Luciferase and photoprotein
The present invention provides a polynucleotide or polynucleotides encoding Oplophorus luciferase which is composed of 19 kDa and 35 kDa proteins, or the 19 kDa photoprotein, the recombinant secretional Oplophorus luciferase or the 19 kDa photoprotein encoded by the polynucleotide(s), an expression vector containing the polynucleotide(s) and a host transformed with the vector. Further, the invention provides a method for producing the recombinant Oplophorus luciferase or the photoprotein. These proteins could be recombinantly produced by culturing the host cell or by in vitro translation system using the recombinant expression vector.
1. An isolated or purified polynucleotide encoding a protein selected from the group consisting of a protein comprising residues 28–196 of SEQ ID NO: 2, and a protein comprising residues 40–359 of SEQ ID NO: 4; or the complete complement of said polynucleotide.
2. The polynucleotide of claim 1 that encodes an Oplophorus luciferase or a subunit thereof.
3. The polynucleotide of claim 1 that encodes an Oplophgrous gracilirostris luciferase.
4. The polynucleotide of claim 1 that encodes a luciferase subunit having a molecular mass of about 19 kDa.
5. The polynucleotide of claim 1 that encodes a luciferase subunit having a molecular mass of about 35 kDa.
6. An isolated or purified that comprises nucleotides 46–633 of SEQ ID NO: 1 luciferase activity.
7. An isolated or purified polynucleotide that encodes a protein comprising residues 28–196 of SEQ ID NO: 2.
8. The complete complement of the polynucleotide of claim 6 .
9. A composition comprising the polynucleotide of claim 6 .
10. A vector comprising the polynucleotide of claim 6 .
11. A host cell comprising the polynucleotide of claim 6 .
12. A method for making a protein having a luciferase activity comprising culturing the host cell of claim 11 under conditions suitable for protein expression and recovering the expressed protein.
13. The method of claim 12 , further comprising renaturing the expressed protein in the presence of one or more polyhydric alcohols.
14. The method of claim 13 , wherein the polyhydric alcohol is selected from the group consisting of glycerol, polyethylene glycol, polypropylene glycol, dextran, mannitol, sorbitol, inositol, xylitol, sucrose, fructose and glucose.
15. An isolated or purified that comprises nucleotides 79–1155 of SEQ ID NO: 3 activity on luciferase.
16. An isolated or purified polynucleotide that encodes a protein comprising residues 40–359 of SEQ ID NO: 4.
17. The complete complement of the polynucleotide of claim 15 .
18. A composition comprising the polynucleotide of claim 15 .
19. A vector comprising the polynucleotide of claim 15 .
20. A host cell comprising the polynucleotide of claim 15 .
21. A method for making a protein having a stabilizing activity on luciferase comprising culturing the host cell of claim 20 under conditions suitable for protein expression.
22. The method of claim 21 , further comprising renaturing the expressed protein in the presence of one or more polyhydric alcohols.
23. The method of claim 22 , wherein the polyhydric alcohol is selected from the group consisting of glycerol, polyethylene glycol, polypropylene glycol, dextran, mannitol, sorbitol, inositol, xylitol, sucrose, fructose and glucose.