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The invention is directed to polypeptides having epoxide hydrolase activity, polynucleotides encoding the polypeptides, antibodies that bind to these polypeptides, and methods for making and using these polynucleotides and polypeptides. The epoxide hydrolases are used to catalyze the hydrolysis of e

The invention is directed to polypeptides having epoxide hydrolase activity, polynucleotides encoding the polypeptides, antibodies that bind to these polypeptides, and methods for making and using these polynucleotides and polypeptides. The epoxide hydrolases are used to catalyze the hydrolysis of epoxides and arene oxides to their corresponding diols.

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1. An isolated or recombinant nucleic acid, wherein the nucleic acid comprises a sequence that hybridizes under stringent conditions to a nucleic acid comprising a sequence as set forth in SEQ ID NO:25 or a sequence encoding a polypeptide having an amino acid sequence as set forth in SEQ ID NO:26 or

1. An isolated or recombinant nucleic acid, wherein the nucleic acid comprises a sequence that hybridizes under stringent conditions to a nucleic acid comprising a sequence as set forth in SEQ ID NO:25 or a sequence encoding a polypeptide having an amino acid sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85, wherein the nucleic acid encodes a polypeptide having an epoxide hydrolase activity.2. The isolated or recombinant nucleic acid of claim 1, wherein the nucleic acid is at least about 100 residues in length.3. The isolated or recombinant nucleic acid of claim 2, wherein the nucleic acid is at least about 200 residues in length.4. The isolated or recombinant nucleic acid of claim 3, wherein the nucleic acid is about 300 residues in length.5. The isolated or recombinant nucleic acid of claim 4, wherein the nucleic acid is at least about 400 residues in length.6. The isolated or recombinant nucleic acid of claim 5, wherein the nucleic acid is at least about 500, 600, 700, 800, 900, or 1000 residues in a length or the full length of a gene or transcript.7. The isolated or recombinant nucleic acid of claim 1, wherein the stringent conditions include a wash step comprising a wash in 0.2×SSC at a temperature of about 65° C. for about 15 minutes.8. An isolated or recombinant nucleic acid having a sequence as set forth in SEQ ID NO:25.9. An isolated or recombinant nucleic acid comprising a sequence encoding a polypeptide having a sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.10. The isolated or recombinant nucleic acid of claim 1, wherein the nucleic acid sequence has at least 95% sequence identity to a sequence as set forth in SEQ ID NO:25, or to a sequence encoding polypeptide having an amino acid sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.11. The isolated or recombinant nucleic acid of claim 10, wherein the nucleic acid sequence has at least 98% sequence identity to a sequence as set forth in SEQ ID NO.25, or to a sequence encoding polypeptide having an amino acid sequence as set forth in SEC ID NO:26 or SEQ ID NO:85.12. The isolated or recombinant nucleic acid of claim 10, wherein the nucleic acid sequence has at least 99% sequence identity to a sequence as set forth in SEQ ID NO:25, or to a sequence encoding polypeptide having an amino acid sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.13. The isolated or recombinant nucleic acid of claim 10, wherein the sequence comparison algorithm is a BLAST version 2.2.2 algorithm where a filtering setting is set to blastall -p blastp -d “nr pataa” -F F, and all other options are set to default.14. The isolated or recombinant nucleic acid of claim 1, wherein the epoxide hydrolase activity comprises catalyzing the addition of water to an oxirane compound.15. The isolated or recombinant nucleic acid of claim 1, wherein the epoxide hydrolase activity further comprises formation of a corresponding diol.16. The isolated or recombinant nucleic acid of claim 1, wherein the epoxide hydrolase activity further comprises formation of an enantiomerically enriched epoxide.17. The isolated or recombinant nucleic acid of claim 14, wherein the oxirane compound comprises an epoxide or arene oxide.18. The isolated or recombinant nucleic acid of claim 14, wherein the oxirane compound or the corresponding diol is optically active.19. The isolated or recombinant nucleic acid of claim 18, wherein the oxirane compound or the corresponding diol is enantiomerically pure.20. The isolated or recombinant nucleic acid of claim 1, wherein the epoxide hydrolase activity is