53 results about "Spermatophyte" patented technology

A method is described for the extraction of products having a pharmacological activity, in particular an anti-tumoral activity, from spermatophyte plants. Said products, which are to be used in the pharmaceutical field, consist of complex mixtures of compounds characterized by one or more stilbene groups, variously hydroxylated and/or glucosidated, and of compounds derived from said group by natural enzymatic biosynthetical processes (stilbenoids). The following compounds are preferred: C-Res, glucosidated C-Res, epsilon-viniferine, H-gnetine, r-2-viniferine, r-viniferine, hopeaphenol, Ampelopepsin A and glucosidated T-Res.

A method for restoring aquatic vegetation in eutrophicated shellow lake features that the hygrophyte, emergent aquatic plant and flootingleaf and floating plants are used to create a biologic fence for improving the local environment of outrophicated water, and the pilot nursing spermatophyte, following equatic and target plants are gradually introduced into the said fence to form a stable cycle of different aquatic plants in the year round.

The invention discloses a specific primer pair for identification of spermatophyte species and applications of the specific primer pair. The invention provides a pair of specific primers consisting of a single stranded DNA (Deoxyribose Nucleic Acid) A and a single stranded DNA B. The single stranded DNA A is 15-40bp and has a DNA fragment same as the DNA fragment shown as a sequence I in a sequence table. The single stranded DNA B is 15-40bp and has a DNA fragment same as the DNA fragment shown as a sequence II of the sequence table. In the invention, with the ycflb gene of a plant to be tested as a template, the DNA fragment obtained by PCR (Polymerase Chain Reaction) amplification with the specific primer pair is also protected. The DNA fragment can be used for assisting identification of the spermatophyte species. The specific primer pair can be used for developing general kits, effectively identifying land plant species, and promoting the development of plant DNA bar codes, contributing to social progress.

The invention relates to a rapid cloning method of plant flowering related gene LFY/FLO homologous fragments and special primers thereof, and relates to the technical field of rapid isolation and cloning of plant homologous genes. The method is characterized in that the used special primer LYF has a nucleotide sequence of 5'-TAYATIAAYAARCCIAARATG-3', and LYR has a nucleotide sequence of 5'-ARIYKIGTIGGIACRTACCA-3'; the primer concentration is 25 muM, and the annealing temperature is 44 DEG C. The method of the invention can clone to obtain homologous fragments of LFY/FLO genes of plants from bryophytes to spermatophytes, and has a wide range of the kinds of applicable plants; the potential problem that a gene fragment is difficult to be amplified due to no expression or low expression of homologous fragments of the LFY/FLO gene when cDNA is used as a template is well avoided; and the method is rapid, simple, economical, and effective.

The invention discloses a grain weight-associated protein originated from soybean and a related biomaterial thereof, and application thereof. The protein provided by the invention is named as GmHSFA2 and is a protein as described in a) or b), wherein a) is a protein with an amino acid sequence as shown in SEQ ID No. 2, and and b) is a protein derived from a) through substitution and/or deletion and/or addition of one or more amino acid residues in the amino acid sequence represented by SEQ ID No. 2 in a sequence table and related to grain weight. Experimental results prove that GmHSFA2 and the biomaterial related to GmHSFA2 can be applied to regulating the grain weight of spermatophytes, especially to increasing of the grain weight of spermatophytes.

The invention provides a natural flower petal lotion and the preparation method thereof. The natural flower petal lotion comprises the following components by weight percentage: 1% to 5% of humectant, 5% of glycerol, 0.01% to 1.25% of antiseptics, 0.01% to 0.05% of buffer, 1% to 15% of plant extractive liquid, 1% to 13% of Spermatophyta plant extract mixture, 2% of chamomile extractive liquid, 2% of green cucumber extractive liquid, 2% of marigold extractive liquid, 3% of aloe extractive liquid, 0.1% to 1% of natural flower petals, 0.1% to 2% of Spermatophyte flower petals, and water in balancing amount. The natural flower petal lotion has the advantages of unique formula, natural active component, no side effect and environmental friendliness; and the lotion is the easy-to-use product which is applied in an appropriate amount to the face without washing, and has significant effect.

Chloropentafluoropropene is employed as a herbicide for the effective control of undesirable spermatophyte growth.

The invention relates to a botanic vegetative growth maintenance gene system, the establishment of a vegetative growth maintenance plant, and a method for utilizing the infinite growth capacity of seed plants. The vegetative growth maintenance gene system comprises a promoter, a cellular lethal factor gene, and a gene device which is arranged when necessary and is used for limiting or eliminating the toxicity of non-target cells of the vegetative growth maintenance gene system; and the utilization of the infinite growth capacity of the seed plants is that the gene system is integrated into a botanic nuclear genome and accurately and correctly begins to perform expression according to given tissues and organs and the specificities of developmental stages. The vegetative growth maintenance gene system can effectively remove cells of reproductive meristems which appear in vegetative apical meristems, and prevent the vegetative meristems from being differentiated, so that a novel, high-yield and high-quality vegetative mass utilization plant, namely the vegetative growth maintenance plant is created; and the vegetative growth maintenance gene system can be applied to all vegetative mass utilization plants, so that the growth speed, production efficiency and yield of vegetative masses of the vegetative mass utilization plants are greatly improved on the original basis.

