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Journal of Bacteriology, January 2001, p. 71-76, Vol. 183, No. 1
Waksman Institute for Microbiology and
Department of Genetics, Rutgers, The State University of New Jersey,
Piscataway, New Jersey 08854,1 and The
Rockefeller University, New York, New York
100212
Received 1 August 2000/Accepted 4 October 2000
The three-dimensional structure of DNA-dependent RNA polymerase
(RNAP) from thermophilic Thermus aquaticus has recently
been determined at 3.3 Å resolution. Currently, very little is known about T. aquaticus transcription and no genetic system to
study T. aquaticus RNAP genes is available. To overcome
these limitations, we cloned and overexpressed T. aquaticus
RNAP genes in Escherichia coli. Overproduced T. aquaticus RNAP subunits assembled into functional RNAP in vitro
and in vivo when coexpressed in E. coli. We used the
recombinant T. aquaticus enzyme to demonstrate that
transcription initiation, transcription termination, and transcription
cleavage assays developed for E. coli RNAP can be adapted
to study T. aquaticus transcription. However, T. aquaticus RNAP differs from the prototypical E. coli
enzyme in several important ways: it terminates transcription less
efficiently, has exceptionally high rate of intrinsic transcript cleavage, and is highly resistant to rifampin. Our results, together with the high-resolution structural information, should now allow a
rational analysis of transcription mechanism by mutation.
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.1.71-76.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Recombinant Thermus aquaticus RNA
Polymerase, a New Tool for Structure-Based Analysis of
Transcription
*
Corresponding author. Mailing address: Waksman
Institute, 190 Frelinghuysen Rd., Piscataway, NJ 08854. Phone: (732)
445-6095. Fax: (732) 445-5735. E-mail:
severik{at}waksman.rutgers.edu.
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