Environmental Control of Vanadium Haloperoxidases and Halocarbon Emissions in Macroalgae

Overview

Journal Mar Biotechnol (NY)

Specialties Biology
Biotechnology

Date 2018 Apr 26

PMID 29691674

Citations 4

Authors

Thillai Punitha

Siew-Moi Phang

Joon Ching Juan

John Beardall

Affiliations

Soon will be listed here.

Abstract

Vanadium-dependent haloperoxidases (V-HPO), able to catalyze the reaction of halide ions (Cl, Br, I) with hydrogen peroxide, have a great influence on the production of halocarbons, which in turn are involved in atmospheric ozone destruction and global warming. The production of these haloperoxidases in macroalgae is influenced by changes in the surrounding environment. The first reported vanadium bromoperoxidase was discovered 40 years ago in the brown alga Ascophyllum nodosum. Since that discovery, more studies have been conducted on the structure and mechanism of the enzyme, mainly focused on three types of V-HPO, the chloro- and bromoperoxidases and, more recently, the iodoperoxidase. Since aspects of environmental regulation of haloperoxidases are less well known, the present paper will focus on reviewing the factors which influence the production of these enzymes in macroalgae, particularly their interactions with reactive oxygen species (ROS).

Citing Articles

Microbial involvement in iodine cycle: mechanisms and potential applications.

Duborska E, Vojtkova H, Matulova M, Seda M, Matus P Front Bioeng Biotechnol. 2023; 11:1279270.

PMID: 38026895 PMC: 10643221. DOI: 10.3389/fbioe.2023.1279270.

Production of Methyl-Iodide in the Environment.

Duborska E, Balikova K, Matulova M, Zverina O, Farkas B, Littera P Front Microbiol. 2022; 12:804081.

PMID: 35003036 PMC: 8733467. DOI: 10.3389/fmicb.2021.804081.

Environmental effects of stratospheric ozone depletion, UV radiation and interactions with climate change: UNEP Environmental Effects Assessment Panel, update 2019.

Bernhard G, Neale R, Barnes P, Neale P, Zepp R, Wilson S Photochem Photobiol Sci. 2020; 19(5):542-584.

PMID: 32364555 PMC: 7442302. DOI: 10.1039/d0pp90011g.

Effect of irradiance on the emission of short-lived halocarbons from three common tropical marine microalgae.

Lim Y, Keng F, Phang S, Sturges W, Malin G, Rahman N PeerJ. 2019; 7:e6758.

PMID: 31041152 PMC: 6476285. DOI: 10.7717/peerj.6758.

References

Strittmatter M, Grenville-Briggs L, Breithut L, van West P, Gachon C, Kupper F . Infection of the brown alga Ectocarpus siliculosus by the oomycete Eurychasma dicksonii induces oxidative stress and halogen metabolism. Plant Cell Environ. 2015; 39(2):259-71. PMC: 4949667. DOI: 10.1111/pce.12533. View

Contreras L, Mella D, Moenne A, Correa J . Differential responses to copper-induced oxidative stress in the marine macroalgae Lessonia nigrescens and Scytosiphon lomentaria (Phaeophyceae). Aquat Toxicol. 2009; 94(2):94-102. DOI: 10.1016/j.aquatox.2009.06.004. View

Gechev T, Van Breusegem F, Stone J, Denev I, Laloi C . Reactive oxygen species as signals that modulate plant stress responses and programmed cell death. Bioessays. 2006; 28(11):1091-101. DOI: 10.1002/bies.20493. View

Coupe E, Smyth M, Fosberry A, Hall R, Littlechild J . The dodecameric vanadium-dependent haloperoxidase from the marine algae Corallina officinalis: cloning, expression, and refolding of the recombinant enzyme. Protein Expr Purif. 2006; 52(2):265-72. DOI: 10.1016/j.pep.2006.08.010. View

Waters C, Bassler B . Quorum sensing: cell-to-cell communication in bacteria. Annu Rev Cell Dev Biol. 2005; 21:319-46. DOI: 10.1146/annurev.cellbio.21.012704.131001. View

Renirie R, Hemrika W, Wever R . Peroxidase and phosphatase activity of active-site mutants of vanadium chloroperoxidase from the fungus Curvularia inaequalis. Implications for the catalytic mechanisms. J Biol Chem. 2000; 275(16):11650-7. DOI: 10.1074/jbc.275.16.11650. View

