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A Sensitive Method Using 4-Methylumbelliferyl-β-Cellobiose as a Substrate To Measure (1,4)-β-Glucanase Activity in Sediments

机译:以4-甲基伞形酮基-β-果糖二糖为底物测量沉积物中(1,4)-β-葡聚糖酶活性的灵敏方法

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A sensitive method to measure (1,4)-β-glucanase activity in organic matter-rich sediments, using 4-methyl-umbelliferyl-β-cellobiose as a substrate, is described. β-Glucosidases, which were also able to hydrolyze this substrate, were inhibited with d-glucono-δ-lactone. The produced 4-methylumbelliferone was recovered quantitatively out of the sediment by an extraction with 80% ethanol. An inhibition experiment with known substrates or inhibitors suggested that at least 59% of the measured activity could be explained by enzymes of the exo-(1,4)-β-glucanase type and that the contribution of endo-(1,4)-β-glucanases was minor. Results of the inhibition experiment also suggested that the measured activity was of bacterial origin in the sediment used. First results of field measurements are given for the sediment from the reed bed of Lake Gooimeer.
机译:描述了一种灵敏的方法,以4-甲基伞形酮基-β-纤维二糖为底物,测量富含有机物的沉积物中的(1,4)-β-葡聚糖酶活性。也能够水解该底物的β-葡萄糖苷酶被d-葡萄糖醛酸-δ-内酯抑制。通过用80%乙醇萃取,从沉淀物中定量回收生成的4-甲基伞形酮。用已知底物或抑制剂进行的抑制实验表明,至少有59%的活性可以用exo-(1,4)-β-葡聚糖酶类型的酶解释,而end-(1,4)- β-葡聚糖酶是次要的。抑制实验的结果还表明,所测得的活性是所用沉积物中的细菌来源。实地测量的最初结果是对古默尔湖芦苇床的沉积物给出的。

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