Patents
Literature
Patsnap Eureka AI that helps you search prior art, draft patents, and assess FTO risks, powered by patent and scientific literature data.

40 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.

Induction culture medium for embryogenic callus of rubber tree variety heat reclamation 628, method for inducing somatic embryogenesis by induction culture medium and application of induction culture medium

The invention belongs to the technical field of plant tissue culture, and particularly relates to an induction culture medium for embryogenic calluses of rubber tree variety thermal reclamation 628, a method for inducing somatic embryogenesis by using the induction culture medium and application of the induction culture medium. According to the induction culture medium, an improved MS culture medium is used as a basic culture medium, and the induction culture medium further comprises 0.1 g / L to 1 g / L of proline, 0.1 g / L to 1 g / L of arginine, 0.1 g / L to 1 g / L of glutamine, 10 mg / L to 70 mg / L of adenine sulfate, 1 mg / L to 10 mg / L of silver nitrate, 0.2 mg / L to 2 mg / L of 2, 4-D, 0.2 mg / L to 2 mg / L of Zetin and 0.2 mg / L to 2 mg / L of Picloram. According to the method, the somatic embryo occurrence rate can be remarkably increased by optimizing the induction culture medium of the embryogenic callus of the heat reclamation 628, the anther somatic embryo occurrence rate of the heat reclamation 628 of the rubber tree variety can be increased to 50% or above by utilizing the induction culture medium, and the cotyledon embryo occurrence rate can be increased to 20% or above.
Owner:RUBBER RES INST CHINESE ACADEMY OF TROPICAL AGRI SCI

Method for cultivating gene-edited pomegranate by two-step somatic embryogenesis technique

The application discloses a method for cultivating and obtaining gene edited Punica granatum by a two-step somatic embryogenesis technique, which comprises the following steps: material obtaining, obtaining of embryogenic callus, preparation of Agrobacterium tumefaciens liquid, pre-culturing of callus, infection, co-culturing, washing, selection culture, subculture and ex vitro rooting, etc. The application firstly takes Punica granatum stem segments as explants to establish a Punica granatum gene editing plant system and obtain Punica granatum gene editing plants, avoids the separation of offspring traits when taking Punica granatum seed hypocotyls as explants, and lays a good foundation for subsequent researches on Punica granatum gene function and fine variety cultivation; in addition, the application further refines the somatic embryogenesis conditions under the selection pressure of Kan and TMT on the basis of the established Punica granatum somatic embryogenesis, directly transforms embryogenic cells by using the bipolar characteristics of somatic embryos, and thus complete and stable Punica granatum gene editing plants are obtained, and the transformation rate is high.
Owner:ANHUI SCI & TECH UNIV

Method for realizing efficient in-vitro regeneration of tea tree cotyledons through somatic embryo indirect generation way

The invention discloses a method for realizing efficient in-vitro regeneration of tea tree cotyledons through a somatic embryo indirect generation way, and belongs to the technical field of plant tissue culture. The tea tree somatic embryo indirect generation system is successfully constructed by screening culture conditions, a culture medium formula and other methods, and a foundation is laid for construction of a tea tree genetic transformation system and industrialized seedling production; according to the method, immature cotyledons of tea trees are used as explants, the cotyledons are induced to generate calluses, then the calluses are proliferated and differentiated to generate somatic embryos, and the somatic embryos are further differentiated to form complete plants, so that efficient and synchronous propagation of tea tree seedlings is realized, and technical support is provided for high-quality variety propagation and new variety breeding of tea trees; the problems of low propagation coefficient, long growth cycle, serious descendant degeneration and the like in traditional seed propagation of tea trees are solved, and the technical bottlenecks of serious explant browning, high bacterial contamination rate, poor plant growth synchronism and the like in other tissue culture technologies are solved.
Owner:ANHUI AGRICULTURAL UNIVERSITY

Psbhlh35 gene and coding protein and application thereof in somatic embryogenesis of tree peony