Malmvarn A, Marsh G, Kautsky L, Athanasiadou M, Bergman A, Asplund L . Hydroxylated and methoxylated brominated diphenyl ethers in the red algae Ceramium tenuicorne and blue mussels from the Baltic Sea. Environ Sci Technol. 2005; 39(9):2990-7. DOI: 10.1021/es0482886. View

Christmann U, Dau H, Haumann M, Kiss E, Liebisch P, Rehder D . Substrate binding to vanadate-dependent bromoperoxidase from Ascophyllum nodosum: a vanadium K-edge XAS approach. Dalton Trans. 2004; (16):2534-40. DOI: 10.1039/B405764C. View

Mata L, Gaspar H, Santos R . CARBON/NUTRIENT BALANCE IN RELATION TO BIOMASS PRODUCTION AND HALOGENATED COMPOUND CONTENT IN THE RED ALGA ASPARAGOPSIS TAXIFORMIS (BONNEMAISONIACEAE)(1). J Phycol. 2016; 48(1):248-53. DOI: 10.1111/j.1529-8817.2011.01083.x. View

10.

Colin C, Leblanc C, Michel G, Wagner E, Leize-Wagner E, Van Dorsselaer A . Vanadium-dependent iodoperoxidases in Laminaria digitata, a novel biochemical function diverging from brown algal bromoperoxidases. J Biol Inorg Chem. 2005; 10(2):156-66. DOI: 10.1007/s00775-005-0626-8. View

11.

Thannickal V, Fanburg B . Reactive oxygen species in cell signaling. Am J Physiol Lung Cell Mol Physiol. 2000; 279(6):L1005-28. DOI: 10.1152/ajplung.2000.279.6.L1005. View

12.

Bouarab K, Adas F, Gaquerel E, Kloareg B, Salaun J, Potin P . The innate immunity of a marine red alga involves oxylipins from both the eicosanoid and octadecanoid pathways. Plant Physiol. 2004; 135(3):1838-48. PMC: 519094. DOI: 10.1104/pp.103.037622. View

13.

Almeida M, Filipe S, Humanes M, Maia M, Melo R, Severino N . Vanadium haloperoxidases from brown algae of the Laminariaceae family. Phytochemistry. 2001; 57(5):633-42. DOI: 10.1016/s0031-9422(01)00094-2. View

14.

Sandy M, Carter-Franklin J, Martin J, Butler A . Vanadium bromoperoxidase from Delisea pulchra: enzyme-catalyzed formation of bromofuranone and attendant disruption of quorum sensing. Chem Commun (Camb). 2011; 47(44):12086-8. DOI: 10.1039/c1cc15605e. View

15.

Kupper F, Carpenter L, McFiggans G, Palmer C, Waite T, Boneberg E . Iodide accumulation provides kelp with an inorganic antioxidant impacting atmospheric chemistry. Proc Natl Acad Sci U S A. 2008; 105(19):6954-8. PMC: 2383960. DOI: 10.1073/pnas.0709959105. View

16.

Leblanc C, Colin C, Cosse A, Delage L, La Barre S, Morin P . Iodine transfers in the coastal marine environment: the key role of brown algae and of their vanadium-dependent haloperoxidases. Biochimie. 2006; 88(11):1773-85. DOI: 10.1016/j.biochi.2006.09.001. View

17.

Blasiak L, Drennan C . Structural perspective on enzymatic halogenation. Acc Chem Res. 2008; 42(1):147-55. PMC: 3980734. DOI: 10.1021/ar800088r. View

18.

Fujimori D, Walsh C . What's new in enzymatic halogenations. Curr Opin Chem Biol. 2007; 11(5):553-60. PMC: 2151916. DOI: 10.1016/j.cbpa.2007.08.002. View

19.

Kousaka K, Ogi N, Akazawa Y, Fujieda M, Yamamoto Y, Takada Y . Novel oxylipin metabolites from the brown alga Eisenia bicyclis. J Nat Prod. 2003; 66(10):1318-23. DOI: 10.1021/np030049t. View

20.

La Barre S, Potin P, Leblanc C, Delage L . The halogenated metabolism of brown algae (Phaeophyta), its biological importance and its environmental significance. Mar Drugs. 2010; 8(4):988-1010. PMC: 2866472. DOI: 10.3390/md8040988. View