Localization and distribution of nickel and other elements in in-vitro grown Alyssum corsicum exhibiting morphological changes in trichomes: initial insights into molecular mechanisms of nickel hyperaccumulation

Alyssum corsicum Duby is a candidate plant used for phytomining and phytoremediation studies with its high Ni-accumulating ability of the aboveground tissues. Metal localization and concentration by hyperaccumulator plants and the physiological basis of these phenomena have been of great interest in recent years. A. corsicum seeds were grown at different concentrations of Ni in Murashige and Skoog medium. Multielement concentrations of the plant roots and shoots were determined by polarized energy dispersive X-ray fluorescence. Ni, Ca, Mg, and Fe localization and concentration at the upper and lower leaf surfaces were determined by scanning electron microscopy coupled with the energy-dispersive X-ray analysis technique (SEM-EDX). Results showed that Ni is accumulated more by the shoots than the roots of the plant and that Ni is concentrated mainly in the trichome and the stoma guard cells of the leaves. Trichome density on the leaves was reduced, and some morphological changes of the trichome structure were also observed with increasing Ni levels. Analysis of antioxidant enzyme activities in roots and shoots was performed. The total leaf proteins of the plant were examined by sodium dodecyl sulfate polyacrylamide gel electrophoresis, and differentially expressed genes were detected by specifically designed primers.

Localization and distribution of nickel and other elements in in-vitro grown Alyssum corsicum exhibiting morphological changes in trichomes: initial insights into molecular mechanisms of nickel hyperaccumulation

Alyssum corsicum Duby is a candidate plant used for phytomining and phytoremediation studies with its high Ni-accumulating ability of the aboveground tissues. Metal localization and concentration by hyperaccumulator plants and the physiological basis of these phenomena have been of great interest in recent years. A. corsicum seeds were grown at different concentrations of Ni in Murashige and Skoog medium. Multielement concentrations of the plant roots and shoots were determined by polarized energy dispersive X-ray fluorescence. Ni, Ca, Mg, and Fe localization and concentration at the upper and lower leaf surfaces were determined by scanning electron microscopy coupled with the energy-dispersive X-ray analysis technique (SEM-EDX). Results showed that Ni is accumulated more by the shoots than the roots of the plant and that Ni is concentrated mainly in the trichome and the stoma guard cells of the leaves. Trichome density on the leaves was reduced, and some morphological changes of the trichome structure were also observed with increasing Ni levels. Analysis of antioxidant enzyme activities in roots and shoots was performed. The total leaf proteins of the plant were examined by sodium dodecyl sulfate polyacrylamide gel electrophoresis, and differentially expressed genes were detected by specifically designed primers.