This application belongs to the field of plant molecular biology technology and specifically provides a PsbHLH35 gene and encoded protein, and their use in tree peony somatic embryogenesis. A PsbHLH35 gene, comprising the nucleotide sequence shown in SEQ ID NO. 1. A protein encoded by the PsbHLH35 gene, comprising the amino acid sequence shown in SEQ ID NO. 2. A method for using the PsbHLH35 gene in tree peony somatic embryogenesis, comprising the following steps: S1) cloning the PsbHLH35 gene into a vector to construct a PsbHLH35 gene overexpression vector; S2) transforming the PsbHLH35 gene overexpression vector into tree peony. The PsbHLH35 gene of this application has a significant promoting effect on tree peony somatic embryogenesis.
Owner:HENAN AGRICULTURAL UNIVERSITY

Pinus koraiensis pkshr gene and application thereof in regulation of somatic embryogenesis of pinus koraiensis

PendingCN122168624APlant peptidesFermentationBiotechnologyPinus koraiensis
This invention relates to the field of plant genetic engineering technology, and in particular to a red pine. PkSHR Genes and their application in regulating somatic embryogenesis in Korean pine. The Korean pine mentioned... PkSHR The nucleotide sequence of the gene is shown in SEQ ID No. 1. The Korean pine provided by this invention... PkSHR Gene regulation of somatic embryogenesis in Korean pine, overexpression of Korean pine PkSHR The gene significantly improves the yield and quality of Korean pine embryos and promotes the growth of Korean pine seedlings.
Owner:BEIJING FORESTRY UNIVERSITY

Method for promoting fir somatic embryogenesis by using histone deacetylase inhibitor

The invention belongs to the field of seed and seedling cultivation, and particularly relates to a method for promoting fir somatic embryogenesis by using a histone deacetylase inhibitor, which comprises the following steps: disinfecting immature zygotic embryos serving as explants, inoculating the immature zygotic embryos to a DCR culture medium to induce calluses, and culturing in the dark for about 30 days to obtain embryogenic calluses; and then transferring to a DCR induction somatic embryo culture medium containing a histone deacetylase inhibitor TSA (final concentration is 0.5 Mm, 2 mu M, 5 mu M, optimally 2 mu M), and culturing in dark for 25-30 days to induce and differentiate the somatic embryo. By accurately regulating and controlling the adding stage and concentration of the TSA, the cedarwood somatic embryo differentiation efficiency is improved to 60% or above from 20% or below in the prior art, the embryogenic state maintaining time can be prolonged, the problems of low efficiency and poor stability in the prior art are solved, operation is easy and convenient, and the method is suitable for large-scale breeding of excellent cedarwood germplasm.
Owner:RES INST OF SUBTROPICAL FORESTRY CHINESE ACAD OF FORESTRY

Genetic transformation method based on pear somatic embryogenesis

The invention discloses a genetic transformation method based on pear somatic embryogenesis, and belongs to the technical field of genetic engineering and molecular breeding. In order to solve the problems that existing pear genetic transformation is low in transformation efficiency, high in chimera rate, long in period, difficult to obtain gene editing regeneration plants and the like, the invention provides two paths: 1, immature zygotic embryos 30-60 days after pear flowering are taken as explants, resistant plants are directly induced through a somatic embryo regeneration path, and the transformation efficiency within 40-60 days reaches 73.91%; secondly, the embryogenic callus with the consistent genetic background is used as an explant for infection, the embryogenic property is maintained and the proliferation efficiency is improved by optimizing a culture medium formula, and a resistant plant with the consistent genetic background can be obtained within 30-50 days. The method overcomes the defect that regeneration plants are difficult to obtain through existing callus transformation, remarkably shortens the breeding period, is high in transformation efficiency, low in chimera rate and controllable in genetic background consistency, and provides technical support for pear functional genomics research and molecular breeding.
Owner:QINGDAO AGRI UNIV

