IP Library Granted Patent US 7,422,868
Granted Patent B2
US 7,422,868 · App. 11/173,092 · Granted Sep 9, 2008

Microbial ATP extraction and detection system

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Quick Facts
Patent No.
US 7,422,868
App. No.
11/173,092
Granted
Sep 9, 2008
Kind
B2
Abstract

The present invention is directed to compositions and methods for single-step extraction and detection of ATP levels from microbial cells. The disclosed compositions are formulated to efficiently elicit bioluminescent detection of ATP among a broad variety of different microorganisms using a common single-step reagent composition. Additional luminescence-based methods are provided for identifying other useful extracting agents or for screening compounds for their pharmaceutical or biological effects on microbial cells.

Claims (44)

1. A composition for extracting ATP from a gram negative microorganism comprising:

(a) a reaction buffer;

(b) one or more ATP extracting agents;

(c) a divalent cation at a first concentration; and

(d) a divalent cation chelator at a second concentration;

wherein the first concentration is at least 10 mM and the second concentration is at least about equal to or greater than the first concentration.

2. The composition of claim 1 , wherein the first concentration is at least 20 mM.

3. The composition of claim 1 , wherein the first concentration is at least about 20 mM and the second concentration is at least about 20 mM.

4. An aqueous composition for detecting ATP in a sample suspected of containing a microorganism comprising:

(a) a reaction buffer;

(b) one or more ATP extracting agents;

(c) a divalent cation at a first concentration

(d) a divalent cation chelator at a second concentration; and

(e) a luciferase enzyme

wherein the second concentration is at least 10 mM and the difference between the first concentration and the second concentration is less than about 5 mM; and

wherein the one or more ATP extracting agents comprises a compound or combination of compounds capable of disrupting the integrity of a bacterium or yeast to effect release of ATP therefrom.

5. The composition of claim 4 , wherein the difference between the first concentration and the second concentration is less than about 2.5 mM.

6. The composition of claim 4 , wherein the difference between the first concentration and the second concentration is less than about 1.0 mM.

7. The composition of claim 4 , wherein the second concentration is greater than the first concentration.

8. The composition of claim 4 , wherein the first concentration is at least about 20 mM and the second concentration is greater than about 20 mM.

9. The composition of claim 4 , wherein the bacterium is a gram negative bacterium.

10. The composition of claim 4 , wherein the one or more ATP extracting agents comprises cetyltrimethylammonium bromide.

11. The composition of claim 4 , wherein the one or more one ATP extracting agents comprises chlorohexidine and a non-ionic detergent.

12. The composition of claim 4 , wherein the one or more ATP extracting agents comprises cetyltrimethylammonium bromide, chlorohexidine, and a non-ionic detergent.

13. The composition of claim 4 , wherein the divalent cation is Mg 2+ , Ca 2+ or Mn 2+ .

14. The composition of claim 4 , wherein the divalent cation chelator is EDTA or CDTA.

15. The composition of claim 4 , wherein the divalent cation is Mg 2+ and the divalent cation chelator is EDTA.

16. An aqueous composition for detecting ATP in a sample suspected of containing a microorganism comprising:

(a) a reaction buffer;

(b) one or more ATP extracting agents;

(c) a divalent cation at a first concentration;

(d) a divalent cation chelator at a second concentration;

wherein the second concentration is greater than the first concentration. wherein the first concentration is at least 10 mM and the difference between the first concentration and the second concentration is less than about 5 mM; and

wherein the one or more ATP extracting agents comprises a compound or combination of compounds capable of disrupting the integrity of a bacterium or yeast to effect release of ATP therefrom.

17. The composition of claim 16 , wherein the difference between the first concentration and the second concentration is less than about 2.5 mM.

18. The composition of claim 16 , wherein the difference between the first concentration and the second concentration is less than about 1.0 mM.

19. The composition of claim 16 , wherein the first concentration is at least about 20 mM and the second concentration is greater than about 20 mM.

20. The composition of claim 16 , wherein the bacterium is a gram negative bacterium.

21. The composition of claim 16 , wherein the one or more ATP extracting agents comprises cetyltrimethylammonium bromide.

22. The composition of claim 16 , wherein the one or more one ATP extracting agents comprises chlorohexidine and a non-ionic detergent.

23. The composition of claim 16 , wherein the one or more ATP extracting agents comprises cetyltrimethylammonium bromide, chlorohexidine, and a non-ionic detergent.

24. The composition of claim 16 , wherein the divalent cation is Mg 2+ , Ca 2+ or Mn 2+ .

25. The composition of claim 16 , wherein the divalent cation chelator is EDTA or CDTA.

26. The composition of claim 16 , wherein the divalent cation is Mg 2+ and the divalent cation chelator is EDTA.

Assignments (2)
SECURITY INTEREST Recorded Apr 3, 2019
From: PROMEGA CORPORATION; PROMEGA BIOSCIENCES, LLC; TERSO SOLUTIONS, INC.; ORION SEVEN, LLC; PROMEGA AVIATION LLC
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 048790/0259 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 28, 2005
From: FAN, FRANK; BUTLER, BRAEDEN; WOOD, KEITH V.
To: PROMEGA CORPORATION
Reel/Frame 017042/0168 →