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Densitometry based microassay for the determination of lipase depolymerizing activity on polyhydroxyalkanoate

机译:基于光度法的微量测定法,用于测定脂肪酶对聚羟基链烷酸酯的解聚活性

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A novel method for the assay of polyhydroxyalkanoate (PHA)-degrading ability of triacylglycerol lipases was developed. By applying the natural affinity of lipases towards hydrophobic interfaces, a sensitive and rapid densitometry analysis for the evaluation of hydrolytic activity of lipase droplets towards PHA-coated surface was successfully carried out. We found that 12 out of 14 tested lipases which are of fungal, bacterial and animal origin were able to hydrolyze P(3HB-co-92 mol% 4HB) thin film. The patterns and opacity of the hydrolysis spots of lipases on PHA films allowed easy comparison of PHA-hydrolytic strength of lipases. Lipase from the bacterium Chromobacterium viscosum exhibited the highest PHA-degrading activity. The hydrolytic activity of lipases on water insoluble PHA, emulsified p-nitrophenyl laurate and olive oil were also compared and interestingly some lipases showed better activity when PHA was used as a substrate.
机译:建立了测定聚羟基链烷酸酯(PHA)降解三酰基甘油脂肪酶能力的新方法。通过应用脂肪酶对疏水界面的天然亲和力,成功进行了灵敏且快速的光密度分析,以评估脂肪酶液滴对PHA涂层表面的水解活性。我们发现,在14种测试的脂肪酶中,其中12种是真菌,细菌和动物来源的脂肪酶,能够水解P(3HB-co-92 mol%4HB)薄膜。脂肪酶在PHA膜上的水解斑点的图案和不透明性使得可以轻松比较脂肪酶的PHA水解强度。来自粘膜色杆菌的脂肪酶表现出最高的PHA降解活性。还比较了脂肪酶对水不溶性PHA,乳化的对硝基苯基月桂酸酯和橄榄油的水解活性,有趣的是,当将PHA用作底物时,某些脂肪酶表现出更好的活性。

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