30results about How to "High rate of adventitious bud induction" patented technology

The invention discloses a method for inducing and multiplying adventitious buds of Cyclocarya paliurus, belonging to the technical field of plant tissue culture. Select the young shoots of Cyclocarya paliurus as explants, before the explants are induced and value-added culture, the explants are first sterilized and disinfected; the sterilized treatment adopts alcohol treatment for 25-30s, sodium hypochlorite treatment for 3-4min; Adventitious bud induction medium formula: WPM+6‑BA+sucrose+agar powder, and adjust pH to 5.75‑5.85; Cyclocarya adventitious bud proliferation medium formula: WPM+IBA+sucrose+agar powder. The present invention obtains a large amount of adventitious bud materials with strong growth, stretched leaves and high growth in a relatively short period of time by optimizing materials, sterilizing treatment and cultivating formula, laying the foundation for establishing an efficient in vitro rapid propagation system of Cyclocarya paliurus, and also It is of great significance to the protection, development and utilization of Cyclocarya paliurus germplasm resources.

The invention discloses a method for tissue culture and rapid propagation of weeping tube flowers, which comprises the following steps: setting a culture medium; selecting and disinfecting explants to ensure that there are no defects in the outer scales; putting the scale buds after the disinfection treatment on the induction medium Carry out the induction culture of adventitious buds; the induced adventitious bud clusters are multiplied by adventitious buds, and the multiplied adventitious bud clusters are divided into individual plants under aseptic conditions and then transferred to the rooting medium for rooting induction culture; After the induction of rooting, the weeping tube flower plants are transplanted and hardened. The invention can obtain a large amount of high-quality and strong seedlings of the weeping tube flower with the same genetic character in a short period of time.

A method for inducing adventitious buds and plant regeneration of Rhododendron Xing'an relates to the field of plant tissue culture, in particular to a method for inducing adventitious buds and plant regeneration. The purpose is to solve the problem that the existing Xing'an Rhododendron tissue culture organ is difficult and takes a long time. Methods: 1. material collection and processing; 2. adventitious bud differentiation induction and proliferation; 3. adventitious bud elongation induction; 4. adventitious bud rooting culture; 5. seedling hardening and transplanting. In the invention, the hydroponic tender buds of wild plants of Rhododendron Xing'an are used as explants, the induction rate of adventitious buds is as high as 100%, the rooting rate of clump seedlings is as high as 99%, and the survival rate of transplanting is as high as 100%. In about 90 days, starting from the second batch, the culture starts directly from proliferation and differentiation, and it only takes 60 days to reach the seedlings. The present invention is used in the field of plant tissue culture.

The invention discloses a method for inducing adventitious buds by utilizing pinus koraiensis germination-accelerated seed germination buds, and relates to the field of forest seedling propagation. The invention aims to solve the problems that current organogenesis of pinus koraiensis is difficult and a differentiation rate of adventitious buds is low. The method comprises the following steps: (1)taking materials of explants and performing disinfection treatment; (2) performing induction differentiation cultivation on the adventitious buds; (3) performing elongation cultivation on the adventitious buds; and (4) performing rooting induction cultivation on regenerated plants. The method specially comprises the following steps: using germination-accelerated pinus koraiensis seeds as the explants, performing inoculation on a differentiation culture medium by the explants, and performing cultivation for 30 days; and after the adventitious buds are obtained, transferring the adventitious buds to an elongation culture medium, continuing cultivation for 60 days (performing subculture once in the process), when cluster seedlings grow to a length of 2-3 cm, performing cutting, performing separation, transferring the separated seedlings to a rooting medium, and performing domestication. According to the method disclosed by the invention, an induction rate of the adventitious buds reaches92.2%, average quantity of buds per explant is 10-12, and after elongation growth cultivation is performed for 60 days, a height of each bud is 3.5 cm, and the rooting rate reaches 52%.

