Real-time monitoring of superoxide anion radical generation in response to wounding: electrochemical study
Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
28761775
PubMed Central
PMC5527980
DOI
10.7717/peerj.3050
PII: 3050
Knihovny.cz E-zdroje
- Klíčová slova
- Electrochemical detection, Polymeric iron-porphyrin-based modified carbon electrode, Superoxide anion radical, Wounding,
- Publikační typ
- časopisecké články MeSH
BACKGROUND: The growth and development of plants is deleteriously affected by various biotic and abiotic stress factors. Wounding in plants is caused by exposure to environmental stress, mechanical stress, and via herbivory. Typically, oxidative burst in response to wounding is associated with the formation of reactive oxygen species, such as the superoxide anion radical (O2•-), hydrogen peroxide (H2O2) and singlet oxygen; however, few experimental studies have provided direct evidence of their detection in plants. Detection of O2•- formation in plant tissues have been performed using various techniques including electron paramagnetic resonance spin-trap spectroscopy, epinephrine-adrenochrome acceptor methods, staining with dyes such as tetrazolium dye and nitro blue tetrazolium (NBT); however, kinetic measurements have not been performed. In the current study, we provide evidence of O2•- generation and its kinetics in the leaves of spinach (Spinacia oleracea) subjected to wounding. METHODS: Real-time monitoring of O2•- generation was performed using catalytic amperometry. Changes in oxidation current for O2•- was monitored using polymeric iron-porphyrin-based modified carbon electrodes (φ = 1 mm) as working electrode with Ag/AgCl as the reference electrode. RESULT: The results obtained show continuous generation of O2•- for minutes after wounding, followed by a decline. The exogenous addition of superoxide dismutase, which is known to dismutate O2•- to H2O2, significantly suppressed the oxidation current. CONCLUSION: Catalytic amperometric measurements were performed using polymeric iron-porphyrin based modified carbon electrode. We claim it to be a useful tool and a direct method for real-time monitoring and precise detection of O2•- in biological samples, with the potential for wide application in plant research for specific and sensitive detection of O2•-.
Biomedical Engineering Research Center Tohoku Institute of Technology Sendai Japan
Department of Pure and Applied Chemistry Tokyo University of Science Noda Chiba Japan
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Alessandro A, Osto LD, Aprile A, Carillo P, Roncaglia E, Cattivelli L, Bassi R. Reactive oxygen species and transcript analysis upon excess light treatment in wild-type Arabidopsis thaliana vs a photosensitive mutant lacking zeaxanthin and lutein. BMC Plant Biology. 2011;11:62. doi: 10.1186/1471-2229-11-62. PubMed DOI PMC
Anderson AA, Rogers K, Tepper CS, Blee K, Cardon J. Timing of molecular events following elicitor treatment of plant cells. Physiology and Molecular Plant Pathology. 1991;38:1–13. doi: 10.1016/S0885-5765(05)80139-0. DOI
Angelini R, Tisi A, Rea G, Chen MM, Botta M, Federico R, Cona A. Involvement of polyamine oxidase in wound healing. Plant Physiology. 2008;146:162–177. doi: 10.1104/pp.107.108902. PubMed DOI PMC
Asada K. Radical production and scavenging in the chloroplasts. In: Baker NR, editor. Photosynthesis and the environment. Kluwer; Dordrecht: 1996. pp. 123–150.
Asada K. Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiology. 2006;141:391–396. doi: 10.1104/pp.106.082040. PubMed DOI PMC
Barber MJ, Kay CJ. Superoxide production during reduction of molecular oxygen by assimilatory nitrate reductase. Archives of Biochemistry and Biophysics. 1996;326:227–232. doi: 10.1006/abbi.1996.0069. PubMed DOI
Bedioui F, Devynck J, Charreton CB. Immobilization of metalloporphyrins in electropolymerized films: design and applications. Accounts of Chemical Research. 1995;28(1):30–36. doi: 10.1021/ar00049a005. DOI
Bedioui F, Trevin S, Devynck J. Chemically modified microelectrodes designed for the electrochemical determination of nitric oxide in biological systems. Electroanalysis. 1996;8:1085–1091. doi: 10.1002/elan.1140081202. DOI
Bhattacharjee S. Sites of generation and physicochemical basis of formation of reactive oxygen species in plant cell. In: Dutta Gupta S, editor. Reactive oxygen species and antioxidants in higher plants. CRC Press; New York: 2010. pp. 1–30.