Application of cobalt chloride in promoting Korean pine somatic embryogenesis

The invention discloses application of cobalt chloride in promoting Korean pine somatic embryogenesis, and belongs to the technical field of plant regeneration. The invention aims to improve the somatic embryo generation efficiency and somatic embryo quality of the Korean pine callus. The invention provides an application of cobalt chloride in promoting Korean pine somatic embryogenesis. The concentration of the cobalt chloride is 50 mu M / L. According to the method, the genetic improvement efficiency of the Korean pine is improved.
Owner:NORTHEAST FORESTRY UNIV

Ailanthus altissima somatic embryogenesis and plant regeneration method

PendingCN121379922APlant tissue cultureHorticulture methodsSomatic embryogenesisAegiceras corniculatum
The invention belongs to the technical field of plant tissue culture, and particularly discloses a somatic embryogenesis and plant regeneration method for ailanthus altissima. The method comprises the following steps: (1) taking a leaf axis, a small leaf or a compound leaf of an ailanthus altissima aseptic seedling as an explant, inoculating the explant on an embryogenic callus induction culture medium, and culturing to form an embryogenic callus; (2) inoculating the embryogenic callus obtained in the step (1) to a somatic embryo induction culture medium for culturing; and (3) selecting embryogenic calluses with good growth vigor and somatic embryos on the surfaces, and subculturing the embryogenic calluses in a somatic embryo germination culture medium to obtain somatic culture seedlings. According to the invention, a somatic embryo regeneration system of Ailanthus altissima is established for the first time, and the problem that the embryonic callus and somatic embryo of Ailanthus altissima are difficult to induce is effectively solved.
Owner:HEBEI ACAD OF FORESTRY SCI

Pinus koraiensis PkDof5.6 gene and application thereof in regulating somatic embryogenesis of pinus koraiensis

PendingCN122012527APlant peptidesFermentationBiotechnologyPinus koraiensis
The invention relates to the technical field of plant genetic engineering, in particular to a pinus koraiensis PkDof5.6 gene and application of the pinus koraiensis PkDof5.6 gene to regulation and control of pinus koraiensis somatic embryogenesis. The nucleotide sequence of the PkDof5.6 gene of the Korean pine is as shown in SEQ ID No. 1 (Sequence Identifier Number 1). The Korean pine PkDof5.6 gene provided by the invention regulates Korean pine somatic embryogenesis, and overexpression of the Korean pine PkDof5.6 gene significantly improves the yield and quality of the Korean pine somatic embryogenesis, and promotes the growth of Korean pine somatic embryogenesis seedlings. The method has important significance in optimizing a Korean pine somatic embryogenesis system and realizing efficient large-scale propagation.
Owner:BEIJING FORESTRY UNIVERSITY

Application of cotton GbCG1 gene in improvement of plant genetic transformation efficiency

The invention discloses an application of a cotton GbCG1 gene in improvement of plant genetic transformation efficiency. Relates to the technical field of transgenosis and provides specific application. According to the invention, a somatic embryo regeneration candidate gene GbCG1 is screened out. The gene is only expressed in sea island cotton, overexpression of GbCG1 in upland cotton can significantly improve the callus differentiation efficiency and shorten the somatic embryo generation period, only 4-5 months are needed from transformation to seedling emergence, the time is 3-5 months faster than that of a control group, and the transformation efficiency is 3.5 times that of the control group. The invention discloses application of a GbCG1 gene in promoting somatic embryogenesis of cotton and improving the gene transformation efficiency, and the callus differentiation efficiency can be remarkably improved by overexpressing the GbCG1 gene. And valuable gene resources are provided for genetic breeding. The method can effectively solve the problem of cotton transformation genotype limitation, and broadens the variety types of cotton genetic transformation receptors.
Owner:INST OF COTTON RES CHINESE ACAD OF AGRI SCI

Application of LhMIR394B gene in enhancing somatic embryogenesis efficiency in hybrid Liriodendron chinense

