Modulation of Dimorphandra wilsonii Rizz. seed germination through H2O2 production in response to Zn interference of the mitochondrial electron transport chain

Environmental and Experimental Botany

Volumn 128, Issue , 2016, Pages 51-58

  Gomes, Marcelo Pedrosa ^a   da Silva Cruz, Fernanda Vieira ^a   Borges, Felipe Viégas ^a   Fonseca, Márcia Bacelar ^b   Garcia, Queila Souza ^a  

^a FEDERAL UNIVERSITY OF MINAS GERAIS   (Brazil)

^b Fundacao Zoo Botanica de Belo Horizonte   (Brazil)

Author keywords

Embryo; Mitochondria; Oxidative stress; Reactive oxygen species; Trace element

Indexed keywords

DOSE-RESPONSE RELATIONSHIP; ELECTRON; EMBRYONIC DEVELOPMENT; ENZYME ACTIVITY; GERMINATION; HYDROGEN PEROXIDE; INHIBITOR; LEGUME; MEMBRANE; MITOCHONDRION; OXYGEN; PLASMA; SECONDARY METABOLITE; SEED; TOXICITY; TRACE ELEMENT; ZINC;

BRAZIL;

DIMORPHANDRA;

EID: 84962798415     PISSN: 00988472     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.envexpbot.2016.04.003     Document Type: Article

References (46)

