Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of the Brazilian Chemical Society (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000800018 |
Resumo: | The biosynthetic origins of the isoprene units of 4-nerolidylcatechol (1), the major constituent of Potomorphe umbellata, have been studied through feeding experiments with [14C]- and [13C]-glucose, and with precursors of the mevalonic acid and triose/pyruvate pathways, namely, [2-14C]-mevalonolactone and [U-14C]-glyceraldehyde-3-phosphate, respectively. The pattern of incorporation of label from [1-13C]-glucose into 1 was determined by quantitative 13C NMR spectroscopy. The labelling pattern revealed that the additive was specifically incorporated, and that the isoprene units of the sesquiterpenoid moiety of 4-nerolidylcatechol were derived from both the mevalonic acid and the triose/pyruvate pathways. The results indicate that both plastidic and cytoplasmic pathways are able to provide isopentenyl diphosphate units for the biosynthesis of 1. |
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Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellataPotomorphe umbellataPiperaceae4-nerolidylcatecholbiosynthesissesquiterpenoidisopentenyl diphosphateThe biosynthetic origins of the isoprene units of 4-nerolidylcatechol (1), the major constituent of Potomorphe umbellata, have been studied through feeding experiments with [14C]- and [13C]-glucose, and with precursors of the mevalonic acid and triose/pyruvate pathways, namely, [2-14C]-mevalonolactone and [U-14C]-glyceraldehyde-3-phosphate, respectively. The pattern of incorporation of label from [1-13C]-glucose into 1 was determined by quantitative 13C NMR spectroscopy. The labelling pattern revealed that the additive was specifically incorporated, and that the isoprene units of the sesquiterpenoid moiety of 4-nerolidylcatechol were derived from both the mevalonic acid and the triose/pyruvate pathways. The results indicate that both plastidic and cytoplasmic pathways are able to provide isopentenyl diphosphate units for the biosynthesis of 1.Sociedade Brasileira de Química2005-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000800018Journal of the Brazilian Chemical Society v.16 n.6b 2005reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532005000800018info:eu-repo/semantics/openAccessBergamo,Debora Cristina B.Kato,Massuo JorgeBolzani,Vanderlan da S.Furlan,Maysaeng2006-01-20T00:00:00Zoai:scielo:S0103-50532005000800018Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2006-01-20T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata |
title |
Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata |
spellingShingle |
Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata Bergamo,Debora Cristina B. Potomorphe umbellata Piperaceae 4-nerolidylcatechol biosynthesis sesquiterpenoid isopentenyl diphosphate |
title_short |
Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata |
title_full |
Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata |
title_fullStr |
Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata |
title_full_unstemmed |
Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata |
title_sort |
Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata |
author |
Bergamo,Debora Cristina B. |
author_facet |
Bergamo,Debora Cristina B. Kato,Massuo Jorge Bolzani,Vanderlan da S. Furlan,Maysa |
author_role |
author |
author2 |
Kato,Massuo Jorge Bolzani,Vanderlan da S. Furlan,Maysa |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Bergamo,Debora Cristina B. Kato,Massuo Jorge Bolzani,Vanderlan da S. Furlan,Maysa |
dc.subject.por.fl_str_mv |
Potomorphe umbellata Piperaceae 4-nerolidylcatechol biosynthesis sesquiterpenoid isopentenyl diphosphate |
topic |
Potomorphe umbellata Piperaceae 4-nerolidylcatechol biosynthesis sesquiterpenoid isopentenyl diphosphate |
description |
The biosynthetic origins of the isoprene units of 4-nerolidylcatechol (1), the major constituent of Potomorphe umbellata, have been studied through feeding experiments with [14C]- and [13C]-glucose, and with precursors of the mevalonic acid and triose/pyruvate pathways, namely, [2-14C]-mevalonolactone and [U-14C]-glyceraldehyde-3-phosphate, respectively. The pattern of incorporation of label from [1-13C]-glucose into 1 was determined by quantitative 13C NMR spectroscopy. The labelling pattern revealed that the additive was specifically incorporated, and that the isoprene units of the sesquiterpenoid moiety of 4-nerolidylcatechol were derived from both the mevalonic acid and the triose/pyruvate pathways. The results indicate that both plastidic and cytoplasmic pathways are able to provide isopentenyl diphosphate units for the biosynthesis of 1. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-11-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000800018 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000800018 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532005000800018 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
dc.source.none.fl_str_mv |
Journal of the Brazilian Chemical Society v.16 n.6b 2005 reponame:Journal of the Brazilian Chemical Society (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
reponame_str |
Journal of the Brazilian Chemical Society (Online) |
collection |
Journal of the Brazilian Chemical Society (Online) |
repository.name.fl_str_mv |
Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
||office@jbcs.sbq.org.br |
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1750318166911746048 |