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Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria

In this work, we carried out studies of the chemical composition of hexane, chloroform and ethanol extracts from two samples of the lichen Parmotrema hypoleucinum collected in Algeria. Each sample of the lichen P. hypoleucinum was collected on two different supports: Olea europaea and Quercus coccif...

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Autores principales: Kerboua, Marwa, Monia, Ali Ahmed, Samba, Nsevolo, Silva, Lúcia, Raposo, Cesar, Díez, David, Rodilla, Jesus Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416662/
https://www.ncbi.nlm.nih.gov/pubmed/36014465
http://dx.doi.org/10.3390/molecules27165229
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author Kerboua, Marwa
Monia, Ali Ahmed
Samba, Nsevolo
Silva, Lúcia
Raposo, Cesar
Díez, David
Rodilla, Jesus Miguel
author_facet Kerboua, Marwa
Monia, Ali Ahmed
Samba, Nsevolo
Silva, Lúcia
Raposo, Cesar
Díez, David
Rodilla, Jesus Miguel
author_sort Kerboua, Marwa
collection PubMed
description In this work, we carried out studies of the chemical composition of hexane, chloroform and ethanol extracts from two samples of the lichen Parmotrema hypoleucinum collected in Algeria. Each sample of the lichen P. hypoleucinum was collected on two different supports: Olea europaea and Quercus coccifera. Hexane extracts were prepared, in Soxhlet; each hexane extract was fractionated by its solubility in methanol; the products soluble in methanol were separated (cold): 1-Hexane, 2-Hexane; and the products insoluble in methanol (cold): 1-Cires, 2-Cires. A diazomethane esterified sample of 1-Hexane, 2-Hexane, 1-Cires and 2-Cires was analyzed by GC-MS, and the components were identified as methyl esters. In the 1-Hexane and 2-Hexane fractions, the methyl esters of the predominant fatty acids in the lichen were identified: palmitic acid, linoleic acid, oleic acid and stearic acid; a hydrocarbon was also identified: 13-methyl-17-norkaur-15-ene and several derivatives of orsellinic acid. In the 1-Cires and 2-Cires fractions, the previous fatty acids were no longer observed, and only the derivatives of orsellinic acid were found. The analysis of the 1-Hexane, 2-Hexane fractions by HPLC-MS/MS allows us to identify different chemical components, and the most characteristic products of the lichen were identified, such as Atranol, Chloroatranol, Atranorin and Chloroatranorin. In the fractions of 1-Cires and 2-Cires, the HPLC-MS/MS analysis reveals that they are very similar in their chemical components; the characteristic products of this lichen in this fraction are Atranorin and Chloroatranorin. In the extracts of chloroform, 1-Chloroform and 2-Chloroform, the analysis carried out by HPLC-MS/MS shows small differences in their chemical composition at the level of secondary products; among the products to be highlighted for this work, we have chloroatranorin, the stictic acid, norstictic acid and other derivatives. In the analysis of the most polar extracts carried out in ethanol: 1-Ethanol and 2-Ethanol, HPLC-MS/MS analysis shows very similar chemical compositions in these two extracts with small differences. In these extracts, the following acids were identified as characteristic compounds of this lichen: constictic acid, stictic acid, substictic acid and methylstictic acid. In the HPLC–MS/MS analysis of all these extracts, alectoronic acid was not found.
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spelling pubmed-94166622022-08-27 Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria Kerboua, Marwa Monia, Ali Ahmed Samba, Nsevolo Silva, Lúcia Raposo, Cesar Díez, David Rodilla, Jesus Miguel Molecules Article In this work, we carried out studies of the chemical composition of hexane, chloroform and ethanol extracts from two samples of the lichen Parmotrema hypoleucinum collected in Algeria. Each sample of the lichen P. hypoleucinum was collected on two different supports: Olea europaea and Quercus coccifera. Hexane extracts were prepared, in Soxhlet; each hexane extract was fractionated by its solubility in methanol; the products soluble in methanol were separated (cold): 1-Hexane, 2-Hexane; and the products insoluble in methanol (cold): 1-Cires, 2-Cires. A diazomethane esterified sample of 1-Hexane, 2-Hexane, 1-Cires and 2-Cires was analyzed by GC-MS, and the components were identified as methyl esters. In the 1-Hexane and 2-Hexane fractions, the methyl esters of the predominant fatty acids in the lichen were identified: palmitic acid, linoleic acid, oleic acid and stearic acid; a hydrocarbon was also identified: 13-methyl-17-norkaur-15-ene and several derivatives of orsellinic acid. In the 1-Cires and 2-Cires fractions, the previous fatty acids were no longer observed, and only the derivatives of orsellinic acid were found. The analysis of the 1-Hexane, 2-Hexane fractions by HPLC-MS/MS allows us to identify different chemical components, and the most characteristic products of the lichen were identified, such as Atranol, Chloroatranol, Atranorin and Chloroatranorin. In the fractions of 1-Cires and 2-Cires, the HPLC-MS/MS analysis reveals that they are very similar in their chemical components; the characteristic products of this lichen in this fraction are Atranorin and Chloroatranorin. In the extracts of chloroform, 1-Chloroform and 2-Chloroform, the analysis carried out by HPLC-MS/MS shows small differences in their chemical composition at the level of secondary products; among the products to be highlighted for this work, we have chloroatranorin, the stictic acid, norstictic acid and other derivatives. In the analysis of the most polar extracts carried out in ethanol: 1-Ethanol and 2-Ethanol, HPLC-MS/MS analysis shows very similar chemical compositions in these two extracts with small differences. In these extracts, the following acids were identified as characteristic compounds of this lichen: constictic acid, stictic acid, substictic acid and methylstictic acid. In the HPLC–MS/MS analysis of all these extracts, alectoronic acid was not found. MDPI 2022-08-16 /pmc/articles/PMC9416662/ /pubmed/36014465 http://dx.doi.org/10.3390/molecules27165229 Text en © 2022 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
Kerboua, Marwa
Monia, Ali Ahmed
Samba, Nsevolo
Silva, Lúcia
Raposo, Cesar
Díez, David
Rodilla, Jesus Miguel
Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria
title Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria
title_full Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria
title_fullStr Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria
title_full_unstemmed Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria
title_short Phytochemical Composition of Lichen Parmotrema hypoleucinum (J. Steiner) Hale from Algeria
title_sort phytochemical composition of lichen parmotrema hypoleucinum (j. steiner) hale from algeria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416662/
https://www.ncbi.nlm.nih.gov/pubmed/36014465
http://dx.doi.org/10.3390/molecules27165229
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