Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários

Detalhes bibliográficos
Ano de defesa: 2018
Autor(a) principal: Formoso, Dianne Dominguez
Orientador(a): Silva, Maria Fátima das Graças Fernandes da lattes
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de São Carlos
Câmpus São Carlos
Programa de Pós-Graduação: Programa de Pós-Graduação em Química - PPGQ
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.ufscar.br/handle/ufscar/10392
Resumo: The order Sapindales, compost for the families Rutaceae, Meliaceae, Burseraceae, Simaroubaceae, Bierbersteiniaceae, Kirkiaceae, Anacardiaceae, Sapindaceae and Nitrariaceae, is rich in various classes of speciais metabolites, being the most frequents: coumarins, alkaloids, flavonoids, quassinoides and limonoides. The family Rutaceae is characterized by a great diversity of those metabolites not common in other families the order (Silva et al., 1988) and is constituted by different genera, of which stands out Hortia, compost for five species distributed from Panama to the state of São Paulo, and some of the area Amazônica (Groppo and Pirani 2012), besides of to be endemic in the area of Minas Gerais, where take the plant as a sample. In this work the endophytic fungus belonging to the family Xylaria, was isolated .This fungus was inoculated in the malt extract agar culture medium, where was produced several secondary metabolites, and between they were separated and identified three compounds: Declorogriseofulvin, Griseofulvina, 3,4-Dihydro-8- hydroxy-3- methylisocouarin-5-carboxylic acid, Spiro[benzofuran-2(3H),1'-[2] cyclohexene]-3,4'- dione, 5-cloro-7-declorogriseofulvina, a compound that is still unpublished and 5- clorogriseofulvin. The second compound is isomer of this last substance and was identified by the NMR and Massa Spectrometry techniques. The hemolytic activity in blood was measured for the substances, resulting the griseofulvin being less toxic in blood than your analogue, as declorogriseofulvin. In addition, the biological activity of the compounds was analyzed against to the strain Staphylococcus aureus, by the Inhibitory Concentration Method for bacteria (MICs) (Barbosa. S et al, 2016), concluding as result that the substances do not have antimicrobial activity against the Gram- positive bacteria.
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spelling Formoso, Dianne DominguezSilva, Maria Fátima das Graças Fernandes dahttp://lattes.cnpq.br/0457632122660653http://lattes.cnpq.br/44822600697248202018-08-21T19:39:42Z2018-08-21T19:39:42Z2018-03-06FORMOSO, Dianne Dominguez. Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários. 2018. Dissertação (Mestrado em Química) – Universidade Federal de São Carlos, São Carlos, 2018. Disponível em: https://repositorio.ufscar.br/handle/ufscar/10392.https://repositorio.ufscar.br/handle/ufscar/10392The order Sapindales, compost for the families Rutaceae, Meliaceae, Burseraceae, Simaroubaceae, Bierbersteiniaceae, Kirkiaceae, Anacardiaceae, Sapindaceae and Nitrariaceae, is rich in various classes of speciais metabolites, being the most frequents: coumarins, alkaloids, flavonoids, quassinoides and limonoides. The family Rutaceae is characterized by a great diversity of those metabolites not common in other families the order (Silva et al., 1988) and is constituted by different genera, of which stands out Hortia, compost for five species distributed from Panama to the state of São Paulo, and some of the area Amazônica (Groppo and Pirani 2012), besides of to be endemic in the area of Minas Gerais, where take the plant as a sample. In this work the endophytic fungus belonging to the family Xylaria, was isolated .This fungus was inoculated in the malt extract agar culture medium, where was produced several secondary metabolites, and between they were separated and identified three compounds: Declorogriseofulvin, Griseofulvina, 3,4-Dihydro-8- hydroxy-3- methylisocouarin-5-carboxylic acid, Spiro[benzofuran-2(3H),1'-[2] cyclohexene]-3,4'- dione, 5-cloro-7-declorogriseofulvina, a compound that is still unpublished and 5- clorogriseofulvin. The second compound is isomer of this last substance and was identified by the NMR and Massa Spectrometry techniques. The hemolytic activity in blood was