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Published January 31, 2015 | Version v1
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Composition of polyphenol and polyamide compounds in common ragweed (Ambrosia artemisiifolia L.) pollen and sub-pollen particles

Authors/Creators

  • 1. Center of Excellence in Molecular Food Sciences, University of Belgrade - Faculty of Chemistry, Belgrade, Serbia

Description

Mihajlovic, Luka, Radosavljevic, Jelena, Burazer, Lidija, Smiljanic, Katarina, Velickovic, Tanja Cirkovic (2015): Composition of polyphenol and polyamide compounds in common ragweed (Ambrosia artemisiifolia L.) pollen and sub-pollen particles. Phytochemistry 109: 125-132, DOI: 10.1016/j.phytochem.2014.10.022, URL: http://dx.doi.org/10.1016/j.phytochem.2014.10.022

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URL
https://www.checklistbank.org/dataset/285456
LSID
urn:lsid:plazi.org:pub:CC7CFFC10E6942029A62FFE0FFF6FFAC
URL
http://publication.plazi.org/id/CC7CFFC10E6942029A62FFE0FFF6FFAC

Cites
Publication: 10.1002/pca.2515 (DOI)
Has part
Taxonomic treatment: 10.5281/zenodo.10522626 (DOI)
Taxonomic treatment: http://treatment.plazi.org/id/304587B90E6842069A35FD52FF18F907 (URL)
Figure: 10.5281/zenodo.10488105 (DOI)
Dataset: 10.5281/zenodo.15155043 (DOI)
Dataset: 10.5281/zenodo.15155045 (DOI)
Figure: 10.5281/zenodo.10488107 (DOI)
Figure: 10.5281/zenodo.10488109 (DOI)
Figure: 10.5281/zenodo.10488111 (DOI)
Figure: 10.5281/zenodo.10488113 (DOI)
Figure: 10.5281/zenodo.10488115 (DOI)
Is source of
Dataset: https://www.gbif.org/dataset/98b8e0f4-8ab4-4c6d-bede-5c94d2ea324b (URL)

