Promoters and proteins from
The present invention relates to an inducible and a high expression nucleic acid promoter isolated from Clostridium thermocellum . These promoters are useful for directing expression of a protein or polypeptide encoded by a nucleic acid molecule operably associated with the nucleic acid promoters. The present invention also relates to nucleic acid constructs including the C. thermocellum promoters, and expression vectors and hosts containing such nucleic acid constructs. The present invention also relates to protein isolated from Clostridium thermocellum , including a repressor protein. The present invention also provides methods of using the isolated promoters and proteins from Clostridium thermocellum , including methods for directing inducible in vitro and in vivo expression of a protein or polypeptide in a host, and methods of producing ethanol from a cellulosic biomass.
1. A nucleic acid construct comprising:
an isolated nucleic acid promoter suitable for directing expression of a protein or polypeptide encoded by a nucleic acid molecule operably associated with the nucleic acid promoter, wherein the nucleic acid promoter has a nucleotide sequence of SEQ ID NO:;
a first nucleic acid molecule, the first nucleic acid molecule encoding the protein or polypeptide;
a first regulatory region;
a second nucleic acid molecule, the second nucleic acid molecule encoding a repressor protein;
a second regulatory region; and
a third regulatory region;
wherein the isolated nucleic acid promoter, the first nucleic acid molecule, and the first regulatory region are operably linked together to allow expression of the protein or polypeptide;
wherein the second nucleic acid molecule, the second regulatory region, and the third regulatory region are operably linked together to allow expression of the repressor protein; and
wherein the second and third regulatory regions are the same regulatory regions linked to the first nucleic acid molecule.
2. The nucleic acid construct according to claim 1 , wherein the first nucleic acid molecule encodes a therapeutic protein or an enzyme.
3. The nucleic acid construct according to claim 2 , wherein the first nucleic acid molecule encodes an enzyme capable of degrading a cellulosic substrate or constituting part of a metabolic pathway.
4. The nucleic acid construct according to claim 3 , wherein the first nucleic acid molecule encodes an enzyme selected from the group consisting of cellulase, hemicellulase, endoglucanase, exoglucanase, xylanase mannanase, lichenase, chitinase, glycosidases, esterases, lyase, lignase, lignin degrading enzyme, alcohol dehydrogenase, and pyruvate decarboxylase.
5. A nucleic acid construct comprising:
an isolated nucleic acid promoter suitable for directing expression of a protein or polypeptide encoded by a nucleic acid molecule operably associated with the nucleic acid promoter, wherein the nucleic acid promoter has a nucleotide sequence of SEQ ID NO:1;
a first nucleic acid molecule, the first nucleic acid molecule encoding the protein or polypeptide;
a first regulatory region;
a second nucleic acid molecule having a nucleotide sequence of SEQ ID NO: 2, the second nucleic acid molecule encoding a repressor protein;
a second regulatory region; and
a third regulatory region;
wherein the isolated nucleic acid promoter, the first nucleic acid molecule, and the first regulatory region are operably linked together to allow expression of the protein or polypeptide; and
wherein the second nucleic acid molecule, the second regulatory region, and the third regulatory region are operably linked together to allow expression of the repressor protein.
6. An expression vector comprising the nucleic acid construct according to claim 5 .
7. A host comprising the expression vector according to claim 6 , wherein the host is a bacterial cell, a yeast cell, a fungal cell, an insect cell, a mammalian cell, or a virus.
8. The host according to claim 7 , wherein the host is a cellulase, hemicellulase, or ethanol producer.
9. The host according to claim 7 , wherein the host is a bacterial cell selected from the group consisting of Clostridium spp., Zymomonas spp., E. coli , or Thermoanaerobacterium saccharolyticum.
10. A method of producing ethanol from a biomass, said method comprising:
providing a first host comprising a first nucleic acid construct, the first nucleic acid construct comprising:
an isolated nucleic acid promoter suitable for directing expression of a protein or polypeptide encoded by a nucleic acid molecule operably associated with the nucleic acid promoter, wherein the nucleic acid promoter has a nucleotide sequence of SEQ ID NO:1;
a first nucleic acid molecule, the first nucleic acid molecule encoding a protein or polypeptide; and
a first regulatory region, wherein the nucleic acid promoter, the first nucleic acid molecule, and the first regulatory region are operably linked together to allow expression of the protein or polypeptide;
providing a second host comprising a second nucleic acid construct, the second nucleic acid construct comprising:
a second nucleic acid molecule, the second nucleic acid molecule encoding a repressor protein having an amino acid sequence of SEQ ID NO:3;
a second regulatory region; and
a third regulatory region, wherein the second and third regulatory regions are operably linked to the second nucleic acid molecule to allow expression of the repressor protein; and
contacting a biomass with the first host and the second host under conditions effective to allow production of ethanol from the biomass.
