Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pH

Detalhes bibliográficos
Autor(a) principal: Leitão, Luís
Data de Publicação: 2012
Outros Autores: Prista, Catarina, Moura, Teresa F., Loureiro-Dias, Maria, Soveral, Graça
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.5/17651
Resumo: Grapevine (Vitis vinifera L.) is one of the oldest and most important perennial crops being considered as a fruit ligneous tree model system in which the water status appears crucial for high fruit and wine quality, controlling productivity and alcohol level. V. vinifera genome contains 28 genes coding for aquaporins, which acting in a concerted and regulated manner appear relevant for plant withstanding extremely unfavorable drought conditions essential for the quality of berries and wine. Several Vv aquaporins have been reported to be expressed in roots, shoots, berries and leaves with clear cultivar differences in their expression level, making their in vivo biochemical characterization a difficult task. In this work V. vinifera cv. Touriga nacional VvTnPIP1;1, VvTnPIP2;2 and VvTnTIP2;1 were expressed in yeast and water transport activity was characterized in intact cells of the transformants. The three aquaporins were localized in the yeast plasma membrane but only VvTnTIP2;1 expression enhanced the water permeability with a concomitant decrease of the activation energy of water transport. Acidification of yeast cytosol resulted in loss of VvTnTIP2;1 activity. Sequence analysis revealed the presence of a His131 residue, unusual in TIPs. By site directed mutagenesis, replacement of this residue by aspartic acid or alanine resulted in loss of pHin dependence while replacement by lysine resulted in total loss of activity. In addition to characterization of VvTn aquaporins, these results shed light on the gating of a specific tonoplast aquaporin by cytosolic pH
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spelling Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pHgrapevineaquaporinsGrapevine (Vitis vinifera L.) is one of the oldest and most important perennial crops being considered as a fruit ligneous tree model system in which the water status appears crucial for high fruit and wine quality, controlling productivity and alcohol level. V. vinifera genome contains 28 genes coding for aquaporins, which acting in a concerted and regulated manner appear relevant for plant withstanding extremely unfavorable drought conditions essential for the quality of berries and wine. Several Vv aquaporins have been reported to be expressed in roots, shoots, berries and leaves with clear cultivar differences in their expression level, making their in vivo biochemical characterization a difficult task. In this work V. vinifera cv. Touriga nacional VvTnPIP1;1, VvTnPIP2;2 and VvTnTIP2;1 were expressed in yeast and water transport activity was characterized in intact cells of the transformants. The three aquaporins were localized in the yeast plasma membrane but only VvTnTIP2;1 expression enhanced the water permeability with a concomitant decrease of the activation energy of water transport. Acidification of yeast cytosol resulted in loss of VvTnTIP2;1 activity. Sequence analysis revealed the presence of a His131 residue, unusual in TIPs. By site directed mutagenesis, replacement of this residue by aspartic acid or alanine resulted in loss of pHin dependence while replacement by lysine resulted in total loss of activity. In addition to characterization of VvTn aquaporins, these results shed light on the gating of a specific tonoplast aquaporin by cytosolic pHPlos ONERepositório da Universidade de LisboaLeitão, LuísPrista, CatarinaMoura, Teresa F.Loureiro-Dias, MariaSoveral, Graça2019-03-21T10:53:56Z20122012-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.5/17651engLeita˜o L, Prista C, Moura TF, Loureiro-Dias MC, Soveral G (2012) Grapevine Aquaporins: Gating of a Tonoplast Intrinsic Protein (TIP2;1) by Cytosolic pH. PLoS ONE 7(3): e33219doi:10.1371/journal.pone.0033219info: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:RCAAP2024-11-20T19:05:16Zoai:repositorio.ul.pt:10400.5/17651Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-11-20T19:05:16Repositório 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 Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pH
title Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pH
spellingShingle Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pH
Leitão, Luís
grapevine
aquaporins
title_short Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pH
title_full Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pH
title_fullStr Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pH
title_full_unstemmed Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pH
title_sort Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pH
author Leitão, Luís
author_facet Leitão, Luís
Prista, Catarina
Moura, Teresa F.
Loureiro-Dias, Maria
Soveral, Graça
author_role author
author2 Prista, Catarina
Moura, Teresa F.
Loureiro-Dias, Maria
Soveral, Graça
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Repositório da Universidade de Lisboa
dc.contributor.author.fl_str_mv Leitão, Luís
Prista, Catarina
Moura, Teresa F.
Loureiro-Dias, Maria
Soveral, Graça
dc.subject.por.fl_str_mv grapevine
aquaporins
topic grapevine
aquaporins
description Grapevine (Vitis vinifera L.) is one of the oldest and most important perennial crops being considered as a fruit ligneous tree model system in which the water status appears crucial for high fruit and wine quality, controlling productivity and alcohol level. V. vinifera genome contains 28 genes coding for aquaporins, which acting in a concerted and regulated manner appear relevant for plant withstanding extremely unfavorable drought conditions essential for the quality of berries and wine. Several Vv aquaporins have been reported to be expressed in roots, shoots, berries and leaves with clear cultivar differences in their expression level, making their in vivo biochemical characterization a difficult task. In this work V. vinifera cv. Touriga nacional VvTnPIP1;1, VvTnPIP2;2 and VvTnTIP2;1 were expressed in yeast and water transport activity was characterized in intact cells of the transformants. The three aquaporins were localized in the yeast plasma membrane but only VvTnTIP2;1 expression enhanced the water permeability with a concomitant decrease of the activation energy of water transport. Acidification of yeast cytosol resulted in loss of VvTnTIP2;1 activity. Sequence analysis revealed the presence of a His131 residue, unusual in TIPs. By site directed mutagenesis, replacement of this residue by aspartic acid or alanine resulted in loss of pHin dependence while replacement by lysine resulted in total loss of activity. In addition to characterization of VvTn aquaporins, these results shed light on the gating of a specific tonoplast aquaporin by cytosolic pH
publishDate 2012
dc.date.none.fl_str_mv 2012
2012-01-01T00:00:00Z
2019-03-21T10:53:56Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.5/17651
url http://hdl.handle.net/10400.5/17651
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Leita˜o L, Prista C, Moura TF, Loureiro-Dias MC, Soveral G (2012) Grapevine Aquaporins: Gating of a Tonoplast Intrinsic Protein (TIP2;1) by Cytosolic pH. PLoS ONE 7(3): e33219
doi:10.1371/journal.pone.0033219
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Plos ONE
publisher.none.fl_str_mv Plos ONE
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv mluisa.alvim@gmail.com
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