References

  • Bacsi, A., Choudhury, B.K., Dharajiya, N., Sur, S., Boldogh, I., 2006. Sub-pollen particles: carriers of allergenic proteins and oxidases. J. Allergy Clin. Immunol. 118, 844-850.
  • Bassard, J.-E., Ullmann, P., Bernier, F., Werck-Reichhart, D., 2010. Phenolamides: bridging polyamines to the phenolic metabolism. Phytochemistry 71, 1808- 1824.
  • Bueb, J.L., Mousli, M., Landry, Y., 1991. Molecular basis for cellular effects of naturally occurring polyamines. Agents Actions 33, 84-87.
  • Chun, O.K., Kim, D.-O., Lee, C.Y., 2003. Superoxide radical scavenging activity of the major polyphenols in fresh plums. J. Agric. Food Chem. 51, 8067-8072.
  • Fabre, N., Rustan, I., de Hoffmann, E., Quetin-Leclercq, J., 2001. Determination of flavone, flavonol, and flavanone aglycones by negative ion liquid chromatography electrospray ion trap mass spectrometry. J. Am. Soc. Mass Spectrom. 12, 707-715.
  • Falasca, G., Franceschetti, M., Bagni, N., Altamura, M.M., Biasi, R., 2010. Polyamine biosynthesis and control of the development of functional pollen in kiwifruit. Plant Physiol. Biochem. 48, 565-573.
  • Ferioli, M.E., Pirona, L., Pinotti, O., 2000. Prolactin and polyamine catabolism: specific effect on polyamine oxidase activity in rat thymus. Mol. Cell. Endocrinol. 165, 51-56.
  • Ferreres, F., Oliveira, A.P., Gil-Izquierdo, A., Valentao, P., Andrade, P.B., 2014. Piper betle leaves: profiling phenolic compounds by HPLC/DAD-ESI/MS and anticholinesterase activity. Phytochem. Anal.. http://dx.doi.org/10.1002/pca.2515.
  • Gonzalez Romano, M.L., Gallego, M.T., Berrens, L., 1996. Extraordinary stability of IgE-binding Parietaria pollen allergens in relation to chemically bound flavonoids. Mol. Immunol. 33, 1287-1293.
  • Grote, M., Vrtala, S., Niederberger, V., Valenta, R., Reichelt, R., 2000. Expulsion of allergen-containing materials from hydrated rye grass (Lolium perenne) pollen revealed by using immunogold field emission scanning and transmission electron microscopy. J. Allergy Clin. Immunol. 105, 1140-1145.
  • Ha, H.C., Yager, J.D., Woster, P.A., Casero Jr., R.A., 1998. Structural specificity of polyamines and polyamine analogues in the protection of DNA from strand breaks induced by reactive oxygen species. Biochem. Biophys. Res. Commun. 244, 298-303.
  • Hendrich, A.B., 2006. Flavonoid -membrane interactions: possible consequences for biological effects of some polyphenolic compounds. Acta Pharmacol. Sin. 27, 27-40.
  • Hoet, P.H., Nemery, B., 2000. Polyamines in the lung: polyamine uptake and polyamine-linked pathological or toxicological conditions. Am. J. Physiol. Lung Cell. Mol. Physiol. 278, L417-L433.
  • Hvattum, E., Ekeberg, D., 2003. Study of the collision-induced radical cleavage of flavonoid glycosides using negative electrospray ionization tandem quadrupole mass spectrometry. J. Mass Spectrom. 38, 43-49.
  • Igarashi, K., Kashiwagi, K., 2010. Modulation of cellular function by polyamines. Int. J. Biochem. Cell Biol. 42, 39-51.
  • Kanter, U., Heller, W., Durner, J., Winkler, J.B., Engel, M., Behrendt, H., Holzinger, A., Braun, P., Hauser, M., Ferreira, F., Mayer, K., Pfeifer, M., Ernst, D., 2013. Molecular and immunological characterization of ragweed (Ambrosia artemisiifolia L.) pollen after exposure of the plants to elevated ozone over a whole growing season. PLoS ONE 8, e61518.
  • Kikuzaki, H., Hisamoto, M., Hirose, K., Akiyama, K., Taniguchi, H., 2002. Antioxidant properties of ferulic acid and its related compounds. J. Agric. Food Chem. 50, 2161-2168.
  • Kite, G.C., Larsson, S., Veitch, N.C., Porter, E.A., Ding, N., Simmonds, M.S., 2013. Acyl spermidines in inflorescence extracts of elder (Sambucus nigra L., Adoxaceae) and elderflower drinks. J. Agric. Food Chem. 61, 3501-3508.
  • Koistinen, K.M., Soininen, P., Venalainen, T.A., Hayrinen, J., Laatikainen, R., Perakyla, M., Tervahauta, A.I., Karenlampi, S.O., 2005. Birch PR-10c interacts with several biologically important ligands. Phytochemistry 66, 2524-2533.
  • Maksimovic, Z., 2008. In vitro antioxidant activity of ragweed (Ambrosia artemisiifolia L., Asteraceae) herb. Ind. Crops Prod. 28, 356-360.
  • March, R.E., Lewars, E.G., Stadey, C.J., Miao, X.-S., Zhao, X., Metcalfe, C.D., 2006. A comparison of flavonoid glycosides by electrospray tandem mass spectrometry. Int. J. Mass Spectrom. 248, 61-85.
  • Narvaez-Cuenca, C.E., Vincken, J.P., Zheng, C., Gruppen, H., 2013. Diversity of (dihydro) hydroxycinnamic acid conjugates in Colombian potato tubers. Food Chem. 139, 1087-1097.
  • Negri, G., Teixeira, E.W., Alves, M.L., Moreti, A.C., Otsuk, I.P., Borguini, R.G., Salatino, A., 2011. Hydroxycinnamic acid amide derivatives, phenolic compounds and antioxidant activities of extracts of pollen samples from Southeast Brazil. J. Agric. Food Chem. 59, 5516-5522.
  • Ognjenovic, J., Stojadinovic, M., Milcic, M., Apostolovic, D., Vesic, J., Stambolic, I., Atanaskovic-Markovic, M., Simonovic, M., Cirkovic Velickovic, T., 2014. Interactions of epigallo-catechin 3-gallate and ovalbumin, the major allergen of egg white. Food Chem. 164, 36-43.
  • Penarrieta, J.M., Alvarado, J.A., Akesson, B., Bergenstahl, B., 2008. Total antioxidant capacity and content of flavonoids and other phenolic compounds in canihua (Chenopodium pallidicaule): an Andean pseudocereal. Mol. Nutr. Food Res. 52, 708-717.
  • Quirantes-Pine, R., Lozano-Sanchez, J., Herrero, M., Ibanez, E., Segura-Carretero, A., Fernandez-Gutierrez, A., 2013. HPLC -ESI -QTOF -MS as a powerful analytical tool for characterising phenolic compounds in olive-leaf extracts. Phytochem. Anal. 24, 213-223.
  • Re, R., Pellegrini, N., Proteggente, A., Pannala, A., Yang, M., Rice-Evans, C., 1999. Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radic. Biol. Med. 26, 1231-1237.
  • Sobolev, V.S., Sy, A.A., Gloer, J.B., 2008. Spermidine and flavonoid conjugates from peanut (Arachis hypogaea) flowers. J. Agric. Food Chem. 56, 2960-2969.
  • Stojadinovic, M., Radosavljevic, J., Ognjenovic, J., Vesic, J., Prodic, I., Stanic-Vucinic, D., Cirkovic Velickovic, T., 2013. Binding affinity between dietary polyphenols and beta-lactoglobulin negatively correlates with the protein susceptibility to digestion and total antioxidant activity of complexes formed. Food Chem. 136, 1263-1271.
  • Tantoush, Z., Stanic, D., Stojadinovic, M., Ognjenovic, J., Mihajlovic, L., AtanaskovicMarkovic, M., Cirkovic Velickovic, T., 2011. Digestibility and allergenicity of β-lactoglobulin following laccase-mediated cross-linking in the presence of sour cherry phenolics. Food Chem. 125, 84-91.
  • Vukics, V., Guttman, A., 2010. Structural characterization of flavonoid glycosides by multi-stage mass spectrometry. Mass Spectrom. Rev. 29, 1-16.
  • Wopfner, N., Jahn-Schmid, B., Schmidt, G., Christ, T., Hubinger, G., Briza, P., Radauer, C., Bohle, B., Vogel, L., Ebner, C., Asero, R., Ferreira, F., Schwarzenbacher, R., 2009. The alpha and beta subchain of Amb a 1, the major ragweed-pollen allergen show divergent reactivity at the IgE and T-cell level. Mol. Immunol. 46, 2090- 2097.
  • Yoon, M.S., Lee, J.S., Choi, B.M., Jeong, Y.I., Lee, C.M., Park, J.H., Moon, Y., Sung, S.C., Lee, S.K., Chang, Y.H., Chung, H.Y., Park, Y.M., 2006. Apigenin inhibits immunostimulatory function of dendritic cells: implication of immunotherapeutic adjuvant. Mol. Pharmacol. 70, 1033-1044.