کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5746076 1618785 2017 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Elucidating mechanisms of toxic action of dissolved organic chemicals in oil sands process-affected water (OSPW)
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست شیمی زیست محیطی
پیش نمایش صفحه اول مقاله
Elucidating mechanisms of toxic action of dissolved organic chemicals in oil sands process-affected water (OSPW)
چکیده انگلیسی


- Six genes were uniquely responsive to acutely toxic extracts of OSPW.
- Gene enrichment analysis demonstrated a role for oxidative stress, protein and DNA damage.
- Roles of sulphur- and nitrogen-containing chemicals in acute toxicities of extracts of OSPW.

Oil sands process-affected water (OSPW) is generated during extraction of bitumen in the surface-mining oil sands industry in Alberta, Canada, and is acutely and chronically toxic to aquatic organisms. It is known that dissolved organic compounds in OSPW are responsible for most toxic effects, but knowledge of the specific mechanism(s) of toxicity, is limited. Using bioassay-based effects-directed analysis, the dissolved organic fraction of OSPW has previously been fractionated, ultimately producing refined samples of dissolved organic chemicals in OSPW, each with distinct chemical profiles. Using the Escherichia coli K-12 strain MG1655 gene reporter live cell array, the present study investigated relationships between toxic potencies of each fraction, expression of genes and characterization of chemicals in each of five acutely toxic and one non-toxic extract of OSPW derived by use of effects-directed analysis. Effects on expressions of genes related to response to oxidative stress, protein stress and DNA damage were indicative of exposure to acutely toxic extracts of OSPW. Additionally, six genes were uniquely responsive to acutely toxic extracts of OSPW. Evidence presented supports a role for sulphur- and nitrogen-containing chemical classes in the toxicity of extracts of OSPW.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemosphere - Volume 186, November 2017, Pages 893-900
نویسندگان
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