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Anchoring plant metallothioneins to the inner face of the plasma membrane of Saccharomyces cerevisiae cells leads to heavy metal accumulation

In this study we engineered yeast cells armed for heavy metal accumulation by targeting plant metallothioneins to the inner face of the yeast plasma membrane. Metallothioneins (MTs) are cysteine-rich proteins involved in the buffering of excess metal ions, especially Cu(I), Zn(II) or Cd(II). The cDN...

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Autores principales: Ruta, Lavinia Liliana, Lin, Ya-Fen, Kissen, Ralph, Nicolau, Ioana, Neagoe, Aurora Daniela, Ghenea, Simona, Bones, Atle M., Farcasanu, Ileana Cornelia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451056/
https://www.ncbi.nlm.nih.gov/pubmed/28562640
http://dx.doi.org/10.1371/journal.pone.0178393
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author Ruta, Lavinia Liliana
Lin, Ya-Fen
Kissen, Ralph
Nicolau, Ioana
Neagoe, Aurora Daniela
Ghenea, Simona
Bones, Atle M.
Farcasanu, Ileana Cornelia
author_facet Ruta, Lavinia Liliana
Lin, Ya-Fen
Kissen, Ralph
Nicolau, Ioana
Neagoe, Aurora Daniela
Ghenea, Simona
Bones, Atle M.
Farcasanu, Ileana Cornelia
author_sort Ruta, Lavinia Liliana
collection PubMed
description In this study we engineered yeast cells armed for heavy metal accumulation by targeting plant metallothioneins to the inner face of the yeast plasma membrane. Metallothioneins (MTs) are cysteine-rich proteins involved in the buffering of excess metal ions, especially Cu(I), Zn(II) or Cd(II). The cDNAs of seven Arabidopsis thaliana MTs (AtMT1a, AtMT1c, AtMT2a, AtMT2b, AtMT3, AtMT4a and AtMT4b) and four Noccaea caerulescens MTs (NcMT1, NcMT2a, NcMT2b and NcMT3) were each translationally fused to the C-terminus of a myristoylation green fluorescent protein variant (myrGFP) and expressed in Saccharomyces cerevisiae cells. The myrGFP cassette introduced a yeast myristoylation sequence which allowed directional targeting to the cytosolic face of the plasma membrane along with direct monitoring of the intracellular localization of the recombinant protein by fluorescence microscopy. The yeast strains expressing plant MTs were investigated against an array of heavy metals in order to identify strains which exhibit the (hyper)accumulation phenotype without developing toxicity symptoms. Among the transgenic strains which could accumulate Cu(II), Zn(II) or Cd(II), but also non-canonical metal ions, such as Co(II), Mn(II) or Ni(II), myrGFP-NcMT3 qualified as the best candidate for bioremediation applications, thanks to the robust growth accompanied by significant accumulative capacity.
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spelling pubmed-54510562017-06-12 Anchoring plant metallothioneins to the inner face of the plasma membrane of Saccharomyces cerevisiae cells leads to heavy metal accumulation Ruta, Lavinia Liliana Lin, Ya-Fen Kissen, Ralph Nicolau, Ioana Neagoe, Aurora Daniela Ghenea, Simona Bones, Atle M. Farcasanu, Ileana Cornelia PLoS One Research Article In this study we engineered yeast cells armed for heavy metal accumulation by targeting plant metallothioneins to the inner face of the yeast plasma membrane. Metallothioneins (MTs) are cysteine-rich proteins involved in the buffering of excess metal ions, especially Cu(I), Zn(II) or Cd(II). The cDNAs of seven Arabidopsis thaliana MTs (AtMT1a, AtMT1c, AtMT2a, AtMT2b, AtMT3, AtMT4a and AtMT4b) and four Noccaea caerulescens MTs (NcMT1, NcMT2a, NcMT2b and NcMT3) were each translationally fused to the C-terminus of a myristoylation green fluorescent protein variant (myrGFP) and expressed in Saccharomyces cerevisiae cells. The myrGFP cassette introduced a yeast myristoylation sequence which allowed directional targeting to the cytosolic face of the plasma membrane along with direct monitoring of the intracellular localization of the recombinant protein by fluorescence microscopy. The yeast strains expressing plant MTs were investigated against an array of heavy metals in order to identify strains which exhibit the (hyper)accumulation phenotype without developing toxicity symptoms. Among the transgenic strains which could accumulate Cu(II), Zn(II) or Cd(II), but also non-canonical metal ions, such as Co(II), Mn(II) or Ni(II), myrGFP-NcMT3 qualified as the best candidate for bioremediation applications, thanks to the robust growth accompanied by significant accumulative capacity. Public Library of Science 2017-05-31 /pmc/articles/PMC5451056/ /pubmed/28562640 http://dx.doi.org/10.1371/journal.pone.0178393 Text en © 2017 Ruta et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ruta, Lavinia Liliana
Lin, Ya-Fen
Kissen, Ralph
Nicolau, Ioana
Neagoe, Aurora Daniela
Ghenea, Simona
Bones, Atle M.
Farcasanu, Ileana Cornelia
Anchoring plant metallothioneins to the inner face of the plasma membrane of Saccharomyces cerevisiae cells leads to heavy metal accumulation
title Anchoring plant metallothioneins to the inner face of the plasma membrane of Saccharomyces cerevisiae cells leads to heavy metal accumulation
title_full Anchoring plant metallothioneins to the inner face of the plasma membrane of Saccharomyces cerevisiae cells leads to heavy metal accumulation
title_fullStr Anchoring plant metallothioneins to the inner face of the plasma membrane of Saccharomyces cerevisiae cells leads to heavy metal accumulation
title_full_unstemmed Anchoring plant metallothioneins to the inner face of the plasma membrane of Saccharomyces cerevisiae cells leads to heavy metal accumulation
title_short Anchoring plant metallothioneins to the inner face of the plasma membrane of Saccharomyces cerevisiae cells leads to heavy metal accumulation
title_sort anchoring plant metallothioneins to the inner face of the plasma membrane of saccharomyces cerevisiae cells leads to heavy metal accumulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451056/
https://www.ncbi.nlm.nih.gov/pubmed/28562640
http://dx.doi.org/10.1371/journal.pone.0178393
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