Materials and methods for detection of oxalate

• US 5,837,833 A
• Filed: 06/20/1995
• Issued: 11/17/1998
• Est. Priority Date: 06/20/1994
• Status: Expired due to Term

• Current Assignee: Knowles Electronics LLC A Delaware Limited Liability Company
• Original Assignee: University of Florida Research Foundation, Incorporated (State University System of Florida)
• Inventors: Peck, Ammon B.
• Primary Examiner(s): Marschel, Ardin H.
• Assistant Examiner(s): Riley, Jezia
• Application Number:
  US08/493,197
• Time in Patent Office: 1,246 Days
• Field of Search: 536/22.1, 536/24.3, 536/24.33, 536/23.7, 435/91.1, 435/91.2, 435/6, 935/76, 935/77, 935/78
• US Class Current: 536/22.1
• CPC Class Codes: C12N 9/10 Transferases (2.) ribonucleases C12N9/22
• CPC Class Codes: C12N 9/1014 Hydroxymethyl-, formyl-transferases (2.1.2)
• CPC Class Codes: C12N 9/88 Lyases (4.)
• 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: C12Q 1/527 involving lyase
• CPC Class Codes: C12Q 1/689 for bacteria

Abstract

The subject invention concerns the novel use of formyl-CoA transferase enzyme together with oxalyl-CoA decarboxylase enzyme for the detection and measurement of oxalate in biological samples. The use of the enzyme system according to the subject invention results in the conversion of oxalate into carbon dioxide and formate. Because the production of formate is directly correlated to the concentration of oxalate present in a sample, the determination of the resulting formate concentration provides an accurate, sensitive and rapid means for detecting even low levels of oxalate. The subject invention further concerns the cloning, sequencing and expression of the genes that encode the formyl-CoA transferase enzyme and the oxalyl-CoA decarboxylase enzyme of Oxalobacter formigenes. The subject invention also concerns a method for detecting the presence of Oxalobacter formigenes organisms in a sample, and the polynucleotide probes and primers used in the detection method.

Claims

1. A method for detecting Oxalobacter formigenes in a sample, comprising the steps of:

(a) amplifying by PCR a DNA fragment of the Oxalobacter formigenes genome in said sample using a polynucleotide PCR primer, said PCR primer comprising a nucleotide sequence that is complementary with a polynucleotide sequence of a formyl-CoA transferase gene of Oxalobacter formigenes, said formyl-CoA transferase gene comprising a polynucleotide sequence selected from the group consisting of SEQ ID. NO. 1, SEQ ID NO. 2 and SEQ ID NO. 3, wherein said PCR primer is capable of specifically priming PCR amplification of said polynucleotide sequence of said formyl-CoA transferase gene;

(b) contacting said amplified DNA fragment with a polynucleotide probe under conditions sufficient for selective hybridizaiton of said polynucleotide probe with said amplified DNA fragment, wherein said polynucleotide probe comprises a nucleotide sequence that is complementary with a polynucleotide sequence of said amplified DNA fragment, said polynucleotide probe comprising a sufficient number of nucleotides to hybridize under high stringency conditions with said polynucleotide sequence of said amplified DNA fragment; and

(c) detecting said polynucleotide probe hybridized to said amplified DNA fragment.

2. The method according to claim 1, wherein said amplified DNA fragment is size-fractionated prior to performing step (b).

3. The method according to claim 1, wherein said amplified DNA fragment is immobilized on a membrane matrix prior to performing step (b).

4. A method for detecting Oxalobacter formigenes in a sample, comprising the steps of:

(a) amplifying by PCR a DNA fragment of the Oxalobacter formigenes genome in said sample using a polynucleotide PCR primer, said PCR primer comprising a nucleotide sequence that is complementary with a polynucleotide sequence of an oxalyl-CoA decarboxylase gene of Oxalobacter formigenes, said oxalyl-CoA decarboxylase gene comprising a polynucleotide sequence of SEQ ID NO. 6, wherein said PCR primer is capable of specifically priming PCR amplification of said polynucleotide sequence of said oxalyl-CoA decarboxylase gene;

(b) contacting said amplified DNA fragment with a polynucleotide probe under conditions sufficient for selective hybridization of said polynucleotide probe with said amplified DNA fragment, wherein said polynucleotide probe comprises a nucleotide sequence that is complementary with a polynucleotide sequence of said amplified DNA fragment, said polynucleotide probe comprising a sufficient number of nucleotides to hybridize under high stringency conditions with said polynucleotide sequence or said amplified DNA fragment; and

(c) detecting said polynucleotide probe hybridized to said amplified DNA fragment.

5. The method according to claim 4, wherein said amplified DNA fragment is size-fractionated prior to performing step (b).

6. The method according to claim 4, wherein said amplified DNA fragment is immobilized on a membrane matrix prior to performing step (b).

7. The method according to claim 4, wherein said polynucleotide probe comprises a nucleotide sequence selected from the group consisting of SEQ ID NO. 8, SEQ ID NO. 9, SEQ ID NO. 10, and SEQ ID NO. 11.

8. A polynucleotide PCR primer comprising a nucleotide sequence that is complementary with a polynucleotide sequence of an oxalyl-CoA decarboxylase gene of Oxalobacter formigenes, said oxalyl-CoA decarboxylase gene comprising a polynucleotide sequence of SEQ ID NO. 6, wherein said PCR primer is capable of specifically priming PCR amplification of said polynucleotide sequence of said oxalyl-CoA decarboxylase gene and comprises a nucleotide sequence selected from the group consisting of SEQ ID NO.10 and SEQ ID NO. 11.