Corrigendum: The involvement of nitric oxide in integration of plant physiological and ultrastructural adjustments in response to arsenic (Front. Plant Sci., (2017) 8, (516), 10.3389/fpls.2017.00516);The involvement of nitric oxide in integration of plant physiological and ultrastructural adjustments in response to arsenic

Frontiers in Plant Science

Volumn 8, Issue , 2017, Pages

  Farnese, Fernanda S ^a   Oliveira, Juraci A ^b   Paiva, Elder A S ^c   Menezes Silva, Paulo E ^a   Da Silva, Adinan A ^b   Campos, Fernanda V ^b   Ribeiro, Cléberson ^b  

^a INSTITUTO FEDERAL GOIANO   (Brazil)

^b FEDERAL UNIVERSITY OF VIÇOSA   (Brazil)

^c FEDERAL UNIVERSITY OF MINAS GERAIS   (Brazil)

Author keywords

Cell signaling; Photosynthesis; Pistia stratiotes; Programmed cell death; Respiration

Indexed keywords

EID: 85018532855     PISSN: None     EISSN: 1664462X     Source Type: Journal    
DOI: 10.3389/fpls.2017.00979     Document Type: Erratum

References (65)

1. Abercrombie, J. M., Halfhill, M. D., Ranjan, P., Rao, M. R., Saxton, A. M., Yuan, J. S., et al. (2008). Transcriptional responses of Arabidopsis thaliana plants to As (V) stress. BMC Plant Biol. 8:87. doi: 10.1186/1471-2229-8-87
2. Alcantara-Martinez, N., Guizar, S., Rivera-Cabrera, F., Anicacio-Acevedo, B. E., Buendia-Gonzalez, L., and Volke-Sepulveda, T. (2016). Tolerance, arsenic uptake, and oxidative stress in acacia farnesiana under arsenate-stress. Int. J. Phytoremediation 18, 671-678. doi: 10.1080/15226514.2015.1118432
3. Andrade, H. M., Oliveira, J. A., Farnese, F. S., Ribeiro, C., Silva, A. A., Campos, F. V., et al. (2016). Arsenic toxicity: cell signalling and the attenuating effect of nitric oxide in Eichhornia crassipes. Biol. Plant. 60, 173-180. doi: 10.1007/s10535-015-0572-4
4. Baker, N. R. (2008). Chlorophyll fluorescence: a probe of photosynthesis in vivo. Annu. Rev. Plant Biol. 59, 89-113. doi: 10.1146/annurev.arplant.59.032607.092759
5. Beligni, M. V., Fath, A., Bethke, P. C., Lamattina, L., and Jones, R. L. (2002). Nitric oxide acts as an antioxidant and delays programmed cell death in barley aleurone layers. Plant Physiol. 129, 1642-1650. doi: 10.1104/pp.002337
6. Biwas, S., Koul, M., and Bhatnagar, A. K. (2015). Effect of arsenic on trichome ultrastructure, essential oil yield and quality of Ocimum basilicum L. J. Med. Plant Res. 5, 1-9. doi: 10.5376/mpr.2015.05.0006 CrossRef Full Text
7. Bolton, M. D. (2009). Primary metabolism and plant defense - fuel for the fire. Mol. Plant Microbe Interact. 22, 487-497. doi: 10.1094/MPMI-22-5-0487
8. Boveris, A., Alvarez, S., Bustamante, J., and Valdez, L. (2002). Measurement of superoxide radical and hydrogen peroxide production in isolated cells and subcellular organelles. Methods Enzymol. 105, 280-287. doi: 10.1016/S0076-6879(02)49342-1
9. Carbonera, D., Gerotto, C., Posocco, B., Giacometti, G. M., and Morosinotto, T. (2012). NPQ activation reduces chlorophyll triplet state formation in the moss Physcomitrella patens. Biochim. Biophys. Acta Bioenerg. 1817, 1608-1615. doi: 10.1016/j.bbabio.2012.05.007
10. Castrillo, G., Sánchez-Bermejo, E., de Lorenzo, L., Crevillén, P., Fraile-Escanciano, A., Tc, M., et al. (2013). WRKY6 transcription factor restricts arsenate uptake and transposon activation in Arabidopsis. Plant Cell 25, 2944-2957. doi: 10.1105/tpc.113.114009
