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      Identification and tissue-specific expression of rutin biosynthetic pathway genes in Capparis spinosa elicited with salicylic acid and methyl jasmonate

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          Abstract

          Capparis spinosa is an edible medicinal plant which is considered as an excellent source of rutin. Rutin is a glycoside of the flavonoid quercetin that has been reported to have a beneficial role in controlling various diseases such as hypertension, arteriosclerosis, diabetes, and obesity. In this study, the partial cDNA of four genes involved in the rutin biosynthetic pathway including 4-coumaroyl CoA ligase (4CL), flavonoid 3′-hydroxylase (F3′H), flavonol synthase (FLS) and flavonol-3-O-glucoside L-rhamnosyltransferase (RT) were identified in C.spinosa plants for the first time. The protein sequences of these genes shared high similarity with the same proteins in other plant species. Subsequently, the expression patterns of these genes as well as rutin accumulation in C.spinosa leaves treated with different concentrations of salicylic acid (SA) and methyl jasmonate (MeJA) and also in different tissues of Caper plants treated with 100 mgL −1 SA and 150 μM MeJA were evaluated. The expression of all four genes was clearly up-regulated and rutin contents increased in response to MeJA and SA treatments after 24 h. The highest rutin contents (5.30 mgg −1 DW and 13.27 mgg −1 DW), as well as the highest expression levels of all four genes, were obtained using 100 mgL −1 SA and 150 μM MeJA, respectively. Among the different tissues, the highest rutin content was observed in young leaves treated with 150 μM MeJA, which corresponded to the expression of related genes, especially RT, as a key gene in the rutin biosynthetic pathway. These results suggest that rutin content in various tissues of C. spinosa can be enhanced to a significant extent by MeJA and SA treatments and the gene expression patterns of rutin-biosynthesis-related genes are regulated by these elicitors.

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          Plant Flavonoids—Biosynthesis, Transport and Involvement in Stress Responses

          This paper aims at analysing the synthesis of flavonoids, their import and export in plant cell compartments, as well as their involvement in the response to stress, with particular reference to grapevine (Vitis vinifera L.). A multidrug and toxic compound extrusion (MATE) as well as ABC transporters have been demonstrated in the tonoplast of grape berry, where they perform a flavonoid transport. The involvement of a glutathione S-transferase (GST) gene has also been inferred. Recently, a putative flavonoid carrier, similar to mammalian bilitranslocase (BTL), has been identified in both grape berry skin and pulp. In skin the pattern of BTL expression increases from véraison to harvest, while in the pulp its expression reaches the maximum at the early ripening stage. Moreover, the presence of BTL in vascular bundles suggests its participation in long distance transport of flavonoids. In addition, the presence of a vesicular trafficking in plants responsible for flavonoid transport is discussed. Finally, the involvement of flavonoids in the response to stress is described.
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            Induction of Abiotic Stress Tolerance by Salicylic Acid Signaling

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              Flavones and flavone synthases.

              Within the secondary metabolite class of flavonoids which consist of more than 9000 known structures, flavones define one of the largest subgroups. Their natural distribution is demonstrated for almost all plant tissues. Various flavone aglyca and their O- or C-glycosides have been described in the literature. The diverse functions of flavones in plants as well as their various roles in the interaction with other organisms offer many potential applications, not only in plant breeding but also in ecology, agriculture and human nutrition and pharmacology. In this context, the antioxidative activity of flavones, their use in cancer prevention and treatment as well as the prevention of coronary heart disease should be emphasized. The therapeutic potential of flavones makes these compounds valuable targets for drug design, including recombinant DNA approaches. The biosynthesis of flavones in plants was found to be catalyzed by two completely different flavone synthase proteins (FNS), a unique feature within the flavonoids. The first, FNS I, a soluble dioxygenase, was only described for members of the Apiaceae family so far. The second, FNS II, a membrane bound cytochrome P450 enzyme, has been found in all other flavone accumulating tissues. This phenomenon is particularly of interest from the evolutionary point of view concerning the flavone biosynthesis and functions in plants. Recently, FNS I and FNS II genes have been cloned from a number of plant species. This now enables detailed biochemical and molecular characterizations and also the development of direct metabolic engineering strategies for modifications of flavone synthesis in plants to improve their nutritional and/or biopharmaceutical value.
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                Author and article information

                Contributors
                m.abdollahi@basu.ac.ir
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                1 June 2020
                1 June 2020
                2020
                : 10
                : 8884
                Affiliations
                [1 ]ISNI 0000 0000 9828 9578, GRID grid.411807.b, Department of Agronomy and Plant Breeding, , Faculty of Agriculture, Bu-Ali Sina University, ; Hamedan, Iran
                [2 ]ISNI 0000 0000 9828 9578, GRID grid.411807.b, Department of Plant Biotechnology, , Faculty of Agriculture, Bu-Ali Sina University, ; Hamedan, Iran
                [3 ]ISNI 0000 0004 0611 9280, GRID grid.411950.8, Medicinal Plants and Natural Products Research Center, Hamadan University of Medical Sciences, ; Hamadan, Iran
                [4 ]ISNI 0000 0004 0611 9280, GRID grid.411950.8, Department of Pharmacognosy and Pharmaceutical Biotechnology, , School of Pharmacy, Hamadan University of Medical Sciences, ; Hamadan, Iran
                [5 ]ISNI 0000 0000 8578 2742, GRID grid.6341.0, Department of Plant Breeding, , Swedish University of Agricultural Sciences, ; Växtskyddsvägen 1, SE-230 53 Alnarp, Sweden
                [6 ]ISNI 0000000121581746, GRID grid.5037.1, KTH Royal Institute of Technology, School of Chemical Science and Engineering, Fibre and Polymer Technology, ; SE-100 44 Stockholm, Sweden
                Article
                65815
                10.1038/s41598-020-65815-2
                7264309
                32483287
                384c4108-7183-420c-8f5c-dbbc45d92720
                © The Author(s) 2020

                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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 29 October 2019
                : 7 May 2020
                Categories
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                © The Author(s) 2020

                Uncategorized
                biotechnology,molecular biology,plant sciences
                Uncategorized
                biotechnology, molecular biology, plant sciences

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