Improved PCR performance and fidelity of double mutant Neq A523R/N540R DNA polymerase

Abstract

We previously reported that Neq A523R DNA polymerase is more efficient in PCR than wild-type Neq DNA polymerase, and amplifies products more rapidly. Neq A523R DNA polymerase also amplifies templates more rapidly than Pfu DNA polymerase, but has a lower fidelity than Pfu DNA polymerase. To improve product yield and the fidelity of amplification simultaneously, we constructed and characterized the double mutant Neq A523R/N540R. The yield of PCR products was greater for Neq A523R/N540R DNA polymerase than wild-type and other mutant DNA polymerases, and the Neq double mutant catalyzed amplification of a 12-kb PCR product from a lambda template with an extension time of 3min. The PCR error rate of Neq A523R/N540R DNA polymerase (6.3×10−5) was roughly similar to that of Pfu DNA polymerase (4.8×10−5), but much lower than those of wild-type Neq DNA polymerase (57.2×10−5), Neq A523R DNA polymerase (13.1×10−5), and Neq N540R DNA polymerase (37.7×10−5). These results indicated that A523R and N540R mutations of Neq DNA polymerase had synergistic effects on its fidelity.