The present invention discloses the application of the hybrid tulipwood LhMIR394B gene in enhancing the efficiency of somatic embryogenesis, and belongs to the field of plant molecular biology. The application of the hybrid tulipwood LhMIR394B gene in enhancing the efficiency of somatic embryogenesis of the present invention, the nucleotide sequence of the hybrid tulipwood LhMIR394B gene is shown in SEQ ID NO.1. The present invention uses hybrid tulipwood leaves as materials, obtains the hybrid tulipwood LhMIR394B gene by cloning, constructs its overexpression vector pBI121-LhMIR394B on this basis, and transfers it into hybrid tulipwood embryonic callus to obtain transgenic plants. The gene function identification results show that the LhMIR394B gene is an important transcription factor that enhances the efficiency of somatic embryogenesis of hybrid tulipwood, and has good application prospects in plant growth and development and breeding.
Owner:NANJING FORESTRY UNIV

Application of LkHY5 gene in regulation of hybrid larch somatic embryogenesis

ActiveCN121538262BPlant peptidesFermentationBiotechnologyExogenous hormones
The present application relates to the technical field of plant genetic engineering, and particularly relates to application of LkHY5 gene in regulation of somatic embryogenesis of hybrid larch. The present application shows that overexpression of LkHY5 gene promotes somatic embryogenesis on a culture medium containing 30 mg / L of exogenous hormone ABA. Overexpression of LkHY5 gene significantly increases expression levels of LkGBSS1-3 and LkTAN1-1. Overexpression of LkHY5 gene significantly increases contents of starch, maltose, glucose and soluble sugar in callus. Overexpression of LkHY5 gene significantly increases microtubule stability in callus.
Owner:NORTHEAST FORESTRY UNIV

Method for establishing hybrid liriodendron somatic embryogenesis system based on LhAHL10 / 15 gene

The invention discloses a method for establishing a hybrid liriodendron somatic embryogenesis system based on an LhAHL10 / 15 gene, and relates to the technical field of plant genetic engineering. According to the method for establishing the hybrid liriodendron somatic embryogenesis system based on the LhAHL10 / 15 gene disclosed by the invention, the purpose of promoting the generation of the hybrid liriodendron somatic embryogenesis is achieved by promoting the LhAHL15 gene or inhibiting the expression of the LhAHL10 gene; the nucleotide sequences of the LhAHL15 gene and the LhAHL10 gene are respectively as shown in SEQ ID NO. 3 and SEQ ID NO. 1. The result shows that overexpression of the LhAHL15 in the hybrid liriodendron is beneficial for improving the indirect somatic embryogenesis efficiency of the hybrid liriodendron. The overexpression of the LhAHL10 in the hybrid liriodendron can also improve the somatic embryo generation efficiency, but can influence the modeling development process of somatic embryos, so that the development of the somatic embryos is stagnated in the globular embryo stage.
Owner:NANJING FORESTRY UNIV +1

A method for inducing somatic embryogenesis by using dendrobium candidum stem segments

The application discloses a method for inducing somatic embryogenesis by using dendrobium candidum stem segments, which comprises the following steps: taking the dendrobium candidum stem segments with dormant buds as explants; disinfecting the explants; uniformly scratching the surface of the disinfected explants; performing skinning treatment on the disinfected explants; performing dormant bud development induction culture on the skinned explants to obtain the dendrobium candidum stem segments with clustered buds; cutting the dendrobium candidum stem segments with clustered buds to remove the bud tips; uniformly scratching the cut surfaces; and performing somatic embryogenesis induction culture to obtain the dendrobium candidum somatic embryos. The method can be used for directly inducing the dendrobium candidum somatic embryos on a large scale by using the dendrobium candidum stem segments, and the induction time is short. The new buds can be used for successfully inducing the somatic embryo clusters in 60-90 days, so that the dendrobium candidum can be rapidly expanded and multiplied. The method is simple in operation, low in cost, and can be used for inducing the dendrobium candidum without seeds. The method is genetically stable, and can be used for large-scale proliferation in a short time according to the requirements.
Owner:HUAQIAO UNIVERSITY

