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Journal of Bacteriology, August 2000, p. 4512-4520, Vol. 182, No. 16
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Inactivation of the Stress- and
Starvation-Inducible gls24 Operon Has a Pleiotrophic Effect
on Cell Morphology, Stress Sensitivity, and Gene Expression in
Enterococcus faecalis
Jean-Christophe
Giard,*
Alain
Rince,
Herve
Capiaux,
Yanick
Auffray, and
Axel
Hartke
Laboratoire de Microbiologie de
l'Environnement, Université de Caen, 14032 Caen, France
Received 3 February 2000/Accepted 1 June 2000
Enterococcus faecalis induces the synthesis of at least
42 proteins during 24 h of glucose starvation. Because of its
induction during carbohydrate and complete starvation (incubation in
tap water) and CdCl2 and bile salts stresses, one of these
proteins (Gls24) was qualified as a "general stress protein" and
was analyzed at the molecular level. Its corresponding gene,
gls24, seems to be the penultimate gene of an operon
composed, altogether, of six open reading frames (ORFs). The ORF
preceding gls24 (orf4) showed very strong
identity with gls24. The deduced polypeptides of these two
genes showed similarity with a 20-kDa hypothetical protein from
Lactococcus lactis and an alkaline stress protein from
Staphylococcus aureus with no previously known biological significance. Data from the operon sequence and Northern analysis led
to the conclusions that (i) gls24 possesses its own
promoter which is especially induced at the onset of starvation and
(ii) the operon promoter is stress inducible in exponential-phase
cells. A mutation in the gls24 gene led to a severe
reduction of growth rate and reduction of survival against 0.3% bile
salts in the 24-h-starved cells compared to the wild-type strain.
Moreover, the chain length of the mutant is significantly reduced
during growth. These results argue strongly for a role of the protein Gls24 and/or GlsB in morphological changes and in stress tolerance in
E. faecalis. Comparison of two-dimensional protein gels
from wild-type cells with those from gls24 mutant cells
revealed a pleiotropic effect of the mutation on gene expression. At
least nine proteins were present in larger amounts in the mutant. For six of them, the corresponding N-terminal microsequence has been obtained. Three of these sequences map in genes coding for
L-lactate dehydrogenase, lipoamide dehydrogenase, and
pyruvate decarboxylase, all involved in pyruvate metabolism.
*
Corresponding author. Mailing address:
Laboratoire de Microbiologie de l'Environnement, Université de
Caen, 14032 Caen Cedex, France. Phone: 2-31-56-54-10. Fax:
2-31-56-53-11. E-mail: giard{at}ibba.unicaen.fr.
Journal of Bacteriology, August 2000, p. 4512-4520, Vol. 182, No. 16
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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