Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinity

Autores
López, Claudia S.; Alice, Alejandro F.; Heras, Horacio; Rivas, Emilio A.; Sánchez Rivas, Carmen
Año de publicación
2006
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
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.
Instituto de Investigaciones Bioquímicas de La Plata
Materia
Ciencias Médicas
anionic phospholipid
Bacillus subtilis
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/83082

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spelling Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinityLópez, Claudia S.Alice, Alejandro F.Heras, HoracioRivas, Emilio A.Sánchez Rivas, CarmenCiencias Médicasanionic phospholipidBacillus subtilisThe importance of the content of anionic phospholipids [cardiolipin (CL) and phosphatidylglycerol (PG)] in the osmotic adaptation and in the membrane structure of <i>Bacillus subtilis</i> cultures was investigated. Insertion mutations in the three putative cardiolipin synthase genes (<i>ywiE</i>, <i>ywnE</i> and <i>ywjE</i>) were obtained. Only the <i>ywnE</i> mutation resulted in a complete deficiency in cardiolipin and thus corresponds to a true <i>clsA</i> gene. The osmotolerance of a <i>clsA</i> 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 <i>clsA</i> 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 <i>clsA</i> 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 <i>clsA</i> mutant strains were studied by Laurdan's steady-state fluorescence spectroscopy. At physiological temperature, the <i>clsA</i> 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 <i>clsA</i> mutant strains increased when they were grown in LBN. In a conditional IPTG-controlled <i>pgsA</i> 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 <i>clsA</i> and <i>pgsA</i> 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 <i>B. subtilis</i> in media containing elevated NaCl concentrations.Instituto de Investigaciones Bioquímicas de La Plata2006info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf605-616http://sedici.unlp.edu.ar/handle/10915/83082enginfo:eu-repo/semantics/altIdentifier/issn/1350-0872info:eu-repo/semantics/altIdentifier/doi/10.1099/mic.0.28345-0info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2026-03-31T12:04:43Zoai:sedici.unlp.edu.ar:10915/83082Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292026-03-31 12:04:44.119SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinity
title Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinity
spellingShingle Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinity
López, Claudia S.
Ciencias Médicas
anionic phospholipid
Bacillus subtilis
title_short Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinity
title_full Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinity
title_fullStr Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinity
title_full_unstemmed Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinity
title_sort Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinity
dc.creator.none.fl_str_mv López, Claudia S.
Alice, Alejandro F.
Heras, Horacio
Rivas, Emilio A.
Sánchez Rivas, Carmen
author López, Claudia S.
author_facet López, Claudia S.
Alice, Alejandro F.
Heras, Horacio
Rivas, Emilio A.
Sánchez Rivas, Carmen
author_role author
author2 Alice, Alejandro F.
Heras, Horacio
Rivas, Emilio A.
Sánchez Rivas, Carmen
author2_role author
author
author
author
dc.subject.none.fl_str_mv Ciencias Médicas
anionic phospholipid
Bacillus subtilis
topic Ciencias Médicas
anionic phospholipid
Bacillus subtilis
dc.description.none.fl_txt_mv The importance of the content of anionic phospholipids [cardiolipin (CL) and phosphatidylglycerol (PG)] in the osmotic adaptation and in the membrane structure of <i>Bacillus subtilis</i> cultures was investigated. Insertion mutations in the three putative cardiolipin synthase genes (<i>ywiE</i>, <i>ywnE</i> and <i>ywjE</i>) were obtained. Only the <i>ywnE</i> mutation resulted in a complete deficiency in cardiolipin and thus corresponds to a true <i>clsA</i> gene. The osmotolerance of a <i>clsA</i> 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 <i>clsA</i> 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 <i>clsA</i> 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 <i>clsA</i> mutant strains were studied by Laurdan's steady-state fluorescence spectroscopy. At physiological temperature, the <i>clsA</i> 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 <i>clsA</i> mutant strains increased when they were grown in LBN. In a conditional IPTG-controlled <i>pgsA</i> 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 <i>clsA</i> and <i>pgsA</i> 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 <i>B. subtilis</i> in media containing elevated NaCl concentrations.
Instituto de Investigaciones Bioquímicas de La Plata
description The importance of the content of anionic phospholipids [cardiolipin (CL) and phosphatidylglycerol (PG)] in the osmotic adaptation and in the membrane structure of <i>Bacillus subtilis</i> cultures was investigated. Insertion mutations in the three putative cardiolipin synthase genes (<i>ywiE</i>, <i>ywnE</i> and <i>ywjE</i>) were obtained. Only the <i>ywnE</i> mutation resulted in a complete deficiency in cardiolipin and thus corresponds to a true <i>clsA</i> gene. The osmotolerance of a <i>clsA</i> 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 <i>clsA</i> 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 <i>clsA</i> 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 <i>clsA</i> mutant strains were studied by Laurdan's steady-state fluorescence spectroscopy. At physiological temperature, the <i>clsA</i> 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 <i>clsA</i> mutant strains increased when they were grown in LBN. In a conditional IPTG-controlled <i>pgsA</i> 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 <i>clsA</i> and <i>pgsA</i> 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 <i>B. subtilis</i> in media containing elevated NaCl concentrations.
publishDate 2006
dc.date.none.fl_str_mv 2006
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status_str publishedVersion
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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
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