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Temporal dynamics of ROS biogenesis under simulated solar radiation in the cyanobacterium Anabaena variabilis PCC 7937

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Abstract

We studied the temporal generation of reactive oxygen species (ROS) in the cyanobacterium Anabaena variabilis PCC 7937 under simulated solar radiation using WG 280, WG 295, WG 305, WG 320, WG 335, WG 345, and GG 400 nm cut-off filters to find out the minimum exposure time and most effective region of the solar spectrum inducing highest level of ROS. There was no significant generation of ROS in all treatments in comparison to the samples kept in the dark during the first 8 h of exposure; however, after 12 h of exposure, ROS were significantly generated in samples covered with 305, 295, or 280 nm cut-off filters. In contrast with ROS, the fragmentation of filaments was predominantly seen in 280 nm cut-off filter covered samples after 12 h of exposure. After 24 h of exposure, ROS levels were significantly higher in all samples than in the dark; however, the ROS signals were more pronounced in 320, 305, 295, or 280 nm cut-off filter covered samples. In contrast, the length of filaments was reduced in 305, 295, or 280 nm cut-off filter covered samples after 24 h of exposure. Thus, fragmentation of the filament was induced by all wavelengths of the UV-B region contrary to the UV-A region where only shorter wavelengths were able to induce the fragmentation. In contrast, ROS were generated by all wavelengths of the solar spectrum after 24 h of exposure; however, shorter wavelengths of both the UV-A and the UV-B regions were more effective in generating ROS in comparison to their higher wavelengths and photosynthetic active radiation (PAR). Moreover, lower wavelengths of UV-B were more efficient than the lower wavelengths of the UV-A radiation. Findings from this study suggest that certain threshold levels of ROS are required to induce the fragmentation of filaments.

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References

  • Cockell CS, Rettberg P, Rabbow E, Olsson-Francis K (2011) Exposure of phototrophs to 548 days in low Earth orbit: Microbial selection pressures in outer space and on early earth. ISME J 5:1671–1682

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • de Almeida SL, Schmidt ÉC, Pereira DT, Kreusch M et al (2013) Effect of ultraviolet-B radiation in laboratory on morphological and ultrastructural characteristics and physiological parameters of selected cultivar of Oryza sativa L. Protoplasma 250:1303–1313

    Article  CAS  PubMed  Google Scholar 

  • Fischer WF (2008) Life before the rise of oxygen. Nature 455:1051–1052

    Article  CAS  PubMed  Google Scholar 

  • Foreman J, Demidchik V, Bothwell JHF, Mylona P, Miedema H, Torresk MA, Linstead P, Costa S, Brownlee C, Jonesk JDG, Davies JM, Dolan L (2003) Reactive oxygen species produced by NADPH oxidase regulate plant cell growth. Nature 422:442–446

    Article  CAS  PubMed  Google Scholar 

  • Foyer CH, Lelandais M, Kunert KJ (1994) Photooxidative stress in plants. Physiol Plant 92:696–717

    Article  CAS  Google Scholar 

  • Gutu A, Kehoe DM (2012) Emerging perspectives on the mechanisms, regulation, and distribution of light color acclimation in cyanobacteria. Mol Plant 5:1–13

    Article  CAS  PubMed  Google Scholar 

  • Häder D-P (2011) Does enhanced solar UV-B radiation affect marine primary producers in their natural habitats? Photochem Photobiol 87:263–266

    Article  PubMed  Google Scholar 

  • Häder D-P, Helbling EW, Williamson CE, Worrest RC (2011) Effects of UV radiation on aquatic ecosystems and interactions with climate change. Photochem Photobiol Sci 10:242–260

    PubMed  Google Scholar 

  • Halliwell B, Gutteridge J (2007) Free radicals in biology and medicine, 4th edn. Oxford University Press, Oxford

    Google Scholar 

  • Hargreaves A, Taiwo FA, Duggan O, Kirk SH, Ahmad SI (2007) Near-ultraviolet photolysis of b-phenylpyruvic acid generates free radicals and results in DNA damage. J Photochem Photobiol B Biol 89:110–116

    Article  CAS  Google Scholar 

  • He Y-Y, Häder D-P (2002) UV-B-induced formation of reactive oxygen species and oxidative damage of the cyanobacterium Anabaena sp: Protective effects of ascorbic acid and n-acetyl-l-cysteine. J Photochem Photobiol B Biol 66:115–124

    Article  CAS  Google Scholar 

  • Karentz D, Cleaver JE, Mitchell DL (1991) DNA damage in the Antarctic. Nature 350:28

    Article  Google Scholar 

  • Kehoe DM (2010) Chromatic adaptation and the evolution of light color sensing in cyanobacteria. Proc Natl Acad Sci U S A 107:9029–9030

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Keshari M, Richa, Sinha RP (2011) Antioxidants as natural arsenal against multiple stresses in cyanobacteria. Int J Pharm Bio Sci 2:B168–B187

  • Lesser MP (2011) Oxidative stress in tropical marine ecosystems. In: Abele D, Vázquez-Medina JP, Zenteno-Savín T (eds) Oxidative stress in aquatic ecosystems. Blackwell Publishing Ltd, Oxford, pp 9–19

    Google Scholar 

  • Ma Z, Gao K (2010) Spiral breakage and photoinhibition of Arthrospira platensis (Cyanophyta) caused by accumulation of reactive oxygen species under solar radiation. Environ Exp Bot 68:208–213

    Article  CAS  Google Scholar 

  • Manney GL, Santee ML, Rex M et al (2011) Unprecedented Arctic ozone loss in 2011. Nature 478:469–475

