Hydrogen peroxide content and vanadium-dependent haloperoxidase activity in thalli of six species of Fucales (Phaeophyceae)

REFERENCES

• Almeida M.G., Humanes M., Melo R., Silva J.A., Fraústo da Silva J.J.R. & Wever R. 2000. Purification and characterization of vanadium haloperoxidases from the brown alga Pelvetia canaliculata. Phytochemistry 54: 5–11.
   Web of Science ®Google Scholar
• Almeida M.G., Filipe S., Humanes M., Maia M.F., Melo R., Severino N., da Silva J.A.L., Fraústo da Silva J.J.R. & Wever R. 2001. Vanadium haloperoxidases from brown algae of the Laminariaceae family. Phytochemistry 57: 633–642.
   PubMed Web of Science ®Google Scholar
• Apel K. & Hirt H. 2004. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annual Review of Plant Biology 55: 373–399.
   PubMed Web of Science ®Google Scholar
• Berglin M., Delage L., Potin P., Vilter H. & Elwing H. 2004. Enzymatic cross-linking of a phenolic polymer extracted from the marine alga Fucus serratus. Biomacromolecules 5: 2376–2383.
   PubMed Web of Science ®Google Scholar
• Bischof K. & Rautenberger R. 2012. Seaweed responses to environmental stress: reactive oxygen and antioxidative strategies. In: Seaweed biology (Ed. by C. Wiencke & K. Bischof), pp. 109–132. Springer-Verlag, Berlin.
   Google Scholar
• Bouarab K., Potin P., Correa J. & Kloareg B. 1999. Sulfated oligosaccharides mediate the interaction between a marine red alga and its green algal pathogenic endophyte. The Plant Cell 11: 1635–1650.
   PubMed Web of Science ®Google Scholar
• Bradford M.M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein–dye binding. Analytical Biochemistry 72: 248–254.
   PubMed Web of Science ®Google Scholar
• Butler A. & Walker J.V. 1993. Marine haloperoxidases. Chemical Reviews 93: 1937–1944.
   Web of Science ®Google Scholar
• Cheeseman J.M. 2006. Hydrogen peroxide concentrations in leaves under natural conditions. Journal of Experimental Botany 57: 2435–2444.
   PubMed Web of Science ®Google Scholar
• Coelho S.M., Taylor A.R., Ryan K.P., Sousa-Pinto I., Brown M.T. & Brownlee C. 2002. Spatiotemporal patterning of reactive oxygen production and Ca2+ wave propagation in Fucus rhizoid cells. The Plant Cell 14: 2369–2381.
   PubMed Web of Science ®Google Scholar
• Colin C., Leblanc C., Wagner E., Delage L., Leize-Wagner E., Van Dorsselaer A., Kloareg B. & Potin P. 2003. The brown algal kelp Laminaria digitata features distinct bromoperoxidase and iodoperoxidase activities. Journal of Biological Chemistry 278: 23545–23552.
   PubMed Web of Science ®Google Scholar
• Colin C., Leblanc C., Michel G., Wagner E., Leize-Wagner E., Van Dorsselaer A. & Potin P. 2005. Vanadium-dependent iodoperoxidases in Laminaria digitata, a novel biochemical function diverging from brown algal bromoperoxidases. Journal of Biological Inorganic Chemistry 10: 156–166.
   PubMed Web of Science ®Google Scholar
• Collén J. & Davison I.R. 1999. Reactive oxygen production and damage in intertidal Fucus spp. (Phaeophyceae). Journal of Phycology 35: 54–61.
   Web of Science ®Google Scholar
• Collén J. & Pedersén M. 1994. A stress-induced oxidative burst in Eucheuma platycladum (Rhodophyta). Physiologia Plantarum 92: 417–422.
   Web of Science ®Google Scholar
• Dring M. 2006. Stress resistance and disease resistance in seaweeds: the role of reactive oxygen metabolism. Advances in Botanical Research 43: 175–207.
   Web of Science ®Google Scholar
• Duroux L. & Welinder K.G. 2003. The peroxidase gene family in plants: a phylogenetic overview. Journal of Molecular Evolution 57: 397–407.
