ISSN: 0973-7510

E-ISSN: 2581-690X

K. Suresh Kumar , P. Ponmurugan1, S. Murugesh2 and R. Indira Priyadarsini3
*Department of Biotechnology, SASTRA University, Thanjavur – 613 402, India.
1Department of Biotechnology, K.S.R. College of Technology, Tiruchengode – 637 215, India.
2Department of Biotechnology, Vivekananda College of Arts and Science, Tiruchengode – 637 215, India.
3Department of Biotechnology, The Oxford College of Engineering, Bangalore- 560 068, India.
J Pure Appl Microbiol. 2011;5(1):77-85
© The Author(s). 2011
Received: 17/05/2010 | Accepted: 01/08/2010| Published: 30/04/2011
Abstract

Pure culture of Acid Black -1 dye degrading bacteria was isolated from azo dye contaminated soil in the industrial zone of Thirupur, Tamil Nadu, India. The bacterium was identified by 16S rRNA as Pseudomonas aeruginosa. The optimization of process conditions (pH, temperature, and carbon source) for dye degradation during incubation with P.aeruginosa was carried out using Response Surface Methodology (RSM) based on a central composite design (CCD). Maximum degradation was achieved at pH 6.5, temperature 350C with carbon source as 1.5 % after 48 hrs of incubation. This design of experiment methodology increased the dye degradation in many folds. The degraded dye sample was assessed by GC – MS, which indicated that the decolorization took place due to dye degradation.

Keywords

16S rRNA,  Pseudomonas aeruginosa, RSM, Biodegradation, GC – MS analysis

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