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        <identifier>oai:figshare.com:article/33793243</identifier>
        <datestamp>2026-09-15T12:50:01Z</datestamp>
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          <dc:title>&lt;p dir="ltr"&gt;&lt;b&gt;A Calcium- and Magnesium-Tolerant Enterobacter sp. MTT Respiratory Inhibition Assay for Rapid Screening of Mercury and Silver in Industrial River Water&lt;/b&gt;&lt;/p&gt;</dc:title>
          <dc:creator>yunus shukor (10052324)</dc:creator>
          <dc:subject>Environmental biotechnology diagnostics (incl. biosensors)</dc:subject>
          <dc:subject>Whole-cell bioassay</dc:subject>
          <dc:subject>Enterobacter</dc:subject>
          <dc:subject>Mercury</dc:subject>
          <dc:subject>Silver</dc:subject>
          <dc:subject>Effect-based monitoring</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;Rapid biological screening can complement instrumental analysis by identifying water samples that warrant priority investigation. This study developed a whole-cell respiratory inhibition assay based on the reduction of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) by a locally isolated bacterium. Enterobacter sp. strain DRY13, retained respiratory activity in the presence of Ca2+ and Mg2+ yet responded strongly to toxic metals. supported tentative placement within Enterobacter. Among 13 metals tested, Ag+ and Hg2+ produced greater than 50% inhibition at 10 mg L−1. One-phase exponential models yielded IC50 values of 0.139 mg L−1 for Ag+ (95% CI, 0.115–0.173 mg L−1) and 0.144 mg L−1 for Hg2+ (95% CI, 0.106–0.221 mg L−1), with R2 values of 0.9842 and 0.999, respectively. The reported limits of detection were 0.0033 mg L−1 for Ag+ and 0.0216 mg L−1 for Hg2+; corresponding limits of quantification were 0.0294 and 0.0386 mg L−1. Most pesticides and solvent-related xenobiotics caused little inhibition at the tested concentrations, whereas sodium dodecyl sulfate was a notable interferent. River and industrial-estate samples inhibited MTT reduction, while tap water did not. Because ICP-AES measures total recoverable metal whereas whole-cell inhibition reflects the combined bioavailable toxic fraction, the assay is best interpreted as a rapid effect-based screen rather than a metal-specific quantitative method. The platform provides a simple basis for prioritizing contaminated samples for confirmatory instrumental analysis.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T12:50:01Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.33793243.v1</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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