   PubMed Web of Science ®Google Scholar
• Fenical W. 1975. Halogenation in the Rhodophyta – a review. Journal of Phycology 11: 245–259.
   Web of Science ®Google Scholar
• Garbary D.J. & Tarakhovskaya E.R. 2013. Marine macroalgae and associated flowering plants from the Keret Archipelago, White Sea, Russia. Algae 28: 267–280.
   Web of Science ®Google Scholar
• Gay C. & Gebicki J.M. 2000. A critical evaluation of the effect of sorbitol on the ferric-xylenol orange hydroperoxide assay. Analytical Biochemistry 284: 217–220.
   PubMed Web of Science ®Google Scholar
• Hiraga S., Sasaki K., Ito H., Ohashi Y. & Matsui H. 2001. A large family of class III plant peroxidases. Plant and Cell Physiology 42: 462–468.
   PubMed Web of Science ®Google Scholar
• Hoidal J.R. 2001. Reactive oxygen species and cell signaling. American Journal of Respiratory Cell and Molecular Biology 25: 661–663.
   PubMed Web of Science ®Google Scholar
• Itoh N., Izumi Y. & Yam H. 1986. Characterization of nonheme type bromoperoxidase in Corallina pilulifera. Journal of Biological Chemistry 261: 5194–5200.
   PubMed Web of Science ®Google Scholar
• Krenn B.E., Tromp M.G.M. & Wever R. 1989. The brown alga Ascophyllum nodosum contains two different vanadium bromoperoxidases. Journal of Biological Chemistry 264: 19287–19292.
   Web of Science ®Google Scholar
• Laturnus F. 2001. Marine macroalgae in polar regions as natural sources for volatile organohalogens. Environmental Science and Pollution Research 8: 103–108.
   PubMed Web of Science ®Google Scholar
• McDowell R.E., Amsler C.D., Dickinson D.A., McClintock J.B. & Baker B.J. 2014. Reactive oxygen species and the Antarctic macroalgal wound response. Journal of Phycology 50: 71–80.
   Web of Science ®Google Scholar
• Mehrtens G. 1994. Haloperoxidase activities in Arctic macroalgae. Polar Biology 14: 351–354.
   Web of Science ®Google Scholar
• Mondal P., Ray M., Kar M. & Sabat S. Ch. 2008. Molecular identification and properties of a light-insensitive rice catalase-B expressed in E. coli. Biotechnology Letters 30: 563–568.
   Web of Science ®Google Scholar
• Passardi F., Bakalovic N., Teixeira F.K., Margis-Pinheiro M., Penel C. & Dunand C. 2007. Prokaryotic origins of the non-animal peroxidase superfamily and organelle-mediated transmission to eukaryotes. Genomics 89: 567–579.
   PubMed Web of Science ®Google Scholar
• Pedreira J., Sanz N., Peña M.J., Sánchez M., Queijeiro E., Revilla G. & Zarra I. 2004. Role of apoplastic ascorbate and hydrogen peroxide in the control of cell growth in pine hypocotyls. Plant and Cell Physiology 45: 530–534.
   Web of Science ®Google Scholar
• Petrov V.D. & Van Breusegem F. 2012. Hydrogen peroxide – a central hub for information flow in plant cells. AoB PLANTS: pls014; doi:10.1093/aobpla/pls014
   Google Scholar
• Potin P. & Leblanc C. 2006. Phenolic-based adhesives of marine brown algae. In: Biological adhesives (Ed. by A.M. Smith & J.A. Callow), pp. 105–124. Berlin, Springer-Verlag.
   Google Scholar
• Queval G., Hager J., Gakière B. & Noctor G. 2008. Why are literature data for H2O2 contents so variable? A discussion of potential difficulties in the quantitative assay of leaf extracts. Journal of Experimental Botany 59: 135–146.
   Web of Science ®Google Scholar
• Ross C., Küpper F.C., Vreeland V., Waite J.H. & Jacobs R.S. 2005. Evidence of a latent oxidative burst in relation to wound repair in the giant unicellular chlorophyte Dasycladus vermicularis. Journal of Phycology 41: 531–541.