enantioselective.21. The isolated or recombinant nucleic acid of claim 1, wherein the epoxide hydrolase activity is thermostable.22. The isolated or recombinant nucleic acid of claim 21, wherein the polypeptide retains an epoxide hydrolase activity under conditions comprising a temperature range of between about 37° C. to about 70° C.23. The isolated or recombinant nucleic acid of claim 1, wherein the epoxide hydrolase activity is thermotolerant.24. The isolated or recombinant nucleic acid of claim 23, wherein the polypeptide retains an epoxide hydrolase activity after exposure to a temperature in the range from greater than 37° C. to about 90° C.25. The isolated or recombinant nucleic acid of claim 24, wherein the polypeptide retains an epoxide hydrolase activity after exposure to a temperature in the range from greater than 37° C. to about 50° C.26. An amplification primer sequence pair for amplifying a nucleic acid encoding a polypeptide having a epoxide hydrolase activity, wherein the primer pair is capable of amplifying a nucleic acid comprising a sequence as set forth in SEQ ID NO:25, or a sequence encoding a polypeptide having an amino acid sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.27. The amplification primer pair of claim 26, wherein each member of the amplification primer sequence pair comprises an oligonucleotide comprising at least about 20 to 50 consecutive bases of the sequence.28. A method of amplifying a nucleic acid encoding a polypeptide having an epoxide hydrolase activity comprising amplification of a template nucleic acid with an amplification primer sequence pair capable of amplifying a nucleic acid sequence as set forth in SEQ ID NO:25, or a sequence encoding a polypeptide having an amino acid sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.29. An expression cassette comprising the nucleic acid of claim 1 .30. The expression cassette of claim 29, wherein the nucleic acid encodes a polypeptide having a sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.31. A vector comprising a nucleic acid comprising:the nucleic acid sequence of claim 1. 32. The vector of claim 31, wherein the nucleic acid encodes a polypeptide having a sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.33. A cloning vehicle comprising the vector is set forth in claim 31 or the nucleic acid as set forth in claim 1, wherein the cloning vehicle comprises a viral vector, a plasmid, a phage, a phagemid, a cosmid, a fosmid, a bacteriophage or an artificial chromosome.34. The cloning vehicle of claim 33, wherein the nucleic acid encodes a polypeptide having a sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.35. The cloning vehicle claim 33, wherein the viral vector comprises an adenovirus vector, a retroviral vector or an adeno-associated viral vector.36. The cloning vehicle of claim 33, comprising a bacterial artificial chromosome (BAC), a P1-derived vector (PAC), a yeast artificial chromosome (YAC), or a mammalian artificial chromosome (MAC).37. A transformed cell comprising a vector, wherein the vector comprises the nucleic acid of claim 1.38. A transformed cell comprisingthe nucleic acid of claim 1. 39. The transformed cell of claim 37 or claim 38, wherein the cell is a bacterial cell, a mammalian cell, a fungal cell, a yeast cell, an insect cell or a plant cell.40. The transformed cell of claim 37 or claim 38, wherein the nucleic acid encodes a polypeptide having a sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.41. An antisense oligonucleotide comprising a nucleic acid sequence complementary to or capable of hybridizing under stringent conditions tothe nucleic acid of claim 1. 42. The antisense oligonucleotide of claim 41, wherein the antisense oligonucleotide is between about 20 to 50, about 20 to 60, about 30 to 70, about 40 to 80, or about 60 to 100 bases in length.43. A method of inhibiting the translation of an epoxide hydrolase message in a cell comprising administering to the cell or expressing in the cell an antisense oligonucleotide comprising a nucleic acid sequence at least 20 residues in length that is complementary to or capable of hybridizing under stringent conditions to a nucleic acid comprisingthe nucleic acid of claim 1. 44. The method of claim 43, wherein the nucleic acid encodes a polypeptide having a sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.45. A method of determining whether a test compound specifically binds to a polypeptide comprising the following steps:(a) expressing a nucleic acid or a vector comprising the nucleic acid under conditions permissive for translation of the nucleic acid to a polypeptide, wherein the nucleic acid has a sequence as set forth in claim 1; (b) providing a test compound; (c) contacting the polypeptide with the test compound; and (d) determining whether the test compound of step (b) specifically binds to the polypeptide. 