ESTUDO QUIMIOTAXONÔMICO DE LIQUENS DO GÊNERO STEREOCAULON E BUSCA DE COMPOSTOS BIOATIVOS

Detalhes bibliográficos
Autor(a) principal: Aline Siqueira Gianini
Data de Publicação: 2022
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UFMS
Texto Completo: https://repositorio.ufms.br/handle/123456789/5009
Resumo: Lichens produce many compounds and those of the polyketide pathway stand out; are phenolic compounds, most of which are exclusive to these organisms, in addition to long-chain fatty acids. These compounds play an important role in the chemotaxonomy of lichens, as they serve as chemical markers for identification at different taxonomic levels. In this work, 151 exsiccates of lichens of the genus Stereocaulon collected in Brazil, Antarctica, Chile and Argentina were analyzed using thin layer-chromatography, high performance liquid chromatography coupled with mass spectrometer, microcrystallization and Nuclear Magnetic Resonance of 1H and 13C. 24 compounds were identified: rangiformic, pseudonorrangiormic, vinapraesorediosic B and bourgeanic acids (fatty acids); lobaric, norstictic, menegazziaic, hypoconstictic, colensoic, stictic acids (depsidones); atranorin, gyrophoric acid, anziaic acid, stenosporic acid, 2-O-methylnorstenosporic acid and perlatolic acid (depsides); strepsilin (dibenzofuran); lobarin (diphenylether), oxysiphulin (chromone) and five new compounds: the depside 1 ´´-oxo -ene''-ene''' perlatolic acid or -ene''-ene''' glomelliferic acid or -ene''-ene''' miriquidic acids and the depsidones: 2''-ene lobaric, 3''-ene lobaric and 4''-ene lobaric and -ene´´´ lobaric acids. The chemical composition together with the morphological analysis of each specimen allowed to identify the species: Stereocaulon corticatulum, Stereocaulon alpinum (3 chemical groups), Stereocaulon melanopotamicum (2 chemical groups), Stereocaulon implexum, Stereocaulon tomentosum (4 chemical groups), Stereocaulon tomentosum var. capitatum (2 chemical groups), Stereocaulon ramulosum and Stereocaulon argus. Extracts of the species S. corticatulum, S. alpinum, S. tomentosum and S. ramulosum were evaluated for antibacterial activity against Staphylococcus aureus (clinical and standard strain), Enterococcus faecium (clinical strain) and Escherichia coli (standard strain), and antioxidant against the free radical DPPH (1,1-diphenyl-2-picrylhydrazyl). The extract of S. ramulosum was the most active, with MIC of 31.25 μg/mL against the two strains of S. aureus; bioautography showed that all substances present in the extract were responsible for the activity. The extracts of the other species showed MIC  125 μg/mL. The evaluation of the antioxidant activity of the extracts indicated more than ten active substances. Our results represent a contribution to the detailed knowledge of the chemical composition of 09 species of lichens of the genus Stereocaulon.
