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Oxidative degradation of polyaromatic hydrocarbons catalyzed by blue laccase from Pleurotus ostreatus Dl in the presence of synthetic mediators

机译:在合成介体的存在下,平菇蓝漆酶催化蓝色漆酶氧化降解多环芳烃。

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摘要

The laccase produced by the white-rot fungus Pleurotus ostreatus Dl (BLPO) under submerged cultivation was purified to homogeneity.Its catalytic activity towards several phenolic compounds,including ABTS (2,2'-azino-bis-(3-ethylbenzthiazoline-6-sulphonic acid) diammonium salt),syringaldazine (4-hydroxy-3,5-dimethoxybenzaldehyde azine),2,6-dimethoxyphenol and catechol was investigated.pH-optima and kinetic constants (K_m and V_(max)) of these reactions were determined.The enzyme was able to degrade the following polyaromatic hydrocarbons (PAHs):anthracene (91%),phenanthrene (72%),fluorene (53.5%),pyrene (65.5%),fluoranthene (69.7%),and perylene (73%) only in the presence of a synthetic mediator.The degradation of phenanthrene in the presence of detergents varied from 49% to 72%,whereas in the absence of any detergent it reached 10%.Investigating the effect of various mediators on PAHs degradation by the BLPO showed that ABTS was a better mediator of anthracene oxidation and HBT (1-hydroxybenzotriazole) was a better mediator of fluorene oxidation.Pyrene and anthracene were degraded more rapidly in a mixture than separately.The effect of different solvents on the activity of the BLPO towards anthracene and fluorene was investigated also.Finally,it was found that in a solution of 30% (v/v) acetonitrile,BLPO could degrade about 56% of the 600 mu M initially added anthracene with the formation of anthraquinone.
机译:深层培养的白腐真菌平菇平菇(BLPO)产生的漆酶被纯化至均质,其对几种酚类化合物的催化活性,包括ABTS(2,2'-azino-bis-(3-ethylbenzthiazoline-6-磺酸),二铵盐),丁香嗪(4-羟基-3,5-二甲氧基苯甲醛嗪),2,6-二甲氧基苯酚和邻苯二酚的研究。确定了这些反应的pH最佳值和动力学常数(K_m和V_(max))该酶能够降解以下多芳烃(PAHs):蒽(91%),菲(72%),芴(53.5%),py(65.5%),荧蒽(69.7%)和per(73%)在去污剂存在下菲的降解率从49%到72%不等,而在没有任何去污剂的情况下菲的降解率达到10%。研究各种媒介物对PAHs降解的影响BLPO表明ABTS是蒽氧化和HBT(1-hydro苯并三唑是更好的芴氧化介质.P和蒽在混合物中的分解速度比单独分解快得多。还研究了不同溶剂对BLPO的蒽和芴活性的影响。在30%(v / v)乙腈溶液中,BLPO可以降解最初添加的蒽中600亩M中的约56%,并形成蒽醌。

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