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329 results about "Somatic embryogenesis" patented technology

Somatic embryogenesis is an artificial process in which a plant or embryo is derived from a single somatic cell. Somatic embryos are formed from plant cells that are not normally involved in the development of embryos, i.e. ordinary plant tissue. No endosperm or seed coat is formed around a somatic embryo. Applications of this process include: clonal propagation of genetically uniform plant material; elimination of viruses; provision of source tissue for genetic transformation; generation of whole plants from single cells called protoplasts; development of synthetic seed technology. Cells derived from competent source tissue are cultured to form an undifferentiated mass of cells called a callus. Plant growth regulators in the tissue culture medium can be manipulated to induce callus formation and subsequently changed to induce embryos to form the callus. The ratio of different plant growth regulators required to induce callus or embryo formation varies with the type of plant. Somatic embryos are mainly produced in vitro and for laboratory purposes, using either solid or liquid nutrient media which contain plant growth regulators (PGR’s). The main PGRs used are auxins but can contain cytokinin in a smaller amount. Shoots and roots are monopolar while somatic embryos are bipolar, allowing them to form a whole plant without culturing on multiple media types. Somatic embryogenesis has served as a model to understand the physiological and biochemical events that occur during plant developmental processes as well as a component to biotechnological advancement. The first documentation of somatic embryogenesis was by Steward et al. in 1958 and Reinert in 1959 with carrot cell suspension cultures.

Preparation method of virus-free seedlings of sweet potato

The invention provides a preparation method of virus-free seedlings of sweet potato. The method comprises the following steps: placing sweet potato blocks that are exposed under the sun and matured banana together for 3 to 5 days; planting the sweet potatoes in sandy soil to accelerate the germination in a culture box; setting relatively high temperature; picking 1-2cm top end of the seedling based on the length; cutting off the visual leaves; disinfecting the surface; rinsing with sterile water; picking off stem tip with 1 to 2 leaf primordium; inoculating to the corresponding culture medium to respectively induce differentiation of adventitious buds and generation of somatic embryogenesis; performing virus detection to a regeneration plant; performing subculture for the virus-free seedling; hardening-seedling; directly planting into a plastic greenhouse; performing flood irrigation with more water; preventing direct exposing under sun at noon in the first two weeks after transplanting; applying urea three weeks after transplanting; watering to obtain virus-free seedlings. According to the preparation method of the virus-free seedlings of sweet potato, the virus-free test-tube plantlets are acclimated and then directly planted into the plastic greenhouse, thus the survival rate is obviously raised, and the operation processes are decreased; the process of acclimating in an acclimating room is saved, and as a result, labor, materials and property are saved.
Owner:QINGDAO AGRI UNIV

Method of somatic embryogenesis of cassava and rapid propagation of regenerated plant

The invention relates to a tissue culture propagating method of Manihot esculenta Crantz. As one of the global three-top tuber crops and the number one alimentarn crop in Africa, the Manihot esculenta Crantz is currently ranked as a vital biological energy crop in our country. Stem section vegetative cottage is commonly adopted for propagation, and the low propagation rate thereof is a restrictive factor for popularizing the new variety and shortening the breeding period. The method of the invention comprises the following steps: the Manihot esculenta Crantz stem section with stem apexes or lateral buds is taken as an explant, and the Manihot esculenta Crantz tissue culture plantlets are quickly obtained in virtue of the micro-propagation method; young leaves, stem apexes and axillary buds of the sterile plantlets obtained from micro-propagation are taken as explants, somatic embryo generation and plant regeneration are induced, thus the Manihot esculenta Crantz somatic cell regeneration system is established. By adopting the method, the Manihot esculenta Crantz has the advantages of high propagation rate, no genotype dependence, and the like; the method has high value on the quick propagation and large-scale production of the Manihot esculenta Crantz improved variety in a short term, and establishes a technical basis for the Manihot esculenta Crantz transgene and other breeding.
Owner:朱文丽 +4