1. Aebi H. Catalase in vitro. Methods Enzymol. 1984, 105:121-126.
2. Apel K., Hirt H. Reactive oxygen species: metabolism oxidative stress, and signal transduction. Annu. Rev. Plant Biol. 2004, 55:373-399.
3. Bailly C., El-Maarouf-Bouteau H., Corbineau F. From intracellular signaling networks to cell death: the dual role of reactive oxygen species in seed physiology. C. R. Biol. 2008, 331:806-814. 10.1016/j.crvi.2008.07.022.
4. Birch-Machin M.A., Howell N., Turnbull D.M. Identification of mitochondrial dysfunction at coupling site II. Methods in Toxicology 1993, 324-328. Academic Press, San Diego. H. Lashand, D.P. Jones (Eds.).
5. Birch-Machin M.A., Jackson S., Kler R.S., Turnbull D.M. Study of skeletal muscle mitochondrial dysfunction. Methods in Toxicology 1993, 58-59. Academic Press, San Diego. L.H. Lashand, D.P. Jones (Eds.).
6. Duarte D.M., Gomes M.P., Barreto L.C., Matheus M.T., Garcia Q.S. Toxic trace elements effects on seed germination of four Brazilian Savanna tree species. Seed Sci. Technol. 2012, 40:425-432.
7. El-Maarouf-Bouteau H., Bailly C. Oxidative signaling in seed germination and dormancy. Plant Signal. Behav. 2008, 175-182.
8. El-Maarouf-Bouteau H., Sajjad Y., Bazin J., Langlade N., Cristescu S.M., Balzergue S., Baudouin E., Bailly C. Reactive oxygen species, abscisic acid and ethylene interact to regulate sunflower seed germination. Plant. Cell Environ. 2015, 38:364-374. 10.1111/pce.12371.
9. Estornell E., Fato R., Palloti F., Lenaz G. Assay conditions for the mitochondrial NADH:coenzyme Q oxidoreductase. FEBS Lett. 1999, 332:127-131.
10. Fernandes F.M., Rego J.O. Dimorphandra wilsonii Rizzini (Fabaceae): distribution, habitat and conservation status. Acta Bot. Bras. 2014, 28:434-444. 10.1590/0102-33062014abb3409.
11. Foyer C.H., Noctor G. Ascorbate and glutathione: the heart of the redox hub. Plant Physiol. 2011, 155:2-18. 10.1104/pp.110.167569.
12. Gill S.S., Tuteja N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol. Biochem. 2010, 48:909-930. 10.1016/j.plaphy.2010.08.016.
13. Gomes M.P., Garcia Q.S. Reactive oxygen species and seed germination. Biologia (Bratisl.) 2013, 68:351-357. 10.2478/s11756-013-0161-y.
14. Gomes M.P., Cristina T., Lanza L., Sá D. Utilization of Willow (Salix humboldtiana Willd.) as a species for phytorremediation of zinc industry waste. Sci. For. 2011, 39:117-123.
15. Gomes M.P., Carneiro M.M.L.C., Nogueira C.O.G., Soares A.M., Garcia Q.S. The system modulating ROS content in germinating seeds of two Brazilian savanna tree species exposed to As and Zn. Acta Physiol. Plant. 2013, 35:1011-1022. 10.1007/s11738-012-1140-6.
16. Grant J.J., Loake G.J. Role of reactive oxygen intermediates and cognate redox signaling in disease resistance. Plant Physiol. 2000, 124:21-30.
17. Hodges D.M., Delong J.M., Forney C.F., Prange R.K. Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta 1999, 1:604-611.
18. IUCN, 2015. The IUCN Red List of Threatened Species [WWW Document]. URL (accessed 31.12.15). http://www.iucnredlist.org.
19. Jaleel C.A., Riadh K., Gopi R., Manivannan P., Ines J., Al-Juburi H.J., Chang-Xing Z., Hong-Bo S., Panneerselvam R. Antioxidant defense responses: physiological plasticity in higher plants under abiotic constraints. Acta Physiol. Plant. 2009, 31:427-436.
20. Kalemba E.M., Jan S., Ewelina R. The role of oxidative stress in determining the level of viability of black poplar (Populus nigra) seeds stored at different temperatures. Funct. Plant Biol. 2015, 42:630-642.
21. 2+ ions on mitochondrial electron transport. Arch. Biol. 1974, 165:121-125.
22. 2+ ions. FEBS J. 1972, 20:229-232.
23. Kranner I., Colville L. Metals and seeds: biochemical and molecular implications and their significance for seed germination. Environ. Exp. Bot. 2011, 72:93-105. 10.1016/j.envexpbot.2010.05.005.
24. Kumar S.P.J., Prasad S.R., Banerjee R., Thammineni C. Seed birth to death: dual functions of reactive oxygen species in seed physiology. Ann. Bot. 2015, 10.1093/aob/mcv098.
25. Li N., Ragheb K., Lawler G., Sturgis J., Rajwa B., Melendez J.A., Robinson J.P. Mitochondrial complex I inhibitor rotenone induces apoptosis through enhancing mitochondrial reactive oxygen species production. J. Biol. Chem. 2003, 278:8516-8525. 10.1074/jbc.M210432200.
