Chromatin-bound DNA polymerase from higher plants |
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Authors: | Stevens Christine Bryant John A. Wyvill P. Carol |
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Affiliation: | (1) Department of Botany, University College, P.O. Box 78, CF1 1XL Cardiff, UK;(2) Present address: Technology Policy Unit, University of Aston, Gosta Green, B4 7ET Birmingham, UK |
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Abstract: | Chromatin-bound DNA polymerase has been extracted from pea (Pisum sativum L.) seedlings, and partially purified by solubilization from chromatin followed by chromatography on columns of either DEAE-cellulose or DEAE-Sephadex. The enzyme elutes from DEAE-cellulose as a single peak, but is fractionated into two peaks, CI and CII, by DEAE-Sephadex chromatography. If the enzyme is stored at-15°C for several days prior to chromatography, a third peak, CIII, derived from CII, is obtained. The polymerase is devoid of nuclease activity, and is relatively insensitive to N-ethyl-maleimide. These features, taken with the ion requirements and with data obtained from other plant species, lead to the suggestion that the chromatin-bound DNA polymerase of higher plants is similar to the DNA polymerase- from vertebrates. |
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Keywords: | Chromatin DNA polymerase
Pisum |
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