首页> 外国专利> Quantitative determn. of adenosine-tri:phosphate - by a bio-luminescent reaction capable of determining ATP in somatic and/or microbial cells

Quantitative determn. of adenosine-tri:phosphate - by a bio-luminescent reaction capable of determining ATP in somatic and/or microbial cells

机译:定量测定。磷酸三磷酸腺苷-通过能够确定体细胞和/或微生物细胞中ATP的生物发光反应

摘要

A process for the quantitative determination of adenosine triphosphate, ATP, in biological material contg. living somatic cells and/or living microbial cells comprises either (i) determining both somatic and microbial cells by (a) obtaining a sample of the biological material; (b) adding at least one detergent to extract the ATP from the somatic cells; (c) adding a reagent for bioluminescent reaction, before, during or after the step (b) extn., which is capable of quantifying the luminescence produced by the non-microbial cells; (d) adding at least one lipid to inhibit inactivation of the bioluminescent reaction and/or the ATP hydrolysis reaction of the detergent; (e) adding at least one enzyme which catalyses hydrolytic cleavage to the mixt. to degrade the ATP form the non-microbial cells; (f) adding a mixt. contg. at least one bactericide to liberate the ATP in the microbial cells and at least one substance which inhibits the activity of the enzyme from (e) but which does not affect the bioluminescent reaction; and (g) quantifying the microbial cells by the bioluminescence produced; or (ii) determining only the microbial cells by carrying out no determination of bioluminescence according to step (c), and then carrying out steps (d), (e), (f) and (g) as above. USE/ADVANTAGE - The process enables ATP to be determined in biological materials such as urine, blood, milk, fruit juices, beer, wine, meat extracts, clear slurry, water, cell cultures, soil samples, foodstuffs and textiles. Mixts. contg. living microorganisms can be analysed even in the presence of living somatic cells.
机译:连续测定生物材料中三磷酸腺苷ATP的方法。活体细胞和/或活微生物细胞包括(i)通过(a)获得生物材料样品来确定体细胞和微生物细胞。 (b)添加至少一种去污剂以从体细胞中提取ATP; (c)在步骤(b)延伸之前,之中或之后添加用于生物发光反应的试剂,该试剂能够定量由非微生物细胞产生的发光; (d)添加至少一种脂质以抑制去污剂的生物发光反应和/或ATP水解反应的失活; (e)将至少一种催化水解切割的酶加入混合物中。从非微生物细胞降解ATP; (f)添加混料。续至少一种在微生物细胞中释放ATP的杀菌剂和至少一种抑制(e)中酶活性但不影响生物发光反应的物质; (g)通过产生的生物发光来定量微生物细胞; (ii)通过不进行根据步骤(c)的生物发光测定,然后如上所述进行步骤(d),(e),(f)和(g),仅确定微生物细胞。使用/优势-该过程使ATP能够在生物材料中测定,例如尿液,血液,牛奶,果汁,啤酒,葡萄酒,肉提取物,净浆,水,细胞培养物,土壤样品,食品和纺织品。混音。续即使存在活体细胞,也可以分析活微生物。

著录项

  • 公开/公告号CH678065A5

    专利类型

  • 公开/公告日1991-07-31

    原文格式PDF

  • 申请/专利权人 HAMILTON BONADUZ AG;

    申请/专利号CH19880001357

  • 发明设计人 SCHRAM ERIC;

    申请日1988-04-13

  • 分类号C12Q1/04;C12Q1/34;C12Q1/66;

  • 国家 CH

  • 入库时间 2022-08-22 05:50:20

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