Abstract:
PURPOSE: A primer set for detecting Pectobacterium wasabiae causing soft rot is provided to quickly and accurately detect Pectobacterium wasabiae and to prevent soft rot. CONSTITUTION: A primer set for detecting Pectobacterium wasabiae contains a primer with nucleic acid sequences of sequence numbers 1 and 2. A method for detecting Pectobacterium wasabiae comprises a step of amplifying DNA isolated from a plant sample and a step of identifying the PCR products. A composition for detecting Pectobacterium wasabiae contains the primer set. A PCR kit contains the primer set.
Abstract:
PURPOSE: A novel antibiotic compound and an antibiotic composition containing the same are provided to suppress bacteria growth and to prevent or treat bacterial infection. CONSTITUTION: A novel antibiotic compound is denoted by chemical formula 7. The compound suppress peptidyl diformylase(PDF) activation. A pharmaceutical composition for preventing or treating infection by pathogen contains the compound of chemical formula 7 and pharmaceutically acceptable carrier. A feed composiiton for preventing or treating infection by pathogen contains the compound of chemical formula 7 and acceptable carriers. An agrochemical composition for preventing or treating infection by plant pathogen contains the compound and agrochemically acceptable carriers.
Abstract:
PURPOSE: A mutant strain which enables xanthan gum containing a mutant gene is provided to massively produce xanthan gum under the conventional technique and installation. CONSTITUTION: A mutant wxoD gene which is related to xanthan gum synthesis is derived from Xanthomonas oryzae strain. The Xanthomonas oryzae strain is Xanthomonas oryzae pv. Oryzae(KACC 10331) strain. The mutant gene wxoD is mutated by inserting the transposon. The mutant gene wxoD contains sequence of sequence number 1. A method for preparing the Xanthomonas sp.(deposit number: KACC91351) comprises: a step of adding transposon to the Xanthomonas sp.; a step of searching the mutant wxo gene using a specific primer; and a step of measuring biosynthesis rate of the xanthangum in the mutant strain and selecting.
Abstract:
본 발명은 서열번호 1의 염기서열을 포함하는 벼흰잎마름병원균의 레이스 판별용 유전자 마커(genetic marker) 및 벼흰잎마름병원균의 레이스의 판별방법에 관한 것으로 보다 상세하게는 서열번호 1의 염기서열을 포함하는 벼흰잎마름병원균의 레이스 판별용 유전자 마커 및 상기 프로브를 제한효소에 의해 절단된 벼흰잎마름병원균 게놈 DNA와 혼성화시키는 것을 특징으로 하는 벼흰잎마름병원균의 레이스의 판별방법에 관한 것이다. 본 발명의 벼흰잎마름병원균의 레이스의 판별방법은 벼흰잎마름병원균의 레이스를 효율적으로 판별할 수 있는 효과를 갖는다. 따라서 본 발명의 판별방법은 벼흰잎마름병원균의 레이스 판별의 목적으로 사용할 수 있다. 벼흰잎마름병, 벼흰잎마름병원균, RFLP, 레이스, 판별
Abstract:
PURPOSE: Primer sets for specific identification of a pathogen, Xanthomonas campestris pv. campestris, and a specific-identification method of the pathogen using the same primers are provided to rapidly and accurately identify Xanthomonas campestris pv. campestris. Therefore, the primer sets can be useful for prevention and control of Xanthomonas campestris pv. campestris. CONSTITUTION: The primer sets for specific identification of a pathogen, Xanthomonas campestris pv. campestris, amplify the total or a portion of 1st to 650th nucleotides in the nucleotide sequence of SEQ ID NO:1 of a gene hrpF, wherein the primer sets have the nucleotide sequences of SEQ ID NO:2 and SEQ ID NO:3. The specific-identification method of Xanthomonas campestris pv. campestris comprises the steps of: (A) extracting the total DNA from a plant sample; (B) PCR amplifying the extracted total DNA; and (C) verifying the amplification of the total or a portion of 1st to 650th nucleotides in the nucleotide sequence of SEQ ID NO:1 of a gene hrpF.
Abstract translation:目的:用于特异性鉴定病原体的引物组,野油菜黄单胞菌(Xanthomonas campestris pv。) 提供了使用相同引物的病原体的特异性鉴定方法,以快速准确地鉴定野油菜黄单胞菌(Xanthomonas campestris pv。 油菜。 因此,引物组可用于预防和控制野油菜黄单胞菌(Xanthomonas campestris pv。 油菜。 构成:用于特异性鉴定病原体的引物组,野油菜黄单胞菌(Xanthomonas campestris pv。 菜籽油,扩增基因hrpF的SEQ ID NO:1的核苷酸序列中第1至第650位核苷酸的总数或部分,其中引物组具有SEQ ID NO:2和SEQ ID NO:3的核苷酸序列。 野油菜黄单胞菌的特异性鉴定方法 营养食品包括以下步骤:(A)从植物样品中提取总DNA; (B)PCR扩增提取的总DNA; 和(C)验证基因hrpF的SEQ ID NO:1的核苷酸序列中第1至第650位核苷酸的总数或部分的扩增。