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spelling 2022-08-03T12:48:38Z2022-08-03T12:48:38Z2022https://repositorio.ufms.br/handle/123456789/5009Lichens produce many compounds and those of the polyketide pathway stand out; are phenolic compounds, most of which are exclusive to these organisms, in addition to long-chain fatty acids. These compounds play an important role in the chemotaxonomy of lichens, as they serve as chemical markers for identification at different taxonomic levels. In this work, 151 exsiccates of lichens of the genus Stereocaulon collected in Brazil, Antarctica, Chile and Argentina were analyzed using thin layer-chromatography, high performance liquid chromatography coupled with mass spectrometer, microcrystallization and Nuclear Magnetic Resonance of 1H and 13C. 24 compounds were identified: rangiformic, pseudonorrangiormic, vinapraesorediosic B and bourgeanic acids (fatty acids); lobaric, norstictic, menegazziaic, hypoconstictic, colensoic, stictic acids (depsidones); atranorin, gyrophoric acid, anziaic acid, stenosporic acid, 2-O-methylnorstenosporic acid and perlatolic acid (depsides); strepsilin (dibenzofuran); lobarin (diphenylether), oxysiphulin (chromone) and five new compounds: the depside 1 ´´-oxo -ene''-ene''' perlatolic acid or -ene''-ene''' glomelliferic acid or -ene''-ene''' miriquidic acids and the depsidones: 2''-ene lobaric, 3''-ene lobaric and 4''-ene lobaric and -ene´´´ lobaric acids. The chemical composition together with the morphological analysis of each specimen allowed to identify the species: Stereocaulon corticatulum, Stereocaulon alpinum (3 chemical groups), Stereocaulon melanopotamicum (2 chemical groups), Stereocaulon implexum, Stereocaulon tomentosum (4 chemical groups), Stereocaulon tomentosum var. capitatum (2 chemical groups), Stereocaulon ramulosum and Stereocaulon argus. Extracts of the species S. corticatulum, S. alpinum, S. tomentosum and S. ramulosum were evaluated for antibacterial activity against Staphylococcus aureus (clinical and standard strain), Enterococcus faecium (clinical strain) and Escherichia coli (standard strain), and antioxidant against the free radical DPPH (1,1-diphenyl-2-picrylhydrazyl). The extract of S. ramulosum was the most active, with MIC of 31.25 μg/mL against the two strains of S. aureus; bioautography showed that all substances present in the extract were responsible for the activity. The extracts of the other species showed MIC  125 μg/mL. The evaluation of the antioxidant activity of the extracts indicated more than ten active substances. Our results represent a contribution to the detailed knowledge of the chemical composition of 09 species of lichens of the genus Stereocaulon.Os liquens produzem muitos compostos e se destacam aqueles da via policetídica; são compostos fenólicos, a maior parte exclusiva desses organismos, além de ácidos graxos de cadeia longa. Esses compostos possuem um papel importante na quimiotaxonomia dos liquens, pois servem como marcadores químicos para identificação em diferentes níveis taxonômicos. Neste trabalho, 151 exsicatas de liquens do gênero Stereocaulon coletados no Brasil, Antártica, Chile e Argentina, foram analisadas através das técnicas de cromatografia em camada delgada, cromatografia líquida de alta eficiência acoplada com espectrômetro de massa, microcristalização e Ressonância Magnética Nuclear de 1H e 13C. Foram identificados 24 compostos: os ácidos rangifórmico, pseudonorrangifórmico, vinapraesorediósico B e bourgeânico (ácidos graxos); os ácidos lobárico, norstítico, menegaziáico, hipoconstítico, colensóico, estítico (depsidonas); atranorina, ácidos girofórico, anziáico, estenospórico, 2-O-metilnorestenospórico e perlatólico (depsídeos), estrepsilina (dibenzofurano), lobarina (éter difenílico), oxisifulina (cromona) e cinco novos compostos, o depsídeo -1’’-oxo-eno’’-eno’’’ perlatólico ou eno’’eno’’’ glomeliférico ou eno’’-eno’’’ miríquidico e as depsidonas, ácidos 2’’-eno lobárico, 3’’-eno lobárico, 4’’eno lobárico e eno’’’ lobárico. A composição química juntamente com a análise morfológica de cada espécime permitiu identificar as espécies: Stereocaulon corticatulum, Stereocaulon alpinum (3 grupos químicos), Stereocaulon melanopotamicum (2 grupos químicos), Stereocaulon implexum, Stereocaulon tomentosum (4 grupos químicos), Stereocaulon tomentosum var. capitatum (2 grupos químicos), Stereocaulon ramulosum e Stereocaulon argus. Os extratos das espécies S. corticatulum, S. alpinum, S. tomentosum e S. ramulosum foram avaliados quanto atividade antibacteriana frente a Staphylococcus aureus (cepa clínica e padrão), Enterococcus faecium (cepa clínica) e Escherichia coli (cepa padrão), e antioxidante frente ao radical livre DPPH (1,1-difenil-2-picrilhidrazil). O extrato de S. ramulosum foi o mais ativo, com CMI de 31,25 μg/mL frente às duas cepas de S. aureus; a bioautografia mostrou que todas as substâncias presentes no extrato foram responsáveis pela atividade. Os extratos das outras espécies apresentaram CMI  125 μg/mL. A avaliação da atividade antioxidante dos extratos indicou mais de dez substâncias ativas. Nossos resultados representam uma contribuição para o conhecimento detalhado da composição química de 09 espécies de liquens do gênero Stereocaulon.Fundação Universidade Federal de Mato Grosso do SulUFMSBrasilStereocaulonliquens, quimiotaxonomiaatividade antibacterianaatividade antioxidante.ESTUDO QUIMIOTAXONÔMICO DE LIQUENS DO GÊNERO STEREOCAULON E BUSCA DE COMPOSTOS BIOATIVOSinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisAna Camila MichelettiAline Siqueira Gianiniinfo:eu-repo/semantics/openAccessporreponame:Repositório Institucional da UFMSinstname:Universidade Federal de Mato Grosso do Sul (UFMS)instacron:UFMSORIGINALTESE_VERSÂO_BIBLIOTECA_FINAL_Aline_Siqueira_Gianini.pdfTESE_VERSÂO_BIBLIOTECA_FINAL_Aline_Siqueira_Gianini.pdfapplication/pdf5919896https://repositorio.ufms.br/bitstream/123456789/5009/-1/TESE_VERS%c3%82O_BIBLIOTECA_FINAL_Aline_Siqueira_Gianini.pdf5e8cb85e8a16342f9740558e80881d40MD5-1123456789/50092022-08-03 08:48:39.051oai:repositorio.ufms.br:123456789/5009Repositório InstitucionalPUBhttps://repositorio.ufms.br/oai/requestri.prograd@ufms.bropendoar:21242022-08-03T12:48:39Repositório Institucional da UFMS - Universidade Federal de Mato Grosso do Sul (UFMS)false
dc.title.pt_BR.fl_str_mv ESTUDO QUIMIOTAXONÔMICO DE LIQUENS DO GÊNERO STEREOCAULON E BUSCA DE COMPOSTOS BIOATIVOS
title ESTUDO QUIMIOTAXONÔMICO DE LIQUENS DO GÊNERO STEREOCAULON E BUSCA DE COMPOSTOS BIOATIVOS
spellingShingle ESTUDO QUIMIOTAXONÔMICO DE LIQUENS DO GÊNERO STEREOCAULON E BUSCA DE COMPOSTOS BIOATIVOS
Aline Siqueira Gianini
Stereocaulon
liquens, quimiotaxonomia
atividade antibacteriana
atividade antioxidante.
title_short ESTUDO QUIMIOTAXONÔMICO DE LIQUENS DO GÊNERO STEREOCAULON E BUSCA DE COMPOSTOS BIOATIVOS
title_full ESTUDO QUIMIOTAXONÔMICO DE LIQUENS DO GÊNERO STEREOCAULON E BUSCA DE COMPOSTOS BIOATIVOS
title_fullStr ESTUDO QUIMIOTAXONÔMICO DE LIQUENS DO GÊNERO STEREOCAULON E BUSCA DE COMPOSTOS BIOATIVOS
title_full_unstemmed ESTUDO QUIMIOTAXONÔMICO DE LIQUENS DO GÊNERO STEREOCAULON E BUSCA DE COMPOSTOS BIOATIVOS
title_sort ESTUDO QUIMIOTAXONÔMICO DE LIQUENS DO GÊNERO STEREOCAULON E BUSCA DE COMPOSTOS BIOATIVOS
author Aline Siqueira Gianini
author_facet Aline Siqueira Gianini
author_role author
dc.contributor.advisor1.fl_str_mv Ana Camila Micheletti
dc.contributor.author.fl_str_mv Aline Siqueira Gianini
contributor_str_mv Ana Camila Micheletti
dc.subject.por.fl_str_mv Stereocaulon
liquens, quimiotaxonomia
atividade antibacteriana
atividade antioxidante.
