Abstract
Nuclear DNA-dependent RNA polymerase II has been purified from leaves of Zea mays by a new procedure that improves enzyme stability and thus permits more manipulation during purification. The purification procedure includes a heating step, gel filtration on Sepharose 6B and 4B, and chromatography on DEAE- and DNA-celluloses. This method of purification yields an enzyme that exhibits maximal activity when denatured DNA is used as a template. Electrophoresis of highly purified enzyme on polyacrylamide gels containing sodium dodecyl sulfate indicates that maize RNA polymerase IIa is composed of several polypeptide subunits. The most highly purified preparations contain polypeptides with molecular weights of 200,000, 160,000, 35,000, 25,000, 20,000, and 17,000.
MeSH Terms
Chromatography
Chromatography, DEAE-Cellulose
DNA
DNA-Directed RNA Polymerases/analysis,isolation & purification
Electrophoresis, Polyacrylamide Gel
Molecular Weight
Peptides/analysis
Plants/enzymology
Templates, Genetic
Zea mays/enzymology
Chemicals
Peptides
DNA
DNA-Directed RNA Polymerases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Mullinix K P
Strain G C
Bogorad L
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