11. Clark, R. B. (1975). Characterization of phosphatase of intact maize roots. J. Agric. Food Chem. 23, 458-460. doi: 10.1021/jf60199a002
12. Corpas, F. J., and Barroso, J. B. (2016). Lead-induced stress, which triggers the production of nitric oxide (NO) and superoxide anion (O2.-) in Arabidopsis peroxisomes, affects catalase activity. Nitric Oxide doi: 10.1016/j.niox.2016.12.010 [Epub ahead of print].
13. de Freitas-Silva, L., de Araújo, T. O., da Silva, L. C., de Oliveira, J. A., and de Araujo, J. M. (2016). Arsenic accumulation in Brassicaceae seedlings and its effects on growth and plant anatomy. Ecotoxicol. Environ. Saf. 124, 1-9. doi: 10.1016/j.ecoenv.2015.09.028
14. Dutilleul, C., Garmier, M., Noctor, G., Mathieu, C., Chétrit, P., Foyer, C. H., et al. (2003). Leaf mitochondria modulate whole cell redox homeostasis, set antioxidant capacity, and determine stress resistance through altered signaling and diurnal regulation. Plant Cell 15, 1212-1226. doi: 10.1105/tpc.009464.2
15. Epron, D., and Dreyer, E. (1993). Long-term effects of drought on photosynthesis of adult oak trees [Quercus petraea (Matt.) Liebl. and Quercus robur L.] in a natural stand. New Phytol. 125, 381-389. doi: 10.1111/j.1469-8137.1993.tb03890.x
16. Fan, H., Du, C., Xu, Y., and Wu, X. (2014). Exogenous nitric oxide improves chilling tolerance of Chinese cabbage seedlings by affecting antioxidant enzymes in leaves. Hortic. Environ. Biotechnol. 55, 159-165. doi: 10.1007/s13580-014-0161-z
17. Farnese, F. S., de Oliveira, J. A., Gusman, G. S., Leão, G. A., Ribeiro, C., Siman, L. I., et al. (2013). Plant responses to arsenic: the role of nitric oxide. Water Air Soil Pollut. 224, 1660. doi: 10.1007/s11270-013-1660-8
18. Farnese, F. S., Menezes-Silva, P. E., Gusman, G. S., and Oliveira, J. A. (2016). When bad guys become good ones: the key role of reactive oxygen species and nitric oxide in the plant responses to abiotic stress. Front. Plant Sci. 7:471. doi: 10.3389/fpls.2016.00471
19. Fernie, A. R., Roscher, A., Ratcliffe, R. G., and Kruger, N. J. (2001). Fructose 2,6-bisphosphate activates pyrophosphate: fructose-6-phosphate 1-phosphotransferase and increases triose phosphate to hexose phosphate cycling heterotrophic cells. Planta 212, 250-263. doi: 10.1007/s004250000386
20. Fernie, A. R., Trethewey, R. N., Krotzky, A. J., and Willmitzer, L. (2004). Metabolite profiling: from diagnostics to systems biology. Nat. Rev. Mol. Cell Biol. 5, 763-769. doi: 10.1038/nrm1451
21. Finnegan, P. M., and Chen, W. (2012). Arsenic toxicity: the effects on plant metabolism. Front. Physiol. 3:182. doi: 10.3389/fphys.2012.00182
22. Gay, C., and Gebicki, J. M. (2000). A critical evaluation of the effect of sorbitol on the ferric-xylenol orange hydroperoxide assay. Anal. Biochem. 284, 217-220. doi: 10.1006/abio.2000.4696
23. Gomes, M. P., Andrade, M. L., Nascentes, C. C., and Scotti, M. R. (2014). Arsenic root sequestration by a tropical woody legume as affected by arbuscular mycorrhizal fungi and organic matter: Implications for land reclamation. Water Air Soil Pollut. 225, 1919. doi: 10.1007/s11270-014-1919-8
