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PMID: 2197183 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Recombinant RNA polymerase: inducible overexpression, purification and assembly of Escherichia coli rpo gene products.

Gene ·Vol. 89 ·No. 1 ·1990-04-30 ·Pages 7-12

Zalenskaya K, Lee J, Gujuluva CN, Shin YK, Slutsky M, Goldfarb A

Abstract

The genes, rpoA, rpoB and rpoC of Escherichia coli, which encode the RNA polymerase alpha-, beta- and beta'-subunits, respectively, have been individually placed on expression plasmids under the control of the bacteriophage T7 promoter. Induction of the T7 RNA polymerase gene in host cells harboring each of the three plasmids resulted in the extensive overproduction of the three polypeptides. The overproduced subunits were purified and assembled into a functional enzyme, whose specific activity and dependence on the sigma-factor were indistinguishable from native RNA polymerase purified by conventional methods.

MeSH Terms
Cloning, Molecular/methods DNA-Directed RNA Polymerases/biosynthesis,genetics,isolation & purification Escherichia coli/enzymology,genetics Gene Expression Genes, Bacterial Kinetics Macromolecular Substances Plasmids Promoter Regions, Genetic Recombinant Proteins/biosynthesis,isolation & purification T-Phages/genetics
Chemicals
Macromolecular Substances Recombinant Proteins DNA-Directed RNA Polymerases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Zalenskaya K
Department of Microbiology, Columbia University College of Physicians and Surgeons, New York, NY 10032.
Lee J
Gujuluva C N
Shin Y K
Slutsky M
Goldfarb A
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
1990-04-30
Pages
7-12
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
Grants
NIGMS NIH HHS · GM30717 · United States
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