   Web of Science ®Google Scholar
• Sáez C.A., Ramesh K., Greco M., Bitonti M.B. & Brown M.T. Enzymatic antioxidant defences are transcriptionally regulated in Es524, a copper-tolerant strain of Ectocarpus siliculosus (Ectocarpales, Phaeophyceae). Phycologia 54: 425–429.
   Web of Science ®Google Scholar
• Schmid M. & Stengel D.B. 2015. Intra-thallus differentiation of fatty acid and pigment profiles in some temperate Fucales and Laminariales. Journal of Phycology 51: 25–36.
   Web of Science ®Google Scholar
• Schopfer P. 1994. Histochemical demonstration and localization of H2O2 in organs of higher plants by tissue printing on nitrocellulose paper. Plant Physiology 104: 1269–1275.
   Web of Science ®Google Scholar
• Suthiphongchai T., Boonsiri P. & Panijpan B. 2008. Vanadium-dependent bromoperoxidases from Gracilaria algae. Journal of Applied Phycology 20: 271–278.
   Web of Science ®Google Scholar
• Takeda T., Yoshimura K., Ishikawa T. & Shigeoka S. 1998. Purification and characterization of ascorbate peroxidase in Chlorella vulgaris. Biochimie 80: 295–301.
   Web of Science ®Google Scholar
• Tarakhovskaya E.R. 2014. Mechanisms of bioadhesion of macrophytic algae. Russian Journal of Plant Physiology 61: 23–30.
   Web of Science ®Google Scholar
• Tarakhovskaya E.R. & Maslov Y.I. 2007. The dynamics of photosynthetic pigments content in ontogenesis of Fucus vesiculosus L. Vestnik Sankt-Peterburgskogo Gosudarstvennogo Universiteta, Seriya 3, Biologiya 4: 111–118. In Russian.
   Google Scholar
• Verhaeghe E., Buisson D., Zekri E., Leblanc C., Potin P. & Ambroise Y. 2008. A colorimetric assay for steady-state analyses of iodo- and bromoperoxidase activities. Analytical Biochemistry 379: 60–65.
   PubMed Web of Science ®Google Scholar
• Vilter H. 1994. Extraction of proteins from sources containing tannins and anionic mucilages. Methods in Enzymology 228: 665–672.
   Web of Science ®Google Scholar
• Vreeland V., Waite J.H. & Epstein L. 1998. Polyphenols and oxidases in substratum adhesion by marine algae and mussels. Journal of Phycology 34: 1–8.
   Web of Science ®Google Scholar
• Wahl M., Jormalainen V., Eriksson B.K., Coyer J.A., Molis M., Schubert H., Dethier M., Karez R., Kruse I., Lenz M., Pearson G., Rohde S., Wikström S.A. & Olsen J.L. 2011. Stress ecology in Fucus: abiotic, biotic and genetic interactions. Advances in Marine Biology 59: 37–106.
   PubMed Web of Science ®Google Scholar
• Weinberger F., Coquempot B., Forner S., Morin P., Kloareg B. & Potin P. 2007. Different regulation of haloperoxidation during agar oligosaccharide-activated defence mechanisms in two related red algae, Gracilaria sp. and Gracilaria chilensis. Journal of Experimental Botany 58: 4365–4372.
   Web of Science ®Google Scholar
• Wever R. 2012. Structure and function of vanadium haloperoxidases. In: Vanadium: biochemical and molecular biological approaches (Ed. by Michibata H.), pp. 995–125. Dordrecht, Springer.
   Google Scholar
• Wever R., Plat H. & de Boer E. 1985. Isolation procedure and some properties of the bromoperoxidase from the seaweed Ascophyllum nodosum. Biochimica et Biophysica Acta 830: 181–186.
   Web of Science ®Google Scholar
• Wolff S.P. 1994. Ferrous ion oxidation in presence of ferric ion indicator xylenol orange for measurement of hydroperoxides. Methods in Enzymology 233: 182–189.
   Web of Science ®Google Scholar