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Detection of Microcystin Producing-Cyanobacteria by PCR

机译:PCR检测微囊藻毒素产生的蓝细菌

摘要

PURPOSE: A detection method of cyanobacteria producing microcystin by using PCR is provided, thereby detecting a small amount of microcystin-producing Cyanobacteria. Therefore, water quality can be appropriately maintained. CONSTITUTION: A primer capable of amplifying a specific region of a peptide synthetase gene that is specifically present in the microcystin producing Cyanobacteria is provided, wherein the specific region of the peptide synthetase gene is adenylation domain; the primer is a pair of primers consisting of one primer selected from MCF-1 having the nucleotide sequence of SEQ ID NO: 1 or MCF-2 having the nucleotide sequence of SEQ ID NO: 2, and another primer selected from MCR-1 having the nucleotide sequence of SEQ ID NO: 3 or MCR-2 having the nucleotide sequence of SEQ ID NO: 4. A detection method of microcystin-producing Cyanobacteria by using PCR comprises the steps of: (1) extracting DNAs from various microorganisms; (2) PCR amplifying the DNAs as template using a primer capable of amplifying a specific region of the peptide synthetase gene; (3) subjecting the amplified genes to electrophoresis; and (4) dyeing of the developed gene to analyze the PCR product.
机译:目的:提供一种利用PCR检测蓝藻产生微囊藻毒素的方法,从而检测出少量产生微囊藻毒素的蓝藻。因此,可以适当地保持水质。组成:提供一种引物,其能够扩增特异性地存在于产生微囊藻毒素的蓝细菌中的肽合成酶基因的特定区域,其中该肽合成酶基因的特定区域为腺苷酸化结构域;所述引物是一对引物,其由选自具有SEQ ID NO:1的核苷酸序列的MCF-1或具有SEQ ID NO:2的核苷酸序列的MCF-2的一个引物和选自具有SEQ ID NO:2的核苷酸序列的MCF-1的另一个引物组成。一种使用PCR的产生微囊藻毒素的蓝细菌的检测方法,包括以下步骤:(1)从各种微生物中提取DNA;以及(3)具有SEQ ID NO:3的核苷酸序列或具有SEQ ID NO:4的核苷酸序列的MCR-2。 (2)使用能够扩增肽合成酶基因的特定区域的引物的PCR,以DNA为模板进行扩增。 (3)对扩增的基因进行电泳; (4)染色所开发的基因以分析PCR产物。

著录项

  • 公开/公告号KR100451062B1

    专利类型

  • 公开/公告日2004-10-02

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20020025356

  • 发明设计人 강종순;오희목;나용주;양규환;

    申请日2002-05-08

  • 分类号C12Q1/68;

  • 国家 KR

  • 入库时间 2022-08-21 22:46:33

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