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Bioassay Guided Fractionation of an Anti-Methicillin-Resistant Staphylococcus aureus Flavonoid From Bromus inermis Leyss Inflorescences
BACKGROUND: Plants are considered as promising sources of new antibacterial agents as well as bioassay guided fractionation. OBJECTIVES: In the present work, the antibacterial properties, especially against methicillin-resistant Staphylococcus aureus (MRSA), of Bromus inermis inflorescence was studi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kowsar
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335569/ https://www.ncbi.nlm.nih.gov/pubmed/25741430 http://dx.doi.org/10.5812/jjm.12739 |
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author | Aliahmadi, Atousa Mirzajani, Fateme Ghassempour, Alireza Sonboli, Ali |
author_facet | Aliahmadi, Atousa Mirzajani, Fateme Ghassempour, Alireza Sonboli, Ali |
author_sort | Aliahmadi, Atousa |
collection | PubMed |
description | BACKGROUND: Plants are considered as promising sources of new antibacterial agents as well as bioassay guided fractionation. OBJECTIVES: In the present work, the antibacterial properties, especially against methicillin-resistant Staphylococcus aureus (MRSA), of Bromus inermis inflorescence was studied, using the bioassay guided fractionation as well as the bio-autographic method. MATERIALS AND METHODS: The plant organic extract was prepared via maceration in methanol, followed by the fractionation using n-hexane. The extracts were subjected for minimum inhibitory concentrations (MICs) against some human pathogenic bacteria via standard broth micro-dilution assay. Thereafter, a bio-autographical method was applied using the high performance thin layer chromatography (HPTLC) coupled with agar overlay assays for the primary characterization and identification of bioactive substance (s). RESULTS: Through the bioassay guided fractionation method, the greatest antibacterial activities were related to the n-hexane extract. It was also revealed that the effective anti-MRSA agent of the assessed plant was a relatively polar substance with an MIC value of about 8 μg/mL against the tested MRSA strain (in comparison with the MIC value of 32 μg/mL for chloramphenicol). CONCLUSIONS: As a result of the full range UV-Vis scanning of the responsible band in the HPTLC experiments (200-700 nm), the flavonoid was the most imaginable natural compound. |
format | Online Article Text |
id | pubmed-4335569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Kowsar |
record_format | MEDLINE/PubMed |
spelling | pubmed-43355692015-03-04 Bioassay Guided Fractionation of an Anti-Methicillin-Resistant Staphylococcus aureus Flavonoid From Bromus inermis Leyss Inflorescences Aliahmadi, Atousa Mirzajani, Fateme Ghassempour, Alireza Sonboli, Ali Jundishapur J Microbiol Research Article BACKGROUND: Plants are considered as promising sources of new antibacterial agents as well as bioassay guided fractionation. OBJECTIVES: In the present work, the antibacterial properties, especially against methicillin-resistant Staphylococcus aureus (MRSA), of Bromus inermis inflorescence was studied, using the bioassay guided fractionation as well as the bio-autographic method. MATERIALS AND METHODS: The plant organic extract was prepared via maceration in methanol, followed by the fractionation using n-hexane. The extracts were subjected for minimum inhibitory concentrations (MICs) against some human pathogenic bacteria via standard broth micro-dilution assay. Thereafter, a bio-autographical method was applied using the high performance thin layer chromatography (HPTLC) coupled with agar overlay assays for the primary characterization and identification of bioactive substance (s). RESULTS: Through the bioassay guided fractionation method, the greatest antibacterial activities were related to the n-hexane extract. It was also revealed that the effective anti-MRSA agent of the assessed plant was a relatively polar substance with an MIC value of about 8 μg/mL against the tested MRSA strain (in comparison with the MIC value of 32 μg/mL for chloramphenicol). CONCLUSIONS: As a result of the full range UV-Vis scanning of the responsible band in the HPTLC experiments (200-700 nm), the flavonoid was the most imaginable natural compound. Kowsar 2014-12-01 /pmc/articles/PMC4335569/ /pubmed/25741430 http://dx.doi.org/10.5812/jjm.12739 Text en Copyright © 2014, Ahvaz Jundishapur University of Medical Sciences; Published by Kowsar. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited. |
spellingShingle | Research Article Aliahmadi, Atousa Mirzajani, Fateme Ghassempour, Alireza Sonboli, Ali Bioassay Guided Fractionation of an Anti-Methicillin-Resistant Staphylococcus aureus Flavonoid From Bromus inermis Leyss Inflorescences |
title | Bioassay Guided Fractionation of an Anti-Methicillin-Resistant Staphylococcus aureus Flavonoid From Bromus inermis Leyss Inflorescences |
title_full | Bioassay Guided Fractionation of an Anti-Methicillin-Resistant Staphylococcus aureus Flavonoid From Bromus inermis Leyss Inflorescences |
title_fullStr | Bioassay Guided Fractionation of an Anti-Methicillin-Resistant Staphylococcus aureus Flavonoid From Bromus inermis Leyss Inflorescences |
title_full_unstemmed | Bioassay Guided Fractionation of an Anti-Methicillin-Resistant Staphylococcus aureus Flavonoid From Bromus inermis Leyss Inflorescences |
title_short | Bioassay Guided Fractionation of an Anti-Methicillin-Resistant Staphylococcus aureus Flavonoid From Bromus inermis Leyss Inflorescences |
title_sort | bioassay guided fractionation of an anti-methicillin-resistant staphylococcus aureus flavonoid from bromus inermis leyss inflorescences |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335569/ https://www.ncbi.nlm.nih.gov/pubmed/25741430 http://dx.doi.org/10.5812/jjm.12739 |
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