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Chemical Composition and Antifungal Activity of Myrcia multiflora and Eugenia florida Essential Oils

The essential oils of three specimens of Myrcia multiflora (A, B and C) and Eugenia florida were extracted by hydrodistillation, and the chemical compositions from the essential oils were identified by gas chromatography and flame ionization detection (CG/MS and CG-FID). The fungicide potential of t...

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Autores principales: Ferreira, Oberdan Oliveira, da Silva, Silvia Helena Marques, de Oliveira, Mozaniel Santana, Andrade, Eloisa Helena de Aguiar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658826/
https://www.ncbi.nlm.nih.gov/pubmed/34885839
http://dx.doi.org/10.3390/molecules26237259
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author Ferreira, Oberdan Oliveira
da Silva, Silvia Helena Marques
de Oliveira, Mozaniel Santana
Andrade, Eloisa Helena de Aguiar
author_facet Ferreira, Oberdan Oliveira
da Silva, Silvia Helena Marques
de Oliveira, Mozaniel Santana
Andrade, Eloisa Helena de Aguiar
author_sort Ferreira, Oberdan Oliveira
collection PubMed
description The essential oils of three specimens of Myrcia multiflora (A, B and C) and Eugenia florida were extracted by hydrodistillation, and the chemical compositions from the essential oils were identified by gas chromatography and flame ionization detection (CG/MS and CG-FID). The fungicide potential of the EOs against five fungicide yeasts was assessed: Candida albicans INCQS-40175, C. tropicalis ATCC 6258, C. famata ATCC 62894, C. krusei ATCC 13803 and C. auris IEC-01. The essential oil of the specimen Myrcia multiflora (A) was characterized by the major compounds: α-bulnesene (26.79%), pogostol (21.27%) and δ-amorphene (6.76%). The essential oil of the specimen M. multiflora (B) was rich in (E)-nerolidol (44.4%), (E)-γ-bisabolene (10.64%) and (E,E)-α-farnesene (8.19%), while (E)-nerolidol (92.21%) was the majority of the specimen M. multiflora (C). The sesquiterpenes seline-3,11-dien-6-α-ol (12.93%), eremoligenol (11%) and γ-elemene (10.70%) characterized the chemical profile of the EOs of E. florida. The fungal species were sensitive to the essential oil of M. multiflora (B) (9–11 mm), and the lowest inhibitory concentration (0.07%) was observed in the essential oil of M. multiflora (A) against the yeasts of C. famata. Fungicidal action was observed in the essential oils of M. multiflora (A) against C. famata, with an MIC of 0.78 µL/mL and 3.12 µL/mL; C. albicans, with an MFC of 50 µL/mL and M. multiflora (C) against C. albicans; and C. krusei, with a MFC of 50 µL/mL.
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spelling pubmed-86588262021-12-10 Chemical Composition and Antifungal Activity of Myrcia multiflora and Eugenia florida Essential Oils Ferreira, Oberdan Oliveira da Silva, Silvia Helena Marques de Oliveira, Mozaniel Santana Andrade, Eloisa Helena de Aguiar Molecules Article The essential oils of three specimens of Myrcia multiflora (A, B and C) and Eugenia florida were extracted by hydrodistillation, and the chemical compositions from the essential oils were identified by gas chromatography and flame ionization detection (CG/MS and CG-FID). The fungicide potential of the EOs against five fungicide yeasts was assessed: Candida albicans INCQS-40175, C. tropicalis ATCC 6258, C. famata ATCC 62894, C. krusei ATCC 13803 and C. auris IEC-01. The essential oil of the specimen Myrcia multiflora (A) was characterized by the major compounds: α-bulnesene (26.79%), pogostol (21.27%) and δ-amorphene (6.76%). The essential oil of the specimen M. multiflora (B) was rich in (E)-nerolidol (44.4%), (E)-γ-bisabolene (10.64%) and (E,E)-α-farnesene (8.19%), while (E)-nerolidol (92.21%) was the majority of the specimen M. multiflora (C). The sesquiterpenes seline-3,11-dien-6-α-ol (12.93%), eremoligenol (11%) and γ-elemene (10.70%) characterized the chemical profile of the EOs of E. florida. The fungal species were sensitive to the essential oil of M. multiflora (B) (9–11 mm), and the lowest inhibitory concentration (0.07%) was observed in the essential oil of M. multiflora (A) against the yeasts of C. famata. Fungicidal action was observed in the essential oils of M. multiflora (A) against C. famata, with an MIC of 0.78 µL/mL and 3.12 µL/mL; C. albicans, with an MFC of 50 µL/mL and M. multiflora (C) against C. albicans; and C. krusei, with a MFC of 50 µL/mL. MDPI 2021-11-30 /pmc/articles/PMC8658826/ /pubmed/34885839 http://dx.doi.org/10.3390/molecules26237259 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ferreira, Oberdan Oliveira
da Silva, Silvia Helena Marques
de Oliveira, Mozaniel Santana
Andrade, Eloisa Helena de Aguiar
Chemical Composition and Antifungal Activity of Myrcia multiflora and Eugenia florida Essential Oils
title Chemical Composition and Antifungal Activity of Myrcia multiflora and Eugenia florida Essential Oils
title_full Chemical Composition and Antifungal Activity of Myrcia multiflora and Eugenia florida Essential Oils
title_fullStr Chemical Composition and Antifungal Activity of Myrcia multiflora and Eugenia florida Essential Oils
title_full_unstemmed Chemical Composition and Antifungal Activity of Myrcia multiflora and Eugenia florida Essential Oils
title_short Chemical Composition and Antifungal Activity of Myrcia multiflora and Eugenia florida Essential Oils
title_sort chemical composition and antifungal activity of myrcia multiflora and eugenia florida essential oils
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658826/
https://www.ncbi.nlm.nih.gov/pubmed/34885839
http://dx.doi.org/10.3390/molecules26237259
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