IP Library Granted Patent US 7,087,376
Granted Patent B2
US 7,087,376 · App. 10/060,618 · Granted Aug 8, 2006

Detection and identification of bacterial strains

Assignee: Profos AG
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Quick Facts
Patent No.
US 7,087,376
App. No.
10/060,618
Granted
Aug 8, 2006
Kind
B2
Abstract

The present invention relates to a method to detect bacteria, the method comprising the following steps: coupling of the bacteriophages and/or bacteriophage proteins to a support, incubating the support coupled with the bacteriophages and/or bacteriophage proteins with a sample, optionally removing the sample and the bacteria in the sample not bound to the bacteriophages and/or bacteriophage proteins, optionally adding substances permeabilizing or destroying the bacterial membrane, and detecting the bacteria in the sample bound to the bacteriophages and/or bacteriophage proteins, wherein the bound bacteria are not subjected to a cultivation step.

Claims (16)

1. A method for the detection of bacteria comprising:

a) coupling at least T4 p12 protein to a support, either by coupling the T4 p12 protein via direct binding to a support or via direct binding of the T4 p12 to a polypeptide, which in turn is immobilized to a support, wherein said T4 p12 lacks enzymatic activity;

b) incubating the support coupled to the T4 p12 with a sample; and

c) detecting bacteria bound to the T4 p12 protein, wherein bound bacteria are not subjected to a cultivation step.

2. The method of claim 1 , further comprising removing unbound sample from the support.

3. The method of claim 1 , further comprising adding to the support one or more substances that permeabilize or destroy bacterial membranes.

4. The method according to claim 1 , wherein detection is performed by immunologic detection of cell components.

5. The method of according to claim 4 , wherein immunologic detection comprises colorimetric detection.

6. The method according to claim 1 , wherein the T4 p12 protein is directly contacted with the support.

7. The method according to claim 6 , wherein the direct contact is by adsorption or chemical bonding.

8. The method according to claim 1 , wherein the T4 p12 protein is bound to said support through a polypeptide immobilized to the support.

9. The method according to claim 8 , wherein the polypeptide immobilized to the support is an antibody, lectin, receptor or anticalin.

10. The method according to claim 1 , wherein the T4 p12 protein exhibits one or more modifications.

11. The method according to claim 1 , wherein at least two distinct bacteriophage proteins, each recognizing distinct types or genera of bacteria, are immobilized to the support.

12. The method according to claim 1 , wherein the support is a microtiter plate, a test stripe, a slide, a wafer, a filter material, or a flow-through cell chamber consisting of polystyrene, polypropylene, polycarbonate, PMMA, cellulose acetate, nitrocellulose, glass, or silicium wafer.

13. The method according to claim 1 , to detect bacteria in the areas of medicine, food industry and analytics, livestock breeding, fresh water or environmental analytics.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 23, 2010
From: PROFOS AG
To: BIOMERIEUX S.A.
Reel/Frame 023836/0551 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2002
From: MILLER, STEFAN
To: PROFOS AG
Reel/Frame 012887/0935 →
Priority Claims (1)
DE 199 36 047 · Feb 8, 2001 · national
Continuity (2)
Continuation PCTDE000249500 · Jul 28, 2000
Related Publication 20020127547A1 · Sep 12, 2002