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Journal of Bacteriology, November 1999, p. 7080-7086, Vol. 181, No. 22
Department of Microbiology and Immunology,
University of Illinois, Chicago, Illinois 60612-7344
Received 27 April 1999/Accepted 7 September 1999
The chromosomal mercury resistance determinant of Bacillus
cereus RC607 confers resistance to inorganic mercury and to
organomercurials. The order of genes in the completed mercury
resistance determinant is operator-promoter 1 (O/P1) merR1
merT open reading frame 3 (ORF3) ORF4 merA O/P2
merR2 merB2 merB1. The previously undetermined 1-kb DNA
sequence between the merA and merB1 genes
includes two significant ORFs, whose predicted protein products are
homologous with MerR (the transcriptional regulator) and MerB (the
organomercurial lyase enzyme). Two transcriptional start sites
(promoters), O/P1 at the beginning of the determinant and O/P2
immediately upstream of the sixth ORF, the newly identified
merR2, were mapped by reverse transcriptase (RT) primer
extension. A long 6.3-kb mRNA traversing all eight ORFs was shown by
RT-PCR. Growth sensitivity measurements in liquid media and cellular
mercury volatization assays characterized inducibility and differences
in functional activity in B. cereus RC607 and after cloning
of the mer determinant into plasmids in Escherichia
coli.
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Mercury Resistance in Bacillus cereus
RC607: Transcriptional Organization and Two New Open Reading
Frames
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, University of Illinois, Room E-704, M/C 790, 835 S. Wolcott Ave., Chicago, IL 60612-7344. Phone: (312) 996-3363. Fax: (312) 996-6415. E-mail: agupta{at}uic.edu.
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