Your browser doesn't support javascript.
loading
Biotransformation of fluorobiphenyl by Cunninghamella elegans.
Amadio, Jessica; Murphy, Cormac D.
Affiliation
  • Amadio J; School of Biomolecular and Biomedical Science, Centre for Synthesis and Chemical Biology, Ardmore House, University College Dublin, Dublin 4, Ireland.
Appl Microbiol Biotechnol ; 86(1): 345-51, 2010 Mar.
Article in En | MEDLINE | ID: mdl-19956946
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 (19)F 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.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Biodegradation, Environmental / Biphenyl Compounds / Cunninghamella Limits: Humans Language: En Year: 2010 Type: Article

Full text: 1 Database: MEDLINE Main subject: Biodegradation, Environmental / Biphenyl Compounds / Cunninghamella Limits: Humans Language: En Year: 2010 Type: Article