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1.
Microbiology (Reading) ; 152(Pt 3): 605-616, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16514141

RESUMO

The importance of the content of anionic phospholipids [cardiolipin (CL) and phosphatidylglycerol (PG)] in the osmotic adaptation and in the membrane structure of Bacillus subtilis cultures was investigated. Insertion mutations in the three putative cardiolipin synthase genes (ywiE, ywnE and ywjE) were obtained. Only the ywnE mutation resulted in a complete deficiency in cardiolipin and thus corresponds to a true clsA gene. The osmotolerance of a clsA mutant was impaired: although at NaCl concentrations lower than 1.2 M the growth curves were similar to those of its wild-type control, at 1.5 M NaCl (LBN medium) the lag period increased and the maximal optical density reached was lower. The membrane of the clsA mutant strain showed an increased PG content, at both exponential and stationary phase, but no trace of CL in either LB or LBN medium. As well as the deficiency in CL synthesis, the clsA mutant showed other differences in lipid and fatty acids content compared to the wild-type, suggesting a cross-regulation in membrane lipid pathways, crucial for the maintenance of membrane functionality and integrity. The biophysical characteristics of membranes and large unilamellar vesicles from the wild-type and clsA mutant strains were studied by Laurdan's steady-state fluorescence spectroscopy. At physiological temperature, the clsA mutant showed a decreased lateral lipid packing in the protein-free vesicles and isolated membranes compared with the wild-type strain. Interestingly, the lateral lipid packing of the membranes of both the wild-type and clsA mutant strains increased when they were grown in LBN. In a conditional IPTG-controlled pgsA mutant, unable to synthesize PG and CL in the absence of IPTG, the osmoresistance of the cultures correlated with their content of anionic phospholipids. The transcriptional activity of the clsA and pgsA genes was similar and increased twofold upon entry to stationary phase or under osmotic upshift. Overall, these results support the involvement of the anionic phospholipids in the growth of B. subtilis in media containing elevated NaCl concentrations.


Assuntos
Adaptação Fisiológica , Bacillus subtilis/fisiologia , Cardiolipinas/metabolismo , Resposta ao Choque Térmico , Fosfatidilgliceróis/metabolismo , Cloreto de Sódio/farmacologia , Bacillus subtilis/química , Bacillus subtilis/genética , Bacillus subtilis/crescimento & desenvolvimento , Proteínas de Bactérias/genética , Proteínas de Bactérias/metabolismo , Membrana Celular/química , Membrana Celular/metabolismo , Ácidos Graxos/análise , Mutação , Concentração Osmolar , Pressão Osmótica , Esporos Bacterianos/fisiologia
2.
Arch Biochem Biophys ; 422(1): 61-70, 2004 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-14725858

RESUMO

The biochemical and biophysical properties of the membrane and some general characteristics of the response of Lactobacillus casei ATCC 393 (reclassified Lactobacillus zeae) to hyperosmotic conditions were studied. Under hypertonic conditions, the hydrophobicity and the bile salt sensitivity of the cultures were increased. The glycolipid AcylH3DG is only present in membranes of NaCl containing medium, whereas, H4DG undergoes a significant increment and H2DG a significant decrease. The fluidity of both the purified membranes and the total lipid vesicles, as determined with the fluorescent probe DPH, did not change in conditions of high salinity. This was coincident with changes in the fatty acid (FA) composition where an increase in the saturated/unsaturated FA ratio was compensated by a rise in the fluidifying 11,12-methyleneoctadecanoic FA (cyc 19:0). Under osmotic stress conditions, Laurdan and acridine orange in total lipid vesicles showed increased lateral lipid packing and proton permeability, respectively.


Assuntos
Lacticaseibacillus casei/química , Lacticaseibacillus casei/fisiologia , Ácidos e Sais Biliares/farmacologia , Membrana Celular/química , Membrana Celular/fisiologia , Permeabilidade da Membrana Celular , Meios de Cultura , Difenilexatrieno/química , Ácidos Graxos/análise , Ácidos Graxos/química , Polarização de Fluorescência , Glicolipídeos/análise , Interações Hidrofóbicas e Hidrofílicas , Lacticaseibacillus casei/genética , Lipossomos/química , Fluidez de Membrana , Lipídeos de Membrana/análise , Pressão Osmótica , Fosfolipídeos/análise , Prótons , Solução Salina Hipertônica/farmacologia
3.
Arch Biochem Biophys ; 408(2): 220-8, 2002 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-12464275

RESUMO

The thermotropic behavior of intact bacterial membranes and vesicles prepared from total and polar lipids isolated from Bacillus subtilis cultures grown at 37 degrees C in normal (LB) and hyperosmotic (LBN) conditions was studied using 1,6-diphenyl-1,3,5-hexatriene (DPH), 1-(4-trimethylammoniumphenyl)-6-phenyl-1,3,5-hexatriene p-toluenesulfonate (TMA-DPH), and 2-diethylamino-6-lauroyl-naphthalene (Laurdan) as fluorescent probes. No phase transition of bulk lipids was observed in these preparations at the range of temperature studied. The anisotropy values (r(s)) for DPH and TMA-DPH in purified membranes showed significant differences between the LB and LBN conditions, suggesting that there was an increase in membrane packing during the adaptation to osmotic stress. Furthermore, generalized polarization (GP) parameters for Laurdan indicated small but significant changes in water relaxation at the membrane hydrophobic/hydrophilic interface. Membrane preparations showed r(s) higher values than those of lipid vesicles and a higher temperature dependence of the Laurdan GP parameter. This fact indicates that membrane proteins increase the lipid packing and keep the membrane more sensitive to temperature changes.


Assuntos
Bacillus subtilis/química , Membrana Celular/química , Difenilexatrieno/análogos & derivados , Polarização de Fluorescência , Bacillus subtilis/fisiologia , Membrana Celular/fisiologia , Difenilexatrieno/química , Corantes Fluorescentes/química , Bicamadas Lipídicas , Pressão Osmótica , Espectrometria de Fluorescência/métodos
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