Thermostable Taq polymerase fragment
It was found that a fragment of native Thermus aquaticus DNA polymerase (TaqWT) lacking 288 N-terminal amino acids (TaqΔ288) possesses an increased thermostability over TaqWT, TaqΔ279, and TaqΔ289. The present invention therefore provides TaqΔ288, recombinant expression vectors encoding the same or derivatives thereof, as well as purification protocols for TaqΔ288. The invention also encompasses kits containing TaqΔ288 as well as the use of TaqΔ288 and kits containing TaqΔ288. In addition, the invention encompasses methods for the sequencing a nucleic acid template and methods for amplifying a target nucleic acid.
1. An isolated polypeptide having DNA polymerase activity and consisting of the amino acid sequence of SEQ ID NO: 2.
2. An isolated polypeptide having DNA polymerase activity and consisting of the amino acid sequence of SEQ ID NO: 4.
3. A fusion polypeptide having the amino acid sequence of SEQ ID NO: 5.
4. The polypeptide of claim 1 covalently coupled to a compound selected from the group consisting of citraconic anhydride, cis-aconitic anhydride, 2,3-dimethylmaleic anhydride, exo-cis-3,6-endoxo-delta 4-tetrahydrophthalic anhydride, and 3,4,5,6-tetrahydrophthalic anhydride.