Antifungal activity of essential oils of Myrcia ovata chemotypes and their major compounds on phytopathogenic fungi

Detalhes bibliográficos
Autor(a) principal: Sampaio, Taís Santos
Data de Publicação: 2020
Outros Autores: Blank, Arie Fitzgerald, Gagliardi, Paulo Roberto, Wisniewski Jr, Alberto, Arrigoni-Blank, Maria de Fátima, Nizio, Daniela Aparecida de Castro, Alves, Mércia Freitas, Nascimento Junior, Alberto Ferreira de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Bioscience journal (Online)
Texto Completo: https://seer.ufu.br/index.php/biosciencejournal/article/view/42315
Resumo: This work evaluated the antifungal activity of essential oils of Myrcia ovata chemotypes (MYRO-175, MYRO-156, MYRO-154, MYRO-165, and MYRO-015) and their major compounds (linalool, geraniol, citral, and (E)-nerolidol) on the phytopathogenic fungi Fusarium pallidoroseum (which causes melon postharvest rot) and Colletotrichum musae (which causes anthracnose in banana). The essential oils were obtained by hydrodistillation and analyzed by GCMS/FID. To evaluate the antifungal activity, the essential oils and their major compounds were tested at different concentrations (0.1; 0.3; 0.4; 0.5; 0.7; 1.0; 3.0, and 5.0 mL/L). The major compounds found in the essential oils were nerolic acid, linalool, geraniol, citral, and (E)-nerolidol. The essential oils of the plants MYRO-154, MYRO-165, and MYRO-015 had the minimum inhibitory concentration (MIC) (0.3 mL/L) for F. pallidoroseum and the lowest minimum fungicidal concentration (MFC) (0.7 mL/L), for C. musae. Geraniol and citral had the lowest MFC (0.5 mL / L) for the two fungi tested. For F. pallidoroseum, the essential oils of the chemotypes were more effective than their major compounds. Conversely, the major compounds geraniol of the chemotype MYRO-156 (74.37%) and citral were more effective than their respective essential oils for C. musae. (E)-nerolidol and geraniol of the chemotype MYRO-015 (33.15%) were responsible for the antifungal activity of the essential oils of their respective chemotypes.
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spelling Antifungal activity of essential oils of Myrcia ovata chemotypes and their major compounds on phytopathogenic fungiAtividade antifúngica dos óleos essenciais de quimiotipos de Myrcia ovata e seus compostos majoritários sobre fungos fitopatogênicosMyrcia ovataVolatile oilFusarium pallidoroseumColletotrichum musaeAgricultural SciencesMyrcia ovata.Fusarium pallidoroseumColletotrichum musae.This work evaluated the antifungal activity of essential oils of Myrcia ovata chemotypes (MYRO-175, MYRO-156, MYRO-154, MYRO-165, and MYRO-015) and their major compounds (linalool, geraniol, citral, and (E)-nerolidol) on the phytopathogenic fungi Fusarium pallidoroseum (which causes melon postharvest rot) and Colletotrichum musae (which causes anthracnose in banana). The essential oils were obtained by hydrodistillation and analyzed by GCMS/FID. To evaluate the antifungal activity, the essential oils and their major compounds were tested at different concentrations (0.1; 0.3; 0.4; 0.5; 0.7; 1.0; 3.0, and 5.0 mL/L). The major compounds found in the essential oils were nerolic acid, linalool, geraniol, citral, and (E)-nerolidol. The essential oils of the plants MYRO-154, MYRO-165, and MYRO-015 had the minimum inhibitory concentration (MIC) (0.3 mL/L) for F. pallidoroseum and the lowest minimum fungicidal concentration (MFC) (0.7 mL/L), for C. musae. Geraniol and citral had the lowest MFC (0.5 mL / L) for the two fungi tested. For F. pallidoroseum, the essential oils of the chemotypes were more effective than their major compounds. Conversely, the major compounds geraniol of the chemotype MYRO-156 (74.37%) and citral were more effective than their respective essential oils for C. musae. (E)-nerolidol and geraniol of the chemotype MYRO-015 (33.15%) were responsible for the antifungal activity of the essential oils of their respective chemotypes.No presente trabalho avaliou-se a atividade antifúngica de óleos essenciais de quimiotipos de Myrcia lundiana (MYRO-175, MYRO-156, MYRO-154, MYRO-165, and MYRO-015) e seus compostos majoritários (linalol, geraniol, citral e (E)-nerolidol) sobre os fungos fitopatogênicos Fusarium pallidoroseum (causa podridão em frutos de melão) e Colletotrichum musae (causa antracnose em frutos de banana). Os óleos essenciais foram obtidos hidrodestilação e analisados por CGEM/DIC. Para avaliação da atividade antifúngica foram testados os óleos essenciais e os compostos majoritários nas concentrações: 0,1; 0,3; 0,4; 0,5; 0,7; 1,0; 3,0 e 5,0 mL/L. Os principais compostos presentes nos óleos essenciais foram o ácido nerólico, o linalol, o geraniol, o citral e o (E)-nerolidol. Os óleos essenciais das plantas MYRO-154, MYRO-165 e MYRO-015 apresentaram CIM de 0,3 mL/L e a planta MYRO-015 apresentou a menor concentração fungicida mínima (CFM) (1,0 mL/L). O geraniol e o citral foram os compostos que apresentaram o menor valor de CFM, 0,5 mL/L, frente aos dois fungos testados. O óleo essencial dos quimiotipos testados foram mais promissores que seus componentes majoritários puros, frente o F. pallidoroseum. Já para o C. musae, os componentes majoritários geraniol do quimiotipo MYRO-156 (74,37%) e o citral foram mais promissores que seus respectivos óleos essenciais. Já o (E)-nerolidol e o geraniol do quimiotipo MYRO-015 (33,15%) foram os responsáveis pela atividade antifúngica apresentada pelos óleos essenciais dos respectivos quimiotipos.EDUFU2020-02-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://seer.ufu.br/index.php/biosciencejournal/article/view/4231510.14393/BJ-v36n2a2020-42315Bioscience Journal ; Vol. 36 No. 2 (2020): Mar./Apr.; 364-375Bioscience Journal ; v. 36 n. 2 (2020): Mar./Abr; 364-3751981-3163reponame:Bioscience journal (Online)instname:Universidade Federal de Uberlândia (UFU)instacron:UFUenghttps://seer.ufu.br/index.php/biosciencejournal/article/view/42315/28086Brazil; ContemporaryCopyright (c) 2020 Taís Santos Sampaio, Arie Fitzgerald Blank, Paulo Roberto Gagliardi, Alberto Wisniewski Jr, Maria de Fátima Arrigoni-Blank, Daniela Aparecida de Castro Nizio, Mércia Freitas Alves, Alberto Ferreira de Nascimento Juniorhttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSampaio, Taís SantosBlank, Arie FitzgeraldGagliardi, Paulo RobertoWisniewski Jr, AlbertoArrigoni-Blank, Maria de FátimaNizio, Daniela Aparecida de CastroAlves, Mércia FreitasNascimento Junior, Alberto Ferreira de2022-06-22T12:27:11Zoai:ojs.www.seer.ufu.br:article/42315Revistahttps://seer.ufu.br/index.php/biosciencejournalPUBhttps://seer.ufu.br/index.php/biosciencejournal/oaibiosciencej@ufu.br||1981-31631516-3725opendoar:2022-06-22T12:27:11Bioscience journal (Online) - Universidade Federal de Uberlândia (UFU)false
dc.title.none.fl_str_mv Antifungal activity of essential oils of Myrcia ovata chemotypes and their major compounds on phytopathogenic fungi
Atividade antifúngica dos óleos essenciais de quimiotipos de Myrcia ovata e seus compostos majoritários sobre fungos fitopatogênicos
title Antifungal activity of essential oils of Myrcia ovata chemotypes and their major compounds on phytopathogenic fungi
spellingShingle Antifungal activity of essential oils of Myrcia ovata chemotypes and their major compounds on phytopathogenic fungi
Sampaio, Taís Santos
Myrcia ovata
Volatile oil
Fusarium pallidoroseum
Colletotrichum musae
Agricultural Sciences
Myrcia ovata.