24. Gupta, B., Huang, B., Gupta, B., and Huang, B. (2014). Mechanism of salinity tolerance in plants: physiological, biochemical, and molecular characterization. Int. J. Genomics 2014, 1-18. doi: 10.1155/2014/701596
25. Gupta, D. K., Inouhe, M., Rodríguez-Serrano, M., Romero-Puertas, M. C., and Sandalio, L. M. (2013). Oxidative stress and arsenic toxicity: role of NADPH oxidases. Chemosphere 90, 1987-1996. doi: 10.1016/j.chemosphere.2012.10.066
26. Hai, L., Yueming, J., Yunbo, L., and Weibo, J. (2006). A simple and rapid determination of ATP, ADP and AMP concentrations in pericarp tissue of litchi fruit by high performance liquid chromatography. Food Technol. Biotechnol. 44, 531-534.
27. Jhanji, S., Setia, R. C., Kaur, N., Kaur, P., and Setia, N. (2012). Role of nitric oxide in cadmium-induced stress on growth, photosynthetic components and yield of Brassica napus L. J. Environ. Biol. 33, 1027-1032.
28. Jin, J., Xu, Y., and Huang, Y. (2010). Protective effect of nitric oxide against arsenic-induced oxidative damage in tall fescue leaves. African J. Biotechnol. 9, 1619-1627. doi: 10.5897/AJB10.1442
29. Kopka, J., Schauer, N., Krueger, S., Birkemeyer, C., Usadel, B., Bergmuller, E., et al. (2005). The Golm metabolome database. Bioinformatics 21, 1635-1638. doi: 10.1093/bioinformatics/bti236
30. Kumar, S., Dubey, R. S., Tripathi, R. D., Chakrabarty, D., and Trivedi, P. K. (2015). Omics and biotechnology of arsenic stress and detoxification in plants: current updates and prospective. Environ. Int. 74, 221-230. doi: 10.1016/j.envint.2014.10.019
31. Kuo, M. C., and Kao, C. H. (2003). Aluminium effects on lipid peroxidation and antioxidative enzyme activities in rice leaves. Biol. Plant. 46, 149-152. doi: 10.1023/A:1022356322373
32. Laloi, C., Przybyla, D., and Apel, K. (2006). A genetic approach towards elucidating the biological activity of different reactive oxygen species in Arabidopsis thaliana. J. Exp. Bot. 57, 1719-1724. doi: 10.1093/jxb/erj183
33. Leão, G. A., de Oliveira, J. A., Felipe, R. T. A., Farnese, F. S., and Gusman, G. S. (2013). Anthocyanins, thiols, and antioxidant scavenging enzymes are involved in Lemna gibba tolerance to arsenic. J. Plant Interact. 9145, 1-9. doi: 10.1080/17429145.2013.784815
34. Leão, G. A., Oliveira, J. A., Farnese, F. S., Gusman, G. S., and Felipe, R. T. A. (2014). Sulfur metabolism: different tolerances of two aquatic macrophytes exposed to arsenic. Ecotoxicol. Environ. Saf. 105, 36-42. doi: 10.1016/j.ecoenv.2014.03.011
35. Li, W. X., Chen, T. B., Huang, Z. C., Lei, M., and Liao, X. Y. (2006). Effect of arsenic on chloroplast ultrastructure and calcium distribution in arsenic hyperaccumulator Pteris vittata L. Chemosphere 62, 803-809. doi: 10.1016/j.chemosphere.2005.04.055
36. Li, Z., Yue, H., and Xing, D. (2013). MAP Kinase 6-mediated activation of vacuolar processing enzyme modulates heat shock-induced programmed cell death in Arabidopsis. New Phytol. 195, 85-96. doi: 10.1111/j.1469-8137.2012.04131.x
37. Lisec, J., Schauer, N., Kopka, J., Willmitzer, L., and Fernie, A. R. (2006). Gas chromatography mass spectrometry-based metabolite profiling in plants. Nat. Protoc. 1, 387-396. doi: 10.1038/nprot.2006.59
38. Liu, S., Yang, R., Pan, Y., Ren, B., Chen, Q., Li, X., et al. (2016). Beneficial behavior of nitric oxide in copper-treated medicinal plants. J. Hazard. Mater. 314, 140-154. doi: 10.1016/j.jhazmat.2016.04.042
