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Optimization of a colorimetric assay for yeast lipase activity in complex systems

机译:比色法测定复杂系统中酵母脂肪酶活性的优化

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The present work describes a simple and sensitive spectrophotometric method based on the release of p-nitrophenyl butyrate (p-NPB) for the estimation of lipase activity. The method was optimized and validated in biphasic complex media containing methyl ricinoleate (MR) or olive mill wastewater (OMW), although it may be used for other biphasic media. Reaction mixtures containing substrate (2.63 mM p-NPB in sodium acetate buffer, 0.05 M and pH 5.6, with 4% (v/v) Triton X-100) and lipase are incubated at 37 °C during 15 minutes. After this time, 2 mL of acetone are added to stop the reaction and the corresponding absorbances are measured at 405 nm in a microplate reader. A linear response was obtained for Candida rugosa lipase concentrations in the range of 0.0054 to 0.1 g L~(-1) and 0.093 to 0.5 g L~(-1) for MR and OMW media, respectively. The method revealed to be more sensitive for MR medium. This conclusion was corroborated by the detection and quantification limits, which were smaller for MR than for OMW medium. The method is precise for both tested media, according to the Horwitz criterion. Besides the simplicity of this method, it is sensitive and precise, and could be adopted for routine analysis, as a tool for screening and detection of lipase activity. In addition, the fact of measuring the absorbances of the samples in a microplate reader, allows to analyze a great number of samples at the same time and to achieve a considerable time saving.
机译:本工作描述了一种简单而灵敏的分光光度法,该方法基于对硝基苯基丁酸(p-NPB)的释放来估算脂肪酶活性。该方法已在包含蓖麻油酸甲酯(MR)或橄榄磨废水(OMW)的双相复杂介质中进行了优化和验证,尽管该方法也可用于其他双相介质。将含有底物(在乙酸钠缓冲液中的2.63 mM p-NPB,0.05 M和pH 5.6,具有4%(v / v)Triton X-100)和脂肪酶的反应混合物在37°C下孵育15分钟。此时间之后,添加2 mL丙酮以终止反应,并在酶标仪中于405 nm处测量相应的吸光度。对于MR和OMW培养基,皱纹念珠菌脂肪酶浓度分别在0.0054至0.1 g L〜(-1)和0.093至0.5 g L〜(-1)范围内获得线性响应。该方法显示对MR介质更敏感。检测和定量限证实了这一结论,MR的检出限和定量限小于OMW培养基。根据Horwitz准则,该方法对于两种被测介质都是精确的。除了该方法的简单性之外,它还灵敏且精确,可作为脂酶活性的筛选和检测工具用于常规分析。另外,在酶标仪中测量样品的吸光度的事实允许同时分析大量样品并节省大量时间。

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