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Biodegradation of Various Aromatic Compounds by Enriched Bacterial Cultures: Part A-Monocyclic and Polycyclic Aromatic Hydrocarbons

机译:丰富的细菌培养物对各种芳香化合物的生物降解作用:A部分-单环和多环芳烃

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摘要

Present study focused on the screening of bacterial consortium for biodegradation of monocyclic aromatic hydrocarbon (MAH) and polycyclic aromatic hydrocarbons (PAHs). Target compounds in the present study were naphthalene, acenaphthene, phenanthrene (PAHs), and benzene (MAH). Microbial consortia enriched with the above target compounds were used in screening experiments. Naphthalene-enriched consortium was found to be the most efficient consortium, based on its substrate degradation rate and its ability to degrade other aromatic pollutants with significantly high efficiency. Substrate degradation rate with naphthalene-enriched culture followed the order benzene > naphthalene > acenaphthene > phenanthrene. Chryseobacterium and Rhodobacter were discerned as the predominant species in naphthalene-enriched culture. They are closely associated to the type strain Chryseobacterium arthrosphaerae and Rhodobacter maris, respectively. Single substrate biodegradation studies with naphthalene (PAH) and benzene (MAH) were carried out using naphthalene-enriched microbial consortium (NAPH). Phenol and 2-hydroxybenzaldehyde were identified as the predominant intermediates during benzene and naphthalene degradation, respectively. Biodegradation of toluene, ethyl benzene, xylene, phenol, and indole by NAPH was also investigated. Monod inhibition model was able to simulate biodegradation kinetics for benzene, whereas multiple substrate biodegradation model was able to simulate biodegradation kinetics for naphthalene.
机译:目前的研究集中于筛选用于单环芳烃(MAH)和多环芳烃(PAHs)生物降解的细菌聚生体。本研究中的目标化合物是萘,,菲(PAHs)和苯(MAH)。筛选实验中使用了富含上述目标化合物的微生物群落。富含萘的财团被发现是最有效的财团,这是由于其底物的降解速率以及其以极高的效率降解其他芳香族污染物的能力。富萘培养物的底物降解速率遵循苯>萘> ena>菲的顺序。在富含萘的培养物中,主要的菌种是金黄色杆菌和红细菌。它们分别与节杆菌属菌株和玛丽红球菌密切相关。使用富含萘的微生物联合体(NAPH)进行了萘(PAH)和苯(MAH)的单底物生物降解研究。在苯和萘降解过程中,苯酚和2-羟基苯甲醛分别被确定为主要中间体。还研究了NAPH对甲苯,乙苯,二甲苯,苯酚和吲哚的生物降解作用。 Monod抑制模型能够模拟苯的生物降解动力学,而多底物生物降解模型能够模拟萘的生物降解动力学。

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