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一株能够代谢阴离子洗涤剂十二烷基硫酸钠(SDS)的恶臭假单胞菌菌株的分离。

Isolation of a strain of Pseudomonas putida capable of metabolizing anionic detergent sodium dodecyl sulfate (SDS).

作者信息

Chaturvedi V, Kumar A

机构信息

School of Biotechnology, Banaras Hindu University, Varanasi-221 005, India.

出版信息

Iran J Microbiol. 2011 Mar;3(1):47-53.

Abstract

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.

摘要

背景与目的

十二烷基硫酸钠(SDS)是应用最为广泛的阴离子洗涤剂之一。本研究旨在从印度瓦拉纳西市受洗涤剂污染的池塘中分离并鉴定能降解SDS的细菌。

材料与方法

采用富集培养技术,在基本培养基(PBM)中从池塘水样中分离出能降解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SDS的降解情况,以确定高效菌株能降解的SDS最大浓度。对粗细胞提取物中的烷基硫酸酯酶活性(SDS降解的关键酶)进行了测定,并通过非变性聚丙烯酰胺凝胶电泳酶谱法研究了烷基硫酸酯酶的多样性。通过16S rRNA序列分析对高效菌株进行了鉴定。

结果

利用以SDS为唯一碳源的基本培养基进行富集培养,最初分离出三株能降解SDS的菌株。然而,只有一株菌株SP3被发现是SDS的高效降解菌。观察发现,该菌株在培养16小时内可完全代谢0.1%的SDS,20小时内可代谢0.2%的SDS,24小时内可代谢0.3%的SDS。烷基硫酸酯酶的比活性为0.087±0.004 μmol SDS/毫克蛋白/分钟,非变性聚丙烯酰胺凝胶电泳酶谱显示存在Rf值为0.21的烷基硫酸酯酶。该菌株被鉴定为恶臭假单胞菌SP3菌株。

结论

本文报道了恶臭假单胞菌SDS降解菌株的分离,该菌株显示出较高的SDS降解率,能降解高达0.3%的SDS。看来该菌株可用于水系统中这种洗涤剂的生物修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f15/3279795/1f47e505f194/IJM-3-047-g001.jpg

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