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Tenuazonic acid from Stemphylium loti inhibits the plant plasma membrane H(+)‐ATPase by a mechanism involving the C‐terminal regulatory domain

Pathogenic fungi often target the plant plasma membrane (PM) H(+)‐ATPase during infection. To identify pathogenic compounds targeting plant H(+)‐ATPases, we screened extracts from 10 Stemphylium species for their effect on H(+)‐ATPase activity. We identified Stemphylium loti extracts as potential H(...

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Autores principales: Bjørk, Peter K., Rasmussen, Silas A., Gjetting, Sisse K., Havshøi, Nanna W., Petersen, Thomas Isbrandt, Ipsen, Johan Ø., Larsen, Thomas O., Fuglsang, Anja T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187312/
https://www.ncbi.nlm.nih.gov/pubmed/31880817
http://dx.doi.org/10.1111/nph.16398
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author Bjørk, Peter K.
Rasmussen, Silas A.
Gjetting, Sisse K.
Havshøi, Nanna W.
Petersen, Thomas Isbrandt
Ipsen, Johan Ø.
Larsen, Thomas O.
Fuglsang, Anja T.
author_facet Bjørk, Peter K.
Rasmussen, Silas A.
Gjetting, Sisse K.
Havshøi, Nanna W.
Petersen, Thomas Isbrandt
Ipsen, Johan Ø.
Larsen, Thomas O.
Fuglsang, Anja T.
author_sort Bjørk, Peter K.
collection PubMed
description Pathogenic fungi often target the plant plasma membrane (PM) H(+)‐ATPase during infection. To identify pathogenic compounds targeting plant H(+)‐ATPases, we screened extracts from 10 Stemphylium species for their effect on H(+)‐ATPase activity. We identified Stemphylium loti extracts as potential H(+)‐ATPase inhibitors, and through chemical separation and analysis, tenuazonic acid (TeA) as a potent H(+)‐ATPase inhibitor. By assaying ATP hydrolysis and H(+) pumping, we confirmed TeA as a H(+)‐ATPase inhibitor both in vitro and in vivo. To visualize in planta inhibition of the H(+)‐ATPase, we treated pH‐sensing Arabidopsis thaliana seedlings with TeA and quantified apoplastic alkalization. TeA affected both ATPase hydrolysis and H(+) pumping, supporting a direct effect on the H(+)‐ATPase. We demonstrated apoplastic alkalization of A. thaliana seedlings after short‐term TeA treatment, indicating that TeA effectively inhibits plant PM H(+)‐ATPase in planta. TeA‐induced inhibition was highly dependent on the regulatory C‐terminal domain of the plant H(+)‐ATPase. Stemphylium loti is a phytopathogenic fungus. Inhibiting the plant PM H(+)‐ATPase results in membrane potential depolarization and eventually necrosis. The corresponding fungal H(+)‐ATPase, PMA1, is less affected by TeA when comparing native preparations. Fungi are thus able to target an essential plant enzyme without causing self‐toxicity.
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spelling pubmed-71873122020-04-28 Tenuazonic acid from Stemphylium loti inhibits the plant plasma membrane H(+)‐ATPase by a mechanism involving the C‐terminal regulatory domain Bjørk, Peter K. Rasmussen, Silas A. Gjetting, Sisse K. Havshøi, Nanna W. Petersen, Thomas Isbrandt Ipsen, Johan Ø. Larsen, Thomas O. Fuglsang, Anja T. New Phytol Research Pathogenic fungi often target the plant plasma membrane (PM) H(+)‐ATPase during infection. To identify pathogenic compounds targeting plant H(+)‐ATPases, we screened extracts from 10 Stemphylium species for their effect on H(+)‐ATPase activity. We identified Stemphylium loti extracts as potential H(+)‐ATPase inhibitors, and through chemical separation and analysis, tenuazonic acid (TeA) as a potent H(+)‐ATPase inhibitor. By assaying ATP hydrolysis and H(+) pumping, we confirmed TeA as a H(+)‐ATPase inhibitor both in vitro and in vivo. To visualize in planta inhibition of the H(+)‐ATPase, we treated pH‐sensing Arabidopsis thaliana seedlings with TeA and quantified apoplastic alkalization. TeA affected both ATPase hydrolysis and H(+) pumping, supporting a direct effect on the H(+)‐ATPase. We demonstrated apoplastic alkalization of A. thaliana seedlings after short‐term TeA treatment, indicating that TeA effectively inhibits plant PM H(+)‐ATPase in planta. TeA‐induced inhibition was highly dependent on the regulatory C‐terminal domain of the plant H(+)‐ATPase. Stemphylium loti is a phytopathogenic fungus. Inhibiting the plant PM H(+)‐ATPase results in membrane potential depolarization and eventually necrosis. The corresponding fungal H(+)‐ATPase, PMA1, is less affected by TeA when comparing native preparations. Fungi are thus able to target an essential plant enzyme without causing self‐toxicity. John Wiley and Sons Inc. 2020-02-03 2020-05 /pmc/articles/PMC7187312/ /pubmed/31880817 http://dx.doi.org/10.1111/nph.16398 Text en © 2019 The Authors New Phytologist © 2019 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research
Bjørk, Peter K.
Rasmussen, Silas A.
Gjetting, Sisse K.
Havshøi, Nanna W.
Petersen, Thomas Isbrandt
Ipsen, Johan Ø.
Larsen, Thomas O.
Fuglsang, Anja T.
Tenuazonic acid from Stemphylium loti inhibits the plant plasma membrane H(+)‐ATPase by a mechanism involving the C‐terminal regulatory domain
title Tenuazonic acid from Stemphylium loti inhibits the plant plasma membrane H(+)‐ATPase by a mechanism involving the C‐terminal regulatory domain
title_full Tenuazonic acid from Stemphylium loti inhibits the plant plasma membrane H(+)‐ATPase by a mechanism involving the C‐terminal regulatory domain
title_fullStr Tenuazonic acid from Stemphylium loti inhibits the plant plasma membrane H(+)‐ATPase by a mechanism involving the C‐terminal regulatory domain
title_full_unstemmed Tenuazonic acid from Stemphylium loti inhibits the plant plasma membrane H(+)‐ATPase by a mechanism involving the C‐terminal regulatory domain
title_short Tenuazonic acid from Stemphylium loti inhibits the plant plasma membrane H(+)‐ATPase by a mechanism involving the C‐terminal regulatory domain
title_sort tenuazonic acid from stemphylium loti inhibits the plant plasma membrane h(+)‐atpase by a mechanism involving the c‐terminal regulatory domain
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187312/
https://www.ncbi.nlm.nih.gov/pubmed/31880817
http://dx.doi.org/10.1111/nph.16398
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