A method to promote somatic embryogenesis and maturation of Cryptomeria japonica

ActiveCN120323326BBreed fastStable genetic traitsPlant tissue cultureHorticulture methodsBiotechnologyGenetic traits
This invention discloses a method for promoting somatic embryogenesis and maturation in Cryptomeria japonica, belonging to the field of somatic embryogenesis technology. The method involves using immature seed embryos as explants to induce embryogenic callus; transferring the proliferated embryogenic callus to a somatic embryogenesis induction medium for further culture to obtain somatic embryos; transferring the somatic embryos to a somatic embryogenesis maturation medium for dark culture to obtain mature cotyledonary embryos; transferring the mature cotyledonary embryos to a somatic embryogenesis basal medium for light culture to obtain somatic embryonic seedlings; and hardening off the seedlings before transplanting to obtain regenerated plants. The results of this application show that embryogenic callus can be stably obtained from different families, with high somatic embryogenesis maturation capacity and rate, enabling the cultivation of a large number of high-quality seedlings with stable genetic traits in a short time; avoiding the phenotypic segregation problem caused by gene recombination during seed propagation, and ensuring that offspring plants inherit the superior characteristics of the parents.
Owner:NANJING FORESTRY UNIV

Method for efficiently obtaining aralia elata tetraploid based on somatic embryogenesis

PendingCN122030260APlant tissue cultureHorticulture methodsAralia elataSomatic embryogenesis
The invention provides a somatic embryogenesis-based aralia elata tetraploid efficient induction method. The method comprises the following steps: taking an aralia elata terminal bud as an explant to induce a callus; after multiple times of subculture, taking the callus and inducing to generate somatic embryos; after the somatic embryos are cultured and treated by 0.02% colchicine for 3 days, the somatic embryos are continuously cultured and induced to generate embryogenic calluses, the somatic embryos are differentiated after proliferation, and regenerated plants are obtained after the somatic embryos are mature. When the regenerated plant grows to 5-10cm, taking the diploid aralia elata plant as a contrast, utilizing a flow cytometry to preliminarily detect the doubled plant, taking the root tip of the doubled plant to identify the number of chromosomes, and screening out the aralia elata tetraploid plant. The morphology of tetraploid and diploid tissue culture seedling and soil culture seedling plants is observed and compared, and it is found that compared with diploid tissue culture seedlings and soil culture seedlings, the tetraploid plants grow shorter on the whole and have thicker stems; the leaves of the tetraploid aralia elata tissue culture seedlings and soil culture seedlings are wider and shorter, the color is darker, and the leaf cracks are more obvious. According to the technical system, the highest induction rate of the aralia elata tetraploid can reach 17.26%, and tetraploid nursery stocks can be obtained after 6 months.
Owner:NORTHEAST FORESTRY UNIV

Pine somatic embryogenesis method

PendingCN121420893APlant tissue cultureHorticulture methodsBiotechnologyForest development
The invention discloses a pine somatic embryogenesis method, and belongs to the technical field of plant tissue culture efficient propagation. According to the method, an immature zygotic embryo is taken as an explant, and after disinfection, a stable regeneration system is established through optimized stages of embryogenic callus induction, proliferation, somatic embryo induction, germination, rooting culture and the like. The culture medium formula in each stage is optimized, and the somatic embryo induction efficiency is high. The method provided by the invention solves the problems of low seed germination rate and inconsistent time of natural breeding of the pine, can be used for germplasm resource protection, genetic improvement, large-scale seedling cultivation, assistance of ecological barrier construction and economic forest development, and lays a foundation for functional verification of stress-resistant genes.
Owner:NORTHEAST FORESTRY UNIV

Application of LkHY5 gene in regulation and control of somatic embryogenesis of hybrid larch

