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4-Chlorophenol degradation by a bacterial consortium: development of a granular activated carbon biofilm reactor
Author(s) -
M.L. Caldeira,
S. Heald,
Maria F. Carvalho,
Isabel Vasconcelos,
Alan T. Bull,
Paula M. L. Castro
Publication year - 1999
Publication title -
applied microbiology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.074
H-Index - 221
eISSN - 1432-0614
pISSN - 0175-7598
DOI - 10.1007/s002530051584
Subject(s) - microbial consortium , biofilm , biodegradation , exopolymer , activated sludge , chemistry , effluent , chlorophenol , adsorption , bioreactor , chromatography , confocal laser scanning microscopy , activated carbon , degradation (telecommunications) , environmental chemistry , nuclear chemistry , microbiology and biotechnology , wastewater , environmental engineering , bacteria , microorganism , organic chemistry , biology , phenol , genetics , engineering , telecommunications , computer science
A bacterial consortium that can degrade chloro- and nitrophenols has been isolated from the rhizosphere of Phragmitis communis. Degradation of 4-chlorophenol (4-CP) by a consortium attached to granular activated carbon (GAC) in a biofilm reactor was evaluated during both open and closed modes of operation. During the operation of the biofilm reactor, 4-CP was not detected in the column effluent, being either adsorbed to the GAC or biodegraded by the consortium. When 4-CP at 100 mg l-1 was fed to the column in open mode operation (20 mg g-1 GAC total supply), up to 27% was immediately available for biodegradation, the rest being adsorbed to the GAC. Biodegradation continued after the system was returned to closed mode operation, indicating that GAC bound 4-CP became available to the consortium. Biofilm batch cultures supplied with 10-216 mg 4-CP g-1 GAC suggested that a residual fraction of GAC-bound 4-CP was biologically unavailable. The consortium was able to metabolise 4-CP after perturbations by the addition of chromium (Cr VI) at 1-5 mg l-1 and nitrate at concentrations up to 400 mg l-1. The development of the biofilm structure was analysed by scanning electron microscopy and confocal laser scanning microscopy (CLSM) techniques. CLSM revealed a heterogeneous structure with a network of channels throughout the biofilm, partially occupied by microbial exopolymer structures.

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