___

  • Abou Auda MM, Symeonidis L, Hatzistavrou E, Yupanis T (2002). Nucleolytic activities and appearance of a new DNase in relation to nickel and manganese accumulation in Alyssum murale. J Plant Physiol 159: 1087–1095.
  • Altınözlü H, Karagöz A, Polat T, Ünver İ (2012). Nickel hyperaccumulation by natural plants in Turkish serpentine soils. Turk J Bot 36: 269–280.
  • Bani A, Echevarria G, Sulçe S, Morel JL, Mullai A (2007). In-situ phytoextraction of Ni by a native population of Alyssum murale on an ultramafic site (Albania). Plant Soil 293: 79–89.
  • Boominathan R, Doran PM (2002). Ni-induced oxidative stress in roots of the Ni hyperaccumulator, Alyssum bertolonii. New Phytol 156: 205–215.
  • Bradford MM (1976). Rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248–254.
  • Broadhurst CL, Chaney J, Angle JS, Erbe EF, Maugel TK (2004). Nickel localization and response to increasing Ni soil levels in leaves of the nickel hyperaccumulator Alyssum murale. Plant Soil 265: 225–242.
  • Broadhurst CL, Tappero RV, Maugel TK, Erbe EF, Sparks DL, Chaney RL (2009). Interaction of nickel and manganese in accumulation and localization in leaves of the Ni hyperaccumulators Alyssum murale and Alyssum corsicum. Plant Soil 314: 35–48.
  • Brooks RR (2000). Phytoarchaelogy and hyperaccumulators. In: Brooks RR, editor. Plants that Hyperaccumulate Heavy Metals: Their Role in Phytoremediation, Microbiology, Archaeology, Mineral Exploration and Phytomining. Cambridge: CAB International, pp. 153–180.
  • Çakmak I (1994). Activity as ascorbate-dependent H 2 O 2 scavenging enzymes and leaf chlorosis are enhanced in magnesium- and potassium-deficient leaves but not in phosphorus-deficient leaves. J Ex Bot 45: 1259–1266.
  • Clemens S (2001). Molecular mechanisms of plant metal tolerance and homeostasis. Planta 212: 475–486.
  • Fatima RA, Ahmad M (2004). Certain antioxidant enzymes of Allium cepa as biomarkers for the detection of toxic heavy metals in wastewater. Sci Total Environ 346: 256–273.
  • Guo TR, Zhang GP, Zhang YH (2007). Physiological changes in barley plants under combined toxicity of aluminum, copper and cadmium. Colloids Surf B 15: 182–188.
  • Hajduch M, Rakwal R, Agrawal R, Yonekura M, Pretova A (2001). High resolution two-dimensional electrophoresis separation of proteins from metal stressed rice (Oryza sativa L.) leaves. Electrophoresis 22: 2824–2831.
  • Heath SM, Southworth D, D’Allura JA (1997). Localization of nickel in epidermal subsidiary cells of leaves of Thlaspi montanum var. Siskiyouense (Brassicacea) using energy dispersive x-ray microanalysis. Int J Plant Sci 158: 184–188.
  • Johnson DM, Hooper PR, Conrey RM (1999). XRF Analysis of Rocks and Minerals for Major and Trace Elements on a Single Low Dilution Li-tetraborate Fused Bead. Newtown Square, PA, USA: International Centre for Diffraction Data.
  • Kerkeb L, Krämer U (2003). The role of free histidine in xylem loading of nickel in Alyssum lesbiacum and Brassica juncea. Plant Physiol 131: 716–724.
  • Krämer U, Charnack JM, Baker AJM (1996). Free histidine as a metal chelator in plants that accumulate nickel. Nature 379: 635–638.
  • Krämer U, Grime GW, Smith JAC, Hawes CR, Baker AJM (1997). Micro-PIXE as a technique for studying nickel localization in leaves of the hyperacccumulator plant Alyssum lesbiacum. Nucl Instrum Methods 130: 346–350.
  • Krämer U, Pickering IJ, Prince RC, Raskin I, Salt DE (2000). Subcellular localization and speciation of nickel in hyperaccumulator and non-hyperaccumulator Thlaspi species. Plant Physiol 122: 1343–1353.
  • Küpper H, Küpper F, Spiller M (1996). Environmental relevance of heavy metal- substituted chlorophylls using the example of water plants. J Ex Bot 47: 259–266.
  • Küpper H, Lombi E, Zhao FJ, Wieshammer G, McGrath SP (2001). Cellular compartmentation of nickel in the hyperaccumulators Alyssum lesbiacum, Alyssum bertolonii and Thlaspi goesingense. J Ex Bot 52: 2291–2300.
  • Laemli UK (1970). Cleavage of structural proteins during the assembly of the head of the bacteriophage T4. Nature 277: 680–684.
  • Margui E, Queralt I, Carvalho ML, Hidalgo M (2005). Comparison of EDXRF and ICP349 after microwave digestion for element determination in plant specimens from an abandoned mining area. Anal Chim Acta 549: 197–204.
  • Marmiroli M, Gonnelli C, Maestr E, Gabbriell R, Marmiroli N (2004). Localisation of nickel and mineral nutrients Ca, K, Fe, Mg by scanning electron microscopy microanalysis in tissues of the nickel-hyperaccumulator Alyssum bertolonii Desv. and the non-accumulator Alyssum montanum. Plant Biosystems 138: 231–243.
  • McNear DH, Peltier E, Everhart J, Chaney RL, Sutton S, Newville M, Rivers M, Sparks DL (2005). Application of quantitative fluorescence and absorption-edge computed microtomography to image metal compartmentalization in Alyssum murale. Environ Sci Technol 39: 2210–2218.
  • Murashige T, Skoog F (1962). A revised medium for rapid growth and bioassays with tobacco tissue culture. Plant Physiol 15: 473–497.
  • Öztürk Ürek R, Tarhan L (2012). The relationship between the antioxidant system and phycocyanin production in Spirulina maxima with respect to nitrate concentration. Turk J Bot 36: 369–377.
  • Pilon-Smits E (2005). Phytoremediation. Annu Rev Plant Biol 56: 15–
  • Prasad MNV (2005). Nickelophilous plants and their significance in phytotechnologies. Braz J Plant Physiol 17: 113–128.
  • Psaras GK, Constantinidis TH, Cotsopoulos B (2000). Relative abundance of nickel in the leaf epidermis of eight hyperaccumulators: evidence that the metal is excluded from both guard cells and trichomes. Ann Bot 86: 73–78.
  • Psaras GK, Manetas Y (2001). Nickel localization in seeds of the metal hyperaccumulator Thlaspi pindicum Hausskn. Ann Bot 88: 513–516.
  • Reeves RD, Adıgüzel N (2008). The nickel hyperaccumulating plants of the serpentines of Turkey and adjacent areas: a review with new data. Turk J Biol 32: 143–153.
  • Robinson BH, Lombi E, Zhao FJ, McGrath SP (2003). Uptake and distribution of nickel and other metals in the hyperaccumulator Berkheya coddii. New Phytol 158: 279–285.
  • Schickler H, Caspi H (1999). Response of antioxidative enzymes to nickel and cadmium stress in hyperaccumulator plants of the genus Alyssum. Phyisol Plant 105: 39–44.
  • Shah K, Kumar RG, Verma S, Dubey RS (2001). Effect of cadmium on lipid peroxidation, superoxide anion generation and activities of antioxidant enzymes in growing rice seedlings. Plant Sci 161: 1135–1144.
  • Tappero R, Peltier E, Gräfe M (2007). Hyperaccumulator Alyssum murale relies on a different metal storage mechanism for cobalt than for nickel. New Phytol 17: 641–654.
  • Timothy E, Tour L (1989). Analysis of rocks using X-ray fluorescence spectrometry. Rigaku Journal 6: 3–9.
Turkish Journal of Botany-Cover
  • ISSN: 1300-008X
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Ranking of 11 coastal halophytes from salt marshes in northwest Turkey according their salt tolerance