ActiveCN121538262APlant peptidesFermentationBiotechnologyExogenous hormones
The invention relates to the technical field of plant genetic engineering, in particular to application of an LkHY5 gene in regulation and control of hybrid larch somatic embryogenesis. Results of the invention show that overexpression of the LkHY5 gene promotes somatic embryogenesis on a culture medium containing 30 mg / L of exogenous hormone ABA. The expression levels of LkGBSS1-3 and LkTAN1-1 are remarkably improved by overexpression of the LkHY5 gene. The overexpression of the LkHY5 gene significantly improves the contents of starch, maltose, glucose and soluble sugar in the callus. The overexpression of the LkHY5 gene significantly improves the stability of the callus microtubules.
Owner:NORTHEAST FORESTRY UNIV

Method for efficiently inducing generation of hybrid liriodendron somatic embryos

The invention discloses a method for efficiently inducing hybrid liriodendron somatic embryogenesis, and belongs to the technical field of plant embryogenesis. The method mainly comprises the following steps: performing callus multiplication culture on embryogenic calluses of hybrid liriodendron in a callus multiplication culture medium containing a DNA methyltransferase inhibitor 5-Aza-dC or Zebularine, then transferring the embryogenic calluses into a somatic embryo induction culture medium for somatic embryo induction, and obtaining mature hybrid liriodendron somatic embryos after somatic embryo induction is completed. The method is easy to operate, and the effects of inhibiting mass proliferation of embryonic tissues, promoting generation and development of somatic embryos and improving the somatic embryo generation efficiency can be achieved only by adding a proper amount of DNA methylated transferase inhibitor in the callus proliferation stage. The method can enhance the somatic embryo induction efficiency of the hybrid liriodendron, provides a new technical scheme for optimizing the somatic embryo generation of the hybrid liriodendron by using an epigenetic regulation means, and has important application value in the field of rapid propagation of the hybrid liriodendron.
Owner:NANJING FORESTRY UNIV

A method for promoting rubber tree somatic secondary somatic embryogenesis and plant regeneration and application thereof

PendingCN122439613ABiotechnologySomatic embryogenesis
The present application relates to the technical field of rubber tree breeding, and particularly relates to a method for promoting rubber tree somatic embryo secondary somatic embryogenesis and plant regeneration and application thereof. The present application provides application of magnesium hydride in promoting rubber tree somatic embryo callus induction, secondary somatic embryogenesis or plant regeneration. Based on the research results, magnesium hydride exhibits a significant regulation effect in the process of rubber tree somatic embryogenesis, development and plant regeneration. Through treatment of magnesium hydride with a suitable concentration, the induction efficiency can be effectively improved, and the growth state of callus is optimized, so that the callus presents a high-quality morphology with loose structure and fresh color. In terms of plant regeneration, magnesium hydride treatment significantly improves the germination rate, promotes the optimization of growth indexes such as plant height, stem diameter, root length and leaf number of regenerated plants, and improves the construction quality and growth potential of plants. In summary, magnesium hydride provides a new technical approach for the establishment of efficient and stable somatic embryogenesis system and plant regeneration of rubber tree.
Owner:RUBBER RES INST CHINESE ACADEMY OF TROPICAL AGRI SCI

A visual detection technique for autophagy activity of cotton callus cells

The application discloses a kind of cotton callus autophagy activity visual detection technology, first using pretreatment buffer to incubate callus, then using PBS buffer transition, using MDC dyeing liquid is dyed, prepare cell suspension, observation.The application increases the level of cell autophagy by pretreatment induction, significantly improves the fluorescence staining intensity, improves the contrast of specific dyed autophagosome and background, so that autophagy in cell is more easily observed;Meanwhile, the pretreatment buffer has the effect of maintaining osmotic pressure, keeping liquid environment pH stable and providing basic nutrition, which can significantly improve the stability of staining.The application uses PBS buffer to wash, which can avoid over-staining and reduce the degree of background clutter.The staining step of the application is more simple, with clear staining levels and clear cell contrast, so that the autophagy phenomenon in plant somatic embryogenesis process is efficiently visualized.
Owner:ZHENGZHOU UNIV +1

GhRCAR3 gene and application thereof in accelerating differentiation of embryogenic callus of cotton

