Novel bioassay for the discovery of inhibitors of the 2-C-Methyl-D-erythritol 4-Phosphate (MEP) and terpenoid pathways leading to carotenoid biosynthesis

Detalhes bibliográficos
Autor(a) principal: Corniani, Natalia [UNESP]
Data de Publicação: 2014
Outros Autores: Velini, Edivaldo Domingues [UNESP], Silva, Ferdinando Marcos Lima [UNESP], Nanayakkara, N. P. Dhammika, Witschel, Matthias, Dayan, Franck E.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1371/journal.pone.0103704
http://hdl.handle.net/11449/117393
Resumo: The 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway leads to the synthesis of isopentenyl diphosphate in plastids. It is a major branch point providing precursors for the synthesis of carotenoids, tocopherols, plastoquinone and the phytyl chain of chlorophylls, as well as the hormones abscisic acid and gibberellins. Consequently, disruption of this pathway is harmful to plants. We developed an in vivo bioassay that can measure the carbon flow through the carotenoid pathway. Leaf cuttings are incubated in the presence of a phytoene desaturase inhibitor to induce phytoene accumulation. Any compound reducing the level of phytoene accumulation is likely to interfere with either one of the steps in the MEP pathway or the synthesis of geranylgeranyl diphosphate. This concept was tested with known inhibitors of steps of the MEP pathway. The specificity of this in vivo bioassay was also verified by testing representative herbicides known to target processes outside of the MEP and carotenoid pathways. This assay enables the rapid screen of new inhibitors of enzymes preceding the synthesis of phytoene, though there are some limitations related to the non-specific effect of some inhibitors on this assay.
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spelling Novel bioassay for the discovery of inhibitors of the 2-C-Methyl-D-erythritol 4-Phosphate (MEP) and terpenoid pathways leading to carotenoid biosynthesisThe 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway leads to the synthesis of isopentenyl diphosphate in plastids. It is a major branch point providing precursors for the synthesis of carotenoids, tocopherols, plastoquinone and the phytyl chain of chlorophylls, as well as the hormones abscisic acid and gibberellins. Consequently, disruption of this pathway is harmful to plants. We developed an in vivo bioassay that can measure the carbon flow through the carotenoid pathway. Leaf cuttings are incubated in the presence of a phytoene desaturase inhibitor to induce phytoene accumulation. Any compound reducing the level of phytoene accumulation is likely to interfere with either one of the steps in the MEP pathway or the synthesis of geranylgeranyl diphosphate. This concept was tested with known inhibitors of steps of the MEP pathway. The specificity of this in vivo bioassay was also verified by testing representative herbicides known to target processes outside of the MEP and carotenoid pathways. This assay enables the rapid screen of new inhibitors of enzymes preceding the synthesis of phytoene, though there are some limitations related to the non-specific effect of some inhibitors on this assay.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Sao Paulo State Univ, Fac Agron Sci, Botucatu, SP, BrazilUniv Mississippi, Sch Pharm, Natl Ctr Nat Prod Res, University, MS 38677 USABASF SE, GVA HC B009, Ludwigshafen, GermanyUSDA ARS, Nat Prod Utilizat Res Unit, University, MS 38677 USASao Paulo State Univ, Fac Agron Sci, Botucatu, SP, BrazilCAPES: BEX 0226/12-2Public Library ScienceUniversidade Estadual Paulista (Unesp)Univ MississippiBASF SEUSDA ARSCorniani, Natalia [UNESP]Velini, Edivaldo Domingues [UNESP]Silva, Ferdinando Marcos Lima [UNESP]Nanayakkara, N. P. DhammikaWitschel, MatthiasDayan, Franck E.2015-03-18T15:56:01Z2015-03-18T15:56:01Z2014-07-31info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article10application/pdfhttp://dx.doi.org/10.1371/journal.pone.0103704Plos One. San Francisco: Public Library Science, v. 9, n. 7, 10 p., 2014.1932-6203http://hdl.handle.net/11449/11739310.1371/journal.pone.0103704WOS:000339954800066WOS000339954800066.pdf98554934481617020000-0003-0431-5942Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPlos One2.7661,164info:eu-repo/semantics/openAccess2024-04-30T15:59:40Zoai:repositorio.unesp.br:11449/117393Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:58:34.690128Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Novel bioassay for the discovery of inhibitors of the 2-C-Methyl-D-erythritol 4-Phosphate (MEP) and terpenoid pathways leading to carotenoid biosynthesis
