Effects of nonpolar mutations in each of the seven Bacillus subtilis mrp genes suggest complex interactions among the gene products in support of Na+and alkali but not cholate resistance

Citation
M. Ito et al., Effects of nonpolar mutations in each of the seven Bacillus subtilis mrp genes suggest complex interactions among the gene products in support of Na+and alkali but not cholate resistance, J BACT, 182(20), 2000, pp. 5663-5670
Citations number
21
Categorie Soggetti
Microbiology
Journal title
JOURNAL OF BACTERIOLOGY
ISSN journal
00219193 → ACNP
Volume
182
Issue
20
Year of publication
2000
Pages
5663 - 5670
Database
ISI
SICI code
0021-9193(200010)182:20<5663:EONMIE>2.0.ZU;2-9
Abstract
The Bacillus subtilis mrp (multiple resistance and pH) operon supports Nat and alkali resistance via an Na+/H+ antiport, as well as cholate efflux and resistance. Among the individual mutants with nonpolar mutations in each o f the seven mrp genes, only the mrpF mutant exhibited cholate sensitivity a nd a cholate efflux defect that were complemented by expression of the dele ted gene in trans. Expression of mrpF in the mrp null (VKN1) strain also re stored cholate transport and increased Na+ efflux, indicating that MrpF doe s not require even low levels of other mrp gene expression for its own func tion, In contrast to MrpF, MrpA function had earlier seemed to depend upon at least modest expression of other mrp genes, i.e., mrpA restored Nat resi stance and efflux to strain VK6 (a polar mrpA mutant which expresses low le vels of mrpB to -G) but not to the null strain VKN1, In a wild-type backgro und, each nonpolar mutation in individual mrp genes caused profound Na+ sen sitivity at both pH 7.0 and 8.3. The mrpA and mrpD mutants were particularl y sensitive to alkaline pH even without added Na+. While transport assays i n membrane vesicles from selected strains indicated that MrpA-dependent ant iport can occur by a secondary, proton motive force-dependent mechanism, th e requirement for multiple mrp gene products suggests that there are featur es of energization, function, or stabilization that differ from typical sec ondary membrane transporters. Northern analyses indicated regulatory relati onships among mrp genes as well, All the mrp mutants, especially the mrpA, -B, -D, -E, and -G mutants, had elevated levels of mrp RNA relative to the wild type, Expression of an upstream gene, maeN, that encodes an Na+/malate symporter, was coordinately regulated with mrp, although it is not part of the operon,