1974•Journal of Biological ChemistryOpen access

Purification and Properties of Deoxyribonucleic Acid-dependent Ribonucleic Acid Polymerases from the Slime Mold Physarum polycephalum

Stella Z. Gornicki, Susan B. Vuturo, Timothy V. West, Robert F. Weaver

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Abstract

The nuclear DNA-dependent RNA polymerases have been partially purified from the slime mold Physarum polycepha-Zum.Two major forms of the enzyme are readily separated upon phosphocellulose chromatography.One of these (R) is resistant to the mushroom toxin cY-amanitin, has a low salt optimum, and has a relatively low preference for denatured DNA over native DNA.This enzyme is therefore probably identifiable with RNA polymerase I from the higher eukaryotes.The other enzyme (S) is sensitive to cr-amanitin, has a relatively high salt optimum, and has a relatively high preference for denatured DNA over native DNA.This enzyme is apparently analogous to RNA polymerase II from the higher eukaryotes.Slime mold RNA polymerase R has been purified to near homogeneity.This enzyme has a sedimentation coefficient of approximately 13.1 S. Polyacrylamide gels run under denaturing conditions reveal a probable subunit structure as follows: 200,

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The nuclear DNA-dependent RNA polymerases have been partially purified from the slime mold Physarum polycepha-Zum.Two major forms of the enzyme are readily separated upon phosphocellulose chromatography.One of these (R) is resistant to the mushroom toxin cY-amanitin, has a low salt optimum, and has a relatively low preference for denatured DNA over native DNA.This enzyme is therefore probably identifiable with RNA polymerase I from the higher eukaryotes.The other enzyme (S) is sensitive to cr-amanitin, has a relatively high salt optimum, and has a relatively high preference for denatured DNA over native DNA.This enzyme is apparently analogous to RNA polymerase II from the higher eukaryotes.Slime mold RNA polymerase R has been purified to near homogeneity.This enzyme has a sedimentation coefficient of approximately 13.1 S. Polyacrylamide gels run under denaturing conditions reveal a probable subunit structure as follows: 200,

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Available abstract

The nuclear DNA-dependent RNA polymerases have been partially purified from the slime mold Physarum polycepha-Zum.Two major forms of the enzyme are readily separated upon phosphocellulose chromatography.One of these (R) is resistant to the mushroom toxin cY-amanitin, has a low salt optimum, and has a relatively low preference for denatured DNA over native DNA.This enzyme is therefore probably identifiable with RNA polymerase I from the higher eukaryotes.The other enzyme (S) is sensitive to cr-amanitin, has a relatively high salt optimum, and has a relatively high preference for denatured DNA over native DNA.This enzyme is apparently analogous to RNA polymerase II from the higher eukaryotes.Slime mold RNA polymerase R has been purified to near homogeneity.This enzyme has a sedimentation coefficient of approximately 13.1 S. Polyacrylamide gels run under denaturing conditions reveal a probable subunit structure as follows: 200,

Key concepts: Physarum polycephalum, Slime mold, DNA, Biochemistry, Chemistry, RNA, Physarum, Polymerase

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Purification and Properties of Deoxyribonucleic Acid-dependent Ribonucleic Acid Polymerases from the Slime Mold Physarum polycephalum — Research Paper | ScholarLens