Mass Spectrometry of flavonoid vicenin-2, based sunlight barriers in Lychnophora species

Scientific Reports

Volumn 4, Issue , 2014, Pages

  Silva, Denise Brentan ^a   Turatti, Izabel Cristina Casanova ^a   Gouveia, Dayana Rubio ^a   Ernst, Madeleine ^a   Teixeira, Simone Pádua ^a   Lopes, Norberto Peporine ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

APIGENIN; APIGENIN-6,8-DI-C-GLYCOPYRANOSIDE; FLAVONOID; GLUCOSIDE; PLANT EXTRACT;

ASTERACEAE; CHEMISTRY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; PLANT LEAF; SUNLIGHT;

APIGENIN; ASTERACEAE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; FLAVONOIDS; GLUCOSIDES; MASS SPECTROMETRY; PLANT EXTRACTS; PLANT LEAVES; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION; SUNLIGHT;

EID: 84896791980     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep04309     Document Type: Article

References (33)

1. Myers, N., Mittermeier, R. A., Mittermeier, C. G., Fonseca, G. A. B. and Kent, J. Biodiversity hotspots for conservation priorities. Nature 403, 853-858 (2000).
2. Joly, C. A. et al. Biodiversity conservation research, training, and policy in Sa?o Paulo. Science 328, 1358-1359 (2010).
3. Forzza, R. C. et al. [As Angiospermas do Brasil] Catalogo de Fungos e Plantas do Brasil [Forzza, R. C. et al. (ed.)] [78-89] (Instituto de pesquisas Jardim Botânico do Rio de Janeiro, Rio de Janeiro, 2010).
4. Keles, L. C. et al. Lychnophorinae (Asteraceae): A Survey of its chemical constituents and biological activities. Quim. Nova 33, 2245-2260 (2010).
5. Simon, M. F. et al. Recent assembly of the Cerrado, a neotropical plant diversity hotspot, by in situ evolution of adaptations to fire. PNAS 106, 20359-20364 (2009).
6. Semir, J., Monge, M., Rezende, A. R. and Lopes, N. P. [Qui'mica de Lychnophora] As Arnicas Endêmicas das Serras do Brasil - Uma Visao Sobre a Biologia e Quimica das Especies de Lychnophora (Asteraceae) [Souza, G. H. B. and Lopes, N. P. (ed.)] [165-189] (UFOP, Ouro Preto, 2012).
7. Gouvea, D. R., Meloni, F., Ribeiro, A. B. B., Lopes, J. L. and Lopes, N. P. A new HPLC-DAD-MS/MS method for the simultaneous determination of major compounds in the crude extract of Lychnophora salicifolia Mart. (Brazilian arnica?o) leaves: application to chemical variability evaluation. Anal. Chim. Acta 748, 28-36 (2012).
8. Gobbo-Neto, L. et al. Evaluation of the Anti-inflammatory and antioxidant activities of di-C-glucosylflavones from Lychnophora ericoides (Asteraceae). Planta Med. 71, 3-6 (2005).
9. Gobbo-Neto, L. et al. Differential metabolic and biological profiles of Lychnophora ericoides Mart. (Asteraceae) from different localities in the Brazilian campos rupestres J. Braz. Chem. Soc. 21, 750-759 (2010).
10. Caprioli, R. M., Farme, T. B. and Gile, J. Molecular imaging of biological samples: Localization of peptides and proteins using MALDI-TOF MS. Anal. Chem. 69, 4751-4760 (1997).
11. Schwamborn, K. and Caprioli, R. M. Molecular imaging by mass spectrometry - looking beyond classical histology. Nat. Rev. Cancer 10, 639-646 (2010).
12. Lee, Y. J., Perdian, D. C., Song, Z., Yeung, E. S. and Nikolau, B. J. Use of mass spectrometry for imaging metabolites in plants. Plant J. 70, 81-95 (2012).
13. Shroff, R., Vergara, F., Muck, A., Svatos, A. and Gershenzon, J. Nonuniform distribution of glucosinolates in Arabidopsis thaliana leaves has important consequences for plant defense. PNAS 105, 6196-6201 (2008).
