Abstract
Original language | English |
---|---|
Pages (from-to) | 104-115 |
Number of pages | 12 |
Journal | New Phytologist |
Volume | 201 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1 Jan 2014 |
Keywords
- Arsenic
- NanoSIMS
- Rice (Oryza sativa)
- Synchrotron XRF
- Trace elements
- Vascular bundle
- cytology
- iron
- manganese
- mass spectrometry
- mobility
- phloem
- phytochemistry
- rice
- trace element
- translocation
- X-ray fluorescence
- Oryza sativa
- article
- blood vessel
- cell vacuole
- cell wall
- fluorescence
- metabolism
- methodology
- plant cell
- plant leaf
- plant structures
- synchrotron
- transport at the cellular level
- X ray
- Biological Transport
- Plant Cells
- Plant Leaves
- Spectrometry, Mass, Secondary Ion
- Synchrotrons
- Vacuoles
- X-Rays
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In: New Phytologist, Vol. 201, No. 1, 01.01.2014, p. 104-115.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Combined NanoSIMS and synchrotron X-ray fluorescence reveal distinct cellular and subcellular distribution patterns of trace elements in rice tissues
AU - Moore, K L
AU - Chen, Y
AU - van de Meene, A M L
AU - Hughes, L
AU - Liu, W
AU - Geraki, T
AU - Mosselmans, F
AU - McGrath, S P
AU - Grovenor, C
AU - Zhao, F J
N1 - Cited By :8 Export Date: 26 January 2015 CODEN: NEPHA Correspondence Address: Moore, K.L.; Department of Materials, University of Oxford, Oxford, OX1 3PH, United Kingdom; email: [email protected] Chemicals/CAS: arsenic, 7440-38-2 References: Becker, M., Asch, F., Iron toxicity in rice-conditions and management concepts (2005) Journal of Plant Nutrition and Soil Science, 168, pp. 558-573; Carey, A.M., Scheckel, K.G., Lombi, E., Newville, M., Choi, Y., Norton, G.J., Charnock, J.M., Meharg, A.A., Grain unloading of arsenic species in rice (2010) Plant Physiology, 152, pp. 309-319; Cobbett, C., Goldsbrough, P., Phytochelatins and metallothioneins: roles in heavy metal detoxification and homeostasis (2002) Annual Review of Plant Biology, 53, pp. 159-182; Conn, S., Gilliham, M., Comparative physiology of elemental distributions in plants (2010) Annals of Botany, 105, pp. 1081-1102; Ha, S.B., Smith, A.P., Howden, R., Dietrich, W.M., Bugg, S., O'Connell, M.J., Goldsbrough, P.B., Cobbett, C.S., Phytochelatin synthase genes from Arabidopsis and the yeast Schizosaccharomyces pombe (1999) Plant Cell, 11, pp. 1153-1163; Hirsch, J., Marin, E., Floriani, M., Chiarenza, S., Richaud, P., Nussaume, L., Thibaud, M.C., Phosphate deficiency promotes modification of iron distribution in Arabidopsis plants (2006) Biochimie, 88, pp. 1767-1771; Khan, M.A., Stroud, J.L., Zhu, Y.G., McGrath, S.P., Zhao, F.J., Arsenic bioavailability to rice is elevated in Bangladeshi paddy soils (2010) Environmental Science & Technology, 44, pp. 8515-8521; Kopittke, P.M., Menzies, N.W., de Jonge, M.D., McKenna, B.A., Donner, E., Webb, R.I., Paterson, D.J., Glover, C.J., In situ distribution and speciation of toxic copper, nickel, and zinc in hydrated roots of cowpea (2011) Plant Physiology, 156, pp. 663-673; Levi-Setti, R.R., Structural and microanalytical imaging of biological materials by scanning microscopy with heavy-ion probes (1988) Annual Review of Biophysics and Biophysical Chemistry, 17, pp. 325-347; Liu, W.J., Wood, B.A., Raab, A., McGrath, S.P., Zhao, F.J., Feldmann, J., Complexation of arsenite with phytochelatins reduces