Isolation and characterization of a bacterial strain for aniline degradation

被引:7
|
作者
Ahmed, Sarfraz [2 ]
Ahmed, Safia [2 ]
Nisar, Muhammad Farrukh [1 ]
Hussain, Khalid [1 ]
Majeed, Abdul [1 ]
Ghumroo, Pir Bakhsh [2 ]
Afghan, Shahid [3 ]
Shahzad, Aamir [3 ]
Nawaz, Khalid [1 ]
Ali, Kazim [3 ]
机构
[1] Univ Gujrat, Dept Bot, Gujrat 50700, Pakistan
[2] Quaid I Azam Univ, Dept Biotechnol, Islamabad 44000, Pakistan
[3] Shakarganj Sugar Res Inst, Jhang, Pakistan
来源
AFRICAN JOURNAL OF BIOTECHNOLOGY | 2010年 / 9卷 / 08期
关键词
Aniline; biodegradation; Staphylococcus aureus; HPLC; plasmid curing; restriction sites; PSEUDOMONAS-PUTIDA; BIODEGRADATION; METABOLISM; TRANSFORMATION; DIVERSITY;
D O I
10.5897/AJB09.1501
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aniline, a serious environmental threat and health risk to living organisms is being released into the soil and water bodies owing to its expanded use in industry. The objective of the present study was to isolate a strain from rhizospheric soil samples of wheat ( Triticum aestivum L.) taken from an agricultural site near the industrial area of Faisalabad, with the capability of degrading aniline with its maximum activity. The isolated strain was identified as Staphylococcus aureus ST1 a newly reported strain for aniline degradation. The strain ST1 showed tolerance up to 2000 ppm for aniline on mineral salt media plates and its degradative ability was checked through shake flasks experiments using HPLC. The strain was capable of degrading aniline and utilizing it as a sole source of carbon and energy. Maximum reduction of aniline concentration in medium up to 59.65% was observed after 72 h. An enhancement in biodegradation was observed using glucose as an additional growth substrate. The degradative products analyzed by HPLC were catechol, phenol and some other unknown compounds. Plasmid curing showed the involvement of plasmid encoded genes which was later followed by the isolation of plasmid DNA, which was found to be a large one of similar to 40 kb having restriction sites for enzymes (EcoRI, BamHI, ClaI, StuI, PstI, and HindIII) used.
引用
收藏
页码:1173 / 1179
页数:7
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