14. Holscher, D. et al. Matrix-free UV-laser desorption/ionization (LDI) mass spectrometric imaging at the single-cell level: distribution of secondary metabolites of Arabidopsis thaliana and Hypericum species. Plant J. 60, 907-918 (2009).
15. Lopes, A. A. et al. A biosynthetic pathway of sesquiterpene lactones in Smallanthus sonchifolius and their localization in leaf tissues by MALDI imaging. Chem. Commun. 49, 9989-9991 (2013).
16. Gobbo-Neto, L. and Lopes, N. P. Online identification of chlorogenic acids, sesquiterpene lactones, and flavonoids in the Brazilian arnica Lychnophora ericoides Mart. (Asteraceae) leaves by HPLC-DAD-MS and HPLC-DAD-MS/MS and a validated HPLC-DAD method for their simultaneous analysis. J. Agric. Food Chem. 56, 1193-1204 (2008).
17. Gobbo-Neto, L., Gates, P. J. and Lopes, N. P. Negative ion 'chip-based' nanospray tandem mass spectrometry for the analysis of flavonoids in glandular trichomes of Lychnophora ericoides Mart. (Asteraceae) Rapid Commun. Mass Spectrom. 22, 3802-3808 (2008).
18. Moraes, S. L., Grego'rio, L. E., Tomaz, J. C. and Lopes, N. P. Rapid screening and identification of polar constituents from Brazilian Arnica Lychnophora sp. by LCUV/ DAD-ESI-MS and LC-UV/DAD-ESI-MS/MS analysis. Chromatographia 69, S157-S165 (2009).
19. Veitch, N. C. and Grayer, R. J. Flavonoids and their glycosides, including anthocyanins. Nat. Prod. Rep. 28, 1626-1695 (2011).
20. Taylor, L. P. and Grotewold, E. Flavonoids as developmental regulators. Curr. Opin. Plant Biol. 8, 317-323 (2005).
21. Domon, B. and Costello, C. A systematic nomenclature for carbohydrate fragmentations in FAB-MS/MS spectra of glycoconjugates. Glycoconj. J. 5, 397-409 (1988).
22. Waridel, P. et al. Evaluation of quadrupole time-of-flight tandem mass spectrometry and ion-trap multiple-stage mass spectrometry for the differentiation of C-glycosidic flavonoid isomers. J. Chromatog. A 926, 29-41 (2001).
23. Tevini, M. and Teramura, A. H. UV-B effects on terrestrial plants. J. Photochem. Photobiol. 50, 479-487 (1989).
24. Treutter, D. Significance of flavonoids in plant resistance and enhancement of their biosynthesis. Plant Biol. 7, 581-591 (2005).
25. Schnitzler, P. P. et al. Tissue localization of UV-B screening pigments and of chalcone synthase mRNA in needles of Scots pine seedlings. New Phytol. 132, 247-258 (1996).
26. Strid, A., Chow, W. S. and Anderson, J. M. UV-B damage and protection at the molecular level in plants. Photosynth. Res. 39, 475-489 (1994).
27. Jenkins, G. I. Signal transduction in responses to UV-B radiation. Annu. Rev. Plant Biol. 60, 407-431 (2009).
28. Stratmann, J. Ultraviolet-B radiation co-opts defense signaling pathways. Trends Plant Sci. 8, 526-533 (2003).
29. Treutter, D. Significance of flavonoids in plant resistance: a review. Environ. Chem. Lett. 4, 147-157 (2006).
30. Beckman, C. B. Phenolic-storing cells: keys to programmed cell death and periderm formation in wilt disease resistance and in general defense responses in plants? Physiol. Mol. Plant Pathol. 57, 101-110 (2000).
31. Peer, W. A. et al. Flavonoid accumulation patterns of transparent testa mutants of Arabidopsis. Plant Physiol. 126, 536-548 (2001).
32. Yin, R. et al. Kaempferol 3-O-rhamnoside-7-O-rhamnoside is an endogenous flavonol inhibitor of polar auxin transport in Arabidopsis shoots. New Phytol. 201, 466-475 (2014).
33. Hutzler, P. et al. Tissue localization of phenolic compounds in plants by confocal laser scanning microscopy. J. Exp. Bot. 49, 953-965 (1998).