The invention discloses a GhRCAR3 gene and application of the GhRCAR3 gene in acceleration of embryogenic callus differentiation of cotton. The nucleotide sequence of the GhRCAR3 gene is as shown in SEQ ID NO. 3. The overexpressed GhRCAR3 gene disclosed by the invention can be used for rapidly inducing the callus to be differentiated into the embryonic callus. Therefore, the GhRCAR3 gene plays an important role in the aspect of somatic embryogenesis of cotton. Therefore, overexpression of the gene and application of the gene to commercial cotton varieties difficult in genetic transformation are beneficial to acceleration of the callus induction process, technical support is provided for cultivation of high-quality cotton germplasm with high yield and stress resistance, and the gene is suitable for popularization and application.
Owner:XINJIANG ACAD OF AGRI SCI (XINJIANG BRANCH OF CHINESE ACAD OF AGRI SCI)

A method for inducing somatic embryogenesis in hypocotyls of grape seedlings

The present application relates to the technical field of plant tissue culture, and particularly discloses a method for establishing a grape seedling hypocotyl induced somatic embryo regeneration system, which comprises the following steps: taking secondary embryos obtained by using seedless grape embryos to rescue deformed seedling hypocotyls as explants, inducing the explants in KBN medium to obtain embryogenic calli, non-embryogenic calli and secondary proembryo groups, inoculating the secondary proembryo groups in X6 medium to proliferate and culture the secondary proembryo groups and somatic embryos, performing secondary induction on the somatic embryos before cotyledon stage to establish a somatic embryo maintaining and proliferating circulation system, inoculating the somatic embryos into X3 medium to differentiate hypocotyls and radicles, and transferring the somatic embryos to WPM medium to grow into seedlings. The present application successfully induces the regeneration system of the secondary proembryo groups obtained by using seedless grape embryos to rescue deformed seedling hypocotyls, and successfully establishes a secondary proembryo group maintaining and proliferating circulation system, which can provide new recipient materials for grape genetic transformation.
Owner:NORTHWEST A & F UNIV

A method for regulating somatic embryogenesis in hybrid tulip trees based on ethephon

ActiveCN118680068BPlant tissue cultureHorticulture methodsBiotechnologySomatic embryogenesis
This invention discloses a method for regulating somatic embryogenesis in hybrid tulip trees based on ethephon, belonging to the field of somatic embryogenesis technology. The method involves inoculating embryogenic callus tissue from hybrid tulip trees into an induction medium containing ethephon or silver nitrate for induction treatment, thereby regulating the somatic embryogenesis efficiency of the hybrid tulip trees. Exogenous application of ethephon promotes the development of XY-TN, LWS-TN, XY-LWS, and XY-LP genotypes; exogenous application of silver nitrate promotes the development of the XY-TN genotype but inhibits the somatic embryogenesis of the LWS-TN, XY-LWS, and XY-LP genotypes. Furthermore, orthogonal experimental results show that the somatic embryogenesis induction effect is best for all genotypes when only ethephon is added without abscisic acid, proving that the combined effect of abscisic acid and ethephon does not enhance the somatic embryogenesis of hybrid tulip trees.
Owner:NANJING FORESTRY UNIV

Application of flavonoids in promoting embryogenic maintenance of korean pine callus and somatic embryogenesis of korean pine

The application discloses application of flavonoids in promoting embryogenic maintenance of Pinus koraiensis callus and somatic embryogenesis of Pinus koraiensis and belongs to the technical field of plant tissue regeneration. The application provides application of flavonoids in promoting embryogenic maintenance of Pinus koraiensis callus, somatic embryogenesis of Pinus koraiensis and reduction of active oxygen, wherein the flavonoids are quercetin, naringenin or catechin. The method improves the genetic improvement efficiency of Pinus koraiensis.
Owner:NORTHEAST FORESTRY UNIV

Taxodium Zhongshanha ThWOX9 gene and application thereof in regulation and control of leaf character size