measured for the substances, resulting the griseofulvin being less toxic in blood than your analogue, as declorogriseofulvin. In addition, the biological activity of the compounds was analyzed against to the strain Staphylococcus aureus, by the Inhibitory Concentration Method for bacteria (MICs) (Barbosa. S et al, 2016), concluding as result that the substances do not have antimicrobial activity against the Gram- positive bacteria.A ordem Sapindales, composto pelas famílias Rutaceae, Meliaceae, Burseraceae, Simaroubaceae, Bierbersteiniaceae, Kirkiaceae, Anacardiaceae, Sapindaceae e Nitrariaceae, é rica em várias classes de metabolitos específicos, sendo os mais freqüentes: cumarinas, alcalóides, flavonóides, quassinoides e limonoides. A família Rutaceae caracteriza-se por uma grande diversidade dos metabólitos não comuns em outras famílias, a ordem (Silva et al., 1988) é constituída por diferentes gêneros, destacando-se Hortia, composto por cinco espécies distribuídas do Panamá até o estado de São Paulo e alguns lugares da Amazônica (Groppo e Pirani 2012), além de serem endêmicos na área de Minas Gerais, onde tomamos a planta como amostra para o estudo de pesquisa. Neste trabalho, isolou-se o fungo endofítico pertencente à família Xylaria. Este fungo foi inoculado no meio de cultura de agar de extrato de malte, onde foram produzidos vários metabolitos secundários e entre eles foram separados e identificados três compostos: Declorogriseofulvin, Griseofulvina, 3, Ácido 4-dihidro-8- hidroxi-3-metilisocouarina-5-carboxílico, Spiro [benzofuran-2 (3H), 1 '- [2] ciclohexeno] -3,4'-diona, 5-cloro-7-declorogriseofulvina, citado pela primera vez nesta tese e 5-clorogriseofulvina. O segundo composto é isómero desta última substância e foi identificado pelastécnicas de RMN e Massa Spectrometry. A atividade hemolítica no sangue foi medida pelas substâncias, resultando em griseofulvina sendo menos tóxico no sangue do que seu análogo, como declorogriseofulvin. Além disso, a atividade biológica dos compostos foi analisada contra a estirpe Staphylococcus aureus, pelo Método de Concentração Inibitória para bactérias (MIC) (Barbosa. S et al, 2016), concluindo como resultado que as substâncias não possuem atividade antimicrobiana contra a bactéria Gram- positiva.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)CNPq: 190126/2015-9porUniversidade Federal de São CarlosCâmpus São CarlosPrograma de Pós-Graduação em Química - PPGQUFSCarGriseofulvina5-clorogriseofulvinaXylareaceaeCIENCIAS EXATAS E DA TERRA::QUIMICAEstudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundáriosStudy of the endophytic fungus isolated from Hortia superba (Rutaceae) in the production of secondary compoundsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisOnlineinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINALfinal 1 (1).pdffinal 1 (1).pdfapplication/pdf3376759https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/10392/1/final%201%20%281%29.pdf0ce355f088086e15b9f3d358d92637dfMD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81957https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/10392/3/license.txtae0398b6f8b235e40ad82cba6c50031dMD53TEXTfinal 1 (1).pdf.txtfinal 1 (1).pdf.txtExtracted texttext/plain137538https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/10392/4/final%201%20%281%29.pdf.txt1a52ae50135eeb98d1181226e65c819fMD54THUMBNAILfinal 1 (1).pdf.jpgfinal 1 (1).pdf.jpgIM Thumbnailimage/jpeg10011https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/10392/5/final%201%20%281%29.pdf.jpgcc2bade8c5f41aa120c406a2a47528fdMD55ufscar/103922019-09-11 03:20:28.786oai:repositorio.ufscar.br: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Repositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestopendoar:43222023-05-25T12:56:22.065321Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false
dc.title.por.fl_str_mv Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários
dc.title.alternative.eng.fl_str_mv Study of the endophytic fungus isolated from Hortia superba (Rutaceae) in the production of secondary compounds
title Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários
spellingShingle Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários
Formoso, Dianne Dominguez
Griseofulvina
