Detecting estrogenic activity in water samples with estrogen-sensitive yeast cells using spectrophotometry and fluorescence microscopy

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dc.contributor.authorWozei, Eleanor
dc.contributor.authorHolman, H-Y.N.
dc.contributor.authorHermanowicz, S.W.
dc.contributor.authorBorglin, S.
dc.date.accessioned2018-04-11T12:51:41Z
dc.date.accessioned2021-12-21T09:35:52Z
dc.date.available2018-04-11T12:51:41Z
dc.date.available2021-12-21T09:35:52Z
dc.date.issued2006-03
dc.descriptionThis article was presented at the SDW Symposium-Mar. 16-17, 2006, and the work was supported by Laboratory Directed Research and Development (LDRD) funding from Berkeley Lab, provided by the Director, Office of Science, of the U.S. Department of Energy under Contract No. DE-AC03-76SF00098 and UC Center for Water Resources Project No. W-944.en_US
dc.description.abstractEnvironmental estrogens are environmental contaminants that can mimic the biological activities of the female hormone estrogen in the endocrine system, i.e. they act as endocrine disrupters. Several substances are reported to have estrogen-like activity or estrogenic activity. These include steroid hormones, synthetic estrogens (xenoestrogens), environmental pollutants and phytoestrogens (plant estrogens). Using the chromogenic substrate ortho-nitrophenyl-β-D-galactopyranoside (ONPG) we show that an estrogen-sensitive yeast strain RMY/ER-ERE, with human estrogen receptor (hERα) gene and the lacZ gene which encodes the enzyme β-galactosidase, is able to detect estrogenic activity in water samples over a wide range of spiked concentrations of the hormonal estrogen 17β-estradiol (E2). Ortho-nitrophenol (ONP), the yellow product of this assay can be detected using spectrophotometry but requires cell lysis to release the enzyme and allow product formation. We improved this aspect in a fluorogenic assay by using fluorescein di-β-D galactopyranoside (FDG) as a substrate. The product was visualized using fluorescence microscopy without the need to kill, fix or lyse the cells. We show that in live yeast cells, the uptake of E2 and the subsequent production of β-galactosidase enzyme occur quite rapidly, with maximum enzyme-catalyzed fluorescent product formation evident after about 30 minutes of exposure to E2. The fluorogenic assay was applied to a selection of estrogenic compounds and the Synchrotron-based Fourier transform infrared (SR-FTIR) spectra of the cells obtained to better understand the yeast whole cell response to the compounds. The fluorogenic assay is most sensitive to E2, but the SR-FTIR spectra suggest that the cells respond to all the estrogenic compounds tested even when no fluorescent response was detected. These findings are promising and may shorten the duration of environmental water screening and monitoring regimes using yeast-based estrogen assays, and the development of biosensors for environmental estrogens designed to complement quantification methods.en_US
dc.identifier.citationWozei, E., Holman, H-Y.N., Hermanowicz, S.W., Borglin S., 2006. Detecting estrogenic activity in water samples with estrogen-sensitive yeast cells using spectrophotometry and fluorescence microscopy.en_US
dc.identifier.urihttps://hdl.handle.net/20.500.11951/197
dc.language.isoenen_US
dc.subjectEstrogenic activityen_US
dc.subjectEstrogenen_US
dc.subjectYeasten_US
dc.subjectAssayen_US
dc.subjectFuorogenic,en_US
dc.subjectChromogenicen_US
dc.subjectEndocrine Disrupting Compounds (EDC)en_US
dc.subjectFourier Transform Infrared Spectromicroscopy (FTIR)en_US
dc.titleDetecting estrogenic activity in water samples with estrogen-sensitive yeast cells using spectrophotometry and fluorescence microscopyen_US
dc.typeArticleen_US
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