Method for efficiently regenerating plant through Hedychium coccineum Buch.-Ham somatic embryogenesis

The invention discloses a method for efficiently regenerating plant through Hedychium coccineum Buch.-Ham somatic embryogenesis. The method comprises the following steps of: inducing calluses by using immature filaments and anthers of Hedychium coccineum Buch.-Ham as explants, conducting optimization, screening and subculture to obtain high-quality embryonic calluses, conducting suspension culture to the embryonic calluses and establishing an embryonic cell suspension culture system of Hedychium coccineum Buch.-Ham. A great number of somatic embryos can be obtained by using embryonic cell suspension cultures for inducing somatic embryos, an optimum effect can be obtained by using SH inorganic salt and 150mug.L<-1> TDZ, and the somatic embryo generation rate can reach 4429/ml SCV (settled cell volume); the obtained somatic embryos can germinate seedlings with buds and roots on somatic embryo germination culture medium; and when SH culture medium is used as basic culture medium and the concentration of 6-BA is 0.5-1.0mg.L<-1>, the germination rate of the somatic embryos can reach 100 percent. Due to the method, a foundation is laid for the in-vitro rapid propagation and the biotechnological breeding of Hedychium coccineum Buch.-Ham, the large-scale popularization and application are facilitated and the application prospect is better.
Owner:GUANGDONG UNIV OF EDUCATION

Induction rapid-propagation culture method for Photinia fraseri in-vitro leaf somatic embryos

The invention provides an induction rapid-propagation culture method for Photinia fraseri in-vitro leaf somatic embryos, comprising the following steps: (1) building a regeneration system of a Photinia fraseri asepsis test tube seedling; (2) building a high-frequency rapid-propagation system induced by an in-vitro somatic embryo and an adventitious bud; and (3) rooting, acclimatizing and transplanting for the test tube seedling. The induction rapid-propagation culture method for Photinia fraseri in-vitro leaf somatic embryos is characterized in that coordinated sets of measures of selecting a proper explant, improving a basic culture medium and ingredients, regulating culture conditions and the like are adopted, and the Photinia fraseri of which the seed is difficult to breed is subjected to path rapid propagation by the somatic embryos; the plant transplantation survival rate is higher than 95%; the germchit grows strongly to solve the problem that an excellent germchit quality degenerates, and a great quantity of purified and rejuvenated detoxification nursery stock with good quality can be provided for production; and in addition, and ideal receptor system is provided for breeding new specimens for Photinia fraseri by genetic transformation or mutation breeding.
Owner:JIANGSU POLYTECHNIC COLLEGE OF AGRI & FORESTRY +1

Micropropagation method of fraxinus rhynchophylla

The invention discloses a micropropagation method of fraxinus rhynchophylla and relates to the micropropagation method. The problems of long reproductive cycle, low reproduction efficiency and poor offspring genetic stability in nursery stock propagation of fraxinus rhynchophylla are solved. The method comprises the following steps of: 1, sterilizing fraxinus rhynchophylla seeds, and culturing single cotyledons of zygotic embryos to obtain cotyledonal cell embryos; 2, performing maturation cultivation on the cotyledonal cell embryos; 3, performing sprouting cultivation on the cotyledonal cellembryos subjected to maturation cultivation to obtain regenerated plants; and 4, transplanting the regenerated plants into a culture medium to culture until new leaves are completely unfolded, and removing a covered plastic thin film. The micropropagation method has the advantages of short nursery stock reproductive cycle, high reproductive rate (culturing for 60 to 70 days) and high reproductionefficiency (each explant can generate 15 to 20 somatic embryos); the germination rate of the somatic embryos is up to 87 to 89.55 percent; the transplanting survival rate of the regenerated plants isup to 75 to 80 percent; and the regeneration plants with the same good characteristics as female parents can be generated in mass.
Owner:NORTHEAST FORESTRY UNIVERSITY +2

