Evaluation of the role of glutathione in the lead-induced toxicity in saccharomyces cerevisiae

Detalhes bibliográficos
Autor(a) principal: Perez, Rita R.
Data de Publicação: 2013
Outros Autores: Sousa, Cátia A., Vankeersbilck, Thomas, Machado, Manuela D., Soares, Eduardo V.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.22/4246
Resumo: The effect of intracellular reduced glutathione (GSH) in the lead stress response of Saccharomyces cerevisiae was investigated. Yeast cells exposed to Pb, for 3 h, lost the cell proliferation capacity (viability) and decreased intracellular GSH level. The Pb-induced loss of cell viability was compared among yeast cells deficient in GSH1 (∆gsh1) or GSH2 (∆gsh2) genes and wild-type (WT) cells. When exposed to Pb, ∆gsh1 and ∆gsh2 cells did not display an increased loss of viability, compared with WT cells. However, the depletion of cellular thiols, including GSH, by treatment of WT cells with iodoacetamide (an alkylating agent, which binds covalently to thiol group), increased the loss of viability in Pb-treated cells. In contrast, GSH enrichment, due to the incubation of WT cells with amino acids mixture constituting GSH (l-glutamic acid, l-cysteine and glycine), reduced the Pb-induced loss of proliferation capacity. The obtained results suggest that intracellular GSH is involved in the defence against the Pb-induced toxicity; however, at physiological concentration, GSH seems not to be sufficient to prevent the Pb-induced loss of cell viability.
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spelling Evaluation of the role of glutathione in the lead-induced toxicity in saccharomyces cerevisiaeThe effect of intracellular reduced glutathione (GSH) in the lead stress response of Saccharomyces cerevisiae was investigated. Yeast cells exposed to Pb, for 3 h, lost the cell proliferation capacity (viability) and decreased intracellular GSH level. The Pb-induced loss of cell viability was compared among yeast cells deficient in GSH1 (∆gsh1) or GSH2 (∆gsh2) genes and wild-type (WT) cells. When exposed to Pb, ∆gsh1 and ∆gsh2 cells did not display an increased loss of viability, compared with WT cells. However, the depletion of cellular thiols, including GSH, by treatment of WT cells with iodoacetamide (an alkylating agent, which binds covalently to thiol group), increased the loss of viability in Pb-treated cells. In contrast, GSH enrichment, due to the incubation of WT cells with amino acids mixture constituting GSH (l-glutamic acid, l-cysteine and glycine), reduced the Pb-induced loss of proliferation capacity. The obtained results suggest that intracellular GSH is involved in the defence against the Pb-induced toxicity; however, at physiological concentration, GSH seems not to be sufficient to prevent the Pb-induced loss of cell viability.SpringerRepositório Científico do Instituto Politécnico do PortoPerez, Rita R.Sousa, Cátia A.Vankeersbilck, ThomasMachado, Manuela D.Soares, Eduardo V.2014-03-25T15:53:16Z20132013-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.22/4246eng0343-865110.1007/s00284-013-0364-zinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-13T12:44:19Zoai:recipp.ipp.pt:10400.22/4246Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:25:09.379149Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Evaluation of the role of glutathione in the lead-induced toxicity in saccharomyces cerevisiae
title Evaluation of the role of glutathione in the lead-induced toxicity in saccharomyces cerevisiae
spellingShingle Evaluation of the role of glutathione in the lead-induced toxicity in saccharomyces cerevisiae
Perez, Rita R.
title_short Evaluation of the role of glutathione in the lead-induced toxicity in saccharomyces cerevisiae
title_full Evaluation of the role of glutathione in the lead-induced toxicity in saccharomyces cerevisiae
title_fullStr Evaluation of the role of glutathione in the lead-induced toxicity in saccharomyces cerevisiae
title_full_unstemmed Evaluation of the role of glutathione in the lead-induced toxicity in saccharomyces cerevisiae
title_sort Evaluation of the role of glutathione in the lead-induced toxicity in saccharomyces cerevisiae
author Perez, Rita R.
author_facet Perez, Rita R.
Sousa, Cátia A.
Vankeersbilck, Thomas
Machado, Manuela D.
Soares, Eduardo V.
author_role author
author2 Sousa, Cátia A.
Vankeersbilck, Thomas
Machado, Manuela D.
Soares, Eduardo V.
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Politécnico do Porto
dc.contributor.author.fl_str_mv Perez, Rita R.
Sousa, Cátia A.
Vankeersbilck, Thomas
Machado, Manuela D.
Soares, Eduardo V.
description The effect of intracellular reduced glutathione (GSH) in the lead stress response of Saccharomyces cerevisiae was investigated. Yeast cells exposed to Pb, for 3 h, lost the cell proliferation capacity (viability) and decreased intracellular GSH level. The Pb-induced loss of cell viability was compared among yeast cells deficient in GSH1 (∆gsh1) or GSH2 (∆gsh2) genes and wild-type (WT) cells. When exposed to Pb, ∆gsh1 and ∆gsh2 cells did not display an increased loss of viability, compared with WT cells. However, the depletion of cellular thiols, including GSH, by treatment of WT cells with iodoacetamide (an alkylating agent, which binds covalently to thiol group), increased the loss of viability in Pb-treated cells. In contrast, GSH enrichment, due to the incubation of WT cells with amino acids mixture constituting GSH (l-glutamic acid, l-cysteine and glycine), reduced the Pb-induced loss of proliferation capacity. The obtained results suggest that intracellular GSH is involved in the defence against the Pb-induced toxicity; however, at physiological concentration, GSH seems not to be sufficient to prevent the Pb-induced loss of cell viability.
publishDate 2013
dc.date.none.fl_str_mv 2013
2013-01-01T00:00:00Z
2014-03-25T15:53:16Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.22/4246
url http://hdl.handle.net/10400.22/4246
dc.language.iso.fl_str_mv eng
language eng
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10.1007/s00284-013-0364-z
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dc.publisher.none.fl_str_mv Springer
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