26. Li C.X., Feng S.L., Shao Y., Jiang L.N., Lu X.Y., Hou X.L. Effects of arsenic on seed germination and physiological activities of wheat seedlings. J. Environ. Sci. 2007, 19:725-732.
27. Liu W., Au D.W.T., Anderson D.M., Lam P.K.S., Wu R.S.S. Effects of nutrients, salinity, pH and light: dark cycle on the production of reactive oxygen species in the alga Chattonella marina. J. Exp. Mar. Biol. Ecol. 2007, 346:76-86. 10.1016/j.jembe.2007.03.007.
28. Marques J., Schulze D., Curi N., Mertzman S. Trace element geochemistry in Brazilian Cerrado soils. Geoderma 2004, 121:31-43.
29. Mohanty N., Vass I., Demeter S. Impairment of photosystem 2 activity at the level of secondary quinone electron acceptor in chloroplasts treated with cobalt, nickel and zinc ions. Physiol. Plant. 1989, 76:386-390. 10.1111/j.1399-3054.1989.tb06208.x.
30. Moreno-Sánchez R., Hernández-Esquivel L., Rivero-Segura N.A., Marín-Hernández A., Neuzil J., Ralph S.J., Rodríguez-Enríquez S. Reactive oxygen species are generated by the respiratory complex II-evidence for lack of contribution of the reverse electron flow in complex I. FEBS J. 2013, 280:927-938. 10.1111/febs.12086.
31. Nakano Y., Asada K. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol. 1981, 22:867-880.
32. Noctor G., De Paepe R., Foyer C.H. Mitochondrial redox biology and homeostasis in plants. Trends Plant Sci. 2007, 12:125-134.
33. Oracz K., El-Maarouf-Bouteau H., Kranner I., Bogatek R., Corbineau F., Bailly C. The mechanisms involved in seed dormancy alleviation by hydrogen cyanide unravel the role of reactive oxygen species as key factors of cellular signaling during germination. Plant Physiol. 2009, 150:494-505. 10.1104/pp.109.138107.
34. Pergo E.M., Ishii-Iwamoto E.L. Changes in energy metabolism and antioxidant defense systems during seed germination of the weed species Ipomoea triloba L. and the responses to allelochemicals. J. Chem. Ecol. 2011, 37:500-513.
35. Polidoros A.N., Scandalios J.G. Role of hydrogen peroxide and different classes of antioxidants in the regulation of catalase and glutathione S-transferase gene expression in maize (Zea mays L.). Plant Physiol. 1999, 106:112-120.
36. Pumphrey A.M., Redfearn E.R. A method for determining the concentration of ubiquinone in mitochondrial preparations. Biochem. J. 1960, 76:61-64.
37. Quinlan C.L., Orr A.L., Perevoshchikova I.V., Treberg J.R., Ackrell B.A., Brand M.D. Mitochondrial Complex II can generate reactive oxygen species at high rates in both the forward and reverse reactions. J. Biol. Chem. 2012, 287:27255-27264. 10.1074/jbc.M112.374629.
38. Rampelotto P.H., de Siqueira Ferreira A., Barboza A.D.M., Roesch L.F.W. Changes in diversity abundance, and structure of soil bacterial communities in Brazilian Savanna under different land use systems. Microb. Ecol. 2013, 66:593-607. 10.1007/s00248-013-0235-y.
39. Rasheed A., Hameed A., Khan M.A., Gul B. Variation in temperature and light but not salinity invokes antioxidant enzyme activities in germinating seeds of Salsola drummondii. Plant Biosyst. 2015, 1-11. (ahead of print). 10.1080/11263504.2014.1001463.
40. Ratter J.A., Ribeiro J.F., Bridgewater S. The Brazilian Cerrado vegetation and threats to its biodiversity. Ann. Bot. 1997, 80:223-230.
41. Rizzini C.T. Espécies novas de árvores do planalto central brasileiro. Acad. Bras. Sci. 1969, 41:239-244.
42. Schopfer P., Liszkay A., Bechtold M., Frahry G., Wagner A. Evidence that hydroxyl radicals mediate auxin-induced extension growth. Planta 2002, 214:821-828. 10.1007/s00425-001-0699-8.
43. Skulachev V.P., Chistyakov V.V., Jasaitis A.A., Smirnova E.G. Inhibition of the respiratory chain by zinc ions. Biochem. Biophys. Res. Commun. 1967, 26.
44. Velikova V., Yordanov I., Edreva A. Oxidative stress and some antioxidant systems in acid rain-treated bean plants: protective role of exogenous polyamines. Plant Sci. 2000, 151:59-66.
45. Vendrame P.R.S., Brito O.R., Quantin C., Becquer T. Disponibilidade de cobre, ferro, manganês e zinco em solos sob pastagens na Região do Cerrado. Pesqui. Agropecu. Bras. 2007, 42:859-864. 10.1590/S0100-204X2007000600013.
46. Weber H., Chételat A., Reymond P., Farmer E.E. Selective and powerful stress gene expression in Arabidopsis in response to malondialdehyde. Plant J. 2004, 37:877-888. 10.1111/j.1365-313X.2003.02013.x.