Journal of Bacteriology, July 2000, p. 3904-3912, Vol. 182, No. 14
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Instituto de Biología Molecular y Celular de Rosario and Departamento de Microbiología, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, 2000 Rosario, Argentina,1 and Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, 28006 Madrid, Spain2
Received 20 January 2000/Accepted 26 April 2000
In this study we describe the expression pattern of the
Leuconostoc paramesenteroides citMCDEFGRP operon in
response to the addition of citrate to the growth medium. An 8.8-kb
polycistronic transcript, which includes the citMCDEFGRP
genes, was identified; its synthesis was dramatically induced upon
addition of citrate to the growth medium. We also found that expression
of the cit operon is subjected to posttranscriptional
regulation, since processing sites included in four complex secondary
structures (I, II, III, and IV) were identified by Northern blot
analysis and mapped by primer extension. Upstream of the
citMCDEFGRP operon a divergent open reading frame, whose
expression was also increased by citrate, was identified by DNA
sequencing and designated citI. The start and end sites of
transcription of the cit operon and citI gene were mapped. The start sites are separated by a stretch of 188 bp with
a very high A+T content of 77% and are preceded by transcriptional promoters. The end sites of the transcripts are located next to the 3'
end of two secondary structures characteristic of
-independent transcriptional terminators. The effect of the citI gene on
expression of the cit operon was studied in
Escherichia coli. The presence of the citI gene
in cis and in trans resulted in increased
activity of the cit promoter. These data provide the first
evidence that citrate fermentation in Leuconostoc is
regulated at the transcriptional level by a transcriptional activator
rather than by a repressor.
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