Brett CMA, Brett AMCFO. Surface modified electrode-reasons and advantages. In: Kossowsky R, Singhal SC, editors. Surface engineering: surface modification of materials. Westinghouse R & D center; Pittsburg: 1984. pp. 656–664.
Choudhury S, Panda P, Sahoo L, Panda SK. Reactive oxygen species signalling in plants under abiotic stress. Plant Signaling & Behaviour. 2013;8:e23681. doi: 10.4161/psb.23681. PubMed DOI PMC
Cona A, Rea G, Botta M, Corelli F, Federico R, Angelini R. Flavin containing polyamine oxidase is a hydrogen peroxide source in the oxidative response to the protein phosphatase inhibitor cantharidin in Zea mays L. Journal of Experimental Botany. 2006;57:2277–2289. doi: 10.1093/jxb/erj195. PubMed DOI
Deronzier A, Moutet JC. Polypyrrole films containing metal complexes: syntheses and applications. Coordination Chemistry Reviews. 1996;147:339–371. doi: 10.1016/0010-8545(95)01130-7. DOI
Di J, Bi S, Zhang M. Third-generation superoxide anion sensor based on superoxide dismutase directly immobilized by sol–gel thin film on gold electrode. Biosensors and Bioelectronics. 2004;19:1479–1486. doi: 10.1016/j.bios.2003.12.006. PubMed DOI
Doke N. Generation of superoxide anion by potato tuber protoplasts during the hypersensitive response to hyphal wall components of Phytophthora infestans and specific inhibition of the reaction by suppressors of hypersensitivity. Physiological Plant Pathology. 1983a;23:359–367. doi: 10.1016/0048-4059(83)90020-6. DOI
Doke N. Involvement of superoxide anion generation in the hypersensitive response of potato tuber tissues to infection with an incompatible race of Phytophthora infestans and to the hyphal wall components. Physiological Plant Pathology. 1983b;23:345–357. doi: 10.1016/0048-4059(83)90019-X. DOI
Doke N. NADPH-dependent O2•− generation in membrane fractions isolated from wounded potato tubers inoculated with Phytophthora infestans. Physiological Plant Pathology. 1985;27:311–322. doi: 10.1016/0048-4059(85)90044-X. DOI
Doke N, Miura J, Sanchez LM, Park HJ, Noritake T, Yoshioka H, Kawakita K. The oxidative burst protects plants against pathogen attack: mechanism and role as an emergency signal for plant bio-defence—a review. Gene. 1996;179:45–51. doi: 10.1016/S0378-1119(96)00423-4. PubMed DOI
Elstner EF. Mechanisms of oxygen activation in different compartments of plant cells. In: Pell EJ, Steffen KL, editors. Active oxygen/oxidative stress and plant metabolism. American Society of Plant Physiologists; Rockville: 1991. pp. 13–25.
Flor-Henry M, McCabe TC, Bruxelles GL de, Roberts MR. Use of a highly sensitive two-dimensional luminescence imaging system to monitor endogenous bioluminescence in plant leaves. BMC Plant Biology. 2004;4:19. doi: 10.1186/1471-2229-4-19. PubMed DOI PMC
Foyer CH, Harbinson J. Oxygen metabolism and the regulation of photosynthetic electron transport. In: Foyer CH, Mullineaux P, editors. Causes of photooxidative stresses and amelioration of defense systems in plants. CRC Press; Boca Raton: 1994. pp. 1–42.
Foyer CH, Noctor G. Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. The Plant Cell. 2005;17:1866–1875. doi: 10.1105/tpc.105.033589. PubMed DOI PMC
Foyer CH, Shigeoka S. Understanding oxidative stress and antioxidant functions to enhance photosynthesis. Plant Physiology. 2011;155:93–100. doi: 10.1104/pp.110.166181. PubMed DOI PMC
Garces H, Durzan D, Pedroso MC. Mechanical stress elicits nitric oxide formation and DNA fragmentation in Arabidopsis thaliana. Annals of Botany. 2001;87:567–574. doi: 10.1006/anbo.2000.1356. DOI
Gill SS, Tuteja N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry. 2010;48:909–930. doi: 10.1016/j.plaphy.2010.08.016. PubMed DOI
Groenendaal Jonas F, Freitag D, Pielartzik H, Reynolds JR. Poly(3,4 ethylenedioxythiophene) and its derivatives: past, present, and future. Advanced Materials. 2000;12:481–494. doi: 10.1002/(SICI)1521-4095(200004)12:7<481::AID-ADMA481>3.0.CO;2-C. DOI
Halliwell B, Gutteridge JMC. Free radicals in biology and medicine. 2nd edition Clarendon Press; Oxford: 1989.
