Abstract:
The present invention relate to a composition for detecting Cochliobolus miyabeanus and a method for detecting Cochliobolus miyabeanus using the same, and more specifically, provides a primer set for detecting Cochliobolus miyabeanus and a probe for quantitative detection of Cochliobolus miyabeanus. When using a primer set and a probe according to the present invention, it is possible to accurately and promptly detect Cochliobolus miyabeanus at high sensitivity and to quantify progress degree of Bipolaris sorokiniana caused by Cochliobolus miyabeanus thereby objectively quantifying, and accordingly it is expected to be established as a molecular biological monitoring system in agriculture.
Abstract translation:本发明涉及一种用于检测曲霉杆菌的组合物和使用该组合物检测曲霉菌的方法,更具体地说,提供了用于检测曲霉菌的引物组和用于定量检测曲霉杆菌的探针。 当使用根据本发明的引物组和探针时,可以高灵敏度准确地并且迅速地检测枸杞子,并且可以量化由Co iana iana iana iana iana of of of ify ify ify ify ify ify ify ify be be be be be be be be be be be 作为农业分子生物学监测系统。
Abstract:
The present invention relates to a composition for controlling bacterial blight comprising Glufosinate ammonium, and a method for controlling bacterial blight by processing the same, which are expected to minimize the damage of agriculture by allowing the effective control of bacterial blight. The composition for controlling bacterial blight contains the Glufosinate ammonium or salt thereof as an effective component. The concentration of the Glufosinate ammonium is less than 5 ppm.
Abstract:
본 발명은 재조합 발현 벡터를 포함하는 아그로박테리아와 공동 배양하기 전에 형질전환 대상 식물체의 배유를 제거하는 단계를 포함하는 것에 특징이 있는 아그로박테리아를 이용한 식물체 형질전환 방법에 관한 것으로써, 본 발명에 따르면 대량의 형질전환을 고속고효율로 안정적으로 수행할 수 있다.
Abstract:
The present invention pertains to an auxin receptor protein involved in activation of proton pump in plasma membrane of a plant derived from rice, a gene encoding the protein, a recombinant vector comprising the gene, a host cell transformed with the recombinant vector, a method of improving traits of a plant by transforming the plant with the recombinant plant expression vector, a plant having improved traits by transformation with the recombinant plant expression vector and seeds of the plant, and a composition comprising the gene of the invention for improving traits of a plant.
Abstract:
PURPOSE: A method for producing transgenic perilla plants and herbicide-resistant perilla plants produced therefrom are provided, thereby easily inserting foreign useful genes into perilla plants, and reducing the production cost and environmental pollution. CONSTITUTION: The method for producing transgenic perilla plants comprises the steps of: (A) constructing an expression vector for transforming plants containing a foreign target gene and a selection maker; (B) introducing the expression vector into Agrobacterium to produce transformed Agrobacterium; (C) co-culturing the transformed Agrobacterium with a tissue section of perilla plants; (D) inducing shoots of the tissue section of perilla plants co-cultured in a selection-shoot inducing medium and subculturing the shoots of perilla plants in a root-inducing medium; and (F) transplanting the root-induced perilla plants in the field.
Abstract:
PURPOSE: A gene which may be involved in signal transduction of disease resistance is provided, which can be useful for development of transgenic plants having disease resistance. CONSTITUTION: The gene which may be involved in signal transduction of disease resistance is DNA encoding a protein having 80% homology to the amino acid sequence set forth in SEQ ID NO: 1 or fragments thereof, wherein DNA has the nucleotide sequence set forth in SEQ ID NO: 2. An expression vector for inducing disease resistance of plants, pQE80L::(a,b,c) contains the gene encoding a protein having 80% homology to the amino acid sequence set forth in SEQ ID NO: 1. A microorganism transformed with the expression vector pQE80L::(a,b,c) is pQE80L:: a/E.coli CF1652(KACC 95010) or pQE80L::(a,b,c) is pQE80L:: b/E.coli CF1652(KACC 95011). A plant having disease resistance which is transformed with the expression vector pQE80L::(a,b,c) is provided.
Abstract translation:目的:提供可能涉及抗病性信号转导的基因,可用于开发具有抗病性的转基因植物。 构成:可能涉及抗病性信号转导的基因是编码与SEQ ID NO:1所示的氨基酸序列或其片段具有80%同源性的蛋白质的DNA,其中DNA具有SEQ所示的核苷酸序列 编号:2.用于诱导植物抗病性的表达载体pQE80L::( a,b,c)含有编码与SEQ ID NO:1所示的氨基酸序列具有80%同源性的蛋白质的基因。 表达载体pQE80L转化的微生物:( a,b,c)是pQE80L :: a /大肠杆菌CF1652(KACC 95010)或pQE80L::( a,b,c)是pQE80L :: b / E.coli CF1652(KACC 95011)。 提供了用表达载体pQE80L转化的具有抗病性的植物:( :( a,b,c))。
Abstract:
본 발명은 DPPH(1,1-diphenyl-2-picrylhydrazyl)를 이용한 항산화물질의 분석방법에 관한 것이다. 좀 더 구체적으로, 본 발명은 유리 라디칼(free radical)인 DPPH와 항산화물질을 반응시켜 DPPH의 보라색이 무색으로 변하는 색깔 변화를 관찰함으로써, 동·식물체 및 미생물 등에 존재하는 항산화물질을 신속·간단하면서도 경제적으로 검출 또는 정량하는 분석방법에 관한 것이다. 본 발명의 방법은 항산화물질의 탐색, 분리·정제에 이용될 수 있으며, 새로운 항산화물질의 개발 및 연구에도 이용될 수 있다.