首页> 外文期刊>Iranian Journal of Microbiology >Isolation of a strain of Pseudomonas putida capable of metabolizing anionic detergent sodium dodecyl sulfate (SDS)
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Isolation of a strain of Pseudomonas putida capable of metabolizing anionic detergent sodium dodecyl sulfate (SDS)

机译:能够代谢阴离子去污剂十二烷基硫酸钠(SDS)的恶臭假单胞菌菌株的分离

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Background and objectives: Sodium Dodecyl Sulfate (SDS) is one of the most widely used anionic detergents. The present study deals with isolation and identification of SDS-degrading bacteria from a detergent contaminated pond situated in Varanasi city, India.Materials and Methods: Employing enrichment technique in minimal medium (PBM), SDS-degrading bacteria were isolated from pond water sample. Rate of degradation of SDS was studied in liquid PBM and also degradation of different concentrations of SDS was also studied to find out maximum concentration of SDS degraded by the potent isolates. Alkyl sulfatase activity (key enzyme in SDS degradation) was estimated in crude cell extracts and multiplicity of alkyl sulfatase was studied by Native PAGE Zymography. The potent isolate was identified by 16S rRNA sequence analysis.Results: Using enrichment technique in minimal medium containing SDS as a sole carbon source, initially three SDS degrading isolates were recovered. However, only one isolate, SP3, was found to be an efficient degrader of SDS. It was observed that this strain could completely metabolize 0.1% SDS in 16 h, 0.2% SDS in 20 h and 0.3% SDS in 24 h of incubation. Specific activity of alkyl sulfatase was 0.087±0.004 μmol SDS/mg protein/min and Native PAGE Zymography showed presence of alkyl sulfatase of Rf value of 0.21. This isolate was identified as Pseudomonas putida strain SP3.Conclusion: This is the report of isolation of SDS-degrading strain of P. putida, which shows high rate of SDS degradation and can degrade up to 0.3% SDS. It appears that this isolate can be exploited for bioremediation of this detergent from water systems.
机译:背景和目的:十二烷基硫酸钠(SDS)是使用最广泛的阴离子洗涤剂之一。本研究从印度瓦拉纳西市一个被去污剂污染的池塘中分离和鉴定降解SDS的细菌。材料与方法:采用基本培养基富集技术,从池塘水样中分离出降解SDS的细菌。研究了液体PBM中SDS的降解速率,还研究了不同浓度的SDS的降解,以找出有效分离物降解的SDS的最大浓度。估计了粗细胞提取物中的烷基硫酸酯酶活性(SDS降解中的关键酶),并通过本机PAGE Zymography研究了烷基硫酸酯酶的多样性。结果:通过富集技术在含有SDS作为唯一碳源的基本培养基中使用富集技术,最初回收了三个降解SDS的分离株。但是,仅发现一种分离物SP3是SDS的有效降解剂。观察到该菌株在温育16小时内可以完全代谢0.1%SDS,在20小时内可以完全代谢0.2%SDS,在24小时内可以完全代谢0.3%SDS。烷基硫酸酯酶的比活为0.087±0.004μmolSDS / mg蛋白质/分钟,Native PAGE Zymography显示存在Rf值为0.21的烷基硫酸酯酶。该分离物被鉴定为恶臭假单胞菌菌株SP3。结论:这是分离出恶臭假单胞菌降解SDS的菌株的报告,该菌株显示出高的SDS降解率,并且可以降解高达0.3%的SDS。看来该分离物可用于从水系统中对该洗涤剂的生物修复。

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