Christian ZÖRB, Ali SÜMER, Ali SUNGUR, Timothy J. FLOWERS, Hasan ÖZCAN

Two new species of Cirsium (Asteraceae) and notes on allies from Turkey

Bayram YILDIZ, Turan ARABACI, Tuncay DİRMENCİ

Genetic fidelity assessment of encapsulated in vitro tissues of Bacopa monnieri after 6 months of storage by using ISSR and RAPD markers

Joe Virgin Largia MUTHIAH, Karutha Pandian SHUNMUGIAH, Ramesh MANIKANDAN

Protective role of foliar-applied nitric oxide in Triticum aestivum under saline stress

Farhana KAUSAR, Muhammad SHAHBAZ, Muhammad ASHRAF

Pollen morphology of Hymenosphace and Aethiopis sections of the genus Salvia (Lamiaceae) in Turkey

Hülya ÖZLER, Sevil PEHLİVAN, Ferhat CELEP, Musa DOĞAN, Ahmet KAHRAMAN

Euglenozoa occurring in Adzopé Reservoir, Côte D’Ivoire

Blé Alexis Tardy KOUASSI, Kouhété Philippe DA, Allassane OUATTARA

Molecular phylogeny of Galanthus (Amaryllidaceae) of Anatolia inferred from multiple nuclear and chloroplast DNA regions

Nivart Taşci MARGOZ, İbrahim Sırrı YÜZBAŞIOĞLU, Zeynep ÇELEN, Tuna EKİM, Ayşe Neşe BİLGİN

Classification of Camellia species from 3 sections using leaf anatomical data with back-propagation neural networks and support vector machines

Wu JIANG, Billur Barshan ÖZAKTAŞ, Nitin MANTRI, Zhengming TAO, Hongfei LU

The revision of genus Seseli (Umbelliferae) in Turkey

Ebru Doğan GÜNER, Hayri DUMAN

Monitoring of vascular plant diversity in a changing climate in the alpine zone of the Central Greater Caucasus

Khatuna GIGAURI, Maia AKHALKATSI, George NAKHUTSRISHVILI, Otar ABDALADZE