46. The method of claim 45, wherein the nucleic acid encodes a polypeptide having a sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.47. A method for identifying a modulator of an epoxide hydrolase activity comprising the following steps:(a) providing a polypeptide encoded by the nucleic acid of claim 1; (b) providing a test compound; (c) contacting the polypeptide of step (a) with the test compound of step (b) and measuring an activity of the epoxide hydrolase, wherein a change in the epoxide hydrolase activity, which is measured in the presence of the test compound, is compared to the epoxide hydrolase activity in the absence of the test compound, thereby providing a determination whether the test compound modulates the epoxide hydrolase activity. 48. The method of claim 47, wherein the nucleic acid encodes a polypeptide having a sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.49. The method of claim 47, wherein the epoxide hydrolase activity is measured by providing an epoxide hydrolase substrated and by detecting a decrease in the amount of the substrate or an increase in the amount of a reaction product, or, by detecting an increase in the amount of the substrate or a decrease in the amount of a reaction product.50. The method of claim 49, wherein decrease in the amount of the substrate or an increase in the amount of the reaction product with the test compound as compared to the amount of substrate or reaction product without the test compound identifies the test compound as an activator of the epoxide hydrolase activity.51. The method of claim 47, wherein an increase in the amount of the substrate or a decrease in the amount of the reaction product with the test compound as compared to the amount of substrate or reaction product without the test compound identifies the test compound as an inhibitor of the epoxide hydrolase activity.52. A method for isolating or recovering a nucleic acid encoding a polypeptide with an epoxide hydrolase activity from an environmental sample comprising the steps of:(a) providing an amplification primer sequence pair as set forth in claim 26; (b) isolating a nucleic acid from the environmental sample or treating the environmental sample so that nucleic acid in the sample is accessible for hybridization to the amplification primer pair; and (c) combining the nucleic acid of step (b) with the amplification primer pair of step (a) and amplifying nucleic acid from the environmental sample, thereby isolating or recovering a nucleic acid encoding a polypeptide with an epoxide hydrolase activity from an environmental sample. 53. The method of claim 52, wherein each member of the amplification primer sequence pair comprises an oligonucleotide comprising at least about 20 to 50 consecutive bases of a sequence as set forth in SEQ ID NO:25, or a sequence encoding a polypeptide having an amino acid sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.54. A method for isolating or recovering a nucleic acid encoding a polypeptide with an epoxide hydrolase activity from an environmental sample comprising the steps of:(a) providing a polynucleotide probe comprising a sequence as set forth in claim 1; (b) isolating a nucleic acid from the environmental sample or treating the environmental sample so that nucleic acid in the sample is accessible for hybridization to polynucleotide probe of step (a); (c) combining the isolated nucleic acid or the treated environmental sample of step (b) with the polynucleotide probe of step (a); and (d) isolating a nucleic acid that specifically hybridizes with the polynucleotide probe of step (a), thereby isolating or recovering a nucleic acid encoding a polypeptide with an epoxide hydrolase activity from an environmental sample. 55. The method of claim 54, wherein the nucleic acid encodes a polypeptide having a sequence as set forth in SEQ ID NO:26 or SEQ ID NO:85.56. The method of claim 52 or claim 54, wherein the environmental sample comprises a water sample, a liquid sample, a soil sample, an air sample or a biological sample.57. The method of claim 56, wherein the biological sample is derived from a bacterial cell, a protozoan cell, an insect cell, a yeast cell, a plant cell, a fungal cell or a mammalian cell.58. An isolated or recombinant nucleic acid comprising a nucleic acid that encodes a polypeptide comprising the amino acid sequence set forth in SEQ ID NO:85.