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Biodegradation and biotransformation of polycyclic non-steroidal anti-inflammatory drugs

机译:多环非甾体抗炎药的生物降解和生物转化

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In recent years the increased use of polycyclic non-steroidal anti-inflammatory drugs has resulted in their presence in the environment. This in turn may cause potential negative effects on living organisms. While the biotransformation mechanisms of polycyclic non-steroidal anti-inflammatory drugs in the human body and in other mammals have been extensively studied, degradation of these drugs by microorganisms has seldom been investigated and is largely unknown. Biotransformation/biodegradation of polycyclic non-steroidal anti-inflammatory drugs is caused by fungal microorganisms, mainly white-rot fungi, and a few strains of bacteria. However, hitherto only complete degradation of olsazine was described. The first step of the transformation is most often hydroxylation catalyzed by cytochrom P-450 monooxygenases, or oxygenation by laccases and three peroxidases: lignin peroxidase, manganese-dependent peroxidase and versatile peroxidase manganese-dependent peroxidase. The aim of this work is to summarize the knowledge about the biotransformation and/or biodegradation of polycyclic non-steroidal anti-inflammatory drugs and to present their biotransformation pathways.
机译:近年来,多环非甾体抗炎药的使用增加,导致其在环境中的存在。反过来,这可能会对生物产生潜在的负面影响。尽管已经广泛研究了多环非甾体抗炎药在人体和其他哺乳动物中的生物转化机理,但很少研究微生物对这些药物的降解,并且在很大程度上尚不清楚。多环非甾体抗炎药的生物转化/生物降解是由真菌微生物(主要是白腐真菌)和一些细菌菌株引起的。然而,迄今仅描述了olsazine的完全降解。转化的第一步通常是由细胞色素P-450单加氧酶催化的羟基化,或由漆酶和三种过氧化物酶的氧化:木质素过氧化物酶,锰依赖性过氧化物酶和通用的过氧化物酶锰依赖性过氧化物酶。这项工作的目的是总结有关多环非甾体抗炎药的生物转化和/或生物降解的知识,并介绍其生物转化途径。

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