The invention aims to provide a Valeriana Fauriei Briq. tissue culture breeding method. The method is as below: 1, using young stems of Valeriana Fauriei as explants and conducting aseptic treatment; 2, placing sterile Valeriana Fauriei stems on a solid culture medium to induce adventitious buds; 3, inoculating the adventitious buds onto the solid medium for rooting and seedling, induced; and 4, transplanting the tissue culture seedlings to the culture medium for hardening seedling cultivation. The invention is not limited or influenced by natural conditions and, has the characteristics of fastness and easiness for large scale. The invention can ease the problem of shortage of wild Valeriana Fauriei resources and of destruction of ecological balance caused by overexploitation.

The invention discloses a melon regeneration in vitro method. The melon regeneration in vitro method provided by the invention comprises the following steps: (1) taking a cotyledon of a melon as an explant, inoculating the explant into a shoot induction medium for culturing to obtain an adventitious bud tussock; (2) placing the adventitious bud tussock obtained in the step (1) to a shoot elongation medium A for culturing to obtain an adventitious bud; (3) placing the adventitious bud obtained in the step (2) into a rooting medium for culturing to obtain a melon regeneration seedling. The melon regeneration in vitro method provided by the invention has the advantages of high adventitious bud inductivity, low vitrification degree, short regeneration period and the like, and by applying the method in the melon genetic transformation, a relatively high transformation rate can be obtained.

The invention discloses a method for regeneration plant of tung oil tree leaf, and belongs to the technology field of rapid propagation of tung oil tree. The method comprises the steps of adventitious bud induction directly by tung oil tree leaf, subculture, multiplication culture, strong seedlings culture, rooting culture, acclimatization and transplantation, which not only provides a path for rapid breeding of excellent tung oil tree plants, and lays a solid foundation for improving resistance of the tung oil tree, tung oil tree output and properties of oil quality later on, and for building a tung oil tree genetic system.

The invention provides a method for improving the seedling rate of tissue culture seedlings of hylocereus undulatus britt. The method comprises the following steps: carrying out adventitious bud induction, synchronous multiplication and rooting seedling culture, wherein hylocereus undulatus britt barbed seats and lignification shoots with small barbs and fluff on the barbed seats are used as explants; when lateral branches of adventitious buds grow, base roots of adventitious bud base parts grow and aerial roots of the lateral branches grow, carrying out hardening seedling; after the hardening seedling, taking out seedlings from a bottle; cutting off the lateral branches with the aerial roots and main stems with the base roots and planting in a culture medium; after the lateral branches and the main stems are survived, growing new roots; and putting the lateral branches and the main stems into pots. According to the method, the production period of the tissue culture seedlings of the hylocereus undulatus britt is short, the adventitious bud induction rate is high, the multiplication and the rooting are synchronous, the multiplication coefficient is more than 5.45 and the rooting rate is 100%; the growth vigor of multiplied seedlings is strong and the transplanting survival rate is more than 95%; one inoculated adventitious bud can grow 3-4 lateral branches with the aerial roots, namely one inoculated adventitious bud can grow 4-5 grown-up seedlings with the roots; the seedling rate of the tissue culture seedlings of the hylocereus undulatus britt is increased by 3-4 times.

The invention discloses an establishing method for an efficient regeneration system for multiple-genotype cowpeas. The method comprises the following steps: pretreatment, induction of adventitious buds, subculturing, adventitious bud elongating, rooting culture, seedling hardening and transplanting. In the pretreatment process, 6-BA with the concentration of 1-4 mg / L or TDZ with the concentration of 0.001-0.1 mg / L is used as a plant growth regulator; the induction process of adventitious buds, a composition of 6-BA and KT or a composition of KT and IBA is used as a plant growth regulator, wherein the concentration of the 6-BA is 0.8-1.2 mg / L, the concentration of the KT is 0.02-2 mg / L, and the concentration of the IBA is 0.15-0.25 mg / L; in the adventitious bud elongating process, 6-BA and IBA are used as a plant growth regulator, wherein the concentration of the 6-BA is 0.5 mg / L, and the concentration of the IBA is 0.1-0.3 mg / L. The efficient regeneration system is not only suitable for regeneration culture of the multiple- genotype cowpeas, but also has the advantages of high induction rate, multiple induced adventitious buds, long adventitious buds, high dry weight of adventitious buds, easy implementation conditions and has a good promotion prospect.

