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Applied and Environmental Microbiology, September 1999, p. 4021-4027, Vol. 65, No. 9
Biological Chemistry,
Received 20 January 1999/Accepted 9 June 1999
The pathways of biotransformation of 4-fluorobiphenyl (4FBP) by the
ectomycorrhizal fungus Tylospora fibrilosa and several other mycorrhizal fungi were investigated by using 19F
nuclear magnetic resonance (NMR) spectroscopy in combination with
14C radioisotope-detected high-performance liquid
chromatography (14C-HPLC). Under the conditions used in
this study T. fibrillosa and some other species degraded
4FBP. 14C-HPLC profiles indicated that there were four
major biotransformation products, whereas 19F NMR showed
that there were six major fluorine-containing products. We confirmed
that 4-fluorobiphen-4'-ol and 4-fluorobiphen-3'-ol were two of the
major products formed, but no other products were conclusively
identified. There was no evidence for the expected biotransformation
pathway (namely, meta cleavage of the less halogenated ring), as none of the expected products of this route were found. To
the best of our knowledge, this is the first report describing intermediates formed during mycorrhizal degradation of halogenated biphenyls.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Degradation of 4-Fluorobiphenyl by Mycorrhizal Fungi as
Determined by 19F Nuclear Magnetic Resonance Spectroscopy
and 14C Radiolabelling Analysis
*
Corresponding author. Mailing address: Biological
Chemistry, Division of Biological Sciences, BMS Building, Imperial
College of Science Technology and Medicine, Exhibition Road, South
Kensington, London, SW7 2AZ, United Kingdom. Phone: 00 44 (0)171 594 3195. Fax: 00 44 (0)171 594 3221. E-mail:
j.nicholson{at}ic.ac.uk.
Applied and Environmental Microbiology, September 1999, p. 4021-4027, Vol. 65, No. 9
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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