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Journal of Bacteriology, April 1999, p. 2050-2058, Vol. 181, No. 7
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Degradation of 1,2-Dibromoethane by
Mycobacterium sp. Strain GP1
Gerrit J.
Poelarends,1
Johan E. T.
van Hylckama Vlieg,1
Julian R.
Marchesi,2
Luisa M.
Freitas Dos Santos,3,
and
Dick B.
Janssen1,*
Department of Biochemistry, Groningen
Biomolecular Sciences and Biotechnology Institute, University of
Groningen, 9747 AG Groningen, The Netherlands,1
and School of Pure and Applied Biology, University of Wales
College of Cardiff, Cardiff CF1 3TL,2 and
Department of Chemical Engineering and Chemical Technology,
Imperial College, London SW7 2BY,3 United
Kingdom
Received 23 September 1998/Accepted 18 January 1999
The newly isolated bacterial strain GP1 can utilize
1,2-dibromoethane as the sole carbon and energy source. On the basis of 16S rRNA gene sequence analysis, the organism was identified as a
member of the subgroup which contains the fast-growing mycobacteria. The first step in 1,2-dibromoethane metabolism is catalyzed by a
hydrolytic haloalkane dehalogenase. The resulting 2-bromoethanol is
rapidly converted to ethylene oxide by a haloalcohol dehalogenase, in
this way preventing the accumulation of 2-bromoethanol and 2-bromoacetaldehyde as toxic intermediates. Ethylene oxide can serve as
a growth substrate for strain GP1, but the pathway(s) by which it is
further metabolized is still unclear. Strain GP1 can also utilize
1-chloropropane, 1-bromopropane, 2-bromoethanol, and 2-chloroethanol as
growth substrates. 2-Chloroethanol and 2-bromoethanol are metabolized
via ethylene oxide, which for both haloalcohols is a novel way to
remove the halide without going through the corresponding acetaldehyde
intermediate. The haloalkane dehalogenase gene was cloned and
sequenced. The dehalogenase (DhaAf) encoded by this gene is
identical to the haloalkane dehalogenase (DhaA) of Rhodococcus
rhodochrous NCIMB 13064, except for three amino acid
substitutions and a 14-amino-acid extension at the C terminus.
Alignments of the complete dehalogenase gene region of strain GP1 with
DNA sequences in different databases showed that a large part of a
dhaA gene region, which is also present in R. rhodochrous NCIMB 13064, was fused to a fragment of a haloalcohol dehalogenase gene that was identical to the last 42 nucleotides of the
hheB gene found in Corynebacterium sp. strain
N-1074.
*
Corresponding author. Mailing address: Department of
Biochemistry, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands. Phone: 31-50-3634209. Fax: 31-50-3634165. E-mail: d.b.janssen{at}chem.rug.nl.
Present address: SmithKline Beecham, Tonbridge TN11 9AN, Kent,
United Kingdom.
Journal of Bacteriology, April 1999, p. 2050-2058, Vol. 181, No. 7
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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