11. The method according to claim 10 , wherein the conditions effective to allow production of ethanol from the biomass comprise contacting the first host with an inducing agent, wherein the inducing agent is lichenan, laminarin, laminaribiose, laminaritriose, laminaritetreose, laminaripentaose, an oligosaccharide containing 1,3 linked sugar residues, a polysaccharide containing 1,3 linked sugar residues, or any analog thereof.
12. The method according to claim 10 , wherein the first host is a yeast cell, a fungal cell, or a bacterial cell.
13. The method according to claim 12 , wherein the first host is a cellulase, hemicellulase, or ethanol producer.
14. The method according to claim 13 , wherein the first host is a bacterial cell selected from the group consisting of Clostridium spp., Zymomonas spp., E. coli , or Thermoanaerobacterium saccharolyticum.
15. The method according to claim 10 , wherein the second host is a yeast cell, a fungal cell, or a bacterial cell.
16. The method according to claim 15 , wherein the second host is a cellulase, hemicellulase, or ethanol producer.
17. The method according to claim 10 , wherein the second host is a bacterial cell selected from the group consisting of Clostridium spp., Zymomonas spp., E. coli , or Thermoanaerobacterium saccharolyticum.
18. The method according to claim 10 , wherein the biomass is a cellulosic substrate.
19. A nucleic acid construct comprising:
a nucleic acid promoter, wherein the nucleic acid promoter has a nucleotide sequence of SEQ ID NO:1;
a first nucleic acid molecule, the first nucleic acid molecule encoding a protein or polypeptide;
a first regulatory region;
a second nucleic acid molecule, the second nucleic acid molecule encoding a repressor protein;
a second regulatory region; and
a third regulatory region;
wherein the nucleic acid promoter, the first nucleic acid molecule, and the first regulatory region are operably linked together to allow expression of the protein or polypeptide;
wherein the second nucleic acid molecule, the second regulatory region, and the third regulatory region are operably linked together to allow expression of the repressor protein; and
wherein the second and third regulatory regions are the same regulatory regions linked to the first nucleic acid molecule.
20. The nucleic acid construct according to claim 19 , wherein the first nucleic acid molecule encodes a therapeutic protein or an enzyme.
21. The nucleic acid construct according to claim 20 , wherein the first nucleic acid molecule encodes an enzyme capable of degrading a cellulosic substrate or constituting part of a metabolic pathway.
22. The nucleic acid construct according to claim 21 , wherein the first nucleic acid molecule encodes an enzyme selected from the group consisting of cellulase, hemicellulase, endoglucanase, exoglucanase, xylanase mannanase, lichenase, chitinase, glycosidases, esterases, lyase, lignase, lignin degrading enzyme, alcohol dehydrogenase, and pyruvate decarboxylase.
23. The nucleic acid construct according to claim 19 , wherein the second nucleic acid molecule has a nucleotide sequence of SEQ ID NO:2.
24. An expression vector comprising the nucleic acid construct according to claim 19 .
25. A host comprising the expression vector according to claim 24 , wherein the host is a bacterial cell, a yeast cell, a fungal cell, an insect cell, a mammalian cell, or a virus.
26. The host according to claim 25 , wherein the host is a cellulase, hemicellulase, or ethanol producer.
27. The host according to claim 25 , wherein the host is a bacterial cell selected from the group consisting of Clostridium spp., Zymomonas spp., E. coli , or Thermoanaerobacterium saccharolyticum.
28. A method for directing expression of a protein or polypeptide in a host, said method comprising:
transforming a host with the nucleic acid construct according to claim 19 to produce a transformed host, under conditions effective to allow expression of the protein or polypeptide in the host.
29. The method according to claim 28 , wherein the conditions effective to allow expression of the protein or polypeptide in the host comprise contacting the host with an inducing agent.
