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Applied and Environmental Microbiology, September 2001, p. 4377-4381, Vol. 67, No. 9
Institute of Microbiology and Molecular
Biology, Ernst Moritz Arndt University of Greifswald, D-17487
Greifswald, Germany
Received 27 February 2001/Accepted 26 June 2001
We have investigated the transformation of chlorinated
hydroxybiphenyls by laccase produced by Pycnoporus
cinnabarinus. The compounds used were transformed to sparingly
water-soluble colored precipitates which were identified by gas
chromatography-mass spectrometry as oligomerization products of the
chlorinated hydroxybiphenyls. During oligomerization of
2-hydroxy-5-chlorobiphenyl and 3-chloro-4-hydroxybiphenyl, dechlorinated C---C-linked dimers were formed, demonstrating the dehalogenation ability of laccase. In addition to these nonhalogenated dimers, both monohalogenated and dihalogenated dimers were identified.
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.9.4377-4381.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Dehalogenation of Chlorinated Hydroxybiphenyls by Fungal
Laccase
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Corresponding author: Mailing address: Institute of
Microbiology and Molecular Biology, Ernst Moritz Arndt University of
Greifswald, Friedrich-Ludwig-Jahn-Str. 15, D-17487 Greifswald, Germany.
Phone: 49-(0)3834-864225. Fax: 49-(0)3834-864202. E-mail:
asgard.schultz{at}web.de.
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