Polymerase compositions and kits, and methods of using and making the same
The present disclosure provides compositions, methods, kits, systems and apparatus that are useful for nucleic acid polymerization. In particular, recombinant polymerases and biologically active fragments thereof are provided that allow for nucleic acid amplification. In some aspects, the disclosure provides recombinant polymerases that yield lower systematic error rates and/or improved accuracy, when used in sequencing by synthesis reactions as compared to a control polymerase. In one aspect, the disclosure relates to recombinant polymerases useful for nucleic acid sequencing, genotyping, copy number variation analysis, paired-end sequencing and other forms of genetic analysis. In another aspect, the recombinant polymerases are useful for the amplification of nucleic acid templates during PCR, emPCR, isothermal amplification, recombinase polymerase amplification, rolling circle amplification, strand displacement amplification and proximity ligation amplification. In some aspects, the disclosure relates to recombinant polymerases useful for the generation of nucleic acid libraries and/or nucleic acid templates.
1. A composition comprising a recombinant DNA polymerase, wherein the recombinant DNA polymerase comprises a polypeptide segment exhibiting polymerase activity, wherein said polypeptide segment has at least 99% identity to SEQ ID NO: 35, and said polypeptide segment has a single amino acid substitution selected from the group consisting of E220K, N234K, N234R, V241K, D264K, E294K, E325R, and N485R, wherein the numbering of said amino acid substitutions in the polypeptide segment is relative to SEQ ID NO: 35 and wherein the polypeptide segment has the amino acid sequence selected from the group consisting of SEQ ID NOs: 79, 81, 82, 86, 94, 101, 111, and 113.
2. The composition of claim 1 , wherein the recombinant DNA polymerase yields a lower error rate, increased signal, and/or improved accuracy when used in a sequencing by synthesis reaction as compared to a reference polymerase having the amino acid sequence of SEQ ID NO: 35.
3. The composition of claim 2 , wherein the sequencing by synthesis reaction includes detection of hydrogen ions.
4. The composition of claim 3 , wherein the detection of hydrogen ions includes an ion-sensitive field effect transistor (ISFET).
5. The composition of claim 1 , wherein at least 90% of the amino acid sequence of the recombinant DNA polymerase is from the polypeptide segment.
6. The composition of claim 1 , wherein at least 60% of the amino acid sequence of the recombinant DNA polymerase is from the polypeptide segment.
7. A method for performing a polymerization reaction, comprising
(a) contacting a recombinant DNA polymerase according to claim 1 with a nucleic acid template in the presence of one or more nucleotides; and
(b) polymerizing at least one of the one or more nucleotides using the recombinant polymerase.
8. The method of claim 7 , wherein the method comprises template-dependent nucleic acid amplification.
9. The method of claim 8 , wherein the amplification comprises polymerization selected from emulsion PCR, bridge PCR, PCR, qPCR, RT-PCR, isothermal amplification, recombinase polymerase amplification, rolling circle amplification, strand displacement amplification and proximity ligation amplification.
10. The method of claim 8 , wherein the method comprises amplifying one or more nucleic acids using a solid support system.
11. The method of claim 10 , wherein the one or more nucleic acids are clonally amplified on the solid support of the solid support system.
12. The method of claim 7 , wherein the recombinant DNA polymerase is contacted with the nucleic acid template in the presence of one or more nucleotides and a salt, wherein the salt is KCl and/or NaCl, and wherein the salt concentration is from 125 mM to 175 mM.
13. A method for obtaining sequence information from a nucleic acid template, comprising:
(a) providing a reaction mixture comprising a template nucleic acid, one or more nucleotides, a sequencing primer and a recombinant DNA polymerase according to claim 1 ;
(b) contacting the template nucleic acid with at least one type of nucleotide, wherein the contacting includes incorporating one or more nucleotides from the at least one type of nucleotide onto the 3′ end of the sequencing primer and generating an extended primer product; and
(c) detecting the presence of the extended primer product in the reaction mixture thereby determining whether nucleotide incorporation has occurred.
14. The method of claim 13 , wherein the detecting the presence of the extended primer product in the reaction mixture comprises detecting the release of hydrogen ions.
15. The method of claim 14 , wherein the detection of hydrogen ions includes an ion-sensitive field effect transistor (ISFET).
16. The method of claim 13 , wherein the recombinant DNA polymerase is contacted with the nucleic acid template in the presence of one or more nucleotides and a salt, wherein the salt is KCl and/or NaCl, and wherein the salt is present at a concentration of between 125 mM and 175 mM.
17. The method of claim 13 , wherein the recombinant DNA polymerase yields a lower error rate, increased signal, and/or improved accuracy when used in a sequencing by synthesis reaction as compared to a reference polymerase having the amino acid sequence of SEQ ID NO: 35.