Metabolic alterations triggered by silicon nutrition: Is there a signaling role for silicon?

Plant Signaling and Behavior

Volumn 8, Issue 1, 2013, Pages 71-74

  Detmann, Kelly C ^a   Araújo, Wagner L ^a   Martins, Samuel C V ^a   Fernie, Alisdair R ^b   DaMatta, Fábio M ^a  

^a FEDERAL UNIVERSITY OF VIÇOSA   (Brazil)

^b MAX PLANCK INSTITUTE OF MOLECULAR PLANT PHYSIOLOGY   (Germany)

Author keywords

Amino acid remobilization; Metabolite profile; Signaling; Silicon (Si)

Indexed keywords

AMINO ACID; CARBON; FERTILIZER; NITROGEN; SILICON;

METABOLISM; PLANT DISEASE; RICE; SIGNAL TRANSDUCTION;

AMINO ACIDS; CARBON; FERTILIZERS; NITROGEN; ORYZA SATIVA; PLANT DISEASES; SIGNAL TRANSDUCTION; SILICON;

EID: 84873505972     PISSN: 15592316     EISSN: 15592324     Source Type: Journal    
DOI: 10.4161/psb.22523     Document Type: Article

References (26)

1. Epstein E. The anomaly of silicon in plant biology. Proc Natl Acad Sci U S A 1994; 91:11-7; PMID:11607449; http://dx.doi.org/10.1073/pnas.91.1.11.
2. Liang Y. Effects of silicon on enzyme activity and sodium, potassium and calcium concentration in barley under salt stress. Plant Soil 1999; 209:217-24; http://dx.doi.org/10.1023/A:1004526604913.
3. Epstein E. SILICON. Annu Rev Plant Physiol Plant Mol Biol 1999; 50:641-64; PMID:15012222.
4. Liang Y, Wong JWC, Wei L. Silicon-mediated enhancement of cadmium tolerance in maize (Zea mays L.) grown in cadmium contaminated soil. Chemosphere 2005; 58:475-83; PMID:15620739; http://dx.doi.org/10.1016/j.chemosphere.2004.09.034.
5. Ma JF. Role of silicon in enhancing the resistance of plants to biotic and abiotic stresses. Soil Sci Plant Nutr 2004; 50:11-8; http://dx.doi.org/10.1080/00380768.2004.10408447.
6. Fauteux F, Rémus-Borel W, Menzies JG, Bélanger RR. Silicon and plant disease resistance against pathogenic fungi. FEMS Microbiol Lett 2005; 249:1-6; PMID:16006059; http://dx.doi.org/10.1016/j.femsle.2005.06.034.
7. Rodrigues FA, Jurick WM, Datnoff LE, Jones JB, Rollins JA. Silicon influences cytological and molecular events in compatible and incompatible rice-Magnaporthe grisea interactions. Physiol Mol Plant Pathol 2005; 66:144-59; http://dx.doi.org/10.1016/j.pmpp.2005.06.002.
8. Ghareeb H, Bozsó Z, Ott PG, Repenning C, Stahl F, Wydra K. Transcriptome of silicon-induced resistance against Ralstonia solanacearum in the silicon non-accumulator tomato implicates priming effect. Physiol Mol Plant Pathol 2011; 75:83-9; http://dx.doi.org/10.1016/j.pmpp.2010.11.004.
9. Shetty R, Fretté X, Jensen B, Shetty NP, Jensen JD, Jørgensen HJL, et al. Silicon-Induced changes in antifungal phenolic acids, flavonoids, and key phenylpropanoid pathway genes during the interaction between miniature roses and the biotrophic pathogen Podosphaera pannosa. Plant Physiol 2011; 157:2194-205; PMID:22021421; http://dx.doi.org/10.1104/pp.111.185215.
10. Epstein E. Silicon: its manifold roles in plants. Ann Appl Biol 2009; 155:155-60; http://dx.doi.org/10.1111/j.1744-7348.2009.00343.x.
11. Tamai K, Ma J. Reexamination of silicon effects on rice growth and production under field conditions using a low silicon mutant. Plant Soil 2008; 307:21-7; http://dx.doi.org/10.1007/s11104-008-9571-y.
12. Detmann KC, Araújo WL, Martins SCV, Sanglard LMVP, Reis JV, Detmann E, et al. Silicon nutrition increases grain yield, which, in turn, exerts a feed-forward stimulation of photosynthetic rates via enhanced mesophyll conductance and alters primary metabolism in rice. New Phytol 2012; 196:752-62; PMID:22994889; http://dx.doi.org/10.1111/j.1469-8137.2012.04299.x.