arsenite efflux and translocation from roots to shoots in Arabidopsis (2010) Plant Physiology, 152, pp. 2211-2221; Lombi, E., Scheckel, K.G., Kempson, I.M., In situ analysis of metal(loid)s in plants: state of the art and artefacts (2011) Environmental and Experimental Botany, 72, pp. 3-17; Lombi, E., Scheckel, K.G., Pallon, J., Carey, A.M., Zhu, Y.G., Meharg, A.A., Speciation and distribution of arsenic and localization of nutrients in rice grains (2009) New Phytologist, 184, pp. 193-201; Ma, L.Q., Komar, K.M., Tu, C., Zhang, W.H., Cai, Y., Kennelley, E.D., A fern that hyperaccumulates arsenic (2001) Nature, 409, p. 579; Ma, J.F., Yamaji, N., Silicon uptake and accumulation in higher plants (2006) Trends in Plant Science, 11, pp. 392-397; Ma, J.F., Yamaji, N., Mitani, N., Xu, X.-Y., Su, Y.-H., McGrath, S.P., Zhao, F.J., Transporters of arsenite in rice and their role in arsenic accumulation in rice grain (2008) Proceedings of the National Academy of Sciences, USA, 105, pp. 9931-9935; Marschner, P., (2012) Marschner's mineral nutrition of higher plants, , London, UK: Academic Press; Matsuo, T.E., Hoshikawa, K.E., (1993) Science of the rice plant. Vol 1, Morphology, , Tokyo, Japan: Food and Agriculture Policy Research Center; Meharg, A.A., Zhao, F.J., (2012) Arsenic & rice, , Dordrecht, the Netherlands: Springer; Mijovilovich, A., Leitenmaier, B., Meyer-Klaucke, W., Kroneck, P.M.H., Gotz, B., Kupper, H., Complexation and toxicity of copper in higher plants. II. Different mechanisms for copper versus cadmium detoxification in the copper-sensitive cadmium/zinc hyperaccumulator Thlaspi caerulescens (Ganges ecotype) (2009) Plant Physiology, 151, pp. 715-731; Moore, K.L., Lombi, E., Zhao, F.J., Grovenor, C.R.M., Elemental imaging at the nanoscale: NanoSIMS and complementary techniques for element localisation in plants (2012) Analytical and Bioanalytical Chemistry, 402, pp. 3263-3273; Moore, K.L., Schröder, M., Grovenor, C.R.M., Imaging secondary ion mass spectrometry (2012) Handbook of nanoscopy, pp. 709-744. , Tendeloo GV, Van Dyck D, Pennycook SJ, eds. Weinheim, Germany: Wiley-VCH; Moore, K.L., Schroder, M., Lombi, E., Zhao, F.J., McGrath, S.P., Hawkesford, M.J., Shewry, P.R., Grovenor, C.R.M., NanoSIMS analysis of arsenic and selenium in cereal grain (2010) New Phytologist, 185, pp. 434-445; Moore, K.L., Schroder, M., Wu, Z., Martin, B., Hawes, C., McGrath, S.P., Hawkesford, M.J., Grovenor, C.R.M., High resolution secondary ion mass spectrometry reveals the contrasting subcellular distribution of arsenic and silicon in rice roots (2011) Plant Physiology, 156, pp. 913-924; Moore, K.L., Zhao, F.-J., Gritsch, C.S., Tosi, P., Hawkesford, M.J., McGrath, S.P., Shewry, P.R., Grovenor, C.R.M., Localisation of iron in wheat grain using high resolution secondary ion mass spectrometry (2012) Journal of Cereal Science, 55, pp. 183-187; Morrissey, J., Guerinot, M.L., Iron uptake and transport in plants: the good, the bad, and the ionome (2009) Chemical Reviews, 109, pp. 4553-4567; Mosselmans, J.F.W., Quinn, P.D., Dent, A.J., Cavill, S.A., Moreno, S.D., Peach, A., Leicester, P.J., Atkinson, K.D., I18-the microfocus spectroscopy beamline at the Diamond Light Source (2009) Journal of Synchrotron Radiation, 16, pp. 818-824; Raab, A., Schat, H., Meharg, A.A., Feldmann, J., Uptake, translocation and transformation of arsenate and arsenite in sunflower (Helianthus