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Phenolic Acids in Jerusalem Artichoke (Helianthus tuberosus L.): Plant Organ Dependent Antioxidant Activity and Optimized Extraction from Leaves

Phenolic acids including chlorogenic acids are major polyphenolic compounds found in Jerusalem artichoke (Helianthus tuberosus L.). The plant itself is an emerging biorefinery crop due to the inulin-rich tubers, a bioethanol feedstock, but the aerial parts represent a rich source of bioactive compou...

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Autores principales: Showkat, Muhammad Mir, Falck-Ytter, Anne Bergljot, Strætkvern, Knut Olav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6766983/
https://www.ncbi.nlm.nih.gov/pubmed/31510058
http://dx.doi.org/10.3390/molecules24183296
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author Showkat, Muhammad Mir
Falck-Ytter, Anne Bergljot
Strætkvern, Knut Olav
author_facet Showkat, Muhammad Mir
Falck-Ytter, Anne Bergljot
Strætkvern, Knut Olav
author_sort Showkat, Muhammad Mir
collection PubMed
description Phenolic acids including chlorogenic acids are major polyphenolic compounds found in Jerusalem artichoke (Helianthus tuberosus L.). The plant itself is an emerging biorefinery crop due to the inulin-rich tubers, a bioethanol feedstock, but the aerial parts represent a rich source of bioactive compounds. We have determined the level of major phenolic acids in extracts of four plant organs: tuber, leaf, flower, and stem. Employing three heating conditions (20 °C, 60 °C, and microwaving), corrected total phenolic content (TPC) was highest in the leaves (4.5–5.7 mg gallic acid equivalents g(−1) dry substance), followed by flower (2.1–2.9), tuber (0.9–1.4), and lowest in stem extracts (0.1–0.2). A previously overlooked interference of the Folin–Ciocalteu assay, namely a signal contribution from ascorbic acid, caused overestimation of TPC in various organs ranging from 65% to 94%. Radical scavenging activity of extracts correlated significantly with TPC, both on corrected (R(2) = 0.841) and uncorrected (R(2) = 0.884) values. Out of the identified phenolic acids determined by quantitative HPLC-UV analysis, chlorogenic and dicaffeoylquinic acids accounted for 72–82% of corrected TPC in leaf and tuber extracts. Optimization of leaf extraction was tested in a 2(3)-factorial Central Composite Face (CCF) design. Temperature was the most important model term, and a solvent strength of less than 50% ethanol promoted the highest TPC yields. Further developments in extraction processing of crop residues may open avenues for improving the utilization of Jerusalem artichoke in valuable products.
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spelling pubmed-67669832019-10-02 Phenolic Acids in Jerusalem Artichoke (Helianthus tuberosus L.): Plant Organ Dependent Antioxidant Activity and Optimized Extraction from Leaves Showkat, Muhammad Mir Falck-Ytter, Anne Bergljot Strætkvern, Knut Olav Molecules Article Phenolic acids including chlorogenic acids are major polyphenolic compounds found in Jerusalem artichoke (Helianthus tuberosus L.). The plant itself is an emerging biorefinery crop due to the inulin-rich tubers, a bioethanol feedstock, but the aerial parts represent a rich source of bioactive compounds. We have determined the level of major phenolic acids in extracts of four plant organs: tuber, leaf, flower, and stem. Employing three heating conditions (20 °C, 60 °C, and microwaving), corrected total phenolic content (TPC) was highest in the leaves (4.5–5.7 mg gallic acid equivalents g(−1) dry substance), followed by flower (2.1–2.9), tuber (0.9–1.4), and lowest in stem extracts (0.1–0.2). A previously overlooked interference of the Folin–Ciocalteu assay, namely a signal contribution from ascorbic acid, caused overestimation of TPC in various organs ranging from 65% to 94%. Radical scavenging activity of extracts correlated significantly with TPC, both on corrected (R(2) = 0.841) and uncorrected (R(2) = 0.884) values. Out of the identified phenolic acids determined by quantitative HPLC-UV analysis, chlorogenic and dicaffeoylquinic acids accounted for 72–82% of corrected TPC in leaf and tuber extracts. Optimization of leaf extraction was tested in a 2(3)-factorial Central Composite Face (CCF) design. Temperature was the most important model term, and a solvent strength of less than 50% ethanol promoted the highest TPC yields. Further developments in extraction processing of crop residues may open avenues for improving the utilization of Jerusalem artichoke in valuable products. MDPI 2019-09-10 /pmc/articles/PMC6766983/ /pubmed/31510058 http://dx.doi.org/10.3390/molecules24183296 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Showkat, Muhammad Mir
Falck-Ytter, Anne Bergljot
Strætkvern, Knut Olav
Phenolic Acids in Jerusalem Artichoke (Helianthus tuberosus L.): Plant Organ Dependent Antioxidant Activity and Optimized Extraction from Leaves
title Phenolic Acids in Jerusalem Artichoke (Helianthus tuberosus L.): Plant Organ Dependent Antioxidant Activity and Optimized Extraction from Leaves
title_full Phenolic Acids in Jerusalem Artichoke (Helianthus tuberosus L.): Plant Organ Dependent Antioxidant Activity and Optimized Extraction from Leaves
title_fullStr Phenolic Acids in Jerusalem Artichoke (Helianthus tuberosus L.): Plant Organ Dependent Antioxidant Activity and Optimized Extraction from Leaves
title_full_unstemmed Phenolic Acids in Jerusalem Artichoke (Helianthus tuberosus L.): Plant Organ Dependent Antioxidant Activity and Optimized Extraction from Leaves
title_short Phenolic Acids in Jerusalem Artichoke (Helianthus tuberosus L.): Plant Organ Dependent Antioxidant Activity and Optimized Extraction from Leaves
title_sort phenolic acids in jerusalem artichoke (helianthus tuberosus l.): plant organ dependent antioxidant activity and optimized extraction from leaves
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6766983/
https://www.ncbi.nlm.nih.gov/pubmed/31510058
http://dx.doi.org/10.3390/molecules24183296
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