Study of a new spectrophotometric end-point assay for lipase activity determination in aqueous media

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• 作者：David Palacios ; Mar铆a D. Busto ; Natividad Ortega
• 关键词：End-point assay ; Emulsifier ; Kinetic study ; Lipases ; pNP-nitrophenyl esters
• 刊名：Lebensmittel-Wissenschaft und -Technologie
• 出版年：March, 2014
• 年：2014
• 卷：55
• 期：2
• 页码：536-542
• 全文大小：957 K

文摘

A new spectrophotometric end-point method to evaluate lipase activity in aqueous media is described. This procedure is based on blocking the enzyme reaction by adding chloroform:isoamyl alcohol (24:1) as a denaturating agent, and removing the precipitate by centrifugation. Emulsifier screening showed that the chemical component with the least effect on lipase activity from Thermomyces lanuginosus, Mucor javanicus, Aspergillus niger, Rhizomucor miehei, Penicillium camemberti and Burkholderia cepacia, in the proposed method, was 0.1% (w/w) gum arabic. In contrast, Triton X-100, SDS, sodium cholate and Tween 80 reduced lipase activity, depending on the microbial source of the latter. A comparative study with other end-point methods based on the addition of chemical reagents (NaOH, Na₂CO₃, THAM or acetone-ethanol) or in thermal treatments (chilling or heating) was performed. The proposed procedure was shown to be more accurate in comparison with other methods that were tested. Furthermore, the effectiveness of the method was demonstrated in a study of the specificity of six commercial lipases toward p-nitrophenyl decanoate (C10) and p-nitrophenyl palmitate (C16). The study also analyzed the kinetic behavior and catalytic efficiency of lipase from T.聽lanuginosus and B.聽cepacia toward p-nitrophenyl decanoate and p-nitrophenyl palmitate.