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Method for removing malt fermented beverage remaining in membrane filter and method for rapid detection of microorganisms in fermented malt beverage

机译:去除残留在膜滤器中的麦芽发酵饮料的方法和快速检测麦芽饮料中微生物的方法

摘要

PPROBLEM TO BE SOLVED: To assay the viable count of a trace amount of bacterial cells mixed in a malt fermented beverage such as beer or a sparkling liquor without performing culture operation. PSOLUTION: The malt fermented beverage remaining on a membrane filter is washed and removed by removing bubbles on the membrane filter and then washing the membrane filter with a weakly alkaline aqueous solution when the malt fermented beverage is filtered through the membrane filter. The membrane filter subjected to the washing and removing treatment is further placed on an adenosine 5'-triphosphate (ATP)-free agar plate for about 1 h to reduce the background noise. The resultant membrane filter is placed in the ATP-free agar plate containing an ATP activator for microorganisms to activate the microorganisms and amplify the ATP in the cells. Thereby, the quantity of ATP emission is increased. As a result, the S/N ratio can remarkably be improved. PCOPYRIGHT: (C)2004,JPO
机译:

要解决的问题:在不进行培养操作的情况下,测定混合在麦芽发酵饮料(如啤酒或起泡酒)中的微量细菌细胞的活力计数。

解决方案:将残留在膜滤器上的麦芽发酵饮料洗涤并除去,方法是除去膜滤器上的气泡,然后在通过膜滤器过滤麦芽发酵饮料时,用弱碱性水溶液洗涤膜滤器。将经过洗涤和去除处理的膜滤器进一步放在无5'-三磷酸腺苷(ATP)的琼脂平板上约1 h,以减少背景噪音。将所得的膜滤器置于不含ATP的琼脂平板中,该琼脂平板含有用于微生物的ATP活化剂,以活化微生物并扩增细胞中的ATP。由此,增加了ATP的发射量。结果,可以显着提高S / N比。

版权:(C)2004,日本特许厅

著录项

  • 公开/公告号JP4145073B2

    专利类型

  • 公开/公告日2008-09-03

    原文格式PDF

  • 申请/专利权人 サッポロビール株式会社;

    申请/专利号JP20020137579

  • 发明设计人 高橋寿洋;

    申请日2002-05-13

  • 分类号C12G3/02;C12C11;C12Q1/06;C12Q1/66;G01N21/77;G01N21/78;G01N33/48;

  • 国家 JP

  • 入库时间 2022-08-21 20:18:49

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