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25 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.

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

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 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

ActiveCN117617120BPlant tissue cultureHorticulture methodsDendrobium candidumSomatic embryogenesis
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

PendingCN121369230APlant tissue cultureHorticulture methodsBiotechnologyTransferase inhibitor
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

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

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 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

A method of pear somatic embryogenesis

ActiveCN119422884BPlant tissue cultureHorticulture methodsSomatic embryogenesisTransgenesis
The present application belongs to the field of biotechnology, and particularly relates to a method for somatic embryogenesis of pear. The method comprises the following steps: fruit collection and explant obtaining; inducing somatic embryogenesis by using immature zygotic embryo as explant; inducing embryogenic callus by using immature zygotic embryo as explant; subculture of embryogenic callus and embryogenic maintenance; somatic embryogenesis of embryogenic callus; strong seedling and rooting culture of regenerated plant; and seedling raising and transplanting. The two somatic embryogenesis induction pathways of the present application, which use immature zygotic embryo and embryogenic callus as explants, have high regeneration efficiency, good genetic stability, good universality, short induction time from explant to regenerated plant, and are a high-efficiency pathway for in vitro rapid propagation of pear. Meanwhile, the method can help to improve the genetic transformation efficiency of pear, enhance the genetic stability of transgenic plants, and reduce the occurrence probability of transgenic plant chimeras.
Owner:QINGDAO AGRI UNIV

Method for promoting regeneration of somatic embryos of sweet sorghum

The invention discloses a method for promoting regeneration of somatic embryos of sweet sorghum. The method comprises the following steps: (1) disinfecting mature sorghum seeds; (2) preparing a culture medium with a first 2, 4-D concentration gradient; (3) sowing sorghum seeds on a first 2, 4-D concentration gradient culture medium, carrying out dark treatment for 1-5 weeks, and inducing to obtain calluses; (4) preparing a culture medium with a second 2, 4-D concentration gradient; and (5) subculturing the callus to the second 2, 4-D concentration gradient culture medium prepared in the step (4), carrying out photoperiod of 16h / 8h and treatment time of 1-5 weeks, and obtaining the type 2 embryogenic callus at the hypocotyl after culture. The method can efficiently and stably promote the regeneration of the somatic embryos of the sweet sorghum, and overcomes the defects of long preparation period and high cost of the immature embryos of the sorghum; the problem of annual supply of sorghum gene editing receptors is solved.
Owner:LIAONING ACAD OF AGRI SCI

LdBBM13 gene for regulating organogenesis and somatic embryogenesis of Lanzhou lily and application of LdBBM13 gene

The invention provides an LdBBM13 gene for regulating organogenesis and somatic embryogenesis of Lanzhou lily and application of the LdBBM13 gene, and belongs to the field of research on growth and development of bulb flower organs. The functions of the LdBBM13 gene in organogenesis and somatic embryogenesis are disclosed by adopting a VIGS silencing technology and a heterologous overexpression method and combining histomorphological observation and transcriptional regulation analysis. Researches show that overexpression of the LdBBM13 gene can significantly improve the induction rate of arabidopsis thaliana calluses, and silencing of the gene can inhibit generation of Lanzhou lily scale induced somatic embryos. The LdBBM13 gene provides a basis for developing a transgenic lily bulb marker gene related to organogenesis by using the LdBBM13 gene, and the Lanzhou lily bulb regeneration and seedling breeding process can be accelerated.
Owner:BIOLOGICAL TECH INST OF FUJIAN ACADEMY OF AGRI SCI

PROPAGATION PROCESS OF EUCHEUM DENTICULATUM (Spiny Seaweed)

This invention proposes a process for propagating spiny cartilage seaweed (E. denticulatum) using callus tissue culture based on a callus-embryo-synthesis-complete seedling regeneration process, allowing for the creation of disease-free, uniform, and high-growth-potential seed sources. The process includes the following steps: acclimatization of broodstock using seawater filtration combined with AgNPs; sterilization and sample preparation; callus induction on solid PES medium; stimulation of somatic embryogenesis using a combination of plant growth regulators NAAA-BAP; and seedling regeneration on a suitable medium. This process increases the multiplication rate, shortens seedling production time, reduces genetic degeneration, and facilitates scaling up production in laboratory and seaweed breeding facilities in Vietnam.
Owner:INST OF OCEANOGRAPHY - VIETNAM ACAD OF SCI & TECH