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PMID: 1696001 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

On the use of T7 RNA polymerase transcripts for physical investigation.

Nucleic acids research ·Vol. 18 ·No. 14 ·1990-07-25 ·Pages 4139-42

Szewczak AA, White SA, Gewirth DT, Moore PB

Abstract

A few years ago we made some observations which raised questions about the accuracy with which T7 RNA polymerase transcribes templates in vitro, and the suitability of its in vitro products for biophysical study (1). The experiments described below demonstrate that there is no reason for concern; the products of T7 RNA polymerase transcription in vitro are as suitable for biophysical characterization as RNAs synthesized in vivo. It is likely that aggregation involving the transcribed portions of the T7 RNA polymerase promoter caused our initial observations.

MeSH Terms
Base Sequence DNA-Directed RNA Polymerases/metabolism Escherichia coli/genetics Magnetic Resonance Spectroscopy Molecular Sequence Data Nucleic Acid Conformation RNA, Bacterial/biosynthesis,genetics T-Phages/enzymology,genetics Templates, Genetic Transcription, Genetic
Chemicals
RNA, Bacterial DNA-Directed RNA Polymerases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Szewczak A A
Department of Chemistry, Yale University, New Haven, CT 06511.
White S A
Gewirth D T
Moore P B
References (14)
14 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1990-07-25
Pages
4139-42
Language
English
Region
England
NLM ID
0411011
PMCID
PMC331170
Subset
IM
Grants
NIAID NIH HHS · AI09167 · United States
NIGMS NIH HHS · GM41651 · United States
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