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Journal of Bacteriology, April 1999, p. 2394-2402, Vol. 181, No. 8
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
mrp, a Multigene, Multifunctional Locus in
Bacillus subtilis with Roles in Resistance to Cholate and to
Na+ and in pH Homeostasis
Masahiro
Ito,1,
Arthur A.
Guffanti,1
Bauke
Oudega,2 and
Terry A.
Krulwich1,*
Department of Biochemistry, Mount Sinai
School of Medicine of the City University of New York, New York,
New York 10029,1 and Molecular
Microbiology, Vrije Universiteit, Amsterdam, The
Netherlands2
Received 22 September 1998/Accepted 2 February 1999
A 5.9-kb region of the Bacillus subtilis chromosome is
transcribed as a single transcript that is predicted to encode seven membrane-spanning proteins. Homologues of the first gene of this operon, for which the designation mrp (multiple
resistance and pH adaptation) is proposed here, have been suggested to
encode an Na+/H+ antiporter or a
K+/H+ antiporter. In the present studies of the
B. subtilis mrp operon, both polar and nonpolar mutations
in mrpA were generated. Growth of these mutants was
completely inhibited by concentrations of added Na+ as low
as 0.3 M at pH 7.0 and 0.03 M at pH 8.3; there was no comparable
inhibition by added K+. A null mutant that was constructed
by full replacement of the mrp operon was even more
Na+ sensitive. A double mutant with mutations
in both mrpA and the multifunctional antiporter-encoding
tetA(L) gene was no more sensitive than the
mrpA mutants to Na+, consistent with a major
role for mrpA in Na+ resistance.
Expression of mrpA from an inducible promoter, upon insertion into the amyE locus, restored significant
Na+ resistance in both the polar and nonpolar
mrpA mutants but did not restore resistance in the null
mutant. The mrpA disruption also resulted in an
impairment of cytoplasmic pH regulation upon a sudden shift in external
pH from 7.5 to 8.5 in the presence of Na+ and, to some
extent, K+ in the range from 10 to 25 mM. By contrast, the
mrpA tetA(L) double mutant, like the tetA(L)
single mutant, completely lost its capacity for both Na+-
and K+-dependent cytoplasmic pH regulation upon
this kind of shift at cation concentrations ranging from 10 to 100 mM;
thus, tetA(L) has a more pronounced involvement than
mrpA in pH regulation. Measurements of Na+
efflux from the wild-type strain, the nonpolar mrpA mutant,
and the complemented mutant indicated that inducible expression of mrpA increased the rate of protonophore- and
cyanide-sensitive Na+ efflux over that in the wild-type
in cells preloaded with 5 mM Na+. The mrpA and
null mutants showed no such efflux in that concentration range. This is
consistent with MrpA encoding a secondary, proton motive
force-energized Na+/H+ antiporter. Studies of a
polar mutant that leads to loss of mrpFG and its
complementation in trans by mrpF or
mrpFG support a role for MrpF as an efflux system for
Na+ and cholate. Part of the Na+ efflux
capacity of the whole mrp operon products is attributable to mrpF. Neither mrpF nor mrpFG
expression in trans enhanced the cholate or Na+
resistance of the null mutant. Thus, one or more other mrp
gene products must be present, but not at stoichiometric levels, for stability, assembly, or function of both MrpF and MrpA expressed in
trans. Also, phenotypic differences among the
mrp mutants suggest that functions in addition to
Na+ and cholate resistance and pH homeostasis will be found
among the remaining mrp genes.
*
Corresponding author. Mailing address: Box 1020, Department of Biochemistry, Mount Sinai School of Medicine,
1 Gustave L. Levy Place, New York, NY 10029. Phone: (212) 241-7280. Fax: (212) 996-7214. E-mail:
terry.krulwich{at}mssm.edu.

Present address: Department of Life Science, Toyo University,
Oura-gun, Gunma 374-01,
Japan.
Journal of Bacteriology, April 1999, p. 2394-2402, Vol. 181, No. 8
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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