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System and methods for the detection of multiple chemical compounds

  • US 9,689,046 B2
  • Filed: 09/19/2014
  • Issued: 06/27/2017
  • Est. Priority Date: 09/20/2013
  • Status: Active Grant
First Claim
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1. A method for simultaneously detecting two parameters in a liquid medium comprising:

  • (i) providing a liquid medium comprising a first and second parameter;

    (ii) contacting in a vessel the liquid medium with cells and a first and second substrate to form an assay mixture, wherein the first substrate comprises a first electroactive analyte chemically linked to a first carrier and the second substrate comprises a second electroactive analyte chemically linked to a second carrier; and

    wherein the cells comprise a chimeric nucleic acid construct comprising in the 5′

    to 3′

    direction of translation as operably linked components a first nucleic acid construct comprising;

    (a) a first promoter inducible by the first parameter; and

    (b) a nucleic acid sequence encoding a first reporter polypeptide comprising a first hydrolase capable of hydrolyzing the first substrate and releasing the first electroactive analyte from the carrier; and

    a second nucleic acid construct comprising;

    (c) a second promoter inducible by the second parameter; and

    (d) a nucleic acid sequence encoding a second reporter polypeptide comprising a second hydrolase capable of hydrolyzing the second substrate and releasing the second electroactive analyte from the carrier;

    (iii) detecting an electrical signal facilitated by the first and second electroactive analyte in the assay mixture, wherein detecting the electrical signal facilitated by the first and second electroactive analyte detects the first and second parameters in the liquid medium;

    wherein the first and second hydrolase are independently selected from the group of hydrolases consisting of β

    -D-glucosidase, β

    -D galactosidase, and β

    -D-glucuronidase;

    wherein the first and second substrate are independently selected from the group of substrates consisting of chlorophenol red-β

    -D-galactopyranoside (CPRG),para-nitrophenol-β

    -D-glucuronide (PNPG), para-aminophenol-β

    -D-galactopyranoside (PAPG) and para-di-phenol-β

    -D-glucopyranoside (PDPG);

    wherein the voltage in step (iii) is applied to the assay mixture by a voltammetric sweep, and wherein the first and second nucleic acid constructs are different.

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