5-clorogriseofulvina
Xylareaceae
CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários
title_full Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários
title_fullStr Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários
title_full_unstemmed Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários
title_sort Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários
author Formoso, Dianne Dominguez
author_facet Formoso, Dianne Dominguez
author_role author
dc.contributor.authorlattes.por.fl_str_mv http://lattes.cnpq.br/4482260069724820
dc.contributor.author.fl_str_mv Formoso, Dianne Dominguez
dc.contributor.advisor1.fl_str_mv Silva, Maria Fátima das Graças Fernandes da
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/0457632122660653
contributor_str_mv Silva, Maria Fátima das Graças Fernandes da
dc.subject.por.fl_str_mv Griseofulvina
5-clorogriseofulvina
Xylareaceae
topic Griseofulvina
5-clorogriseofulvina
Xylareaceae
CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.cnpq.fl_str_mv CIENCIAS EXATAS E DA TERRA::QUIMICA
description The order Sapindales, compost for the families Rutaceae, Meliaceae, Burseraceae, Simaroubaceae, Bierbersteiniaceae, Kirkiaceae, Anacardiaceae, Sapindaceae and Nitrariaceae, is rich in various classes of speciais metabolites, being the most frequents: coumarins, alkaloids, flavonoids, quassinoides and limonoides. The family Rutaceae is characterized by a great diversity of those metabolites not common in other families the order (Silva et al., 1988) and is constituted by different genera, of which stands out Hortia, compost for five species distributed from Panama to the state of São Paulo, and some of the area Amazônica (Groppo and Pirani 2012), besides of to be endemic in the area of Minas Gerais, where take the plant as a sample. In this work the endophytic fungus belonging to the family Xylaria, was isolated .This fungus was inoculated in the malt extract agar culture medium, where was produced several secondary metabolites, and between they were separated and identified three compounds: Declorogriseofulvin, Griseofulvina, 3,4-Dihydro-8- hydroxy-3- methylisocouarin-5-carboxylic acid, Spiro[benzofuran-2(3H),1'-[2] cyclohexene]-3,4'- dione, 5-cloro-7-declorogriseofulvina, a compound that is still unpublished and 5- clorogriseofulvin. The second compound is isomer of this last substance and was identified by the NMR and Massa Spectrometry techniques. The hemolytic activity in blood was measured for the substances, resulting the griseofulvin being less toxic in blood than your analogue, as declorogriseofulvin. In addition, the biological activity of the compounds was analyzed against to the strain Staphylococcus aureus, by the Inhibitory Concentration Method for bacteria (MICs) (Barbosa. S et al, 2016), concluding as result that the substances do not have antimicrobial activity against the Gram- positive bacteria.
publishDate 2018
dc.date.accessioned.fl_str_mv 2018-08-21T19:39:42Z
dc.date.available.fl_str_mv 2018-08-21T19:39:42Z
dc.date.issued.fl_str_mv 2018-03-06
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
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dc.identifier.citation.fl_str_mv FORMOSO, Dianne Dominguez. Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários. 2018. Dissertação (Mestrado em Química) – Universidade Federal de São Carlos, São Carlos, 2018. Disponível em: https://repositorio.ufscar.br/handle/ufscar/10392.
dc.identifier.uri.fl_str_mv https://repositorio.ufscar.br/handle/ufscar/10392
identifier_str_mv FORMOSO, Dianne Dominguez. Estudo químico do fungo endofítico isolado de Hortia superba (Rutaceae) na produção de compostos secundários. 2018. Dissertação (Mestrado em Química) – Universidade Federal de São Carlos, São Carlos, 2018. Disponível em: https://repositorio.ufscar.br/handle/ufscar/10392.
url https://repositorio.ufscar.br/handle/ufscar/10392
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dc.publisher.none.fl_str_mv Universidade Federal de São Carlos
Câmpus São Carlos
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Química - PPGQ
dc.publisher.initials.fl_str_mv UFSCar
publisher.none.fl_str_mv Universidade Federal de São Carlos
Câmpus São Carlos
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