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Biotransformation of fluorobiphenyl by Cunninghamella elegans
Author(s)
Date Issued
2010
Date Available
2012-09-04T15:59:46Z
Abstract
The fungus Cunninghamella elegans is a useful model of human catabolism of xenobiotics. In this paper, the biotransformation of fluorinated biphenyls by C. elegans was investigated by analysis of the culture supernatants with a variety of analytical techniques. 4-Fluorobiphenyl was principally transformed to 4-fluoro-4′-hydroxybiphenyl, but other mono- and dihydroxylated compounds were detected in organic extracts by gas chromatography–mass spectrometry. Additionally, fluorinated water-soluble products were detected by 19F NMR and were identified as sulphate and β-glucuronide conjugates. Other fluorobiphenyls (2-fluoro-, 4,4′-difluoro- and 2,3,4,5,6-pentafluoro-biphenyl) were catabolised by C. elegans, yielding mono- and dihydroxylated products, but phase II metabolites were detected from 4,4′-difluorobiphenyl only.
Sponsorship
Other funder
Other Sponsorship
EPA
Type of Material
Journal Article
Publisher
Springer
Journal
Applied Microbiology and Biotechnology
Volume
86
Issue
1
Start Page
345
End Page
351
Copyright (Published Version)
2009 Springer-Verlag
Subject – LCSH
Fluorine
Biphenyl compounds
Biotransformation (Metabolism)
Mucorales
Language
English
Status of Item
Peer reviewed
This item is made available under a Creative Commons License
File(s)
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Name
FBph manuscript revision.doc
Size
946 KB
Format
Microsoft Word
Checksum (MD5)
2072988917920dc68342bea7276253d6
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