Abstract
The Brassicaceae are known for their capacity to produce and accumulate the sulfur (S)-rich glucosinolates, which have appreciable human health benefits. Selenium (Se) is chemically very similar to S and many plant enzymes appear unable to distinguish between these two elements. Thus Se may be metabolized through many of the S uptake and assimilation pathways. We were interested in the effect of Se-fertilization on the production of glucosinolate compounds in Brassicaceae. We fertilized broccoli, cauliflower and forage rape with Na2SeO4 and examined the glucosinolates produced in four tissues (tap root, stem, leaf and floret) of these plants using liquid chromatography–mass spectrometry (LC-MS). Several Se-containing glucosinolates were identified and measured. In each case, the Se atom substituted for the S atom normally found in the methylthioalkyl moiety of the glucosinolate and was presumably donated by selenomethionine. The highest concentration of these new Se-containing glucosinolates was in broccoli florets and forage rape roots. In forage rape leaves the majority of the methylthio class of glucosinolates was selenized. Se fertilization also appeared to increase the concentration of the non-selenized methylthioglucosinolates in the shoot tissues of these Brassica species. Our results show that Se and S metabolism of Brassica tissues vary in their responses to Se fertilization and that several enzymes of the glucosinolate biosynthetic and metabolism pathways can use Se in place of S to generate Se-containing glucosinolates.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
References
Broadley MR, White PJ, Bryson RJ, Meacham MC, Bowen HC, Johnson SE, Hawkesford MJ, McGrath SP, Zhao FJ, Breward N, Harriman M, Tucker M (2006) Biofortification of UK food crops with selenium. Proc Nutr Soc 65:169–181
Charron CS, Kopsell DA, Randle WM, Sams CE (2001) Sodium selenate fertilisation increases selenium accumulation and decreases glucosinolate concentration in rapid-cycling Brassica oleracea. J Sci Food Agric 81:962–966
Collins R, Johansson A-L, Karlberg T, Markova N, van den Berg S, Olesen K, Hammarstrom M, Flores A, Schuler H, Schiavone LH, Brzezinski P, Arner ESJ, Hogbom M (2012) Biochemical discrimination between selenium and sulfur 1: a single residue provides selenium specificity to human selenocysteine lyase. PLoS One 7(1):e30581
Emmert SW, Desai D, Amin S, Richie JP (2010) Enhanced Nrf2-dependent induction of glutathione in mouse embryonic fibroblasts by isoselenocyanate analog of sulforaphane. Bioorg Med Chem Lett 20:2675–2679
Galeas ML, Zhang LH, Freeman JL, Wegner M, Pilon-Smits EAH (2007) Seasonal fluctuations of selenium and sulfur accumulation in selenium hyperaccumulators and related nonaccumulators. New Phytol 173:517–525
Harris J, Schneberg KA, Pilon-Smits EAH (2014) Sulfur-selenium-molybdenum interactions distinguish selenium hyperaccumulator Stanleya pinnata from non-hyperaccumulator Brassica juncea (Brassicaceae). Planta 239:479–491
Hsu FC, Wirtz M, Heppel SC, Bogs J, Kramer U, Khan MS, Bub A, Hell R, Rausch T (2011) Generation of Se-fortified broccoli as functional food: impact of Se fertilization on S metabolism. Plant Cell Environ 34:192–207
Ip C, Hayes C, Budnick RM, Ganther HE (1991) Chemical form of selenium, critical metabolites, and cancer prevention. Cancer Res 51:595–600
Kryukov GV, Castellano S, Novoselov SV, Lobanov AV, Zehtab O, Guigo R, Gladyshev VN (2003) Characterization of mammalian selenoproteomes. Science 300:1439–1443
Matich AJ, McKenzie MJ, Lill RE, Brummell DA, McGhie TK, Chen RKY, Rowan DD (2012) Selenoglucosinolates and their metabolites produced in Brassica spp. fertilised with sodium selenate. Phytochemistry 75:140–152
Neuhierl B, Bock A (1996) On the mechanism of selenium tolerance in selenium-accumulating plants – purification and characterization of a specific selenocysteine methyltransferase from cultured cells of Astragalus bisculatus. Eur J Biochem 239:235–238
Robbins RJ, Keck AS, Banuelos G, Finley JW (2005) Cultivation conditions and selenium fertilization alter the phenolic profile, glucosinolate, and sulforaphane content of broccoli. J Med Food 8:204–214
Sharma A, Sharma AK, Madhunapantula SV, Desai D, Huh SJ, Mosca P, Amin S, Robertson GP (2009) Targeting Akt3 signaling in malignant melanoma using isoselenocyanates. Clin Cancer Res 15:1674–1685
Sors TG, Ellis DR, Salt DE (2005) Selenium uptake, translocation, assimilation and metabolic fate in plants. Photosynth Res 86:373–389
Stoner GD, Morse MA (1997) Isothiocyanates and plant polyphenols as inhibitors of lung and esophageal cancer. Cancer Lett 114:113–119
Thomson CD (2004) Selenium and iodine intakes and status in New Zealand and Australia. Br J Nutr 91:661–672
Toler HD, Charron CS, Sams CE, Randle WR (2007) Selenium increases sulfur uptake and regulates glucosinolate metabolism in rapid-cycling Brassica oleracea. J Am Soc Hortic Sci 132:14–19
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2015 Springer International Publishing Switzerland
About this chapter
Cite this chapter
McKenzie, M.J., Matich, A.J., Chen, R.KY., Lill, R.E., McGhie, T.K., Rowan, D.D. (2015). Identification and Distribution of Selenium-Containing Glucosinolate Analogues in Tissues of Three Brassicaceae Species. In: De Kok, L., Hawkesford, M., Rennenberg, H., Saito, K., Schnug, E. (eds) Molecular Physiology and Ecophysiology of Sulfur. Proceedings of the International Plant Sulfur Workshop. Springer, Cham. https://doi.org/10.1007/978-3-319-20137-5_26
Download citation
DOI: https://doi.org/10.1007/978-3-319-20137-5_26
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-20136-8
Online ISBN: 978-3-319-20137-5
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)