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Analysis of radical scavenging active components in the fermented mycelia of Ophiocordyceps formosana
The rates of 1,1-diphenyl-2-picryhydrazyl (DPPH)-free radical scavenging and hydroxyl radical eliminating were employed as indexes to qualitatively and quantitatively analyse the radical scavenging activity of the extracts with different solvents from fermented mycelia of Hirsutella huangshanensis R...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059058/ https://www.ncbi.nlm.nih.gov/pubmed/30123647 http://dx.doi.org/10.1080/21501203.2017.1383318 |
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author | Li, Yang-mei Cheng, Wen-ming Da, Zi-fei Hu, Fenglin Li, Chun-ru |
author_facet | Li, Yang-mei Cheng, Wen-ming Da, Zi-fei Hu, Fenglin Li, Chun-ru |
author_sort | Li, Yang-mei |
collection | PubMed |
description | The rates of 1,1-diphenyl-2-picryhydrazyl (DPPH)-free radical scavenging and hydroxyl radical eliminating were employed as indexes to qualitatively and quantitatively analyse the radical scavenging activity of the extracts with different solvents from fermented mycelia of Hirsutella huangshanensis RCEF0868, the anamorph of Ophiocordyceps formosana (FMOF). The results showed that both the aqueous extract and the methanol extract had significant radical scavenging activity. The half maximal inhibitory concentrations (IC(50)) of the aqueous extract on DPPH-free radical and hydroxyl radical are 0.85 and 1.37 mg/mL, respectively, while the IC(50) of methanol extract is 1.23 and 2.91 mg/mL, respectively. The combined liquid chromatography-diode array detector-high resolution mass spectrometer(HRMS) analysis and activity determination revealed that the molecular formulas of three radical scavengers in aqueous extract were C(6)H(14)O(6)(1), C(14)H(17)N(5)O(8)(2) and C(20)H(33)N(5)O(9)(3). In addition to the compound 1, the methanol extract had another three radical scavengers as C(30)H(22)O(11)(4), C(30)H(22)O(10)(5) and C(30)H(18)O(10)(6). All the six kinds of components exhibited the DPPH radical scavenging activity, and compounds 1, 4 and 5 also showed the hydroxyl radical eliminating activity at the same time. By querying the database of natural products and reference to the relevant reports, compound 3 may be a new entity. The others were respectively cordycepic acid, succinoadenosine, 4α-oxyrugulosin, rugulosin and skyrin and, among them, succinoadenosine and 4α-oxyrugulosin were found in entomogenous fungi for the first time. |
format | Online Article Text |
id | pubmed-6059058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-60590582018-08-17 Analysis of radical scavenging active components in the fermented mycelia of Ophiocordyceps formosana Li, Yang-mei Cheng, Wen-ming Da, Zi-fei Hu, Fenglin Li, Chun-ru Mycology Article The rates of 1,1-diphenyl-2-picryhydrazyl (DPPH)-free radical scavenging and hydroxyl radical eliminating were employed as indexes to qualitatively and quantitatively analyse the radical scavenging activity of the extracts with different solvents from fermented mycelia of Hirsutella huangshanensis RCEF0868, the anamorph of Ophiocordyceps formosana (FMOF). The results showed that both the aqueous extract and the methanol extract had significant radical scavenging activity. The half maximal inhibitory concentrations (IC(50)) of the aqueous extract on DPPH-free radical and hydroxyl radical are 0.85 and 1.37 mg/mL, respectively, while the IC(50) of methanol extract is 1.23 and 2.91 mg/mL, respectively. The combined liquid chromatography-diode array detector-high resolution mass spectrometer(HRMS) analysis and activity determination revealed that the molecular formulas of three radical scavengers in aqueous extract were C(6)H(14)O(6)(1), C(14)H(17)N(5)O(8)(2) and C(20)H(33)N(5)O(9)(3). In addition to the compound 1, the methanol extract had another three radical scavengers as C(30)H(22)O(11)(4), C(30)H(22)O(10)(5) and C(30)H(18)O(10)(6). All the six kinds of components exhibited the DPPH radical scavenging activity, and compounds 1, 4 and 5 also showed the hydroxyl radical eliminating activity at the same time. By querying the database of natural products and reference to the relevant reports, compound 3 may be a new entity. The others were respectively cordycepic acid, succinoadenosine, 4α-oxyrugulosin, rugulosin and skyrin and, among them, succinoadenosine and 4α-oxyrugulosin were found in entomogenous fungi for the first time. Taylor & Francis 2017-10-10 /pmc/articles/PMC6059058/ /pubmed/30123647 http://dx.doi.org/10.1080/21501203.2017.1383318 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Li, Yang-mei Cheng, Wen-ming Da, Zi-fei Hu, Fenglin Li, Chun-ru Analysis of radical scavenging active components in the fermented mycelia of Ophiocordyceps formosana |
title | Analysis of radical scavenging active components in the fermented mycelia of Ophiocordyceps formosana |
title_full | Analysis of radical scavenging active components in the fermented mycelia of Ophiocordyceps formosana |
title_fullStr | Analysis of radical scavenging active components in the fermented mycelia of Ophiocordyceps formosana |
title_full_unstemmed | Analysis of radical scavenging active components in the fermented mycelia of Ophiocordyceps formosana |
title_short | Analysis of radical scavenging active components in the fermented mycelia of Ophiocordyceps formosana |
title_sort | analysis of radical scavenging active components in the fermented mycelia of ophiocordyceps formosana |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059058/ https://www.ncbi.nlm.nih.gov/pubmed/30123647 http://dx.doi.org/10.1080/21501203.2017.1383318 |
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