title Novel bioassay for the discovery of inhibitors of the 2-C-Methyl-D-erythritol 4-Phosphate (MEP) and terpenoid pathways leading to carotenoid biosynthesis
spellingShingle Novel bioassay for the discovery of inhibitors of the 2-C-Methyl-D-erythritol 4-Phosphate (MEP) and terpenoid pathways leading to carotenoid biosynthesis
Corniani, Natalia [UNESP]
title_short Novel bioassay for the discovery of inhibitors of the 2-C-Methyl-D-erythritol 4-Phosphate (MEP) and terpenoid pathways leading to carotenoid biosynthesis
title_full Novel bioassay for the discovery of inhibitors of the 2-C-Methyl-D-erythritol 4-Phosphate (MEP) and terpenoid pathways leading to carotenoid biosynthesis
title_fullStr Novel bioassay for the discovery of inhibitors of the 2-C-Methyl-D-erythritol 4-Phosphate (MEP) and terpenoid pathways leading to carotenoid biosynthesis
title_full_unstemmed Novel bioassay for the discovery of inhibitors of the 2-C-Methyl-D-erythritol 4-Phosphate (MEP) and terpenoid pathways leading to carotenoid biosynthesis
title_sort Novel bioassay for the discovery of inhibitors of the 2-C-Methyl-D-erythritol 4-Phosphate (MEP) and terpenoid pathways leading to carotenoid biosynthesis
author Corniani, Natalia [UNESP]
author_facet Corniani, Natalia [UNESP]
Velini, Edivaldo Domingues [UNESP]
Silva, Ferdinando Marcos Lima [UNESP]
Nanayakkara, N. P. Dhammika
Witschel, Matthias
Dayan, Franck E.
author_role author
author2 Velini, Edivaldo Domingues [UNESP]
Silva, Ferdinando Marcos Lima [UNESP]
Nanayakkara, N. P. Dhammika
Witschel, Matthias
Dayan, Franck E.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Univ Mississippi
BASF SE
USDA ARS
dc.contributor.author.fl_str_mv Corniani, Natalia [UNESP]
Velini, Edivaldo Domingues [UNESP]
Silva, Ferdinando Marcos Lima [UNESP]
Nanayakkara, N. P. Dhammika
Witschel, Matthias
Dayan, Franck E.
description The 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway leads to the synthesis of isopentenyl diphosphate in plastids. It is a major branch point providing precursors for the synthesis of carotenoids, tocopherols, plastoquinone and the phytyl chain of chlorophylls, as well as the hormones abscisic acid and gibberellins. Consequently, disruption of this pathway is harmful to plants. We developed an in vivo bioassay that can measure the carbon flow through the carotenoid pathway. Leaf cuttings are incubated in the presence of a phytoene desaturase inhibitor to induce phytoene accumulation. Any compound reducing the level of phytoene accumulation is likely to interfere with either one of the steps in the MEP pathway or the synthesis of geranylgeranyl diphosphate. This concept was tested with known inhibitors of steps of the MEP pathway. The specificity of this in vivo bioassay was also verified by testing representative herbicides known to target processes outside of the MEP and carotenoid pathways. This assay enables the rapid screen of new inhibitors of enzymes preceding the synthesis of phytoene, though there are some limitations related to the non-specific effect of some inhibitors on this assay.
publishDate 2014
dc.date.none.fl_str_mv 2014-07-31
2015-03-18T15:56:01Z
2015-03-18T15:56:01Z
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://dx.doi.org/10.1371/journal.pone.0103704
Plos One. San Francisco: Public Library Science, v. 9, n. 7, 10 p., 2014.
1932-6203
http://hdl.handle.net/11449/117393
10.1371/journal.pone.0103704
WOS:000339954800066
WOS000339954800066.pdf
9855493448161702
0000-0003-0431-5942
url http://dx.doi.org/10.1371/journal.pone.0103704
http://hdl.handle.net/11449/117393
identifier_str_mv Plos One. San Francisco: Public Library Science, v. 9, n. 7, 10 p., 2014.
1932-6203
10.1371/journal.pone.0103704
WOS:000339954800066
WOS000339954800066.pdf
9855493448161702
0000-0003-0431-5942
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Plos One
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application/pdf
dc.publisher.none.fl_str_mv Public Library Science
publisher.none.fl_str_mv Public Library Science
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reponame:Repositório Institucional da UNESP
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