The invention provides an application of protein in regulating and controlling the selenium content of plant tissues and/or organs. The protein is any one of the following proteins: a) protein with anamino acid sequence as shown in SEQ ID No.7; b) fusion protein obtained by connecting a label to an N terminal or/and C terminal of the protein as shown in SEQ ID No.7; and c) protein related to selenium metabolism and obtained by substituting and/or deleting and/or adding one or more amino acid residues to the amino acid sequence as shown in SEQ ID No.7. The selenium content of the plant tissuesand/or organs is regulated and controlled to increase the selenium content of the plant tissues and/or organs. The selenium content in the plant tissues and/or organs is regulated and controlled to increase the selenium content in the plant tissues and/or organs. The organs are seeds; and plants are spermatophytes.

The invention discloses a specific expression promoter for a plant embryo and application thereof. The promoter is derived from (1) a DNA (Deoxyribonucleic Acid) sequence shown as a sequence 1 in a sequence table, (2) a DNA sequence having over 70 percent of homology with the DNA sequence defined by the sequence 1 in the sequence table and having the function of a specific expression promoter forthe plant embryo, and (3) a nucleotide sequence which can be hybridized with the DNA sequence defined by the sequence 1 in the sequence table under a highly serious condition. The promoter can be used for promoting specific expression of an exogenous gene in the plant embryo, and is suitable for any seed plant.

The invention discloses a specific expression promoter for a plant embryo and application thereof. The promoter is derived from (1) a DNA (Deoxyribonucleic Acid) sequence shown as a sequence 1 in a sequence table, (2) a DNA sequence having over 70 percent of homology with the DNA sequence defined by the sequence 1 in the sequence table and having the function of a specific expression promoter forthe plant embryo, and (3) a nucleotide sequence which can be hybridized with the DNA sequence defined by the sequence 1 in the sequence table under a highly serious condition. The promoter can be used for promoting specific expression of an exogenous gene in the plant embryo, and is suitable for any seed plant.

A method for reducing salinity stress symptoms in a seed plant, comprising the step of adding carbon-based nanomaterials into a salinity growth medium in which the seed plant is cultivated, the salinity growth medium is in a salinity condition which causes the seed plant cultivated in the growth medium demonstrates the salinity stress symptom.

The invention is in the field of Brassica carinata breeding (i.e. Ethiopian mustard breeding), specifically relating to Brassica carinata variety DH-153.113. The present invention relates to seeds, plants or parts thereof, cells, methods of making, and uses of this variety and its progeny.

The invention is in the field of Brassica carinata breeding (i.e. Ethiopian mustard breeding), specifically relating to Brassica carinata variety DH-140.356. The present invention relates to seeds, plants or parts thereof, cells, methods of making, and uses of this variety and its progeny.

The present disclosure provides alfalfa plants exhibiting broad spectrum resistance to Race 1, Race 2, and Race 5 anthracnose. Such plants may comprise novel introgressed genomic regions associated with disease resistance from Race 1, Race 2, and Race 5 anthracnose. In certain aspects, compositions, including novel polymorphic markers and methods for producing, breeding, identifying, and selecting plants or germplasm with a disease resistance phenotype are provided. Also provided are alfalfa varieties designated as C0416C4164 and H0415C4114. Provided by the invention are the seeds, plants and derivatives of alfalfa varieties C0416C4164 and H0415C4114. Also provided by the invention are tissue cultures of alfalfa varieties C0416C4164 and H0415C4114, and the plants regenerated therefrom. Still further provided by the invention are methods for producing alfalfa plants by crossing alfalfa variety C0416C4164 or H0415C4114 with itself or another alfalfa variety and plants produced by such methods.

The invention is in the field of Brassica carinata breeding (i.e. Ethiopian mustard breeding), specifically relating to Brassica carinata variety DH-129.B036. The present invention relates to seeds, plants or parts thereof, cells, methods of making, and uses of this variety and its progeny.

In an embodiment, the invention relates to the seeds, plants, and plant parts of canola variety SCV299420 and to methods for producing a canola plant produced by crossing canola variety SCV299420 with itself or with another canola variety. The invention also relates to methods for producing a canola plant containing in its genetic material one or more transgenes and to the transgenic canola plants and plant parts produced by those methods. This invention also relates to canola varieties or breeding lines and plant parts derived from canola variety SCV299420, to methods for producing other canola varieties, lines or plant parts derived from canola variety SCV299420 and to the canola plants, varieties, and their parts derived from use of those methods. The invention further relates to hybrid canola seeds, plants and plant parts produced by crossing the variety SCV299420 with another canola variety.

A new and distinct watermelon variety NUN 11802 WMW is disclosed as well as seeds and plants and fruits thereof. NUN 11802 is a round oval, diploid watermelon variety of the mini-seeded type, comprising resistance to Fusarium oxysporum f. s.p niveum Race 0 and Race 1.

A new and distinct hybrid watermelon variety NUN 11801 WMW is disclosed as well as seeds and plants and fruits thereof. NUN 11801 is an oval small, diploid watermelon varieties of the mini-seeded type, comprising resistance to Fusarium oxysporum f s.p niveum Race 0 and Race 1.