DNA Polymerase I (Escherichia coli)
Source: Escherichia coli
DNA Polymerase I is a mezophilic, DNA-dependent DNA polymerase with inherent 3'-> 5' and 5'-> 3' exonuclease activity.
Description:
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Exhibits the 5'-> 3' polymerase activity.
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Exhibits the 5'-> 3' exonuclease activity, active only on duplex DNA.
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Contains the 3'-> 5' exonuclease, primarily active on single-stranded DNA (1).
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Ultrapure recombinant enzyme.
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Used to prepare radioactive probes by nick translation (2) and random priming (3).
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Useful for end-labeling of DNA molecules with 3’ and 5’ protruding tails or blunt-ended.
Unit Definition: One unit is defined as the amount of enzyme required to incorporate 10 nmoles of total deoxyribonucleotide into acid-insoluble material in 30 min at 37°C with DNase I-activated DNA as the template primer.
Storage Conditions: Store at -20°C.
Storage Buffer: 50 mM potassium phosphate (pH 7.0), 0.25 mM dithiothreitol and 50% (v/v) glycerol.
Assay Conditions: 67 mM potassium phosphate (pH 7.4), 6.7 mM MgCl2, 1 mM dithiothreitol, 0.033 mM each dCTP, dGTP, dTTP and [ α-³²P]dATP, 4.5 µg activated DNA. Incubation is at 37°C for 30 min in a reaction volume of 100 µl.
Quality Control: All preparations are assayed for contaminating endonuclease activity. Typical preparations are greater than 95% pure, as judged by SDS polyacrylamide gel electrophoresis.
References:
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Lehman, I.R. (1981) Enzymes 14, 15-37.
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Rigby, P.W.J., Diekmann, M., Rhodes, C. and Berg, P. (1977) J. Mol. Biol. 113, 237-251.
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Hartman, C.P. and Robussay, D. (1981) Gene Amplification and Analysis (Chirikjian, J.G. and Papas, T.S., eds.) 2, 17-39, Elsevier/North Holland, New York.