Higdon A, Diers AR, Oh J, Landar Y, Darley-Usmar VM. Cell signalling by reactive lipid species: new concepts and molecular mechanisms. Biochemical Journal. 2012;442:453–464. doi: 10.1042/BJ20111752. PubMed DOI PMC
Jih PJ, Chen YC, Jeng ST. Involvement of hydrogen peroxide and nitric oxide in expression of the ipomoelin gene from sweet potato. Plant Physiology. 2003;132:381–389. doi: 10.1104/pp.102.015701. PubMed DOI PMC
John M, Rohrig G, Schmidt J, Walden R, Schell J. Cell signaling by oligosaccharides. Trends in Plant Science. 1997;2:111–115. doi: 10.1016/S1360-1385(97)01005-4. DOI
Laloi C, Havaux M. Key players of singlet oxygen-induced cell death in plants. Frontiers in Plant Science. 2015;6 doi: 10.3389/fpls.2015.00039. Article 39. PubMed DOI PMC
Ledford HK, Chin BL, Niyogi KK. Acclimation to singlet oxygen stress in Chlamydomonas reinhardtii. Eukaryotic Cell. 2007;6:919–930. doi: 10.1128/EC.00207-06. PubMed DOI PMC
Legendre L, Rueter S, Heinstein PF, Low PS. Characterization of the oligogalacturonide-induced oxidative cells. Plant Physiology. 1993;102:233–240. doi: 10.1104/pp.102.1.233. PubMed DOI PMC
Li JLY, Sulaiman M, Beckett RP, Minibayeva FV. Cell wall peroxidases in the liverwort Dumortiera hirsuta are responsible for extracellular superoxide production, and can display tyrosinase activity. Physiologia Plantarum. 2010;138:474–484. doi: 10.1111/j.1399-3054.2009.01318.x. PubMed DOI
Liers C, Ullrich C, Hofrichter M, Minibayeva FV, Beckett RP. Oxidoreductases from lichenized ascomycetes: purification and characterization of a heme-peroxidase from Leptogium saturninum that oxidizes high-redox potential substrates. Fungal Genetics and Biology. 2011;48:1139–1145. doi: 10.1016/j.fgb.2011.10.004. PubMed DOI
Liu Y, Ren D, Pike S, Pallardy S, Gassmann W, Zhang S. Chloroplast-generated reactive oxygen species are involved in hypersensitive response-like cell death mediated by a mitogen-activated protein kinase cascade. Plant Journal. 2007;51:941–954. doi: 10.1111/j.1365-313X.2007.03191.x. PubMed DOI
Matsuoka R, Igarashi M, Kondo T, Aikawa T, Yuasa M. Biomimetic antithrombogenic electrochemical superoxide anion radical sensor. Journal of the Electrochemical Society. 2014;161(6):B163–B166. doi: 10.1149/2.099403jes. DOI
McDowell RE, Amsler MO, Li Q, Lancaster Jr JR, Amsler CD. The immediate wound induced oxidative burst of Saccharina latissimi depends on light via photosynthetic electron transport. Journal of Phycology. 2015;51:431–441. doi: 10.1111/jpy.12302. PubMed DOI
Miller G, Schlauch K, Tam R, Cortes D, Torres MA, Shulaev V, Dangl JL, Mittler R. The plant NADPH oxidase RBOHD mediates rapid systemic signaling in response to diverse stimuli. Science Signaling. 2009;2(84):45–49. doi: 10.1126/scisignal.2000448. PubMed DOI
Miller G, Shulaev V, Mittler R. Reactive oxygen signaling and abiotic stress. Physiologia Plantarum. 2008;133(3):481–489. doi: 10.1111/j.1399-3054.2008.01090.x. PubMed DOI
Minibayeva F, Kolesnikov O, Chasov A, Beckett RP, Luthje S, Vylegzhanina N, Buck F, Bottger M. Wound-induced apoplastic peroxidases activities: their roles in the production and detoxification of reactive oxygen species. Plant Cell Environment. 2009;32:497–508. doi: 10.1111/j.1365-3040.2009.01944.x. PubMed DOI
Misra HR, Fridovich I. The univalent reduction of oxygen by reduced flavins and quinones. The Journal of Biological Chemistry. 1972;247:188–192. PubMed
Morker KH, Roberts MR. Light as both an input and an output of wound-induced reactive oxygen formation in Arabidopsis leaves. Plant Signaling and Behaviour. 2011;6(8):1–3. doi: 10.4161/psb.6.1.13880. PubMed DOI PMC
Murphy MP. How mitochondria produce reactive oxygen species. Biochemical Journal. 2009;417:1–13. doi: 10.1042/BJ20081386. PubMed DOI PMC
Murphy TM, Asard H, Cross AR. Possible sources of reactive oxygen during the oxidative burst in plants. In: Asard H, Berczi A, editors. Plasma membrane redox systems and their role in biological stresses and disease. Kluwer Academic Publishers; Dordrecht: 1998. pp. 215–246.