annuus): formation of arsenic-phytochelatin complexes during exposure to high arsenic concentrations (2005) New Phytologist, 168, pp. 551-558; Rauser, W.E., Structure and function of metal chelators produced by plants - the case for organic acids, amino acids, phytin, and metallothioneins (1999) Cell Biochemistry and Biophysics, 31, pp. 19-48; Ryan, B.M., Kirby, J.K., Degryse, F., Harris, H., McLaughlin, M.J., Scheiderich, K., Copper speciation and isotopic fractionation in plants: uptake and translocation mechanisms (2013) New Phytologist, 199, pp. 367-378; Salt, D.E., Prince, R.C., Baker, A.J.M., Raskin, I., Pickering, I.J., Zinc ligands in the metal hyperaccumulator Thlaspi caerulescens as determined using X-ray absorption spectroscopy (1999) Environmental Science & Technology, 33, pp. 713-717; Savant, N.K., Snyder, G.H., Datnoff, L.E., Silicon management and sustainable rice production (1997) Advances in Agronomy, 58, pp. 151-199; Smart, K.E., Smith, J.A.C., Kilburn, M.R., Martin, B.G.H., Hawes, C., Grovenor, C.R.M., High-resolution elemental localization in vacuolate plant cells by nanoscale secondary ion mass spectrometry (2010) Plant Journal, 63, pp. 870-879; Sole, V.A., Papillon, E., Cotte, M., Walter, P., Susini, J., A multiplatform code for the analysis of energy-dispersive X-ray fluorescence spectra (2007) Spectrochimica Acta Part B-Atomic Spectroscopy, 62, pp. 63-68; Song, W.Y., Park, J., Mendoza-Cozatl, D.G., Suter-Grotemeyer, M., Shim, D., Hortensteiner, S., Geisler, M., Rentsch, D., Arsenic tolerance in Arabidopsis is mediated by two ABCC-type phytochelatin transporters (2010) Proceedings of the National Academy of Sciences, USA, 107, pp. 21187-21192; White, P.J., Broadley, M.R., Biofortification of crops with seven mineral elements often lacking in human diets - iron, zinc, copper, calcium, magnesium, selenium and iodine (2009) New Phytologist, 182, pp. 49-84; (2002) World Health Report 2002. Reducing risks, promoting healthy life, , WHO. Geneva, Switzerland: World Health Organization; Yamaguchi, N., Ishikawa, S., Abe, T., Baba, K., Arao, T., Terada, Y., Role of the node in controlling traffic of cadmium, zinc, and manganese in rice (2012) Journal of Experimental Botany, 63, pp. 2729-2737; Yamaji, N., Ma, J.F., A transporter at the node responsible for intervascular transfer of silicon in rice (2009) Plant Cell, 21, pp. 2878-2883; Zhao, F.J., McGrath, S.P., Meharg, A.A., Arsenic as a food chain contaminant: mechanisms of plant uptake and metabolism and mitigation strategies (2010) Annual Review of Plant Biology, 61, pp. 535-559; Zhao, F.J., Stroud, J.L., Khan, M.A., McGrath, S.P., Arsenic translocation in rice investigated using radioactive As-73 tracer (2012) Plant and Soil, 350, pp. 413-420; Zheng, L.Q., Huang, F.L., Narsai, R., Wu, J.J., Giraud, E., He, F., Cheng, L.J., Whelan, J., Physiological and transcriptome analysis of iron and phosphorus interaction in rice seedlings (2009) Plant Physiology, 151, pp. 262-274
