Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)

Detalhes bibliográficos
Autor(a) principal: Leite, Ana C. [UNESP]
Data de Publicação: 2007
Outros Autores: Lopes, Adriana A. [UNESP], Kato, Massuo J., Bolzani, Vanderlan da Silva [UNESP], Furlan, Maysa [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S0103-50532007000800008
http://hdl.handle.net/11449/70063
Resumo: Metabolic studies involving the incorporation of [1-13C]-D- glucose into intact leaves of Piper aduncum (Piperaceae) have indicated that both the mevalonate (MVA) and the pyruvate-triose (MEP) non-mevalonate pathways are implicated in the biosynthesis of isoprene moieties present in methyl 2,2-dimethyl-2H-1-chromene-6-carboxylate (1) and methyl 2,2-dimethyl-8- (3′-methyl-2′-butenyl)-2H-1-chromene-6-carboxylate (2). The pattern of incorporation of label from [1-13C]-D-glucose into these chromenes was determined by quantitative 13C NMR spectroscopy. The results confirmed that biosynthetic compartment of 1 and 2 could either be the plastid and/ or the cytosol or, possibly, an additional compartment such as the plastid inter-membrane space. ©2007 Sociedade Brasileira de Química.
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spelling Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)2-C-methyl-D-erythritol-4-phosphate pathway[1-13C]-D-glucoseChromenesMevalonate pathwayPiper aduncumMetabolic studies involving the incorporation of [1-13C]-D- glucose into intact leaves of Piper aduncum (Piperaceae) have indicated that both the mevalonate (MVA) and the pyruvate-triose (MEP) non-mevalonate pathways are implicated in the biosynthesis of isoprene moieties present in methyl 2,2-dimethyl-2H-1-chromene-6-carboxylate (1) and methyl 2,2-dimethyl-8- (3′-methyl-2′-butenyl)-2H-1-chromene-6-carboxylate (2). The pattern of incorporation of label from [1-13C]-D-glucose into these chromenes was determined by quantitative 13C NMR spectroscopy. The results confirmed that biosynthetic compartment of 1 and 2 could either be the plastid and/ or the cytosol or, possibly, an additional compartment such as the plastid inter-membrane space. ©2007 Sociedade Brasileira de Química.Instituto de Química Universidade Estadual Paulista, 14801-970 Araraquara-SPInstituto de Química Universidade de São Paulo, 05599-970 São Paulo-SPInstituto de Química Universidade Estadual Paulista, 14801-970 Araraquara-SPUniversidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Leite, Ana C. [UNESP]Lopes, Adriana A. [UNESP]Kato, Massuo J.Bolzani, Vanderlan da Silva [UNESP]Furlan, Maysa [UNESP]2014-05-27T11:22:40Z2014-05-27T11:22:40Z2007-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1500-1503application/pdfhttp://dx.doi.org/10.1590/S0103-50532007000800008Journal of the Brazilian Chemical Society, v. 18, n. 8, p. 1500-1503, 2007.0103-50531678-4790http://hdl.handle.net/11449/7006310.1590/S0103-50532007000800008S0103-50532007000800008WOS:0002528597000082-s2.0-375490241892-s2.0-37549024189.pdf448408368525167313080427947868721308042794786872Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of the Brazilian Chemical Society1.4440,3570,357info:eu-repo/semantics/openAccess2023-10-16T06:03:42Zoai:repositorio.unesp.br:11449/70063Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:04:37.263781Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)
title Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)
spellingShingle Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)
Leite, Ana C. [UNESP]
2-C-methyl-D-erythritol-4-phosphate pathway
[1-13C]-D-glucose
Chromenes
Mevalonate pathway
Piper aduncum
title_short Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)
title_full Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)
title_fullStr Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)
title_full_unstemmed Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)
title_sort Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)
author Leite, Ana C. [UNESP]
author_facet Leite, Ana C. [UNESP]
Lopes, Adriana A. [UNESP]
Kato, Massuo J.
Bolzani, Vanderlan da Silva [UNESP]
Furlan, Maysa [UNESP]
author_role author
author2 Lopes, Adriana A. [UNESP]
Kato, Massuo J.
Bolzani, Vanderlan da Silva [UNESP]
Furlan, Maysa [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Leite, Ana C. [UNESP]
Lopes, Adriana A. [UNESP]
Kato, Massuo J.
Bolzani, Vanderlan da Silva [UNESP]
Furlan, Maysa [UNESP]
dc.subject.por.fl_str_mv 2-C-methyl-D-erythritol-4-phosphate pathway
[1-13C]-D-glucose
Chromenes
Mevalonate pathway
Piper aduncum
topic 2-C-methyl-D-erythritol-4-phosphate pathway
[1-13C]-D-glucose
Chromenes
Mevalonate pathway
Piper aduncum
description Metabolic studies involving the incorporation of [1-13C]-D- glucose into intact leaves of Piper aduncum (Piperaceae) have indicated that both the mevalonate (MVA) and the pyruvate-triose (MEP) non-mevalonate pathways are implicated in the biosynthesis of isoprene moieties present in methyl 2,2-dimethyl-2H-1-chromene-6-carboxylate (1) and methyl 2,2-dimethyl-8- (3′-methyl-2′-butenyl)-2H-1-chromene-6-carboxylate (2). The pattern of incorporation of label from [1-13C]-D-glucose into these chromenes was determined by quantitative 13C NMR spectroscopy. The results confirmed that biosynthetic compartment of 1 and 2 could either be the plastid and/ or the cytosol or, possibly, an additional compartment such as the plastid inter-membrane space. ©2007 Sociedade Brasileira de Química.
publishDate 2007
dc.date.none.fl_str_mv 2007-12-01
2014-05-27T11:22:40Z
2014-05-27T11:22:40Z
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/10.1590/S0103-50532007000800008
Journal of the Brazilian Chemical Society, v. 18, n. 8, p. 1500-1503, 2007.
0103-5053
1678-4790
http://hdl.handle.net/11449/70063
10.1590/S0103-50532007000800008
S0103-50532007000800008
WOS:000252859700008
2-s2.0-37549024189
2-s2.0-37549024189.pdf
4484083685251673
1308042794786872
1308042794786872
url http://dx.doi.org/10.1590/S0103-50532007000800008
http://hdl.handle.net/11449/70063
identifier_str_mv Journal of the Brazilian Chemical Society, v. 18, n. 8, p. 1500-1503, 2007.
0103-5053
1678-4790
10.1590/S0103-50532007000800008
S0103-50532007000800008
WOS:000252859700008
2-s2.0-37549024189
2-s2.0-37549024189.pdf
4484083685251673
1308042794786872
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of the Brazilian Chemical Society
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0,357
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dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1500-1503
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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