<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Roggo, Clémence</dc:creator>
  <dc:creator>Picioreanu, Cristian</dc:creator>
  <dc:creator>Richard, Xavier</dc:creator>
  <dc:creator>Mazza, Christian</dc:creator>
  <dc:creator>Lintel, Harald van</dc:creator>
  <dc:creator>Meer, Jan Roelof van der</dc:creator>
  <dc:date>2018</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Whole-cell bacterial bioreporters are proposed as alternatives to chemical analysis of,  for example, pollutants in environmental compartments. Commonly based on reporter  gene induction, bioreporters produce a detectable signal within 30 min to a few hours  after exposure to the chemical target, which is impractical for applications aiming at a  fast response. In an attempt to attain faster readout but maintain flexibility of chemical  targeting, we explored the concept for quantitative chemical sensing by bacterial  chemotaxis. Chemotaxis was quantified from enrichment of cells across a 600 µm- wide chemical gradient stabilized by parallel flow in a microfluidic chip, further  supported by transport and chemotaxis steady state and kinetic modelling. As proof- of-concept, we quantified Escherichia coli chemotaxis towards serine, aspartate and  methylaspartate as a function of attractant concentration and exposure time. E. coli  chemotaxis enrichment increased sharply between 0 and 10 µM serine, before  saturating at 100 µM. The chemotaxis accumulation rate was maximal at 10 µM  serine, leading to observable cell enrichment within 5 min. The potential application  for biosensing of environmental toxicants was investigated by quantifying chemotaxis  of Cupriavidus pinatubonensis JMP134 towards the herbicide 2,4- dichlorophenoxyacetate. Our results show that bacterial chemotaxis can be quantified  on a scale of minutes and may be used for developing faster bioreporter assays.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/306522</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306522/files/maz_qcb.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306522/files/maz_qcb_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1111/1462-2920.13982</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Environmental Microbiology. - 2018, vol. 20, no. 1, p. 241–258</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Quantitative chemical biosensing by bacterial chemotaxis in microfluidic chips: Chemotaxis-microfluidic biosensor</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
