Arilpropan?ides em Embryobionta

Detalhes bibliográficos
Ano de defesa: 1975
Autor(a) principal: Marx, Maria Claudia lattes
Orientador(a): Rezende, Ceres Maria Andrade da Mata
Banca de defesa: Rezende, Ceres Maria Andrade da Mata
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal Rural do Rio de Janeiro
Programa de Pós-Graduação: Programa de P?s-Gradua??o em Qu?mica
Departamento: Instituto de Ci?ncias Exatas
País: Brasil
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: https://tede.ufrrj.br/jspui/handle/jspui/4351
Resumo: Lignins are among the most abundant organic products on earth. Their polyarylpropanoid molecules were, for this reason, subject of many investigations. In opposition, relatively little is known about bisarylpropanoids (lignans, neolignans) and arylpropanoids (propenylphenols, allylphenols). These metabolites function in Embryobionta as social hormones. Their evolutive potentiation led to the derivatives of the biogenetic group of benzyltetrahydroisoquinoline. Mapping of the biosynthetic routes which lead to these alcaloids (in previous work), as well as to mono- and bisarylpropanoids, starts from phenylalanine and makes possible not only the classification, but also the rational codification of all skeleta involved. The analysis of the aromatic oxygenation pattern of each of the classes of lignans and neolignans suggests details of the oxidative coupling mechanisms. In the case of propenylphenols and allylphenols, such an analysis, associated with consideration of the natural distribution of the derivatives, does not corroborate in vivo evidence on the biosynthesis of allylphenols, recently obtained in Italy. The structural variation, of lignins, lignans, and neolignans through 350 x 106 years of plant evolution can be accompanied, paying attention to one of the basic principles of Biochemical Systematics: evolution of a biogenetic group of metabolites operates through gradual diversification of skeleta and their derivatives up to a maximum, initiating, in sequence, gradual retraction of the number of skeleta and number of corresponding derivatives. The different classes of arylpropanoids, can, for this reason, in combination with the benzyltetrahydroisoquinoline group, be used as chemosystematic markers, a fact which, in the present case, served to suggest the singular taxonomic position of the subclass Magnoliidae and the phylogenetic relation of its families.
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spelling Rezende, Ceres Maria Andrade da MataGottlieb, Otto RichardRezende, Ceres Maria Andrade da Matahttp://lattes.cnpq.br/3354457350968761Marx, Maria Claudia2021-01-27T17:20:53Z1975-06-27MARX, Maria Claudia. Arilpropan?ides em Embryobionta. 1975. 127 f. Disserta??o (Programa de P?s-Gradua??o em Qu?mica) - Instituto de Ci?ncias Exatas, Universidade Federal Rural do Rio de Janeiro, Serop?dica - RJ, 1975.https://tede.ufrrj.br/jspui/handle/jspui/4351Lignins are among the most abundant organic products on earth. Their polyarylpropanoid molecules were, for this reason, subject of many investigations. In opposition, relatively little is known about bisarylpropanoids (lignans, neolignans) and arylpropanoids (propenylphenols, allylphenols). These metabolites function in Embryobionta as social hormones. Their evolutive potentiation led to the derivatives of the biogenetic group of benzyltetrahydroisoquinoline. Mapping of the biosynthetic routes which lead to these alcaloids (in previous work), as well as to mono- and bisarylpropanoids, starts from phenylalanine and makes possible not only the classification, but also the rational codification of all skeleta involved. The analysis of the aromatic oxygenation pattern of each of the classes of lignans and neolignans suggests details of the oxidative coupling mechanisms. In the case of propenylphenols and allylphenols, such an analysis, associated with consideration of the natural distribution of the derivatives, does not corroborate in vivo evidence on the biosynthesis of allylphenols, recently obtained in Italy. The structural variation, of lignins, lignans, and neolignans through 350 x 106 years of plant evolution can be accompanied, paying attention to one of the basic principles of Biochemical Systematics: evolution of a biogenetic group of metabolites operates through gradual diversification of skeleta and their derivatives up to a maximum, initiating, in sequence, gradual retraction of the number of skeleta and number of corresponding derivatives. The different classes of arylpropanoids, can, for this reason, in combination with the benzyltetrahydroisoquinoline group, be used as chemosystematic markers, a fact which, in the present case, served to suggest the singular taxonomic position of the subclass Magnoliidae and the phylogenetic relation of its families.As ligninas figuram entre os mais abundantes produtos org?nicos na Terra. Suas mol?culas poliarilpropano?dicas foram por isto objetivo de muitos estudos. Em contraste, ? diminuto o n?mero de informa??es sobre bisarilpropan?ides (lignanas, neolignanas) e arilpropan?ides (propenilfen?is, alilfen?is). Estes metab?litos desempenham em Embryobionta papel de horm?nios sociais. Sua potencia??o evolutiva levou aos derivados do grupo biogen?tico da benziltetrahidroisoquinolina. O mapeamento dos caminhos biossint?ticos, que leva a estes alcal?ides (efetuado em trabalho anterior), como aos mono- e bisarilpropan?ides