Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)
Autor(a) principal: | |
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Data de Publicação: | 2007 |
Outros Autores: | , , , |
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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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 1.444 0,357 0,357 |
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 |
|
_version_ |
1808128454940426240 |