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Overexpression of chalcone isomerase A gene in Astragalus trigonus for stimulating apigenin

Apigenin is one of the most studied flavonoids and is widely distributed in the plant kingdom. Apigenin exerts important antioxidant, antibacterial, antifungal, antitumor activities, and anti-inflammatory effects in neurological or cardiovascular disease. Chalcone isomerase A (chiA) is an important...

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Autores principales: Elarabi, Nagwa I., Abdelhadi, Abdelhadi A., Sief-Eldein, Ahmed G. M., Ismail, Ismail A., Abdallah, Naglaa A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683443/
https://www.ncbi.nlm.nih.gov/pubmed/34921216
http://dx.doi.org/10.1038/s41598-021-03704-y
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author Elarabi, Nagwa I.
Abdelhadi, Abdelhadi A.
Sief-Eldein, Ahmed G. M.
Ismail, Ismail A.
Abdallah, Naglaa A.
author_facet Elarabi, Nagwa I.
Abdelhadi, Abdelhadi A.
Sief-Eldein, Ahmed G. M.
Ismail, Ismail A.
Abdallah, Naglaa A.
author_sort Elarabi, Nagwa I.
collection PubMed
description Apigenin is one of the most studied flavonoids and is widely distributed in the plant kingdom. Apigenin exerts important antioxidant, antibacterial, antifungal, antitumor activities, and anti-inflammatory effects in neurological or cardiovascular disease. Chalcone isomerase A (chiA) is an important enzyme of the flavonoid biosynthesis pathway. In order to enhance the apigenin production, the petunia chi A gene was transformed for Astragalus trigonus. Bialaphos survived plants were screened by PCR, dot blot hybridization and RT-PCR analysis. Also, jasmonic acid, salicylic acid, chitosan and yeast extract were tested to evaluate their capacity to work as elicitors for apigenin. Results showed that yeast extract was the best elicitor for induction of apigenin with an increase of 3.458 and 3.9 fold of the control for calli and cell suspension culture, respectively. Transformed cell suspension showed high apigenin content with a 20.17 fold increase compared to the control and 6.88 fold more than the yeast extract treatment. While, transformed T(1) calli derived expressing chiA gene produced apigenin 4.2 fold more than the yeast extract treatment. It can be concluded that the highest accumulation of apigenin was obtained with chiA transgenic cell suspension system and it can be utilized to enhancement apigenin production in Astragalus trigonus.
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spelling pubmed-86834432021-12-20 Overexpression of chalcone isomerase A gene in Astragalus trigonus for stimulating apigenin Elarabi, Nagwa I. Abdelhadi, Abdelhadi A. Sief-Eldein, Ahmed G. M. Ismail, Ismail A. Abdallah, Naglaa A. Sci Rep Article Apigenin is one of the most studied flavonoids and is widely distributed in the plant kingdom. Apigenin exerts important antioxidant, antibacterial, antifungal, antitumor activities, and anti-inflammatory effects in neurological or cardiovascular disease. Chalcone isomerase A (chiA) is an important enzyme of the flavonoid biosynthesis pathway. In order to enhance the apigenin production, the petunia chi A gene was transformed for Astragalus trigonus. Bialaphos survived plants were screened by PCR, dot blot hybridization and RT-PCR analysis. Also, jasmonic acid, salicylic acid, chitosan and yeast extract were tested to evaluate their capacity to work as elicitors for apigenin. Results showed that yeast extract was the best elicitor for induction of apigenin with an increase of 3.458 and 3.9 fold of the control for calli and cell suspension culture, respectively. Transformed cell suspension showed high apigenin content with a 20.17 fold increase compared to the control and 6.88 fold more than the yeast extract treatment. While, transformed T(1) calli derived expressing chiA gene produced apigenin 4.2 fold more than the yeast extract treatment. It can be concluded that the highest accumulation of apigenin was obtained with chiA transgenic cell suspension system and it can be utilized to enhancement apigenin production in Astragalus trigonus. Nature Publishing Group UK 2021-12-17 /pmc/articles/PMC8683443/ /pubmed/34921216 http://dx.doi.org/10.1038/s41598-021-03704-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Elarabi, Nagwa I.
Abdelhadi, Abdelhadi A.
Sief-Eldein, Ahmed G. M.
Ismail, Ismail A.
Abdallah, Naglaa A.
Overexpression of chalcone isomerase A gene in Astragalus trigonus for stimulating apigenin
title Overexpression of chalcone isomerase A gene in Astragalus trigonus for stimulating apigenin
title_full Overexpression of chalcone isomerase A gene in Astragalus trigonus for stimulating apigenin
title_fullStr Overexpression of chalcone isomerase A gene in Astragalus trigonus for stimulating apigenin
title_full_unstemmed Overexpression of chalcone isomerase A gene in Astragalus trigonus for stimulating apigenin
title_short Overexpression of chalcone isomerase A gene in Astragalus trigonus for stimulating apigenin
title_sort overexpression of chalcone isomerase a gene in astragalus trigonus for stimulating apigenin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683443/
https://www.ncbi.nlm.nih.gov/pubmed/34921216
http://dx.doi.org/10.1038/s41598-021-03704-y
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