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Applied and Environmental Microbiology, November 1998, p. 4396-4402, Vol. 64, No. 11
Marine Biotechnology Institute, Kamaishi
Laboratories, Heita, Kamaishi City, Iwate, Japan
Received 26 March 1998/Accepted 19 August 1998
DNA was isolated from phenol-digesting activated sludge, and
partial fragments of the 16S ribosomal DNA (rDNA) and the gene encoding
the largest subunit of multicomponent phenol hydroxylase (LmPH)
were amplified by PCR. An analysis of the amplified fragments by temperature gradient gel electrophoresis (TGGE) demonstrated that
two major 16S rDNA bands (bands R2 and R3) and two major LmPH gene
bands (bands P2 and P3) appeared after the activated sludge became
acclimated to phenol. The nucleotide sequences of these major bands
were determined. In parallel, bacteria were isolated from the activated
sludge by direct plating or by plating after enrichment either in batch
cultures or in a chemostat culture. The bacteria isolated were
classified into 27 distinct groups by a repetitive extragenic
palindromic sequence PCR analysis. The partial nucleotide
sequences of 16S rDNAs and LmPH genes of members of these 27 groups
were then determined. A comparison of these nucleotide
sequences with the sequences of the major TGGE bands indicated that the
major bacterial populations, R2 and R3, possessed major LmPH genes P2
and P3, respectively. The dominant populations could be isolated either
by direct plating or by chemostat culture enrichment but not by batch
culture enrichment. One of the dominant strains (R3) which
contained a novel type of LmPH (P3), was closely related to
Valivorax paradoxus, and the result of a kinetic analysis
of its phenol-oxygenating activity suggested that this strain was the
principal phenol digester in the activated sludge.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Molecular Detection, Isolation, and Physiological
Characterization of Functionally Dominant Phenol-Degrading
Bacteria in Activated Sludge
*
Corresponding author. Mailing address: Marine
Biotechnology Institute, Kamaishi Laboratories, 3-75-1 Heita, Kamaishi
City, Iwate 026-0001, Japan. Phone: 81 193 26 6537. Fax: 81 193 26 6584. E-mail: kazwata{at}kamaishi.mbio.co.jp.
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