parte da fenilalanina e permite n?o s? a classifica??o, como ainda a codifica??o racional de todos os esqueletos envolvidos. O estudo do padr?o de oxigena??o arom?tico de cada uma das classes de lignanas e de neolignanas revela min?cias do mecanismo do acoplamento oxidativo. No caso de propenilfen?is e alilfen?is, tal estudo, associado ? considera??o da distribui??o natural dos derivados, n?o ap?ia evidentemente, a bioss?ntese de alilfen?is obtida recentemente in vivo na It?lia, A varia??o estrutural de ligninas, lignanas e neolignanas atrav?s de 350 x 106 anos de evolu??o vegetal, pode ser acompanhada, atentando para um dos princ?pios b?sicos da Sistem?tica Bioqu?mica: evolu??o de um grupo biogen?tico de metab?litos opera por gradual diversifica??o de esqueletos e de seus derivados at? um m?ximo, iniciando-se a seguir, retra??o em n?mero de esqueletos e n?mero de derivados correspondentes. Por esta raz?o, podem as diversas classes de arilpropan?ides serem utilizadas, em conjunto com o grupo da benziltetrahidroisoquinolina, como marcadores quimiossistem?ticos, fato que, no caso presente, serviu para destacar a posi??o taxon?mica singular da subclasse Magnoliidae e a rela??o filogen?tica de suas fam?lias.Submitted by Jorge Silva (jorgelmsilva@ufrrj.br) on 2021-01-27T17:20:53Z No. of bitstreams: 1 1975 - Maria Cl?udia Marx.pdf: 1878078 bytes, checksum: 4ef9de9b01d64983be2ff22d8415de4b (MD5)Made available in DSpace on 2021-01-27T17:20:53Z (GMT). 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dc.title.por.fl_str_mv Arilpropan?ides em Embryobionta
title Arilpropan?ides em Embryobionta
spellingShingle Arilpropan?ides em Embryobionta
Marx, Maria Claudia
Embryobionta
Arilpropanoides
Lignoides
Alil- e propenilfen?is
Quimiosistematica
Qu?mica
title_short Arilpropan?ides em Embryobionta
title_full Arilpropan?ides em Embryobionta
title_fullStr Arilpropan?ides em Embryobionta
title_full_unstemmed Arilpropan?ides em Embryobionta
title_sort Arilpropan?ides em Embryobionta
author Marx, Maria Claudia
author_facet Marx, Maria Claudia
author_role author
dc.contributor.advisor1.fl_str_mv Rezende, Ceres Maria Andrade da Mata
dc.contributor.advisor-co1.fl_str_mv Gottlieb, Otto Richard
dc.contributor.referee1.fl_str_mv Rezende, Ceres Maria Andrade da Mata
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/3354457350968761
dc.contributor.author.fl_str_mv Marx, Maria Claudia
contributor_str_mv Rezende, Ceres Maria Andrade da Mata
Gottlieb, Otto Richard
Rezende, Ceres Maria Andrade da Mata
dc.subject.por.fl_str_mv Embryobionta
Arilpropanoides
Lignoides
Alil- e propenilfen?is
Quimiosistematica
topic Embryobionta
Arilpropanoides
Lignoides
Alil- e propenilfen?is
Quimiosistematica
Qu?mica
dc.subject.cnpq.fl_str_mv Qu?mica
description Lignins are among the most abundant organic products on earth. Their polyarylpropanoid molecules were, for this reason, subject of many investigations. In opposition, relatively little is known about bisarylpropanoids (lignans, neolignans) and arylpropanoids (propenylphenols, allylphenols). These metabolites function in Embryobionta as social hormones. Their evolutive potentiation led to the derivatives of the biogenetic group of benzyltetrahydroisoquinoline. Mapping of the biosynthetic routes which lead to these alcaloids (in previous work), as well as to mono- and bisarylpropanoids, starts from phenylalanine and makes possible not only the classification, but also the rational codification of all skeleta involved. The analysis of the aromatic oxygenation pattern of each of the classes of lignans and neolignans suggests details of the oxidative coupling mechanisms. In the case of propenylphenols and allylphenols, such an analysis, associated with consideration of the natural distribution of the derivatives, does not corroborate in vivo evidence on the biosynthesis of allylphenols, recently obtained in Italy. The structural variation, of lignins, lignans, and neolignans through 350 x 106 years of plant evolution can be accompanied, paying attention to one of the basic principles of Biochemical Systematics: evolution of a biogenetic group of metabolites operates through gradual diversification of skeleta and their derivatives up to a maximum, initiating, in sequence, gradual retraction of the number of skeleta and number of corresponding derivatives. The different classes of arylpropanoids, can, for this reason, in combination with the benzyltetrahydroisoquinoline group, be used as chemosystematic markers, a fact which, in the present case, served to suggest the singular taxonomic position of the subclass Magnoliidae and the phylogenetic relation of its families.
publishDate 1975
dc.date.issued.fl_str_mv 1975-06-27
dc.date.accessioned.fl_str_mv 2021-01-27T17:20:53Z
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dc.identifier.citation.fl_str_mv MARX, Maria Claudia. Arilpropan?ides em Embryobionta. 1975. 127 f. Disserta??o (Programa de P?s-Gradua??o em Qu?mica) - Instituto de Ci?ncias Exatas, Universidade Federal Rural do Rio de Janeiro, Serop?dica - RJ, 1975.
dc.identifier.uri.fl_str_mv https://tede.ufrrj.br/jspui/handle/jspui/4351
identifier_str_mv MARX, Maria Claudia. Arilpropan?ides em Embryobionta. 1975. 127 f. Disserta??o (Programa de P?s-Gradua??o em Qu?mica) - Instituto de Ci?ncias Exatas, Universidade Federal Rural do Rio de Janeiro, Serop?dica - RJ, 1975.
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