4.7 Article

Biotransformation of fluorobiphenyl by Cunninghamella elegans

Journal

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
Volume 86, Issue 1, Pages 345-351

Publisher

SPRINGER
DOI: 10.1007/s00253-009-2346-4

Keywords

Fluorine; Biphenyl; Metabolism; F-19 NMR

Funding

  1. Environmental Protection Agency STRIVE Programme

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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 F-19 NMR and were identified as sulphate and beta-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.

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