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Journal of Bacteriology, February 1999, p. 764-771, Vol. 181, No. 3
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Molecular Characterization of the Lactococcus
lactis ptsHI Operon and Analysis of the Regulatory Role of
HPr
Evert J.
Luesink,
Christel
M. A.
Beumer,
Oscar P.
Kuipers,* and
Willem M.
De Vos
Microbial Ingredients Section, NIZO Food
Research, 6710 BA Ede, The Netherlands
Received 27 July 1998/Accepted 21 September 1998
The Lactococcus lactis ptsH and ptsI genes,
encoding the general proteins of the phosphoenolpyruvate-dependent
phosphotransferase system, HPr and enzyme I, respectively, were cloned,
and the regulatory role of HPr was studied by mutational analysis of
its gene. A promoter sequence was identified upstream of the
ptsHI operon, and the transcription start site was mapped
by primer extension. The results of Northern analyses showed the
presence of two glucose-inducible transcripts, one of 0.3 kb containing
ptsH and a second of 2.0 kb containing both
ptsH and ptsI. Disruption of the
ptsH and ptsI genes in strain NZ9800 resulted
in a reduced growth rate at the expense of glucose, but no growth at
the expense of sucrose and fructose, confirming the dominant role of
the phosphotransferase system in the uptake of these sugars in L. lactis. Complementation of the ptsH and
ptsI mutants with the intact genes under the control of a
regulated promoter resulted in the restoration of the wild-type phenotype. The role of HPr(Ser-P) in the recently established CcpA-mediated control of galactose metabolism as well as glycolysis was
analyzed by producing an HPr mutant carrying an aspartic acid on
residue 46 which mimicks a phosphorylated serine. The results of these
experiments demonstrated the role of HPr(Ser-P) as corepressor in the
catabolite repression of the gal operon. Furthermore, we show for the first time that HPr(Ser-P) functions as a coactivator in
the CcpA-mediated catabolite activation of the pyruvate kinase and
L-lactate dehydrogenase genes.
*
Corresponding author. Mailing address: Microbial
Ingredients Section, NIZO Food Research, P.O. Box 20, 6710 BA Ede, The
Netherlands. Phone: 31-318-659525. Fax: 31-31-650400. E-mail:
kuipers{at}nizo.nl.
Journal of Bacteriology, February 1999, p. 764-771, Vol. 181, No. 3
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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