30. The method according to claim 29 , wherein the inducing agent is lichenan, laminarin, laminaribiose, laminaritriose, laminaritetreose, laminaripentaose, a synthetic inducer, an oligosaccharide containing 1 , 3 linked sugar residues, a polysaccharide containing 1,3 linked sugar residues, or any analog thereof
31. The method according to claim 28 , wherein the host is a bacterial cell, a fungal cell, a yeast cell, an insect cell, a mammalian cell, or a virus.
32. The method according to claim 31 , wherein the host is a bacterial cell selected from the group consisting of Clostridium spp., Zymomonas spp., E. coli , or Thermoanaerobacterium saccharolyticum.
33. A method for directing in vitro expression of a protein or polypeptide, said method comprising:
providing a cell-free transcription-translation system;
providing a nucleic acid template for the cell-free transcription-translation system using the nucleic acid construct according to claim 19 ; and
combining the nucleic acid template with the cell-free transcription-translation system under conditions effective to allow expression of the protein or polypeptide in vitro.
34. A method for directing inducible in vivo expression of a protein or polypeptide in a host, said method comprising:
transforming a host with the nucleic acid construct according to claim 19 to produce a transformed host, under conditions effective to allow expression of the protein or polypeptide in the host.
35. The method according to claim 34 , wherein the conditions effective to allow expression of the protein or polypeptide in the host comprise contacting the host with an inducing agent, wherein the inducing agent is lichenan, laminarin, laminaribiose, laminaritriose, laminaritetreose, laminaripentaose, a synthetic inducer, an oligosaccharide containing 1,3 linked sugar residues, a polysaccharide containing 1,3 linked sugar residues, or any analog thereof.
36. The method according to claim 34 , wherein the host is a bacterial cell, a fungal cell, a yeast cell, an insect cell, a mammalian cell, or a virus.
37. The method according to claim 36 , wherein the host is a bacterial cell selected from the group consisting of Clostridium spp., Zymomonas spp., E. coli , or Thermoanaerobacterium saccharolyticum.
38. A method of producing ethanol from a biomass, said method comprising:
providing a host according to claim 25 , and
contacting a biomass with the host under conditions effective to allow the host to convert the biomass to ethanol, thereby producing ethanol from the biomass.
39. The method according to claim 38 , wherein the conditions effective to allow the host to convert the biomass to ethanol comprise contacting the host with an inducing agent wherein the inducing agent is lichenan, laminarin, laminaribiose, laminaritriose, laminaritetreose, laminaripentaose, an oligosaccharide containing 1,3 linked sugar residues, a polysaccharide containing 1,3 linked sugar residues, or any analog thereof.
40. The method according to claim 38 , wherein the host is a yeast cell, a fungal cell, or a bacterial cell.
41. The method according to claim 40 , wherein the host is a cellulase, hemicellulase, or ethanol producer.
42. The method according to claim 38 , wherein the host is co-cultured with another organism.
43. The method according to claim 41 , wherein the host is a bacterial cell selected from the group consisting of Clostridium spp., Zymomonas spp., E. coli , or Thermoanaerobacterium saccharolyticum.
44. The method according to claim 41 , wherein the biomass is a cellulosic substrate.
45. An expression vector comprising the nucleic acid construct according to claim 1 .
46. A host comprising the expression vector according to claim 45 , wherein the host is a bacterial cell, a yeast cell, a fungal cell, an insect cell, a mammalian cell, or a virus.
47. The host according to claim 46 , wherein the host is a cellulase, hemicellulase, or ethanol producer.
48. The host according to claim 46 , wherein the host is a bacterial cell selected from the group consisting of Clostridium spp., Zymomonas spp., E. coli , or Thermoanaerobacterium saccharolyticum.
49. The nucleic acid construct according to claim 5 , wherein the first nucleic acid molecule encodes a therapeutic protein or an enzyme.
50. The nucleic acid construct according to claim 49 , wherein the first nucleic acid molecule encodes an enzyme capable of degrading a cellulosic substrate or constituting part of a metabolic pathway.
51. The nucleic acid construct according to claim 50 , wherein the first nucleic acid molecule encodes an enzyme selected from the group consisting of cellulase, hemicellulase, endoglucanase, exoglucanase, xylanase mannanase, lichenase, chitinase, glycosidases, esterases, lyase, lignase, lignin degrading enzyme, alcohol dehydrogenase, and pyruvate decarboxylase.