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Improved Productivity of Naringin Oleate with Flavonoid and Fatty Acid by Efficient Enzymatic Esterification
Naringin is a flavonoid found in citrus fruits. It exhibits biological activities, such as anticancer and antioxidant effects, but it suffers from low solubility and low stability in lipophilic systems. These drawbacks lead to difficulties in the commercial application of naringin, but they can be o...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868195/ https://www.ncbi.nlm.nih.gov/pubmed/35204125 http://dx.doi.org/10.3390/antiox11020242 |
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author | Lee, Jonghwa Kim, Kyeonga Son, Jemin Lee, Hyeseon Song, Jin Han Lee, Taek Jeon, Heungbae Kim, Hyun Soo Park, Si Jae Yoo, Hah Young Park, Chulhwan |
author_facet | Lee, Jonghwa Kim, Kyeonga Son, Jemin Lee, Hyeseon Song, Jin Han Lee, Taek Jeon, Heungbae Kim, Hyun Soo Park, Si Jae Yoo, Hah Young Park, Chulhwan |
author_sort | Lee, Jonghwa |
collection | PubMed |
description | Naringin is a flavonoid found in citrus fruits. It exhibits biological activities, such as anticancer and antioxidant effects, but it suffers from low solubility and low stability in lipophilic systems. These drawbacks lead to difficulties in the commercial application of naringin, but they can be overcome through esterification. In this study, naringin oleate was synthesized by enzymatic esterification and optimal conditions for the reaction were investigated. Experiments were conducted focusing on the following parameters: enzyme type, enzyme concentration, molar ratio of naringin to oleic acid, reaction temperature, and reaction solvent. We further confirmed the degree of esterification based on the difference in the initial and the final naringin concentrations. A conversion of 93.10% was obtained under optimized conditions (Lipozyme TL IM 10 g/L, molar ratio 1:20, reaction temperature 40 °C, acetonitrile as solvent, and 48 h reaction time). Thus, naringin oleate, a high value-added material that overcomes the low hydrophobicity of naringin and enhances its performance, was obtained through esterification of naringin using oleic acid. This study presented a method for the efficient enzymatic synthesis that could ensure high conversion within a shorter reaction time compared with that required in previously reported methods. |
format | Online Article Text |
id | pubmed-8868195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88681952022-02-25 Improved Productivity of Naringin Oleate with Flavonoid and Fatty Acid by Efficient Enzymatic Esterification Lee, Jonghwa Kim, Kyeonga Son, Jemin Lee, Hyeseon Song, Jin Han Lee, Taek Jeon, Heungbae Kim, Hyun Soo Park, Si Jae Yoo, Hah Young Park, Chulhwan Antioxidants (Basel) Article Naringin is a flavonoid found in citrus fruits. It exhibits biological activities, such as anticancer and antioxidant effects, but it suffers from low solubility and low stability in lipophilic systems. These drawbacks lead to difficulties in the commercial application of naringin, but they can be overcome through esterification. In this study, naringin oleate was synthesized by enzymatic esterification and optimal conditions for the reaction were investigated. Experiments were conducted focusing on the following parameters: enzyme type, enzyme concentration, molar ratio of naringin to oleic acid, reaction temperature, and reaction solvent. We further confirmed the degree of esterification based on the difference in the initial and the final naringin concentrations. A conversion of 93.10% was obtained under optimized conditions (Lipozyme TL IM 10 g/L, molar ratio 1:20, reaction temperature 40 °C, acetonitrile as solvent, and 48 h reaction time). Thus, naringin oleate, a high value-added material that overcomes the low hydrophobicity of naringin and enhances its performance, was obtained through esterification of naringin using oleic acid. This study presented a method for the efficient enzymatic synthesis that could ensure high conversion within a shorter reaction time compared with that required in previously reported methods. MDPI 2022-01-27 /pmc/articles/PMC8868195/ /pubmed/35204125 http://dx.doi.org/10.3390/antiox11020242 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 Lee, Jonghwa Kim, Kyeonga Son, Jemin Lee, Hyeseon Song, Jin Han Lee, Taek Jeon, Heungbae Kim, Hyun Soo Park, Si Jae Yoo, Hah Young Park, Chulhwan Improved Productivity of Naringin Oleate with Flavonoid and Fatty Acid by Efficient Enzymatic Esterification |
title | Improved Productivity of Naringin Oleate with Flavonoid and Fatty Acid by Efficient Enzymatic Esterification |
title_full | Improved Productivity of Naringin Oleate with Flavonoid and Fatty Acid by Efficient Enzymatic Esterification |
title_fullStr | Improved Productivity of Naringin Oleate with Flavonoid and Fatty Acid by Efficient Enzymatic Esterification |
title_full_unstemmed | Improved Productivity of Naringin Oleate with Flavonoid and Fatty Acid by Efficient Enzymatic Esterification |
title_short | Improved Productivity of Naringin Oleate with Flavonoid and Fatty Acid by Efficient Enzymatic Esterification |
title_sort | improved productivity of naringin oleate with flavonoid and fatty acid by efficient enzymatic esterification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868195/ https://www.ncbi.nlm.nih.gov/pubmed/35204125 http://dx.doi.org/10.3390/antiox11020242 |
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