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Applied and Environmental Microbiology, November 2008, p. 6563-6569, Vol. 74, No. 21
0099-2240/08/$08.00+0 doi:10.1128/AEM.00624-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Jae-Geun Song,
Ki Hoon Nam,
Jong Il Lee,
Heejin Bae,
Gun A. Kim,
Younguk Sun, and
Suk-Tae Kwon*
Department of Genetic Engineering, Sungkyunkwan University, 300 Cheoncheon-Dong, Jangan-Gu, Suwon 440-746, Republic of Korea
Received 14 March 2008/ Accepted 30 August 2008
The known archaeal family B DNA polymerases are unable to participate in the PCR in the presence of uracil. Here, we report on a novel archaeal family B DNA polymerase from Nanoarchaeum equitans that can successfully utilize deaminated bases such as uracil and hypoxanthine and on its application to PCR. N. equitans family B DNA polymerase (Neq DNA polymerase) produced
DNA fragments up to 10 kb with an approximately 2.2-fold-lower error rate (5.53 x 10–6) than Taq DNA polymerase (11.98 x 10–6). Uniquely, Neq DNA polymerase also amplified
DNA fragments using dUTP (in place of dTTP) or dITP (partially replaced with dGTP). To increase PCR efficiency, Taq and Neq DNA polymerases were mixed in different ratios; a ratio of 10:1 efficiently facilitated long PCR (20 kb). In the presence of dUTP, the PCR efficiency of the enzyme mixture was two- to threefold higher than that of either Taq and Neq DNA polymerase alone. These results suggest that Neq DNA polymerase and Neq plus DNA polymerase (a mixture of Taq and Neq DNA polymerases) are useful in DNA amplification and PCR-based applications, particularly in clinical diagnoses using uracil-DNA glycosylase.
Published ahead of print on 12 September 2008.
J.J.C. and J.-G.S. contributed equally to this work.
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