Fusarium pallidoroseum
Colletotrichum musae.
title_short Antifungal activity of essential oils of Myrcia ovata chemotypes and their major compounds on phytopathogenic fungi
title_full Antifungal activity of essential oils of Myrcia ovata chemotypes and their major compounds on phytopathogenic fungi
title_fullStr Antifungal activity of essential oils of Myrcia ovata chemotypes and their major compounds on phytopathogenic fungi
title_full_unstemmed Antifungal activity of essential oils of Myrcia ovata chemotypes and their major compounds on phytopathogenic fungi
title_sort Antifungal activity of essential oils of Myrcia ovata chemotypes and their major compounds on phytopathogenic fungi
author Sampaio, Taís Santos
author_facet Sampaio, Taís Santos
Blank, Arie Fitzgerald
Gagliardi, Paulo Roberto
Wisniewski Jr, Alberto
Arrigoni-Blank, Maria de Fátima
Nizio, Daniela Aparecida de Castro
Alves, Mércia Freitas
Nascimento Junior, Alberto Ferreira de
author_role author
author2 Blank, Arie Fitzgerald
Gagliardi, Paulo Roberto
Wisniewski Jr, Alberto
Arrigoni-Blank, Maria de Fátima
Nizio, Daniela Aparecida de Castro
Alves, Mércia Freitas
Nascimento Junior, Alberto Ferreira de
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Sampaio, Taís Santos
Blank, Arie Fitzgerald
Gagliardi, Paulo Roberto
Wisniewski Jr, Alberto
Arrigoni-Blank, Maria de Fátima
Nizio, Daniela Aparecida de Castro
Alves, Mércia Freitas
Nascimento Junior, Alberto Ferreira de
dc.subject.por.fl_str_mv Myrcia ovata
Volatile oil
Fusarium pallidoroseum
Colletotrichum musae
Agricultural Sciences
Myrcia ovata.
Fusarium pallidoroseum
Colletotrichum musae.
topic Myrcia ovata
Volatile oil
Fusarium pallidoroseum
Colletotrichum musae
Agricultural Sciences
Myrcia ovata.
Fusarium pallidoroseum
Colletotrichum musae.
description This work evaluated the antifungal activity of essential oils of Myrcia ovata chemotypes (MYRO-175, MYRO-156, MYRO-154, MYRO-165, and MYRO-015) and their major compounds (linalool, geraniol, citral, and (E)-nerolidol) on the phytopathogenic fungi Fusarium pallidoroseum (which causes melon postharvest rot) and Colletotrichum musae (which causes anthracnose in banana). The essential oils were obtained by hydrodistillation and analyzed by GCMS/FID. To evaluate the antifungal activity, the essential oils and their major compounds were tested at different concentrations (0.1; 0.3; 0.4; 0.5; 0.7; 1.0; 3.0, and 5.0 mL/L). The major compounds found in the essential oils were nerolic acid, linalool, geraniol, citral, and (E)-nerolidol. The essential oils of the plants MYRO-154, MYRO-165, and MYRO-015 had the minimum inhibitory concentration (MIC) (0.3 mL/L) for F. pallidoroseum and the lowest minimum fungicidal concentration (MFC) (0.7 mL/L), for C. musae. Geraniol and citral had the lowest MFC (0.5 mL / L) for the two fungi tested. For F. pallidoroseum, the essential oils of the chemotypes were more effective than their major compounds. Conversely, the major compounds geraniol of the chemotype MYRO-156 (74.37%) and citral were more effective than their respective essential oils for C. musae. (E)-nerolidol and geraniol of the chemotype MYRO-015 (33.15%) were responsible for the antifungal activity of the essential oils of their respective chemotypes.
publishDate 2020
dc.date.none.fl_str_mv 2020-02-11
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://seer.ufu.br/index.php/biosciencejournal/article/view/42315
10.14393/BJ-v36n2a2020-42315
url https://seer.ufu.br/index.php/biosciencejournal/article/view/42315
identifier_str_mv 10.14393/BJ-v36n2a2020-42315
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://seer.ufu.br/index.php/biosciencejournal/article/view/42315/28086
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.coverage.none.fl_str_mv Brazil; Contemporary
dc.publisher.none.fl_str_mv EDUFU
publisher.none.fl_str_mv EDUFU
dc.source.none.fl_str_mv Bioscience Journal ; Vol. 36 No. 2 (2020): Mar./Apr.; 364-375
Bioscience Journal ; v. 36 n. 2 (2020): Mar./Abr; 364-375
1981-3163
reponame:Bioscience journal (Online)
instname:Universidade Federal de Uberlândia (UFU)
instacron:UFU
instname_str Universidade Federal de Uberlândia (UFU)
instacron_str UFU
institution UFU
reponame_str Bioscience journal (Online)
collection Bioscience journal (Online)
repository.name.fl_str_mv Bioscience journal (Online) - Universidade Federal de Uberlândia (UFU)
repository.mail.fl_str_mv biosciencej@ufu.br||
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