J Bacteriol, May 1998, p. 2599-2608, Vol. 180, No. 10
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
andLaboratoire de Génétique Moléculaire des Microorganismes et des Interactions Cellulaires, CNRS UMR 5577, Institut National des Sciences Appliquées, F-69621 Villeurbanne Cedex, France
Received 26 November 1997/Accepted 16 March 1998
The divergent structural operons caiTABCDE and
fixABCX of Escherichia coli are required for
anaerobic carnitine metabolism. Transcriptional monocopy
lacZ fusion studies showed that both operons are
coexpressed during anaerobic growth in the presence of carnitine,
respond to common environmental stimuli (like glucose and nitrate), and
are modulated positively by the same general regulators, CRP and FNR,
and negatively by H-NS. Overproduction of the CaiF specific regulatory
protein mediating the carnitine signal restored induction in an
fnr mutant, corresponding to its role as the primary target
for anaerobiosis. Transcript analysis identified two divergent
transcription start points initiating 289 bp apart. DNase I
footprinting revealed three sites with various affinities for the
binding of the cAMP-CRP complex inside this regulatory region.
Site-directed mutagenesis experiments indicated that previously
reported perfect CRP motif 1, centered at
41.5 of the cai
transcriptional start site, plays a direct role in the sole
cai activation. In contrast, mutation in CRP site 2, positioned at
69.5 of the fix promoter, caused only a
threefold reduction in fix expression. Thus, the role of
the third CRP site, located at
126.5 of fix, might be to
reinforce the action of site 2. A critical 50-bp cis-acting
sequence overlapping the fix mRNA start site was found, by
deletion analysis, to be necessary for cai transcription.
This region is thought to be involved in transduction of the signal
mediated by the CaiF regulator.
Present address: BASF AG, Zentrale Forschung Feinchemie, D-67056
Ludwigshafen, Germany.
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