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Biodegradation of the Anionic Surfactant Linear Alkylbenzene Sulfonate (LAS) by Autochthonous Pseudomonas sp.

机译:假单胞菌属假单胞菌对阴离子表面活性剂线性烷基苯磺酸盐(LAS)的生物降解。

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Anionic surfactants, the earliest and the most common surfactants in detergent and cosmetic product formulations contribute significantly to the pollution profile of the ecosystem. Linear alkylbenzene sulfonates (LAS), a major chemical constituent of detergents, forms an imperative group of anionic surfactants. Bioremediation of LAS by conventional processes such as activated sludge is ineffective due to the low kinetics of degradation by unsuitable organisms and foam production. Hence this study was focused on isolating and characterizing indigenous LAS-degrading bacteria from soil. Twenty different LAS-degrading bacteria were isolated from detergent-contaminated soil by enrichment culture technique and degradation efficiency was assessed by Methylene Blue Active Substances (MBAS) assay and by reverse-phase high-performance liquid chromatogra-phy (HPLC) analysis. The most efficient LAS-degrading isolates, L9 (81.33±0.7) and L12 (81.81 ± 0.8), were selected and identified as Pseudomonas nitroreducens (MTCC 10463) and Pseudomonas aer-uginosa (MTCC 10462). The 16S rDNA sequences of the isolates were deposited in NCBI GenBank under the accession numbers HQ 271083 (L9) and HQ 271084 (LI2). The isolates were capable of degrading 0.05 g/I LAS at 25 °C and pH 7.0-7.5. Presence of a solid support caused biofilm formation which in turn enhanced LAS degradation. The isolates tend to display diauxic growth with alternate carbon source such as dextrose. These isolates also have the capability to degrade other xenobiotics like hydrocarbons and pesticides. Since xenobiotic pollutants in nature occur as a mixture of compounds rather than single pollutants, the potential of these two indigenous LAS-degrading isolates to degrade multiple xenobiotics gains relevance.
机译:阴离子表面活性剂是洗涤剂和化妆品配方中最早,最常见的表面活性剂,对生态系统的污染状况有很大贡献。线性烷基苯磺酸盐(LAS)是清洁剂的主要化学成分,形成了阴离子表面活性剂的重要基团。由于不适当的生物体降解和泡沫产生的动力学较低,通过常规方法(例如活性污泥)对LAS进行生物修复是无效的。因此,这项研究的重点是从土壤中分离和鉴定降解本地LAS的细菌。通过富集培养技术从洗涤剂污染的土壤中分离出20种不同的LAS降解细菌,并通过亚甲基蓝活性物质(MBAS)分析和反相高效液相色谱(HPLC)分析来评估降解效率。选择最有效的LAS降解分离株L9(81.33±0.7)和L12(81.81±0.8),鉴定为硝基假单胞菌(MTCC 10463)和铜绿假单胞菌(MTCC 10462)。分离物的16S rDNA序列以登录号HQ 271083(L9)和HQ 271084(LI2)保藏在NCBI GenBank中。分离物能够在25°C和pH 7.0-7.5下降解0.05 g / I LAS。固体支持物的存在导致生物膜的形成,继而增强了LAS的降解。分离株倾向于显示出具有替代碳源的右旋糖生长,例如葡萄糖。这些分离物还具有降解其他异质生物的能力,例如碳氢化合物和农药。由于自然界中的异源生物污染物是化合物的混合物而不是单一污染物,因此,这两种降解本地LAS的分离株降解多种异源生物的潜力具有相关性。

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