39. Lu, Q., He, Z. L., Graetz, D. A., Stoffella, P. J., and Yang, X. (2011). Upatake and distribution of metal by water lettuce (Pistia stratiotes L.). Environ. Sci. Pollut. Res. 18, 978-986. doi: 10.1007/s11356-011-0453-0
40. Luedemann, A., Strassburg, K., Erban, A., and Kopka, J. (2008). TagFinder for the quantitative analysis of gas chromatography - Mass spectrometry (GC-MS)-based metabolite profiling experiments. Bioinformatics 24, 732-737. doi: 10.1093/bioinformatics/btn023
41. Marin, A. R., Pezeshki, S. R., Masschelen, P. H., and Choi, H. S. (1993). Effect of dimethylarsenic acid (DMAA) on growth, tissue arsenic and photosynthesis in rice plants. J. Plant Nut. 16, 865-880. doi: 10.1080/01904169309364580
42. Martins, S. C. V., Galmés, J., Molins, A., and Damatta, F. M. (2013). Improving the estimation of mesophyll conductance to CO2: On the role of electron transport rate correction and respiration. J. Exp. Bot. 64, 3285-3298. doi: 10.1093/jxb/ert168
43. Maxwell, K., and Johnson, G. N. (2000). Chlorophyll fluorescence-a practical guide. J. Exp. Bot. 51, 659-668. doi: 10.1093/jexbot/51.345.659
44. Millar, A. H., Whelan, J., Soole, K. L., and Dayl, D. A. (2011). Organization and regulation of mitochondrial respiration in plants. Annu. Rev. Plant Biol. 62, 79-104. doi: 10.1146/annurev-arplant-042110-103857
45. Mishra, S., Stärk, H.-J., and Küpper, H. (2014). A different sequence of events than previously reported leads to arsenic-induced damage in Ceratophyllum demersum L. Metallomics 6, 444-454. doi: 10.1039/c3mt00317e
46. Mohammadi, M., and Karr, A. L. (2001). Superoxide anion generation in effective and ineffective soybean root nodules. J. Plant Physiol. 158, 1023-1029. doi: 10.1078/S0176-1617(04)70126-1
47. Moore, S. A., Moennich, D. M., and Gresser, M. J. (1983). Synthesis and hydrolysis of ADP-arsenate by beef heart submitochondrial particles. J. Biol. Chem. 25, 6266-6271.
48. Novitskaya, L., Trevanion, S. J., Driscoll, S., Foyer, C. H., and Noctor, G. (2002). How does photorespiration modulate leaf amino acid contents? A dual approach through modelling and metabolite analysis. Plant Cell Environ. 25, 821-835. doi: 10.1046/j.1365-3040.2002.00866.x
49. Ortega-Galisteo, A. P., Rodríguez-Serrano, M., Pazmiño, D. M., Gupta, D. K., Sandalio, L. M., and Romero-Puertas, M. C. (2012). S-Nitrosylated proteins in pea (Pisum sativum L.) leaf peroxisomes: changes under abiotic stress. J. Exp. Bot. 63, 2089-2103. doi: 10.1093/jxb/err414
50. Osakabe, Y., Osakabe, K., Shinozaki, K., and Tran, L.-S. P. (2014). Response of plants to water stress. Front. Plant Sci. 5:86. doi: 10.3389/fpls.2014.00086
51. Reynolds, E. S. (1963). The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J. Cell Biol. 17, 208-212. doi: 10.1083/jcb.17.1.208
52. Rofkar, J. R., Dwyer, D. F., and Bobak, D. M. (2014). Uptake and toxicity of arsenic, copper, and silicon in Azolla caroliniana and Lemna minor. Int. J. Phytoremediation 16, 155-166. doi: 10.1080/15226514.2012.759534
53. Saeid, Z. D., Zahra, A., and Abdolhamid, N. S. (2014). Investigation of synergistic action between coronatine and nitric oxide in alleviating arsenic-induced toxicity in sweet basil seedlings. Plant Growth Regul. 74, 119-130. doi: 10.1007/s10725-014-9903-2
