ISSN: 0973-7510

E-ISSN: 2581-690X

Lichun Jiang , Qiping Ruan and Chunxiang Bian
1Key Laboratory for Molecular Biology and Biopharmaceutics, Mianyang Normal University, Mianyang, Sichuan 621000, P. R. China.
J Pure Appl Microbiol. 2014;8(3):1883-1892
© The Author(s). 2014
Received: 09/10/2013 | Accepted: 30/12/2013 | Published: 31/06/2014
Abstract

Degradation of increasing phenol and phenolic wastes by some bacteria has become more important these days. 26 bacteria from activated sludge in an insulating material plant of China were isolated to investigate phenol degrading activity in minimal salt medium (MSM) containing 0.5 g/L phenol. 6 isolates showed high phenol activity after 6 cycles each consisting of 120 hours’ incubation. The isolate with the highest phenol degrading activity was subsequently identified as Pseudomonas sp. DHS3Y based on morphological, physiological, biochemical and 16S rRNA molecular phylogeny. A PCR product encoding the phenol hydroxylase gene was successfully obtained from Strain DHS3Y. The optimum conditions for achieving high phenol degradation were pH 7.5, 2.0 % (w/v) NaCl and temperature of 32°C. Pseudomonas sp. DHS3Y was found to degrade phenol of up to 0.9 g/L concentrations under the optimal conditions. The isolation of Pseudomonas sp. DHS3Y is a potential alternative for the bioremediation of phenol contaminated environment.

Keywords

Phenol, Pseudomonas sp. DHS3Y, Phenol degrading activity, Bioremediation

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