Fusion protein having luminescence activity
The fusion protein comprising (1) a first region comprising the amino acid sequence of SEQ ID NO: 18 and (2) a second region comprising an amino acid sequence for a polypeptide containing at least one cysteine residue for binding to other useful compound via the thiol group can be modified by chemical modification, and thus has a high catalytic ability for a luminescence activity and is highly available for general purposes.
1. A polynucleotide comprising a polynucleotide encoding the fusion protein comprising:
(1) a first region selected from the group consisting of (a) to (d) below:
(a) a region consisting of the amino acid sequence of SEQ ID NO: 18;
(b) a region consisting of the amino acid sequence of SEQ ID NO: 18 wherein 1 to 10 amino acids are deleted, substituted, inserted and/or added and having a catalytic ability for a luminescence activity with a luciferin which is a substrate;
(c) a region consisting of an amino acid sequence having at least 90% homology to the amino acid sequence of SEQ ID NO: 18 and having a catalytic ability for a luminescence activity with a luciferin which is a substrate; and,
(d) a region consisting of an amino acid sequence encoded by a polynucleotide which hybridizes under high stringent conditions to a polynucleotide consisting of a nucleotide sequence complementary to the nucleotide sequence of SEQ ID NO: 17 and having a catalytic ability for a luminescence activity with a luciferin which is a substrate, wherein the high stringent conditions are 5×SSC, 5×Denhardt's solution, 0.5% (w/v) SDS, 50% (v/v) formamide and 50° C.; and,
(2) a second region consisting of an amino acid sequence for a polypeptide having at least one cysteine residue for binding to other useful compound via its thiol group, wherein the second region is selected from the group consisting of (e) to (h) below:
(e) a region consisting of the amino acid sequence of SEQ ID NO: 20;
(f) a region comprising the amino acid sequence of SEQ ID NO: 20 wherein 1 to 3 amino acids are deleted, substituted, inserted and/or added and having at least one cysteine residue for binding to other useful compound via the thiol group;
(g) a region comprising an amino acid sequence having at least 90% homology to the amino acid sequence of SEQ ID NO: 20 and having at least one cysteine residue for binding to other useful compound via the thiol group; and,
(h) a region comprising an amino acid sequence encoded by a polynucleotide which hybridizes under high stringent conditions to a polynucleotide consisting of a nucleotide sequence complementary to the nucleotide sequence of SEQ ID NO: 19 and having at least one cysteine residue for binding to other useful compound via the thiol group, wherein the high stringent conditions are 5×SSC, 5×Denhardt's solution, 0.5% (w/v) SDS, 50% (v/v) formamide and 50° C.
2. A polynucleotide comprising:
(1) a first coding sequence selected from the group consisting of (a) to (d) below:
(a) a coding sequence consisting of a polynucleotide consisting of the nucleotide sequence of SEQ ID NO: 17;
(b) a coding sequence consisting of a polynucleotide which hybridizes under high stringent conditions to a polynucleotide consisting of a nucleotide sequence complementary to the nucleotide sequence of SEQ ID NO: 17 and encodes a region having a catalytic ability for a luminescence activity with a luciferin which is a substrate, wherein the high stringent conditions are 5×SSC, 5×Denhardt's solution, 0.5% (w/v) SDS, 50% (v/v) formamide and 50° C.;
(c) a coding sequence consisting of a polynucleotide encoding a region consisting of the amino acid sequence of SEQ ID NO: 18; and,
(d) a coding sequence consisting of a polynucleotide encoding a region consisting of the amino acid sequence of SEQ ID NO: 18 wherein 1 to 10 amino acids are deleted, substituted, inserted and/or added and having a catalytic ability for a luminescence activity with a luciferin which is a substrate; and,
(2) a second coding sequence consisting of a polynucleotide encoding a polypeptide having at least one cysteine residue for binding to other useful compound via the thiol group, wherein the second coding sequence is selected from the group consisting of (e) to (h) below:
(e) a coding sequence consisting of a polynucleotide encoding a region consisting of the nucleotide sequence of SEQ ID NO: 19;
(f) a coding sequence consisting of a polynucleotide which hybridizes under high stringent conditions to a polynucleotide consisting of a nucleotide sequence complementary to the nucleotide sequence of SEQ ID NO: 19 and encodes a region having at least one cysteine residue for binding to other useful compound via the thiol group, wherein the high stringent conditions are 5×SSC, 5×Denhardt's solution, 0.5% (w/v) SDS, 50% (v/v) formamide and 50° C.;
(g) a coding sequence consisting of a polynucleotide encoding a region consisting of the amino acid sequence of SEQ ID NO: 20; and,
(h) a coding sequence consisting of a polynucleotide encoding a region consisting of the amino acid sequence of SEQ ID NO: 20 wherein 1 to 3 amino acids are deleted, substituted, inserted and/or added and having at least one cysteine residue for binding to other useful compound via the thiol group.
3. The polynucleotide according to claim 2 , wherein:
(1) the first coding sequence is a coding sequence consisting of a polynucleotide consisting of the nucleotide sequence of SEQ ID NO: 17; and,
(2) the second coding sequence is a coding sequence consisting of a polynucleotide consisting of the nucleotide sequence of SEQ ID NO: 19.
4. A polynucleotide comprising a polynucleotide consisting of the nucleotide sequence of SEQ ID NO: 3, 5 or 7.
5. A recombinant vector comprising the polynucleotide according to claim 1 .
6. A transformant transformed with the recombinant vector according to claim 5 .