PendingCN120795109ABacteriaMicroorganism based processesBiotechnologySomatic embryogenesis
The invention belongs to the technical field of plant genetic engineering, and particularly relates to a taxodium Zhongshanha ThWOX9 gene and application thereof in regulation and control of leaf character size. The invention provides a ThWOX9 gene for regulating and controlling the shape and / or size of a Taxodium Zhongshanha leaf. An amino acid sequence coded by the ThWOX9 gene is as shown in SEQ ID NO: 2. Experiments show that through overexpression of the ThWOX9 gene in crop arabidopsis thaliana, the leaf size of the crop can be reduced, the leaf is curled, and the somatic embryogenesis rate of the crop is increased. Therefore, the ThWOX9 gene screened by the invention provides a new thought for crop breeding.
Owner:INST OF BOTANY JIANGSU PROVINCE & CHINESE ACADEMY OF SCI

Method for promoting oil palm callus proliferation and somatic embryo induction by utilizing baicalin

ActiveCN121942578AIncrease callus proliferation rateReduce the risk of subsequent regenerative deformitiesPlant tissue cultureHorticulture methodsBiotechnologyPlant hormone
The invention discloses a method for promoting oil palm callus proliferation and somatic embryo induction by utilizing baicalin. Oil palm tender yellow leaves are used as tissue culture explants, a Y3 culture medium is used as a basic culture medium, and baicalin is added to promote oil palm callus induced proliferation and somatic embryogenesis. Wherein 0.5 mg / L of baicalin is added in the callus induction proliferation stage, the effect of part of 2, 4-D or dicamba can be replaced, the dosage of 2, 4-D or dicamba is reduced, the risk of subsequent regeneration malformation is reduced, the callus induction time is shortened by 20 days, and the callus proliferation rate is increased by 48.19%; 0.3 mg / L of baicalin is added in the somatic embryo induction stage, so that plant hormone 6-BA can be completely replaced, meanwhile, the somatic embryo induction time is shortened by 31 days, and the somatic embryo induction rate is increased by 5%. Therefore, by adding the baicalin into the culture medium, the callus proliferation and somatic embryo induction efficiency of the oil palm can be improved, the induction time is shortened, and the method has good popularization and application prospects in the field of tissue culture and rapid propagation of the oil palm.
Owner:SANYA RES INST OF CHINESE ACAD OF TROPICAL AGRI +1

Application of CsFIP37 gene in regulating somatic embryogenesis in citrus

The present invention relates to the application of CsFIP37 gene in regulating citrus somatic embryogenesis, by constructing m 6 A modified A-modified overexpression vector for CsFIP37, a key component of the methyltransferase complex, was transformed into calli of the cultivar 'Guoqing No. 1,' which has lost its ability to produce somatic embryos. The study revealed that CsFIP37 promotes somatic embryogenesis in citrus. This study provides insights into the regulatory mechanisms of somatic embryogenesis, providing new insights into fundamental aspects of somatic embryogenesis and potentially significant for improving the yield and quality of agronomically important crops.
Owner:HUAZHONG AGRI UNIV

Application of a CseIF5A2 gene and its encoded protein in citrus somatic embryogenesis

This invention provides an application of the CseIF5A2 gene and its encoded protein in citrus somatic embryogenesis. The invention identified the protein CseIF5A2 in sweet orange, constructed an RNA interference vector to transform 'Folengxia' embryogenic callus, and specifically interfered with CseIF5A2 gene expression, significantly enhancing its somatic embryogenesis ability. After interfering with CseIF5A2 expression, the mRNA content of key somatic embryogenesis genes such as LEC1, AGL15, and HB1 in the translational state increased, indicating that CseIF5A2 negatively regulates the translation efficiency of these genes, inhibiting somatic embryogenesis. Mechanistically, interfering with CseIF5A2 expression mainly affects the translational level rather than the transcriptional level. Furthermore, CseIF5A2 participates in this process by regulating the autophagy-mediated starch metabolism pathway. This invention provides a new target and application strategy for improving citrus regeneration efficiency, yield, and quality.
Owner:HUAZHONG AGRI UNIV