54. Sanglard, L. M. V., Martins, S. C. V., Detmann, K. C., Silva, P. E. M., Lavinsky, A. O., Detmann, E., et al. (2014). Silicon nutrition alleviates the negative impacts of arsenic on the photosynthetic apparatus of rice leaves: an analysis of the key limitations of photosynthesis. Physiol. Plant. 152, 355-366. doi: 10.1111/ppl.12178
55. Schneider, J., Labory, C. R. G., Rangel, W. M., Alves, E., and Guilherme, L. R. G. (2013). Anatomy and ultrastructure alterations of Leucaena leucocephala (Lam.) Inoculated with mycorrhizal fungi in response to arsenic-contaminated soil. J. Hazard. Mater. 262, 1245-1258. doi: 10.1016/j.jhazmat.2012.05.091
56. Schussler, E. E., and Longstreth, D. J. (1996). Aerenchyma develops by cell lysis in roots and cell separation in leaf petioles in Sagittaria lancifolia (Alismataceae). Am. J. Bot. 83, 1266-1273. doi: 10.2307/2446110
57. Shan, C., He, F., Xu, G., Han, R., and Liang, Z. (2012). Nitric oxide is involved in the regulation of ascorbate and glutathione metabolism in Agropyron cristatum leaves under water stress. Biol. Plant. 56, 187-191. doi: 10.1007/s10535-012-0040-3
58. Shukla, P., Singh, S., Dubey, P., Singh, A., and Singh, A. K. (2015). Nitric oxide mediated amelioration of arsenic toxicity which alters the alternative oxidase (Aox1) gene expression in Hordeum vulgare L. Ecotoxicol. Environ. Saf. 120, 59-65. doi: 10.1016/j.ecoenv.2015.05.030
59. Silveira, N. M., de Oliveira, J. A., Ribeiro, C., Canatto, R. A., Siman, L., Cambraia, J., et al. (2015). Nitric oxide attenuates oxidative stress induced by arsenic in lettuce (Lactuca sativa) leaves. Water Air Soil Pollut. 226, 379. doi: 10.1007/s11270-015-2630-0
60. Srivastava, S., Srivastava, A. K., Singh, B., Suprasanna, P., and D’souza, S. F. (2013). The effect of arsenic on pigment composition and photosynthesis in Hydrilla verticillata. Biol. Plant. 57, 385-389. doi: 10.1007/s10535-012-0288-7
61. Valentini, R., Epron, D., Deangelis, P., Matteucci, G., and Dreyer, E. (1995). In-situ estimation of net Co2 assimilation, photosynthetic electron flow and photorespiration in Turkey Oak (Q-Cerris L) leaves - diurnal cycles under different levels of water-supply. Plant Cell Environ. 18, 631-640. doi: 10.1111/j.1365-3040.1995.tb00564.x
62. van Kooten, O., and Snel, J. F. H. (1990). The use of chlorophyll fluorescence nomenclature in plant stress physiology. Photosynth. Res. 25, 147-150. doi: 10.1007/BF00033156
63. Wang, S., and Blumwald, E. (2014). Stress-induced chloroplast degradation in Arabidopsis is regulated via a process independent of autophagy and senescence-associated vacuoles. Plant Cell 26, 4875-4888. doi: 10.1105/tpc.114.133116
64. Wellburn, A. R. (1994). The spectral determination of chlorophylls a and b, as well as total carotenoids, using various solvents with spectrophotometers of different resolution. Plant Physiol. 144, 307-313. doi: 10.1016/S0176-1617(11)81192-2
65. Xing, F., Li, Z., Sun, A., and Xing, D. (2013). Reactive oxygen species promote chloroplast dysfunction and salicylic acid accumulation in fumonisin B1-induced cell death. FEBS Lett. 587, 2164-2172. doi: 10.1016/j.febslet.2013.05.034