topic Stereocaulon
liquens, quimiotaxonomia
atividade antibacteriana
atividade antioxidante.
description Lichens produce many compounds and those of the polyketide pathway stand out; are phenolic compounds, most of which are exclusive to these organisms, in addition to long-chain fatty acids. These compounds play an important role in the chemotaxonomy of lichens, as they serve as chemical markers for identification at different taxonomic levels. In this work, 151 exsiccates of lichens of the genus Stereocaulon collected in Brazil, Antarctica, Chile and Argentina were analyzed using thin layer-chromatography, high performance liquid chromatography coupled with mass spectrometer, microcrystallization and Nuclear Magnetic Resonance of 1H and 13C. 24 compounds were identified: rangiformic, pseudonorrangiormic, vinapraesorediosic B and bourgeanic acids (fatty acids); lobaric, norstictic, menegazziaic, hypoconstictic, colensoic, stictic acids (depsidones); atranorin, gyrophoric acid, anziaic acid, stenosporic acid, 2-O-methylnorstenosporic acid and perlatolic acid (depsides); strepsilin (dibenzofuran); lobarin (diphenylether), oxysiphulin (chromone) and five new compounds: the depside 1 ´´-oxo -ene''-ene''' perlatolic acid or -ene''-ene''' glomelliferic acid or -ene''-ene''' miriquidic acids and the depsidones: 2''-ene lobaric, 3''-ene lobaric and 4''-ene lobaric and -ene´´´ lobaric acids. The chemical composition together with the morphological analysis of each specimen allowed to identify the species: Stereocaulon corticatulum, Stereocaulon alpinum (3 chemical groups), Stereocaulon melanopotamicum (2 chemical groups), Stereocaulon implexum, Stereocaulon tomentosum (4 chemical groups), Stereocaulon tomentosum var. capitatum (2 chemical groups), Stereocaulon ramulosum and Stereocaulon argus. Extracts of the species S. corticatulum, S. alpinum, S. tomentosum and S. ramulosum were evaluated for antibacterial activity against Staphylococcus aureus (clinical and standard strain), Enterococcus faecium (clinical strain) and Escherichia coli (standard strain), and antioxidant against the free radical DPPH (1,1-diphenyl-2-picrylhydrazyl). The extract of S. ramulosum was the most active, with MIC of 31.25 μg/mL against the two strains of S. aureus; bioautography showed that all substances present in the extract were responsible for the activity. The extracts of the other species showed MIC  125 μg/mL. The evaluation of the antioxidant activity of the extracts indicated more than ten active substances. Our results represent a contribution to the detailed knowledge of the chemical composition of 09 species of lichens of the genus Stereocaulon.
publishDate 2022
dc.date.accessioned.fl_str_mv 2022-08-03T12:48:38Z
dc.date.available.fl_str_mv 2022-08-03T12:48:38Z
dc.date.issued.fl_str_mv 2022
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
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dc.identifier.uri.fl_str_mv https://repositorio.ufms.br/handle/123456789/5009
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dc.publisher.none.fl_str_mv Fundação Universidade Federal de Mato Grosso do Sul
dc.publisher.initials.fl_str_mv UFMS
dc.publisher.country.fl_str_mv Brasil
publisher.none.fl_str_mv Fundação Universidade Federal de Mato Grosso do Sul
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMS
instname:Universidade Federal de Mato Grosso do Sul (UFMS)
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institution UFMS
reponame_str Repositório Institucional da UFMS
collection Repositório Institucional da UFMS
bitstream.url.fl_str_mv https://repositorio.ufms.br/bitstream/123456789/5009/-1/TESE_VERS%c3%82O_BIBLIOTECA_FINAL_Aline_Siqueira_Gianini.pdf
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