摘要:
The present invention discloses a polynucleotide sequence for an insect salivary glucose oxidase enzyme and the amino acid sequence of the enzyme itself. It also provides recombinant polynucleotide vector systems designed to express the enzyme in a variety of host organisms. The invention also discloses a method for creating transgenic plants having increased resistance to insect predation resulting from the expression of the foreign glucose oxidase protein. The presence of the insect glucose oxidase enzyme triggers a plant's defensive mechanisms and results in increased resistance to insects.
摘要:
The present invention relates to new genes encoding for the production of novel nox enzyme proteins involved in generation of reactive oxygen intermediates that affect cell division. The present invention also provides vectors containing these genes, cells transfected with these vectors, antibodies raised against these novel proteins, kits for detection, localization and measurement of these genes and proteins, and methods to determine the activity of drugs to affect the activity of the proteins of the present invention.
摘要:
The present invention relates to a composition for selectively detecting an extremely small amount of peptidoglycan in sample, a preparation method of the composition, and a detection kit for peptidoglycan. It is possible to quantify a small amount of peptidoglycan contained in human blood, tissue, body fluid, water or food, and to diagnose an infection of microorganism with peptidoglycan as a component of cell wall using the composition and the detection kit. In addition, the composition can be applied for a diagnosis reagent of detecting an infection of Gram-positive bacteria in animal or human being in advance, and thus, can be used for the prevention or treatment of food poisonings and Bacterial sepsis.
摘要:
Methods and compositions for stabilizing opsin protein in a vertebrate visual system are provided by administration of opsin-binding synthetic retinoids.
摘要:
The present invention relates to methods for reducing plant sensitivity to diseases and attacks from pathogenic organisms. The methods according to the invention comprises overexpressing an inducible lipoxygenase in plants in order to improve their response to diseases and pathogens. The invention also relates to expression cassettes for overexpressing lipoxygenases in plants, and also to transformed plants.
摘要:
Mutated p53 proteins comprising amino acids deletion were disclosed herein. The mutant p53 exhibits high cellular retention and is capable of rendering tumor cells sensitive to apoptotic inducing agents such as null-irradiation or chemotherapeutic agents. The mutant p53 protein can be delivered separately or in combination with apoptotic inducing agents via aerosol liposome/transfection/infection methods to treat cellular proliferative diseases and disorders in humans and animals.
摘要:
The invention relates to biocatalysts showing alcohol dehydrogenase activity obtainable from Rhodococcus ruber, their preparation, their use in the oxidation of secondary alcohols and/or the reduction of ketones, as well as nucleic acids coding for these alcohol dehydrogenases and microorganisms transformed with nucleic acids coding for these biocatalysts and their use for producing the biocatalyst or oxidizing secondary alcohols and/or reducing ketones.
摘要:
The cell lines comprises a DNA construct that comprises all or part of a promoter sequence of the gene coding for cyclooxygenase 2 (cox-2) and a reporter gene, operatively joined to each other, such that said promoter sequence of the cox-2 gene controls the expression of said reporter gene in response to a suitable stimulus. The assay method comprises bringing said cell line into contact with the compound to be assayed and determining the existence of a signal indicative of the expression of activity due to the reporter gene. This method is suitable for the induction at a transcriptional level of cox-2 by suitable stimuli.
摘要:
Polynucleotides that comprise regulatory regions of the yeast alcohol oxidase 1 promoter are provided. Isolated polynucleotides, recombinant polynucleotides, vectors, expression cassettes and transformed cells containing the regulatory regions are disclosed. Proteins produced by the transformed cells are also provided.
摘要:
The present invention concerns a nucleic acid that codes for a plant allene oxide cyclase (AOC). The provision of the new cDNA clone now permits for the first time the production of jasmonic acid in large quantities and of great purity by biotechnological means.