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Combined Effect of Cultivar and Peel Chromaticity on Figs’ Primary and Secondary Metabolites: Preliminary Study Using Biochemical and FTIR Fingerprinting Coupled to Chemometrics

SIMPLE SUMMARY: Primary and secondary metabolites are among the markers for addressing fig chemotypic variability. These compounds are mainly driven by the cultivar factor besides chromatic coordinates color as they are highly correlated to these biomarkers. Combined use of chemical analytical proce...

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Autores principales: Hssaini, Lahcen, Elfazazi, Kaoutar, Razouk, Rachid, Ouaabou, Rachida, Hernandez, Francisca, Hanine, Hafida, Charafi, Jamal, Houmanat, Karim, Aboutayeb, Rachid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301012/
https://www.ncbi.nlm.nih.gov/pubmed/34201443
http://dx.doi.org/10.3390/biology10070573
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author Hssaini, Lahcen
Elfazazi, Kaoutar
Razouk, Rachid
Ouaabou, Rachida
Hernandez, Francisca
Hanine, Hafida
Charafi, Jamal
Houmanat, Karim
Aboutayeb, Rachid
author_facet Hssaini, Lahcen
Elfazazi, Kaoutar
Razouk, Rachid
Ouaabou, Rachida
Hernandez, Francisca
Hanine, Hafida
Charafi, Jamal
Houmanat, Karim
Aboutayeb, Rachid
author_sort Hssaini, Lahcen
collection PubMed
description SIMPLE SUMMARY: Primary and secondary metabolites are among the markers for addressing fig chemotypic variability. These compounds are mainly driven by the cultivar factor besides chromatic coordinates color as they are highly correlated to these biomarkers. Combined use of chemical analytical procedures and vibrational spectroscopy is of great importance for a better understanding of network connections within the dataset. In this study, we screened 11 fig tree cultivars for their biochemical and spectral fingerprints in a comparative scheme for high resolution discrimination. Analytical methods herein used were also evaluated for their greenness aspects using GAPI eco-scale tool. ABSTRACT: Figs are a traditional pantry staple for healthy eating in Middle Eastern and North African countries as fig trees grow abundantly in such hot and dry climates. Despite the importance of this species, chemotypic diversity has gone unheeded and therefore its valorization pathways remain poorly documented. For this reason, high-pressure liquid chromatography (HPLC) alongside vibrational spectroscopy were used to investigate the changes of antiradical potency and primary and secondary metabolites in fresh figs with regard to the combined effect of the cultivar factor and the fruit peel chromatic coordinates. Fourier-transform infrared spectroscopy (FTIR) fingerprinting displayed six major peaks assigned to functional groups of the investigated samples with significant differences in their vibration intensities. Biochemical screening revealed highly significant variability (p < 0.05) among the investigated cultivars. Antioxidant activity was found to be higher in free radical scavenging using 2,2-diphenyl-1-picrylhydrazyl (DPPH) compared to ferric reducing ability (FRAP). Chemometric investigations of both biochemical and FTIR fingerprinting showed satisfactory resolutions, and the total phenol contents and chromatic coordinates had the highest scores in the dataset. However, the cultivars’ geographical origin seemed not to have a clear impact on the clustering results. The aforementioned analytical procedures were found to be equally important and can be jointly used for high-resolution screening and discrimination of fig trees.
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spelling pubmed-83010122021-07-24 Combined Effect of Cultivar and Peel Chromaticity on Figs’ Primary and Secondary Metabolites: Preliminary Study Using Biochemical and FTIR Fingerprinting Coupled to Chemometrics Hssaini, Lahcen Elfazazi, Kaoutar Razouk, Rachid Ouaabou, Rachida Hernandez, Francisca Hanine, Hafida Charafi, Jamal Houmanat, Karim Aboutayeb, Rachid Biology (Basel) Article SIMPLE SUMMARY: Primary and secondary metabolites are among the markers for addressing fig chemotypic variability. These compounds are mainly driven by the cultivar factor besides chromatic coordinates color as they are highly correlated to these biomarkers. Combined use of chemical analytical procedures and vibrational spectroscopy is of great importance for a better understanding of network connections within the dataset. In this study, we screened 11 fig tree cultivars for their biochemical and spectral fingerprints in a comparative scheme for high resolution discrimination. Analytical methods herein used were also evaluated for their greenness aspects using GAPI eco-scale tool. ABSTRACT: Figs are a traditional pantry staple for healthy eating in Middle Eastern and North African countries as fig trees grow abundantly in such hot and dry climates. Despite the importance of this species, chemotypic diversity has gone unheeded and therefore its valorization pathways remain poorly documented. For this reason, high-pressure liquid chromatography (HPLC) alongside vibrational spectroscopy were used to investigate the changes of antiradical potency and primary and secondary metabolites in fresh figs with regard to the combined effect of the cultivar factor and the fruit peel chromatic coordinates. Fourier-transform infrared spectroscopy (FTIR) fingerprinting displayed six major peaks assigned to functional groups of the investigated samples with significant differences in their vibration intensities. Biochemical screening revealed highly significant variability (p < 0.05) among the investigated cultivars. Antioxidant activity was found to be higher in free radical scavenging using 2,2-diphenyl-1-picrylhydrazyl (DPPH) compared to ferric reducing ability (FRAP). Chemometric investigations of both biochemical and FTIR fingerprinting showed satisfactory resolutions, and the total phenol contents and chromatic coordinates had the highest scores in the dataset. However, the cultivars’ geographical origin seemed not to have a clear impact on the clustering results. The aforementioned analytical procedures were found to be equally important and can be jointly used for high-resolution screening and discrimination of fig trees. MDPI 2021-06-23 /pmc/articles/PMC8301012/ /pubmed/34201443 http://dx.doi.org/10.3390/biology10070573 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
Hssaini, Lahcen
Elfazazi, Kaoutar
Razouk, Rachid
Ouaabou, Rachida
Hernandez, Francisca
Hanine, Hafida
Charafi, Jamal
Houmanat, Karim
Aboutayeb, Rachid
Combined Effect of Cultivar and Peel Chromaticity on Figs’ Primary and Secondary Metabolites: Preliminary Study Using Biochemical and FTIR Fingerprinting Coupled to Chemometrics
title Combined Effect of Cultivar and Peel Chromaticity on Figs’ Primary and Secondary Metabolites: Preliminary Study Using Biochemical and FTIR Fingerprinting Coupled to Chemometrics
title_full Combined Effect of Cultivar and Peel Chromaticity on Figs’ Primary and Secondary Metabolites: Preliminary Study Using Biochemical and FTIR Fingerprinting Coupled to Chemometrics
title_fullStr Combined Effect of Cultivar and Peel Chromaticity on Figs’ Primary and Secondary Metabolites: Preliminary Study Using Biochemical and FTIR Fingerprinting Coupled to Chemometrics
title_full_unstemmed Combined Effect of Cultivar and Peel Chromaticity on Figs’ Primary and Secondary Metabolites: Preliminary Study Using Biochemical and FTIR Fingerprinting Coupled to Chemometrics
title_short Combined Effect of Cultivar and Peel Chromaticity on Figs’ Primary and Secondary Metabolites: Preliminary Study Using Biochemical and FTIR Fingerprinting Coupled to Chemometrics
title_sort combined effect of cultivar and peel chromaticity on figs’ primary and secondary metabolites: preliminary study using biochemical and ftir fingerprinting coupled to chemometrics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301012/
https://www.ncbi.nlm.nih.gov/pubmed/34201443
http://dx.doi.org/10.3390/biology10070573
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