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Virtual screening and docking analysis of novel ligands for selective enhancement of tea (Camellia sinensis) flavonoids
Flavour of tea is mainly contributed by a group of polyphenols – flavonoids. However, the content of flavonoid fluctuates seasonally and is found to be higher in the first flush of tea, when compared to the second flush. This disparity in the flavonoid content, and hence taste, incurs heavy economic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039891/ https://www.ncbi.nlm.nih.gov/pubmed/35498963 http://dx.doi.org/10.1016/j.fochx.2022.100212 |
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author | Majumder, Anusha Kanti Mondal, Sunil Mukhoty, Samyabrata Bag, Sagar Mondal, Anupam Begum, Yasmin Sharma, Kalpna Banik, Avishek |
author_facet | Majumder, Anusha Kanti Mondal, Sunil Mukhoty, Samyabrata Bag, Sagar Mondal, Anupam Begum, Yasmin Sharma, Kalpna Banik, Avishek |
author_sort | Majumder, Anusha |
collection | PubMed |
description | Flavour of tea is mainly contributed by a group of polyphenols – flavonoids. However, the content of flavonoid fluctuates seasonally and is found to be higher in the first flush of tea, when compared to the second flush. This disparity in the flavonoid content, and hence taste, incurs heavy economic losses to the tea plantation industry each harvest season. For our present study, four key product-specific enzymes (PAL, FNS, FLS and ANS) of the tea-specific flavonoid pathway were selected to perform molecular docking studies with specific virtually screened allosteric modulators. Results of docking analyses showed Naringenin, 2-Morpholin-4-ium-4-ylethanesulfonate, 6-C-Glucosylquercetin, 2-Oxoglutaric acid, 3,5,7,3′,4′-pentahydroxyflavone to be capable of improving the spontaneity of the enzyme-substrate reactions in terms of docking score, RMSD values, and non-covalent interactions (H-bond,hydrophobic interaction, Π-stacking, salt bridge, etc.). Further, the evolutionary relationship of tea flavonoid pathway enzymes was constructed and compared with related taxa. The codon usage-based of tea flavonoid biosynthetic genes indicated the non-biasness of their nucleotide composition. Overall this study will provide a direction towards putative ligand-dependent enhancement of flavonoid content, irrespective of seasonal variation. |
format | Online Article Text |
id | pubmed-9039891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90398912022-04-27 Virtual screening and docking analysis of novel ligands for selective enhancement of tea (Camellia sinensis) flavonoids Majumder, Anusha Kanti Mondal, Sunil Mukhoty, Samyabrata Bag, Sagar Mondal, Anupam Begum, Yasmin Sharma, Kalpna Banik, Avishek Food Chem X Article(s) from the Special Issue on Recovery and application of high-value resources from foods and food by-products by Mauricio Rostagno and Juliane Viganó Flavour of tea is mainly contributed by a group of polyphenols – flavonoids. However, the content of flavonoid fluctuates seasonally and is found to be higher in the first flush of tea, when compared to the second flush. This disparity in the flavonoid content, and hence taste, incurs heavy economic losses to the tea plantation industry each harvest season. For our present study, four key product-specific enzymes (PAL, FNS, FLS and ANS) of the tea-specific flavonoid pathway were selected to perform molecular docking studies with specific virtually screened allosteric modulators. Results of docking analyses showed Naringenin, 2-Morpholin-4-ium-4-ylethanesulfonate, 6-C-Glucosylquercetin, 2-Oxoglutaric acid, 3,5,7,3′,4′-pentahydroxyflavone to be capable of improving the spontaneity of the enzyme-substrate reactions in terms of docking score, RMSD values, and non-covalent interactions (H-bond,hydrophobic interaction, Π-stacking, salt bridge, etc.). Further, the evolutionary relationship of tea flavonoid pathway enzymes was constructed and compared with related taxa. The codon usage-based of tea flavonoid biosynthetic genes indicated the non-biasness of their nucleotide composition. Overall this study will provide a direction towards putative ligand-dependent enhancement of flavonoid content, irrespective of seasonal variation. Elsevier 2022-01-18 /pmc/articles/PMC9039891/ /pubmed/35498963 http://dx.doi.org/10.1016/j.fochx.2022.100212 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article(s) from the Special Issue on Recovery and application of high-value resources from foods and food by-products by Mauricio Rostagno and Juliane Viganó Majumder, Anusha Kanti Mondal, Sunil Mukhoty, Samyabrata Bag, Sagar Mondal, Anupam Begum, Yasmin Sharma, Kalpna Banik, Avishek Virtual screening and docking analysis of novel ligands for selective enhancement of tea (Camellia sinensis) flavonoids |
title | Virtual screening and docking analysis of novel ligands for selective enhancement of tea (Camellia sinensis) flavonoids |
title_full | Virtual screening and docking analysis of novel ligands for selective enhancement of tea (Camellia sinensis) flavonoids |
title_fullStr | Virtual screening and docking analysis of novel ligands for selective enhancement of tea (Camellia sinensis) flavonoids |
title_full_unstemmed | Virtual screening and docking analysis of novel ligands for selective enhancement of tea (Camellia sinensis) flavonoids |
title_short | Virtual screening and docking analysis of novel ligands for selective enhancement of tea (Camellia sinensis) flavonoids |
title_sort | virtual screening and docking analysis of novel ligands for selective enhancement of tea (camellia sinensis) flavonoids |
topic | Article(s) from the Special Issue on Recovery and application of high-value resources from foods and food by-products by Mauricio Rostagno and Juliane Viganó |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039891/ https://www.ncbi.nlm.nih.gov/pubmed/35498963 http://dx.doi.org/10.1016/j.fochx.2022.100212 |
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