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Summary: The cellular and subcellular distributions of trace elements can provide important clues to understanding how the elements are transported and stored in plant cells, but mapping their distributions is a challenging task. The distributions of arsenic, iron, zinc, manganese and copper, as well as physiologically related macro-elements, were mapped in the node, internode and leaf sheath of rice (Oryza sativa) using synchrotron X-ray fluorescence (S-XRF) and high-resolution secondary ion mass spectrometry (NanoSIMS). Although copper and silicon generally showed cell wall localization, arsenic, iron and zinc were strongly localized in the vacuoles of specific cell types. Arsenic was highly localized in the companion cell vacuoles of the phloem in all vascular bundles, showing a strong co-localization with sulfur, consistent with As(III)-thiol complexation. Within the node, zinc was localized in the vacuoles of the parenchyma cell bridge bordering the enlarged and diffuse vascular bundles, whereas iron and manganese were localized in the fundamental parenchyma cells, with iron being strongly co-localized with phosphorus in the vacuoles. The highly heterogeneous and contrasting distribution patterns of these elements imply different transport activities and/or storage capacities among different cell types. Sequestration of arsenic in companion cell vacuoles may explain the limited phloem mobility of arsenite. © 2013 New Phytologist Trust.
AB - Summary: The cellular and subcellular distributions of trace elements can provide important clues to understanding how the elements are transported and stored in plant cells, but mapping their distributions is a challenging task. The distributions of arsenic, iron, zinc, manganese and copper, as well as physiologically related macro-elements, were mapped in the node, internode and leaf sheath of rice (Oryza sativa) using synchrotron X-ray fluorescence (S-XRF) and high-resolution secondary ion mass spectrometry (NanoSIMS). Although copper and silicon generally showed cell wall localization, arsenic, iron and zinc were strongly localized in the vacuoles of specific cell types. Arsenic was highly localized in the companion cell vacuoles of the phloem in all vascular bundles, showing a strong co-localization with sulfur, consistent with As(III)-thiol complexation. Within the node, zinc was localized in the vacuoles of the parenchyma cell bridge bordering the enlarged and diffuse vascular bundles, whereas iron and manganese were localized in the fundamental parenchyma cells, with iron being strongly co-localized with phosphorus in the vacuoles. The highly heterogeneous and contrasting distribution patterns of these elements imply different transport activities and/or storage capacities among different cell types. Sequestration of arsenic in companion cell vacuoles may explain the limited phloem mobility of arsenite. © 2013 New Phytologist Trust.
KW - Arsenic
KW - NanoSIMS
KW - Rice (Oryza sativa)
KW - Synchrotron XRF
KW - Trace elements
KW - Vascular bundle
KW - cytology
KW - iron
KW - manganese
KW - mass spectrometry
KW - mobility
KW - phloem
KW - phytochemistry
KW - rice
KW - trace element
KW - translocation
KW - X-ray fluorescence
KW - Oryza sativa
KW - article
KW - blood vessel
KW - cell vacuole
KW - cell wall
KW - fluorescence
KW - metabolism
KW - methodology
KW - plant cell
KW - plant leaf
KW - plant structures
KW - synchrotron
KW - transport at the cellular level
KW - X ray
KW - Biological Transport
KW - Plant Cells
KW - Plant Leaves
KW - Spectrometry, Mass, Secondary Ion
KW - Synchrotrons
KW - Vacuoles
KW - X-Rays
U2 - 10.1111/nph.12497
DO - 10.1111/nph.12497
M3 - Article
SN - 1469-8137
VL - 201
SP - 104
EP - 115
JO - New Phytologist
JF - New Phytologist
IS - 1
ER -