Abstract:
PURPOSE: A cultivation method of arachis hypogaea sprouts containing the massive amount of resveratrol is provided to cultivate arachis hypogaea seeds at 26~30deg C in the dark condition for reducing the cultivation period. CONSTITUTION: A cultivation method of arachis hypogaea sprouts containing the massive amount of resveratrol comprises the following steps: cultivating arachis hypogaea seeds at 26~30deg C in the dark condition; and automatically supplying 6~10ml of water to the seeds for 1~3minutes every hour. The cultivation period for the arachis hypogaea seeds is 4~6days.
Abstract:
PURPOSE: A composition containing Perilla frutescens var. frutescens extract with neuraminidase activity is provided to prevent and teat influenza. CONSTITUTION: A Perilla frutescens var. frutescens extract has an activity of suppressing neuraminidase. The Perilla frutescens var. frutescens are Perilla frutescens var. crispa, Perilla citriodora, Perilla hirtella, or Perilla setoyensis. The extract is crude extract of Perilla frutescens var. frutescens. The extract is polyphenol compounds. The polyphenol compounds are hydroxyflavone, 3',4'5,7-tetrahydroxy flavone, or 2R-2[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-prophenyl]oxy]-3-(3,4-dihydroxyphenyl)propanoic acid. A pharmaceutical, food, or livestock feed for preventing or treating influenza contains the extract as an active ingredient.
Abstract:
The present invention relates to a bean composition containing conjugated linoleic acid (CLA) and a method for producing the same. More specifically, the bean composition is produced in which linoleic acid is converted into CLA by adding microorganisms in a bean pulverized material so that the utilization of beans is maximized. Accordingly, the domestic production rate of beans is increased. CLA components are contained in biological activity functions of microorganisms which are beneficial for the human body so as to enhance efficiency in weight loss, cholesterol decrease, hyperlipidemia alleviation, and atherosclerosis alleviation. Accordingly, the bean composition can be utilized as functional food and a medical product.
Abstract:
PURPOSE: A Vigna nakashimae-derived compound and a composition containing the same are provided to strongly prevent enzyme activation and to prevent or treat alpha-glucosidase related diseases. CONSTITUTION: A pharmaceutical composition for preventing or treating alpha-glucosidase related diseases contains a compound of chemical formulas 1-3 as an active ingredient. The diseases are diabetic disease or obesity. The composition additionally contains pharmaceutically acceptable carriers. A food composition for preventing or treating the diseases contains the compound of chemical formula 1-3 as an active ingredient. A method for preparing the extract comprises: a step of extracting Vigna nakashimae with low carbon number alcohol of C1-C4, water, or a mixture solvent thereof; a step of fractioning the extract with ethanol, chloroform, methanol, or water; and a step of performing the fraction by column chromatography.
Abstract:
PURPOSE: A method for detecting DNA polymorphism by real time PCR using SSR primer pair is provided to effectively detect DNA amplification polymorphism and to use in determining the species of Vigna angularis (Willd.) Ohwi and Ohashi. CONSTITUTION: A method for detecting DNA polymorphism comprises: a step of isolating genome DNA from Vigna angularis (Willd.) Ohwi and Ohashi; a step of performing real time PCR using SSR primer pair; and a step of separating PCR product. An SSR primer pair is a primer pair of sequence number 1 and 2, sequence numbers 3 and 4, or sequence numbers 5 and 6. The primer pair is derived from Vigna angularis (Willd.) Ohwi and Ohashi.
Abstract:
PURPOSE: An SSR primer isolated from Arachis hypogaea L. is provided to effectively detect the DNA polymorphism of peanuts and to be used for a DNA profile of Arachis hypogaea L. CONSTITUTION: An SSR primer pair isolated from Arachis hypogaea L. is a primer pair of sequence numbers 9 and 10, sequence numbers 11 and 12, sequence numbers 13 and 14, sequence numbers 15 and 16, sequence number 17 and 18, sequence numbers 19 and 20, sequence numbers 21 and 22, or sequence numbers 23 and 24. A method for detecting the DNA polymorphism of Arachis hypogaea L. comprises: a step of isolating a genome DNA from Arachis hypogaea L.; a step of performing PCR using an SSR primer pair; and a step of separating a PCR product.