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Functional characterization of two flavone synthase II members in citrus
Polymethoxylated flavones (PMFs), the main form of flavones in citrus, are derived from the flavone branch of the flavonoid biosynthesis pathway. Flavone synthases (FNSs) are enzymes that catalyze the synthesis of flavones from flavanones. However, the FNS in citrus has not been characterized yet. H...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419818/ https://www.ncbi.nlm.nih.gov/pubmed/37577395 http://dx.doi.org/10.1093/hr/uhad113 |
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author | Zheng, Juan Zhao, Chenning Liao, Zhenkun Liu, Xiaojuan Gong, Qin Zhou, Chenwen Liu, Yilong Wang, Yue Cao, Jinping Liu, Lili Wang, Dengliang Sun, Chongde |
author_facet | Zheng, Juan Zhao, Chenning Liao, Zhenkun Liu, Xiaojuan Gong, Qin Zhou, Chenwen Liu, Yilong Wang, Yue Cao, Jinping Liu, Lili Wang, Dengliang Sun, Chongde |
author_sort | Zheng, Juan |
collection | PubMed |
description | Polymethoxylated flavones (PMFs), the main form of flavones in citrus, are derived from the flavone branch of the flavonoid biosynthesis pathway. Flavone synthases (FNSs) are enzymes that catalyze the synthesis of flavones from flavanones. However, the FNS in citrus has not been characterized yet. Here, we identified two type II FNSs, designated CitFNSII-1 and CitFNSII-2, based on phylogenetics and transcriptome analysis. Both recombinant CitFNSII-1 and CitFNSII-2 proteins directly converted naringenin, pinocembrin, and liquiritigenin to the corresponding flavones in yeast. In addition, transient overexpression of CitFNSII-1 and CitFNSII-2, respectively, in citrus peel significantly enhanced the accumulation of total PMFs, while virus-induced CitFNSII-1 and CitFNSII-2 genes silencing simultaneously significantly reduced the expression levels of both genes and total PMF content in citrus seedlings. CitFNSII-1 and CitFNSII-2 presented distinct expression patterns in different cultivars as well as different developmental stages. Methyl salicylate (MeSA) treatment reduced the CitFNSII-2 expression as well as the PMFs content in the peel of Citrus sinensis fruit but did not affect the CitFNSII-1 expression. These results indicated that both CitFNSII-1 and CitFNSII-2 participated in the flavone biosynthesis in citrus while the regulatory mechanism governing their expression might be specific. Our findings improved the understanding of the PMFs biosynthesis pathway in citrus and laid the foundation for further investigation on flavone synthesis regulation. |
format | Online Article Text |
id | pubmed-10419818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104198182023-08-12 Functional characterization of two flavone synthase II members in citrus Zheng, Juan Zhao, Chenning Liao, Zhenkun Liu, Xiaojuan Gong, Qin Zhou, Chenwen Liu, Yilong Wang, Yue Cao, Jinping Liu, Lili Wang, Dengliang Sun, Chongde Hortic Res Article Polymethoxylated flavones (PMFs), the main form of flavones in citrus, are derived from the flavone branch of the flavonoid biosynthesis pathway. Flavone synthases (FNSs) are enzymes that catalyze the synthesis of flavones from flavanones. However, the FNS in citrus has not been characterized yet. Here, we identified two type II FNSs, designated CitFNSII-1 and CitFNSII-2, based on phylogenetics and transcriptome analysis. Both recombinant CitFNSII-1 and CitFNSII-2 proteins directly converted naringenin, pinocembrin, and liquiritigenin to the corresponding flavones in yeast. In addition, transient overexpression of CitFNSII-1 and CitFNSII-2, respectively, in citrus peel significantly enhanced the accumulation of total PMFs, while virus-induced CitFNSII-1 and CitFNSII-2 genes silencing simultaneously significantly reduced the expression levels of both genes and total PMF content in citrus seedlings. CitFNSII-1 and CitFNSII-2 presented distinct expression patterns in different cultivars as well as different developmental stages. Methyl salicylate (MeSA) treatment reduced the CitFNSII-2 expression as well as the PMFs content in the peel of Citrus sinensis fruit but did not affect the CitFNSII-1 expression. These results indicated that both CitFNSII-1 and CitFNSII-2 participated in the flavone biosynthesis in citrus while the regulatory mechanism governing their expression might be specific. Our findings improved the understanding of the PMFs biosynthesis pathway in citrus and laid the foundation for further investigation on flavone synthesis regulation. Oxford University Press 2023-05-31 /pmc/articles/PMC10419818/ /pubmed/37577395 http://dx.doi.org/10.1093/hr/uhad113 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nanjing Agricultural University. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Zheng, Juan Zhao, Chenning Liao, Zhenkun Liu, Xiaojuan Gong, Qin Zhou, Chenwen Liu, Yilong Wang, Yue Cao, Jinping Liu, Lili Wang, Dengliang Sun, Chongde Functional characterization of two flavone synthase II members in citrus |
title | Functional characterization of two flavone synthase II members in citrus |
title_full | Functional characterization of two flavone synthase II members in citrus |
title_fullStr | Functional characterization of two flavone synthase II members in citrus |
title_full_unstemmed | Functional characterization of two flavone synthase II members in citrus |
title_short | Functional characterization of two flavone synthase II members in citrus |
title_sort | functional characterization of two flavone synthase ii members in citrus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419818/ https://www.ncbi.nlm.nih.gov/pubmed/37577395 http://dx.doi.org/10.1093/hr/uhad113 |
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