Murphy TM, Auh CK. The superoxide synthases of plasma membrane preparations from cultured rose cells. Plant Physiology. 1996;110:621–629. doi: 10.1104/pp.110.2.621. PubMed DOI PMC
Olson JS, Ballou DP, Palmer GS, Massey V. The reaction of xanthine oxidase with molecular oxygen. The Journal of Biological Chemistry. 1974;249:4350–4362. PubMed
Porras AG, Olson JS, Palmer G. The reaction of reduced xanthine oxidase with oxygen. Kinetics of peroxide and superoxide formation. The Journal of Biological Chemistry. 1981;256:9096–9103. PubMed
Pospíšil P, Prasad A, Rác M. Role of reactive oxygen species in ultra-weak photon emission in biological systems. Journal of Photochemistry and Photobiology B. 2014;139:11–23. doi: 10.1016/j.jphotobiol.2014.02.008. PubMed DOI
Prasad A, Pospíšil P. Ultraweak photon emission induced by visible light and ultraviolet A radiation via photoactivated skin chromophores: in vivo charge coupled device imaging. Journal of Biomedical Optics. 2012;17(8) doi: 10.1117/1.JBO.17.8.085004. Article 85004. PubMed DOI
Prasad A, Pospíšil P. Towards the two-dimensional imaging of spontaneous ultra-weak photon emission from microbial, plant and animal cells. Scientific Reports. 2013;3 doi: 10.1038/srep01211. Article 1211. PubMed DOI PMC
Rea G, Metoui O, Infantino A, Federico R, Angelini R. Copper amine oxidase expression in defense responses to wounding and Ascochyta rabiei invasion. Plant Physiology. 2002;128:865–875. doi: 10.1104/pp.010646. PubMed DOI PMC
Richter C. Redox intermediates between O2 and H2O. In: Carafoli E, Semenza G, editors. Membrane biochemistry. A laboratory manual on transport and bioenergetics. New York: Springer-Verlag; 1979.
Roach T, Beckett RP, Minibayeva FV, Colville L, Whitaker C, Chen H, Bailly C, Kranner I. Extracellular superoxide production, viability and redox poise in response to desiccation in recalcitrant Castanea sativa seeds. Plant Cell Environment. 2009;33:59–75. PubMed
Roach T, Colville L, Beckett RP, Minibayeva FV, Havaux M, Kranner I. A proposed interplay between peroxidase, amine oxidase and lipoxygenase in the wounding-induced oxidative burst in Pisum sativum seedlings. Phytochemistry. 2015;112:130–138. doi: 10.1016/j.phytochem.2014.06.003. PubMed DOI
Roy P, Roy SK, Mitra A, Kulkarni AP. Superoxide generation by lipoxygenase in the presence of NADH and NADPH. Biochimica et Biophysica Acta. 1994;1214:171–179. doi: 10.1016/0005-2760(94)90041-8. PubMed DOI
Stennis M, Chandra S, Ryan C, Low P. Systemin potentiates the oxidative burst in cultured tomato cells. Plant Physiology. 1998;117:1031–1036. doi: 10.1104/pp.117.3.1031. PubMed DOI PMC
Tripathy BC, Oelmüller R. Reactive oxygen species generation and signaling in plants. Plant Signaling and Behavior. 2012;7(12):1621–1633. doi: 10.4161/psb.22455. PubMed DOI PMC
Turrens JF. Mitochondrial formation of reactive oxygen species. Journal of Physiology. 2003;552:335–344. doi: 10.1113/jphysiol.2003.049478. PubMed DOI PMC
Upchurch RG. Fatty acid unsaturation, mobilization, and regulation in the response of plants to stress. Biotechnology Letters. 2008;30:967–977. doi: 10.1007/s10529-008-9639-z. PubMed DOI
