8
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Analysis of Flavonoid Metabolites in Buckwheat Leaves Using UPLC-ESI-MS/MS

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Flavonoids from plants are particularly important in our diet. Buckwheat is a special crop that is rich in flavonoids. In this study, four important buckwheat varieties, including one tartary buckwheat and three common buckwheat varieties, were selected as experimental materials. The total flavonoid content of leaves from red-flowered common buckwheat was the highest, followed by tartary buckwheat leaves. A total of 182 flavonoid metabolites (including 53 flavone, 37 flavonol, 32 flavone C-glycosides, 24 flavanone, 18 anthocyanins, 7 isoflavone, 6 flavonolignan, and 5 proanthocyanidins) were identified based on Ultra Performance Liquid Chromatography–Electrospray Ionization–Tandem Mass Spectrometry (UPLC-ESI-MS/MS) system. Through clustering analysis, principal component analysis (PCA), and orthogonal signal correction and partial least squares-discriminant analysis (OPLS-DA), different samples were clearly separated. Considerable differences were observed in the flavonoid metabolites between tartary buckwheat leaves and common buckwheat leaves, and both displayed unique metabolites with important biological functions. This study provides new insights into the differences of flavonoid metabolites between tartary buckwheat and common buckwheat leaves and provides theoretical basis for the sufficient utilization of buckwheat.

          Related collections

          Most cited references48

          • Record: found
          • Abstract: found
          • Article: not found

          The effects of plant flavonoids on mammalian cells: implications for inflammation, heart disease, and cancer.

          Flavonoids are nearly ubiquitous in plants and are recognized as the pigments responsible for the colors of leaves, especially in autumn. They are rich in seeds, citrus fruits, olive oil, tea, and red wine. They are low molecular weight compounds composed of a three-ring structure with various substitutions. This basic structure is shared by tocopherols (vitamin E). Flavonoids can be subdivided according to the presence of an oxy group at position 4, a double bond between carbon atoms 2 and 3, or a hydroxyl group in position 3 of the C (middle) ring. These characteristics appear to also be required for best activity, especially antioxidant and antiproliferative, in the systems studied. The particular hydroxylation pattern of the B ring of the flavonoles increases their activities, especially in inhibition of mast cell secretion. Certain plants and spices containing flavonoids have been used for thousands of years in traditional Eastern medicine. In spite of the voluminous literature available, however, Western medicine has not yet used flavonoids therapeutically, even though their safety record is exceptional. Suggestions are made where such possibilities may be worth pursuing.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Signature-Discovery Approach for Sample Matching of a Nerve-Agent Precursor Using Liquid Chromatography−Mass Spectrometry, XCMS, and Chemometrics

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Identification and expression of isoflavone synthase, the key enzyme for biosynthesis of isoflavones in legumes.

              Isoflavones have drawn much attention because of their benefits to human health. These compounds, which are produced almost exclusively in legumes, have natural roles in plant defense and root nodulation. Isoflavone synthase catalyzes the first committed step of isoflavone biosynthesis, a branch of the phenylpropanoid pathway. To identify the gene encoding this enzyme, we used a yeast expression assay to screen soybean ESTs encoding cytochrome P450 proteins. We identified two soybean genes encoding isoflavone synthase, and used them to isolate homologous genes from other leguminous species including red clover, white clover, hairy vetch, mung bean, alfalfa, lentil, snow pea, and lupine, as well as from the nonleguminous sugarbeet. We expressed soybean isoflavone synthase in Arabidopsis thaliana, which led to production of the isoflavone genistein in this nonlegume plant. Identification of the isoflavone synthase gene should allow manipulation of the phenylpropanoid pathway for agronomic and nutritional purposes.
                Bookmark

                Author and article information

                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                03 April 2019
                April 2019
                : 24
                : 7
                : 1310
                Affiliations
                College of Agronomy, Northwest A & F University, State Key Laboratory of Crop Stress Biology for Arid Areas, Yangling, Xianyang 712000, China; lijing1993@ 123456nwafu.edu.cn (J.L.); yangpu@ 123456nwsuaf.edu.cn (P.Y.); 2016060037@ 123456nwsuaf.edu.cn (Q.Y.); gxw199308@ 123456163.com (X.G.); mhcnzb@ 123456163.com (H.M.); dangke4718@ 123456163.com (K.D.); ghchen2017@ 123456163.com (G.C.); gao2123@ 123456nwsuaf.edu.cn (X.G.)
                Author notes
                [* ]Correspondence: fengbaili@ 123456nwsuaf.edu.cn ; Tel.: +86 029 8708 2889
                Author information
                https://orcid.org/0000-0003-0743-7291
                https://orcid.org/0000-0002-8213-7478
                Article
                molecules-24-01310
                10.3390/molecules24071310
                6479795
                30987158
                9605a110-7d93-4661-ac1d-aced69d10253
                © 2019 by the authors.

                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 ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 19 March 2019
                : 01 April 2019
                Categories
                Article

                tartary buckwheat,common buckwheat,flavonoid metabolites,pca,opls-da,uplc-esi-ms/ms

                Comments

                Comment on this article