the following steps: A, completely soaking pretreated ardisia maclurei seeds into a kinetin solution, wherein the concentration of the kinetin solution is 10-100 mg/ L, and the soaking time is 1-24 hours; B, performing constant temperature incubation on the soaked ardisia maclurei seeds. By the method, the germination rate of the ardisia maclurei seeds can be as high as 92%; the method is simple and convenient to operate, low in cost, high in practicality, free of pollution and easy to popularize; by the method, the germination of the ardisia maclurei seeds can be effectively promoted; the method has the advantages of short germination time and tidy germination; the method has very important ecological and economic significances in protecting ardisia maclurei seed resources in China and prompting large-scale artificial cultivation of ardisia maclurei.

The invention provides a carrot seed germination accelerating method comprising seed selection, seed soaking with a seed soaking agent, microwave nutrient solution seed soaking, refrigerator temperature-varying seed storage, rare earth seed dressing, and finally germination accelerating. The germination accelerating method breaks a dormancy period of seeds, and has the advantages of fast germination, neat heights of germinated seedlings, strong seedlings and high content of trace elements; carbosulfan, maleic hydrazide, thiamethoxam, kinetin KT and the like are added into the seed soaking agent, so that a bactericidal effect is played, at the same time, seed germination is accelerated, and field pests and diseases are fewer after seedlings are transplanted.

The invention provides a formula of an induction medium for efficiently inducing anther culture of japonica rice. The formula of the induction medium comprises the following components in certain proportions: KNO3, (NH4)2SO4, KH2PO4, CaCl2.2H2O, MgSO4.7H2O, Na2-EDTA, FeSO4.7H2O, MnSO4.4H2O, ZnSO4.7H2O, H3BO3, KI, glycerol, Na3C6H5O7.H2O, folic acid, glycine, alanine, lysine, vitamin B1, vitamin B6, niacin, 2-hydroxyethyl trimethyl ammonium chloride, sucrose, plant gel, 2,4-D, NAA, phthalocyanine complex nucleic acid, protolysate, activated carbon, taurine, biotin and plant sulfide kinetin alpha. The induction medium has the advantages that callus of anther of japonica rice can be efficiently induced, the browning can be lowered, and the culture efficiency of the anther of japonica rice can be substantially improved.

The application discloses a composite nutrient solution for adjusting the growth of crops, a preparation method and an application thereof. The composite nutrient solution comprises the following main active components in parts by weight: 0.05-5 parts of kinetin, 0.05-5 parts of 6-benayl aminopurine, 0.05-5 parts of zeatin, 0.01-1 part of diethyl aminoethyl hexanoate and 0.001-0.1 part of brassinolide. The composite nutrient solution disclosed by the application is used for the reproductive growth stage of the crops and can be used for carrying out high-efficiency adjustment on the crops; the composite nutrient solution has the beneficial effects that not only can the set flowers and set fruits be increased and can the effective pollination be improved, but also the stress resistance can be effectively improved, the premature senescence of the crops can be prevented and finally the purpose of increasing the yield of the crops is achieved. The composite nutrient solution has the advantages that the functions are diversified, the use efficiency is high and the use cost is effectively reduced.