Method and culture device for detecting yeasts and molds

• US 10,640,743 B2
• Filed: 01/25/2018
• Issued: 05/05/2020
• Est. Priority Date: 02/04/2013
• Status: Active Grant

• Current Assignee: Neogen Food Safety US Holdco Corporation (Neogen Corporation)
• Original Assignee: 3M Innovative Properties Company (3M Company)
• Inventors: Chandrapati, Sailaja, Nordby, Tera M.
• Primary Examiner(s): Afremova, Vera
• Application Number:
  US15/879,582
• Publication Number:
  US 20180148675A1
• Time in Patent Office: 831 Days
• Field of Search: None
• CPC Class Codes: C12M 23/04 Flat or tray type, drawers C12M23/10, C12M23/12, C12M23/16 take precedence
• CPC Class Codes: C12M 23/20 Material Coatings immunocoatings C12M25/00
• CPC Class Codes: C12M 23/24 Gas permeable parts
• CPC Class Codes: C12Q 1/04 Determining presence or kind of microorganism; Use of selective media for testing antibiotics or bacteriocides; Compositions containing a chemical indicator therefor C12Q1/6897 takes precedence
• CPC Class Codes: G01N 33/52 Use of compounds or compositions for colorimetric, spectrophotometric or fluorometric investigation, e.g. use of reagent paper and including single- and multilayer analytical elements immunological elements G01N33/54386; involving labelled immunochemicals G01N33/58; for haemoglobin or occult blood G01N33/72

Abstract

A thin film culture device for detecting yeast and mold microorganisms in a sample is provided. The culture device comprises a body comprising a self-supporting substrate having a first major surface and a second major surface; a first adhesive composition disposed on a portion of the first major surface of the substrate; a substantially dry, cold-water-soluble first hydrogel-forming composition adhered to the first adhesive composition; and a plurality of indicator agents. The plurality of indicator agents comprises three indicator agents for detecting distinct glycosidase enzyme activities, an indicator agent for detecting an alkyl esterase enzyme activity, and an indicator agent for detecting a phosphatase enzyme activity, wherein each of the plurality of indicator agents comprises a detectable reporter group. A method of using the culture device is also provided.

Claims

1. A culture device, comprising:

a body comprising a self-supporting substrate having a first major surface and a second major surface;

a first adhesive composition disposed on a portion of the first major surface of the substrate;

a substantially dry, cold-water-soluble first hydrogel-forming composition adhered to the first adhesive composition; and

a plurality of indicator agents, the plurality of indicator agents comprising;

5-bromo-4-chloro-3-indolyl acetate, 5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside, 5-bromo-4-chloro-3-indolyl-beta-D-glucopyranoside, 5-bromo-4-chloro-3-indolyl-alpha-D-glucopyranoside, and 5-bromo-4-chloro-3-indolyl phosphate para-toluidine salt; and

a cover sheet attached to the body member, wherein

the cover sheet comprises a first major surface facing the body member, and

wherein the culture device also comprises a second adhesive composition disposed on a portion of the first major surface of the cover sheet and a substantially dry, cold-water-soluble second hydrogel-forming composition adhered to the second adhesive composition;

wherein at least three of the 5-bromo-4-chloro-3-indolyl acetate, 5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside, 5-bromo-4-chloro-3-indolyl-beta-D-glucopyranoside, 5-bromo-4-chloro-3-indolyl-alpha-D-glucopyranoside, and 5-bromo-4-chloro-3-indolyl phosphate para-toluidine salt are disposed in the first adhesive composition and/or the second adhesive composition.

2. The culture device of claim 1, wherein the 5-bromo-4-chloro-3-indolyl acetate, 5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside, 5-bromo-4-chloro-3-indolyl-beta-D-glucopyranoside, 5-bromo-4-chloro-3-indolyl-alpha-D-glucopyranoside, and 5-bromo-4-chloro-3-indolyl phosphate para-toluidine salt are disposed in the first adhesive composition and/or the second adhesive composition.

3. The culture device of claim 1, further comprising a water-insoluble spacer having an aperture, the spacer being attached to the body member or the coversheet and the entire aperture being positioned between the body member and the cover sheet.

5. A method of detecting yeast or mold in a sample, comprising:

contacting a sample and an aqueous liquid with the gelling agent disposed on the first or second adhesive composition of the culture device of claim 1 to form an inoculated culture device;

incubating the inoculated culture device for a period of time; and

detecting a yeast or mold colony in the culture device.

6. The method of claim 5, wherein detecting a yeast or mold colony in the culture device comprises detecting in the culture device a presence or an absence of the detectable reporter group of at least one of the indicator agents, wherein detecting the presence of the detectable reporter group is indicative of a presence of a colony of yeast or mold microorganisms.

7. The method of claim 5, wherein contacting a sample with the gelling agent disposed on the first or second adhesive composition of the culture device comprises placing the sample in fluid communication with the at least one nutrient.

8. The method of claim 5, wherein incubating the inoculated culture device comprises incubating the inoculated culture device at a temperature between about 20°

C. and about 32°

C., inclusive.

9. The method of claim 5, wherein incubating the inoculated culture device for a period of time comprises incubating the inoculated culture device for up to about 72 hours.

10. The method of claim 8, wherein incubating the inoculated culture device for a period of time comprises incubating the inoculated culture device for up to about 60 hours.

11. The method of claim 5, further comprising enumerating yeast or mold colonies present in the inoculated culture device after incubating the inoculated culture device.

4. The culture device of embodiment 21, further comprising a predefined volume of aqueous liquid disposed between the body member and the coversheet, wherein the aqueous liquid and gelling agent form a hydrogel.