<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li P</submitter><funding>Fundamental Research Funds for the Central Universities</funding><funding>Tsinghua University</funding><funding>Beijing Municipal Commission of Education</funding><pagination>100092</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9488089</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6</volume><pubmed_abstract>In this study, an &lt;i>Escherichia coli&lt;/i> (&lt;i>E. coli&lt;/i>) whole-cell biosensor for the specific detection of bioavailable arsenic was developed by placing a green fluorescent protein (GFP) reporter gene under the control of the ArsR1 (GSU2952) regulatory circuit from &lt;i>Geobacter sulfurreducens&lt;/i>. &lt;i>E. coli&lt;/i> cells only emitted green fluorescence in the presence of arsenite and were more sensitive to arsenite when they were grown in M9 supplemented medium compared to LB medium. Under optimal test conditions, the &lt;i>Geobacter arsR1&lt;/i> promoter had a detection limit of 0.01 μM arsenite and the GFP expression was linear within a range of 0.03-0.1 μM (2.25-7.5 μg/l). These values were well below World Health Organization's drinking water quality standard, which is 10 μg/l. The feasibili</pubmed_abstract><journal>Environmental science and ecotechnology</journal><pubmed_title>Development of a whole-cell biosensor based on an ArsR-P &lt;sub>&lt;i>ars&lt;/i>&lt;/sub> regulatory circuit from &lt;i>Geobacter sulfurreducens&lt;/i>.</pubmed_title><pmcid>PMC9488089</pmcid><funding_grant_id>BLX201934</funding_grant_id><funding_grant_id>2019ZY19</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Fu X</pubmed_authors><pubmed_authors>Sun D</pubmed_authors><pubmed_authors>Li P</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Yuan X</pubmed_authors><pubmed_authors>Dang Y</pubmed_authors><pubmed_authors>Holmes DE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of a whole-cell biosensor based on an ArsR-P &lt;sub>&lt;i>ars&lt;/i>&lt;/sub> regulatory circuit from &lt;i>Geobacter sulfurreducens&lt;/i>.</name><description>In this study, an &lt;i>Escherichia coli&lt;/i> (&lt;i>E. coli&lt;/i>) whole-cell biosensor for the specific detection of bioavailable arsenic was developed by placing a green fluorescent protein (GFP) reporter gene under the control of the ArsR1 (GSU2952) regulatory circuit from &lt;i>Geobacter sulfurreducens&lt;/i>. &lt;i>E. coli&lt;/i> cells only emitted green fluorescence in the presence of arsenite and were more sensitive to arsenite when they were grown in M9 supplemented medium compared to LB medium. Under optimal test conditions, the &lt;i>Geobacter arsR1&lt;/i> promoter had a detection limit of 0.01 μM arsenite and the GFP expression was linear within a range of 0.03-0.1 μM (2.25-7.5 μg/l). These values were well below World Health Organization's drinking water quality standard, which is 10 μg/l. The feasibili</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-21T14:26:31.971Z</modification><creation>2025-04-21T14:26:31.971Z</creation></dates><accession>S-EPMC9488089</accession><cross_references><pubmed>36159180</pubmed><doi>10.1016/j.ese.2021.100092</doi></cross_references></HashMap>