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

• Current Assignee: Fredsense Technologies Corp.
• Original Assignee: Fredsense Technologies Corp.
• Inventors: Mayall, Robert Matthew, Hicks, Emily Candice, Renaud-Young, Margaret Mary-Flora, Lloyd, David Christopher, Oberding, Lisa Kara, George, Iain Fraser Scotney
• Primary Examiner(s): Noakes, Suzanne M
• Assistant Examiner(s): Lee, Jae W
• Application Number:
  US14/491,367
• Publication Number:
  US 20150083612A1
• Time in Patent Office: 1,012 Days
• Field of Search: None
• CPC Class Codes: C12Q 1/34 involving hydrolase
• CPC Class Codes: C12Q 1/6897 involving reporter genes operably linked to promoters
• CPC Class Codes: G01N 2333/938 acting on beta-galactose-glycoside bonds, e.g. beta-galactosidase
• CPC Class Codes: G01N 2333/942 acting on beta-1, 4-glucosidic bonds, e.g. cellulase
• CPC Class Codes: G01N 2458/30 Electrochemically active labels

Abstract

Methods that may be used for the electrochemical detection of multiple parameters, including chemical compounds. Further provided are cells that may be used in the electrochemical detection of multiple parameters, including chemical compounds, as well as a kit for the electrochemical detection of multiple parameters, including chemical compounds.

Claims

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.

2. The method according to claim 1 wherein the β

-D-galactosidase comprises SEQ ID NO;

2, the β

-D glucuronidase comprises SEQ ID NO;

4, and the β

-D-glucosidase comprises SEQ ID NO;

6.

3. A method of simultaneously detecting a first and second parameter in a liquid medium, the method comprising:

(i) contacting in a vessel the liquid medium and (a) a first substrate comprising a first electroactive analyte chemically linked to a first carrier;

(b) a second substrate comprising a second electroactive analyte chemically linked to a second carrier;

(c) a first reporter polypeptide comprising a first hydrolase; and

(d) a second reporter polypeptide comprising a second hydrolase, to form an assay mixture, wherein the first hydrolase is capable of hydrolyzing the first substrate and releasing the first electroactive analyte from the carrier and the second hydrolase is capable of hydrolyzing the second substrate and releasing the second electroactive analyte from the carrier; and

(ii) detecting an electrical signal facilitated by the first and second electroactive analyte in the assay mixture, wherein detecting the electrical signal is 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 detecting the electrical signal is performed by applying a voltage to the assay mixture by a voltammetric sweep, and wherein the first and second reporter polypeptides are different.

4. The method according to claim 3 wherein the β

-D-galactosidase comprises SEQ ID NO;

2, the β

-D glucuronidase comprises SEQ ID NO;

4, and the β

-D-glucosidase comprises SEQ ID NO;

6.