The invention discloses a method for rapidly breeding paris polyphylla, mainly aiming at solving the problem of the existing paris polyphylla tuber breeding way in the prior art that, only one bud can be bred by using one tuber, a smaller root is formed, and growing is slow, so that the demand of the existing market on polyphylla breeding cannot be met. The perennial and robust paris polyphylla rhizomes which are not damaged and do not have plant diseases and insect pests are selected as a provenance for breeding; the method comprises the steps of digging out the fresh paris polyphylla rhizomes, washing and then drying in the air, and cutting off adventitious roots on the rhizomes; after that, washing stem internodes with sterile water, then cutting off buds on the stem internodes, and cutting the stem internodes of the rhizomes into blocky structures; inoculating the blocky structures into a breeding culture medium for culturing; when a first true leaf and five adventitious roots grow on one blocky structure, transplanting the blocky structure into soft soil for growing. After the scheme is adopted, the aims of rapidly breeding the paris polyphylla and enabling the paris polyphylla to take more roots are achieved.

The invention belongs to the technical field of plant cultivation, and in particular relates to a method for tissue culture and rapid propagation of Polygonatum long-stalked. A method for tissue culture and rapid propagation of Polygonatum long-stemmed Polygonatum, the method comprising the following steps: (1) disinfection and inoculation of flower buds of Polygonatum long-stemmed; (2) induction of clustered buds; (3) proliferation of adventitious buds; (4) Rooting culture of regenerated plants; (5) Hardening and transplanting. By adopting the method of the present invention, compared with the reported literature, the pretreatment time can be shortened, the explant contamination rate is low, and the adventitious bud generation time can be shortened, thereby obtaining long-stalked Polygonatum regenerated plants faster, which is beneficial to industrial production. By adopting the method of the present invention, the induction rate of adventitious buds of long-stemmed Polygonatum polygonatum clustered buds is as high as 90.0%, the number of adventitious buds is 8.4, the multiplying multiple of adventitious buds can reach 7.7, and the survival rate of transplanted plants can reach more than 95%.

The invention discloses a method for inducing and cultivating hybrid liquidambar tetraploids, which comprises the steps of carrying out pre-differentiation culture treatment on the leaves and petioles of the isolated aseptic plants of the hybrid liquid sweetgum respectively, and then treating the pre-differentiated cultured The leaves and petioles were induced by colchicine respectively. The method of the present invention has a high induction rate of the hybrid liquidambar tetraploid, and a high rate of obtaining the hybrid liquidambar tetraploid, and adopts the method of the present invention to induce and obtain the hybrid liquidambar artificial allotetraploid for the first time, and the number of two heterologous chromosomes Being copied, it has both hybridization effect and ploidy effect, and can produce variation to a greater extent, which provides the possibility to further improve the genetic gain of liquidambar and the selection of improved varieties.

The invention discloses a method for tissue culture and rapid propagation of A. japonica, which comprises the following steps in turn: (1) Disinfection and inoculation of the stem section of A. japonica; (2) induction of clustered buds; (3) proliferation of adventitious buds; (4) rooting culture of regenerated plants; (5) transplanting of hardened seedlings. In the above steps, culture media with different components and ratios are used. By adopting the method of the invention, it is possible to quickly obtain the bubble plant in the field, which is beneficial to industrialized production. By adopting the method of the present invention, the induction rate of adventitious buds of clustered buds of the transplanted bubble can reach as high as 92.5%, the multiplying multiple of adventitious buds can reach 7.2, and the transplanting survival rate of plants can reach more than 95%.