13. Sweetlove LJ, Fernie AR. Regulation of metabolic networks: understanding metabolic complexity in the systems biology era. New Phytol 2005; 168:9-24; PMID:16159317; http://dx.doi.org/10.1111/j.1469-8137.2005.01513.x.
14. Less H, Galili G. Principal transcriptional programs regulating plant amino acid metabolism in response to abiotic stresses. Plant Physiol 2008; 147:316-30; PMID:18375600; http://dx.doi.org/10.1104/pp.108.115733.
15. Meitzel T, Radchuk R, Nunes-Nesi A, Fernie AR, Link W, Weschke W, et al. Hybrid embryos of Vicia faba develop enhanced sink strength, which is established during early development. Plant J 2011; 65:517-31; PMID:21235645; http://dx.doi.org/10.1111/j.1365-313X.2010.04450.x.
16. Araújo WL, Ishizaki K, Nunes-Nesi A, Larson TR, Tohge T, Krahnert I, et al. Identification of the 2-hydroxyglutarate and isovaleryl-CoA dehydrogenases as alternative electron donors linking lysine catabolism to the electron transport chain of Arabidopsis mitochondria. Plant Cell 2010; 22:1549-63; PMID:20501910; http://dx.doi.org/10.1105/tpc.110.075630.
17. Araújo WL, Tohge T, Ishizaki K, Leaver CJ, Fernie AR. Protein degradation-an alternative respiratory substrate for stressed plants. Trends Plant Sci 2011; 16:489-98; PMID:21684795.
18. Barneix AJ. Physiology and biochemistry of source-regulated protein accumulation in the wheat grain. J Plant Physiol 2007; 164:581-90; PMID:16690166; http://dx.doi.org/10.1016/j.jplph.2006.03.009.
19. Winter H, Lohaus G, Heldt HW. Phloem transport of amino acids in relation to their cytosolic levels in barley leaves. Plant Physiol 1992; 99:996-1004; PMID:16669030; http://dx.doi.org/10.1104/pp.99.3.996.
20. Hodges M. Enzyme redundancy and the importance of 2-oxoglutarate in plant ammonium assimilation. J Exp Bot 2002; 53:905-16; PMID:11912233; http://dx.doi.org/10.1093/jexbot/53.370.905.
21. Fauteux F, Chain F, Belzile F, Menzies JG, Bélanger RR. The protective role of silicon in the Arabidopsis-powdery mildew pathosystem. Proc Natl Acad Sci U S A 2006; 103:17554-9; PMID:17082308; http://dx.doi.org/10.1073/pnas.0606330103.
22. Armengaud P, Sulpice R, Miller AJ, Stitt M, Amtmann A, Gibon Y. Multilevel analysis of primary metabolism provides new insights into the role of potassium nutrition for glycolysis and nitrogen assimilation in Arabidopsis roots. Plant Physiol 2009; 150:772-85; PMID:19346439; http://dx.doi.org/10.1104/pp.108.133629.
23. Dallagnol LJ, Rodrigues FA, DaMatta FM, Mielli MVB, Pereira SC. Deficiency in silicon uptake affects cytological, physiological, and biochemical events in the rice-Bipolaris oryzae interaction. Phytopathology 2011; 101:92-104; PMID:20879842; http://dx.doi.org/10.1094/PHYTO-04-10-0105.
24. Fleck AT, Nye T, Repenning C, Stahl F, Zahn M, Schenk MK. Silicon enhances suberization and lignification in roots of rice (Oryza sativa). J Exp Bot 2011; 62:2001-11; PMID:21172812; http://dx.doi.org/10.1093/jxb/erq392.
25. Morillo SA, Tax FE. Functional analysis of receptor-like kinases in monocots and dicots. Curr Opin Plant Biol 2006; 9:460-9; PMID:16877029; http://dx.doi.org/10.1016/j.pbi.2006.07.009.
26. Vij S, Giri J, Dansana PK, Kapoor S, Tyagi AK. The receptor-like cytoplasmic kinase (OsRLCK) gene family in rice: organization, phylogenetic relationship, and expression during development and stress. Mol Plant 2008; 1:732-50; PMID:19825577; http://dx.doi.org/10.1093/mp/ssn047.