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Journal of Bacteriology, January 1999, p. 426-433, Vol. 181, No. 2
Department of Microbiology and Immunology,
Emory University School of Medicine, Atlanta, Georgia 30322
Received 8 September 1998/Accepted 5 November 1998
We have identified a locus essential for galacturonate utilization
in Bacillus subtilis. Genes homologous to Escherichia
coli and Erwinia chrysanthemi glucuronate and
galacturonate metabolic genes were found in a cluster consisting of 10 open reading frames (ORFs) in the B. subtilis chromosome. A
mutant of B. subtilis containing a replacement of the
second and third ORFs was unable to grow with galacturonate as its
primary carbon source. Galacturonate induced expression from a
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Regulation of Hexuronate Utilization in
Bacillus subtilis

and
A-dependent promoter, exuP1, located
upstream from the first ORF. The eighth ORF in this cluster (the
exu locus) encodes a LacI and GalR homolog that negatively
regulated expression from exuP1. A 26-bp inverted repeat
sequence centered 15 bp downstream from the exuP1 start
point of transcription acted in cis to negatively regulate
expression from exuP1 under noninducing conditions.
Expression from the exuP1 promoter was repressed by high
levels of glucose, which is probably mediated by CcpA (catabolite
control protein A). A
E-dependent promoter,
exuP2, was localized between the second and third ORFs and
was active during sporulation.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, Emory University School of Medicine,
Atlanta, GA 30322. Phone: (404) 727-5969. Fax: (404) 727-3659. E-mail: Moran{at}microbio.emory.edu.
Present address: Department of Microbiology, University of
Minnesota, Minneapolis, MN 55455.
Present address: Respiratory Diseases Branch, Centers for Disease
Control and Prevention, Atlanta, GA 30333.
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