| Literature DB >> 8819983 |
Y Ishino1, A Takahashi-Fujii, T Uemori, M Imamura, I Kato, H Doi.
Abstract
We studied the 5' --> 3' exonuclease activity of Bacillus caldotenax DNA polymerase by site-directed mutagenesis. Among seven mutants constructed, two mutant DNA polymerases with an amino acid substitution of Gly184 --> Asp or Gly192 --> Asp were confirmed to be deficient in this exonuclease. The two positions corresponded to those of the Escherichia coli DNA polymerase I mutants defective in 5' --> 3' exonuclease, polA480ex and polA214. These results provide experimental support for the proposed amino acid sequence essential for the 5' --> 3' exonuclease activity associated with eubacterial polymerase I-like DNA polymerases (family A), including E.coli and Thermus aquaticus.Entities:
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Year: 1995 PMID: 8819983 DOI: 10.1093/protein/8.11.1171
Source DB: PubMed Journal: Protein Eng ISSN: 0269-2139