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Journal of Bacteriology, April 2000, p. 2345-2349, Vol. 182, No. 8
Center of Marine Biotechnology, University of
Maryland Biotechnology Institute, Baltimore, Maryland 21202
Received 8 October 1999/Accepted 26 January 2000
A DNA library of pRJ28, a large linear plasmid encoding mercury
resistance, was constructed, and the mercury resistance genes were
cloned. The 5,921-bp sequence was analyzed and showed a high degree of
similarity to the Streptomyces lividans 1326 mercury resistance operon. Genes merR, merT,
merP, and orfIV were found in a similar order
and in a single transcription unit. merA and merB were found to be transcribed in the opposite direction
to genes merR, merT, merP, and
orfIV, as in S. lividans 1326. A novel putative
regulatory gene, orfX, was found 22 bp downstream of merA. orfX encodes a 137-amino acid protein
with a potential helix-turn-helix motif in the N-terminal domain,
characteristic of the MerR family of transcriptional regulators.
Transcriptional studies showed that orfX is cotranscribed
with merA and merB. It is hypothesized that
orfX plays a role in the regulation of the mercury
resistance operon, probably by binding at the MerR operator site.
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Cloning and Sequence Analysis of the Mercury
Resistance Operon of Streptomyces sp. Strain CHR28 Reveals a
Novel Putative Second Regulatory Gene

*
Corresponding author. Mailing address: Center of Marine
Biotechnology, Columbus Center, Suite 236, 701 East Pratt St.,
Baltimore, MD 21202. Phone: (410) 234-8883. Fax: (410) 234-8896. E-mail: hillr{at}umbi.umd.edu.
Contribution no. 517 from the Center of Marine Biotechnology.
Present address: Chemistry Department, The Johns Hopkins
University, Baltimore, MD 21218.
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