Von GM, Schlosser E, Neubacher H. Evidence from electron-spin resonance for the formation of free radicals during infection of Avena sativa by Drechslera spp. Physiology and Molecular Plant Pathology. 1993;42:405–412. doi: 10.1006/pmpp.1993.1030. DOI
Vylegzhaninat NN, Gordon LK, Minibayeva FV, Kolesnikov OP. Superoxide production as a stress response of wounded root cells: ESR spin-trap and acceptor methods. Applied Magnetic Resonance. 2001;21:63–70. doi: 10.1007/BF03162440. DOI
Watanabe T, Sakai S. Effects of active oxygen species and methyl jasmonate on expression of the gene for a wound-inducible 1-aminocyclopropane-1-carboxylate synthase in winter squash (C. maxima) Planta. 1998;206:570–576. doi: 10.1007/s004250050434. DOI
Whitaker C, Beckett RP, Minibayeva FV, Kranner I. Production of reactive oxygen species in excised, desiccated and cryopreserved explants of Trichiliadregeana. South African Journal of Botany. 2010;76:112–118. doi: 10.1016/j.sajb.2009.09.008. DOI
Wohlgemuth H, Mittelstrass K, Kschieschan S, Bender J, Weigel HJ, Overmyer K, Kangasjärvi J, Sandermann H, Langebartels C. Activation of an oxidative burst is a general feature of sensitive plants exposed to the air pollutant ozone. Plant Cell Environment. 2002;25:717–726. doi: 10.1046/j.1365-3040.2002.00859.x. DOI
Yim HS, Kibbey CE, Ma SC, Kliza DM, Liu D, Park SB, Terre CE, Meyerhoff ME. Polymer membrane-based ion-, gas- and bio-selective potentiometric sensors. Biosensors and Bioelectronics. 1993;8:1–38. doi: 10.1016/0956-5663(93)80041-M. PubMed DOI
Yoda H, Hiroi Y, Sano H. Polyamine oxidase is one of the key elements for oxidative burst to induce programmed cell death in tobacco cultured cells. Plant Physiology. 2006;142:193–206. doi: 10.1104/pp.106.080515. PubMed DOI PMC
Yuasa M, Oyaizu K. Electrochemical detection and sensing of reactive oxygen species. Current Organic Chemistry. 2005;9:1685–1697. doi: 10.2174/138527205774610921. DOI
Yuasa M, Oyaizu K, Yamaguchi A, Ishikawa M, Eguchi K, Kobayashi T, Toyoda Y, Tsutsui S. Electrochemical sensor for superoxide anion radical using polymeric iron porphyrin complexes containing axial 1-methylimidazole ligand as cytochrome c mimics. Polymers for Advanced Technologies. 2005;16:287–292. doi: 10.1002/pat.590. DOI
Zuo L, Christofi FL, Wright VP, Bao S, Clanton TL. Lipoxygenase-dependent superoxide release in skeletal muscle. Journal of Applied Physiology. 2004;97(2):661–668. doi: 10.1152/japplphysiol.00096.2004. PubMed DOI
Zuo L, Hallman AH, Roberts WJ, Wagner PD, Hogan MC. Superoxide release from contracting skeletal muscle in pulmonary TNF-α overexpression mice. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 2014;306(1):R75–R81. doi: 10.1152/ajpregu.00425.2013. PubMed DOI PMC
Zuo L, Nogueira L, Hogan MC. Reactive oxygen species formation during tetanic contractions in single isolated Xenopus myofibers. Journal of Applied Physiology. 2011;111:898–904. doi: 10.1152/japplphysiol.00398.2011. PubMed DOI PMC
Zuo L, Shiah A, Roberts WJ, Chien MT, Wagner PD, Hogan MC. Low PO2 conditions induce reactive oxygen species formation during contractions in single skeletal muscle fibers. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 2013;304(11):R1009–R1016. doi: 10.1152/ajpregu.00563.2012. PubMed DOI PMC
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