Appl Environ Microbiol, July 1998, p. 2566-2571, Vol. 64, No. 7
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Environmental Technology,
Received 29 December 1997/Accepted 17 April 1998
A new aerobic bacterium was isolated from the sediment of a
freshwater pond close to a contaminated site at Amponville (France). It
was enriched in a fixed-bed reactor fed with 2,6-dichlorophenol (2,6-DCP) as the sole carbon and energy source at pH 7.5 and room temperature. The degradation of 2,6-DCP followed Monod kinetics at low
initial concentrations. At concentrations above 300 µM (50 mg
· liter
1), 2,6-DCP increasingly inhibited its own
degradation. The base sequence of the 16S ribosomal DNA allowed us to
assign the bacterium to the genus Ralstonia (formerly
Alcaligenes). The substrate spectrum of the bacterium
includes toluene, benzene, chlorobenzene, phenol, and all four
ortho- and para-substituted mono- and
dichlorophenol isomers. Substituents other than chlorine prevented
degradation. The capacity to degrade 2,6-DCP was examined in two
fixed-bed reactors. The microbial population grew on and completely
mineralized 2,6-DCP at 2,6-DCP concentrations up to 740 µM in
continuous reactor culture supplied with H2O2
as an oxygen source. Lack of peroxide completely stopped
further degradation of 2,6-DCP. Lowering the acid-neutralizing capacity
of the medium to 1/10th the original capacity led to a decrease in the
pH of the effluent from 7 to 6 and to a significant reduction in the
degradation activity. A second fixed-bed reactor successfully removed
low chlorophenol concentrations (20 to 26 µM) with
hydraulic residence times of 8 to 30 min.
*
Corresponding author. Mailing address: Ciba Specialty
Chemicals Inc., WS-2090.K1.26, CH-4133 Pratteln, Switzerland. Phone: 41 61 468 23 46. Fax: 41 61 468 21 65. E-mail:
patrick.steinle{at}cibasc.com.
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