Somatic embryogenesis method for cunninghamia lanceolata

The invention discloses a somatic embryogenesis method for cunninghamia lanceolata, which comprises the steps of initial induction of an embryogenic suspensor cell mass, maintenance and multiplication of an ESM (embryogenic suspensor mass), and development and maturity of a somatic embryo, wherein the development and maturity of the somatic embryo can adopt an indirect somatic embryogenesis way or a direct somatic embryogenesis way. With the adoption of the somatic embryogenesis method for the cunninghamia lanceolata, browning in an establishment process of the conventional liquid suspension system can be effectively improved, cell division under a low density condition is started, and the stability of suspensor cells is maintained, so that a stable multiplication liquid suspension cell line is established. The somatic embryogenesis frequency of the cunninghamia lanceolata can be increased by about 20 times at most through the direct and indirect somatic embryogenesis ways, the problem of low somatic embryogenesis frequency caused by an incomplete somatic embryogenesis system of the cunninghamia lanceolata can be well solved, the cost is saved, conditions are prepared for factory production of the cunninghamia lanceolata, and a pace of industrial production of the cunninghamia lanceolata is accelerated.
Owner:NANJING FORESTRY UNIV

Method for rapidly propagating aralia elata through somatic embryo and secondary somatic embryogenesis

The present invention provides a method for rapidly propagating aralia elata through somatic embryo and secondary somatic embryogenesis. The invention uses the leaf, petiole and root segment of young seedling of aralia elata as explants. The explants are dark-cultivated for 35 days in the SH cultivation with 3.0mg/L, 2.0mg/L and 0.3mg/L of IBA concentration respectively and 2% of sucrose. The somatic embryo inductivities of three explants can equally obtain 100%. Furthermore each explant generates more somatic embryos (8.6-11.3). The sucrose concentration and IBA can equally affect the generation of secondary somatic embryo. After the explants are dark-cultivated for 4 weeks in the cultivation condition of 3.0mg/L IBA+ 2% of sucrose+ SH culture medium, 100% of somatic embryos are generated with secondary somatic embryos. The obtained mature primary somatic embryos and secondary somatic embryos are transferred to a WPM culture medium with no hormone. The mature primary somatic embryos and secondary somatic embryos can quickly germinate and grow to seedling. The robust seedling with length about 5cm is transplanted into the soil, and the survival rate can obtain 89%. The method which is provided by the invention and has the advantages of simple culturing, short regenerate cycle and capability for continuously obtaining the regenerated plant can be used for the industrial production of aralia elata seedling.
Owner:NORTHEAST FORESTRY UNIVERSITY +1

High-frequency somatic embryo regeneration culture method for overcoming alfalfa variety genotype limitation

InactiveCN101926285AOvercome different breedsOvercoming the genotype restriction problemHorticulture methodsPlant tissue cultureHypocotylSomatic embryogenesis
The invention discloses a high-frequency somatic embryo regeneration culture method for overcoming alfalfa variety genotype limitation, which comprises the following steps of: (1) selecting materials: selecting three explants of the epicotyl, the hypocotyl and the regenerated plant blade of an aseptic seedling after flushing, sterilizing and disinfecting as well as drying a mature alfalfa seed; (2) inoculating the selected explants onto a somatic embryogenesis induced culture medium for culture; (3) inoculating the explants subjected to somatic embryogenesis induced culture onto an embryo successive formation culture medium for culture; (4) inoculating the explants subjected to embryo successive formation culture onto an embryo maturation germination seeding-formation culture medium for culture to form a seedling; (5) carrying out seedling strengthening and rooting culture; and (6) transplanting a regenerated plant to survive. The invention can effectively overcome the problems of different varieties and genotype limitation in alfalfa high-frequency somatic embryo regeneration culture, greatly improves the somatic embryogenesis frequency and the plant regeneration frequency and improves the breeding efficiency.
Owner:JIANGSU POLYTECHNIC COLLEGE OF AGRI & FORESTRY +1
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