    Article  CAS  PubMed  Google Scholar 

  • Parmar A, Singh NK, Pandey A, Gnansounou E, Madamwar D (2011) Cyanobacteria and microalgae: a positive prospect for biofuels. Bioresour Technol 102:10163–10172

    Article  CAS  PubMed  Google Scholar 

  • Pospíšil P (2009) Production of reactive oxygen species by photosystem II. Biochim Biophys Acta Bioenerg 1787:1151–1160

    Article  Google Scholar 

  • Rastogi RP, Sinha RP (2009) Biotechnological and industrial significance of cyanobacterial secondary metabolites. Biotechnol Adv 27:521–539

    Article  CAS  PubMed  Google Scholar 

  • Rastogi RP, Singh SP, Häder D-P, Sinha RP (2010) Detection of reactive oxygen species (ROS) by the oxidant-sensing probe 2′,7′-dichlorodihydrofluorescein diacetate in the cyanobacterium Anabaena variabilis PCC 7937. Biochem Biophys Res Commun 397:603–607

    Article  CAS  PubMed  Google Scholar 

  • Rastogi RP, Singh SP, Häder D-P, Sinha RP (2011) Ultraviolet-B-induced DNA damage and photo repair in the cyanobacterium Anabaena variabilis PCC 7937. Environ Exp Bot 74:280–288

    Article  CAS  Google Scholar 

  • Rastogi RP, Kumari S, Richa, Han T, Sinha RP (2012) Molecular characterization of hot spring cyanobacteria and evaluation of their photoprotective compounds. Can J Microbiol 58:719–727

  • Richa, Rastogi RP, Kumari S, Singh KL, Kannaujiya VK, Singh G, Kesheri M, Sinha RP (2011) Biotechnological potential of mycosporine-like amino acids and phycobiliproteins of cyanobacterial origin. Biotechnol Bioinforma Bioeng 1:159–171

  • Rinalducci S, Pedersen JZ, Zolla L (2008) Generation of reactive oxygen species upon strong visible light irradiation of isolated phycobilisomes from Synechocystis PCC 6803. Biochim Biophys Acta Bioenerg 1777:417–424

    Article  CAS  Google Scholar 

  • Safferman RS, Morris ME (1964) Growth characteristics of the blue-green algal virus LPP1. J Bacteriol 88:771–775

    CAS  PubMed Central  PubMed  Google Scholar 

  • Sicora CI, Appleton SE, Brown CM, Chung J, Chandler J, Cockshutt AM, Vass I, Campbell DA (2006) Cyanobacterial psbA families in Anabaena and Synechocystis encode trace, constitutive and UVB-induced D1 isoforms. Biochim Biophys Acta Bioenerg 1757:47–56

    Article  CAS  Google Scholar 

  • Singh SP, Montgomery BL (2011) Determining cell shape: Adaptive regulation of cyanobacterial cellular differentiation and morphology. Trends Microbiol 19:278–285

    Article  CAS  PubMed  Google Scholar 

  • Singh SP, Häder D-P, Sinha RP (2010) Cyanobacteria and ultraviolet radiation (UVR) stress: Mitigation strategies. Ageing Res Rev 9:79–90

    Article  CAS  PubMed  Google Scholar 

  • Singh G, Babele PK, Sinha RP, Tyagi MB, Kumar A (2013) Enzymatic and non-enzymatic defense mechanisms against ultraviolet-B radiation in two Anabaena species. Process Biochem 48:796–802

    Article  CAS  Google Scholar 

  • Stanier RY, Cohen-Bazire G (1977) Phototrophic prokaryotes: the cyanobacteria. Annu Rev Microbiol 31:225–274

    Article  CAS  PubMed  Google Scholar 

  • Van Breusegem F, Dat JF (2006) Reactive oxygen species in plant cell death. Plant Physiol 141:384–390

    Article  PubMed Central  PubMed  Google Scholar 

  • Vincent WF, Neale PJ (2000) Mechanisms of UV damage to aquatic organisms. In: de Mora SJ, Demers S, Vernet M (eds) The effects of UV radiation on marine ecosystems. Cambridge Univ. Press, Cambridge, pp 149–176

    Chapter  Google Scholar 

  • Xie Z, Wang Y, Liu Y, Liu Y (2009) Ultraviolet-B exposure induces photo-oxidative damage and subsequent repair strategies in a desert cyanobacterium Microcoleus vaginatus Gom. Eur J Soil Biol 45:377–382

    Article  CAS  Google Scholar 

  • Yadav S, Sinha RP, Tyagi MB, Kumar A (2011) Cyanobacterial secondary metabolites. Int J Pharma Bio Sci 2:B144–B167

    Google Scholar 

  • Zehr JP (2011) Nitrogen fixation by marine cyanobacteria. Trends Microbiol 19:162–173

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

R.P. Rastogi is thankful to University Grants Commission, New Delhi, India, for financial support in the form of a fellowship. We are also thankful to Dr. Peter Richter, Friedrich-Alexander Universität, Erlangen-Nürnberg, Germany, for his help during the microscopic analysis.

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The authors declare no conflict of interest.

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Correspondence to Rajeshwar P. Sinha.

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Handling Editor: Néstor Carrillo

Shailendra P. Singh and Rajesh P. Rastogi contributed equally to the MS.

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Singh, S.P., Rastogi, R.P., Häder, DP. et al. Temporal dynamics of ROS biogenesis under simulated solar radiation in the cyanobacterium Anabaena variabilis PCC 7937. Protoplasma 251, 1223–1230 (2014). https://doi.org/10.1007/s00709-014-0630-3

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  • DOI: https://doi.org/10.1007/s00709-014-0630-3

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