Ability of leaf mesophyll to retain potassium correlates with salinity tolerance in wheat and barley

This work investigated the importance of the ability of leaf mesophyll cells to control K+ flux across the plasma membrane as a trait conferring tissue tolerance mechanism in plants grown under saline conditions. Four wheat (Triticum aestivum and Triticum turgidum) and four barley (Hordeum vulgare)...

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Published inPhysiologia plantarum Vol. 149; no. 4; pp. 515 - 527
Main Authors Wu, Honghong, Shabala, Lana, Barry, Karen, Zhou, Meixue, Shabala, Sergey
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.12.2013
Blackwell
Wiley Subscription Services, Inc
Subjects
apoplast
Barley
Biological and medical sciences
breeding
cell viability
correlation
epicuticular wax
epidermis (plant)
Fluctuations
Fundamental and applied biological sciences. Psychology
Genotype
Genotypes
greenhouse experimentation
Hordeum - drug effects
Hordeum - genetics
Hordeum - physiology
Hordeum vulgare
hydrogen ions
ion transport
Leaves
mesophyll
Mesophyll Cells - metabolism
Organic solvents
osmosis
pharmacology
Phenotype
Plant Leaves - drug effects
Plant Leaves - genetics
Plant Leaves - physiology
Plant physiology and development
plasma membrane
potassium
Potassium - metabolism
potassium channels
Salinity
Salinity tolerance
salt stress
Salt-Tolerance
screening
shoots
sodium
Sodium - metabolism
Sodium chloride
Sodium Chloride - pharmacology
solvents
Triticum - drug effects
Triticum - genetics
Triticum - physiology
Triticum aestivum
Triticum turgidum
waxes
Wheat
Ability
Halotolerance
Monocotyledones
Hordeum vulgare
Plant leaf
Cereal crop
Salinity
Triticum
Mesophyll
Plant physiology
Gramineae
Angiospermae
Spermatophyta
Potassium
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Abstract This work investigated the importance of the ability of leaf mesophyll cells to control K+ flux across the plasma membrane as a trait conferring tissue tolerance mechanism in plants grown under saline conditions. Four wheat (Triticum aestivum and Triticum turgidum) and four barley (Hordeum vulgare) genotypes contrasting in their salinity tolerance were grown under glasshouse conditions. Seven to 10‐day‐old leaves were excised, and net K+ and H+ fluxes were measured from either epidermal or mesophyll cells upon acute 100 mM treatment (mimicking plant failure to restrict Na+ delivery to the shoot) using non‐invasive microelectrode ion flux estimation (the MIFE) system. To enable net ion flux measurements from leaf epidermal cells, removal of epicuticular waxes was trialed with organic solvents. A series of methodological experiments was conducted to test the efficiency of different methods of wax removal, and the impact of experimental procedures on cell viability, in order to optimize the method. A strong positive correlation was found between plants' ability to retain K+ in salt‐treated leaves and their salinity tolerance, in both wheat and especially barley. The observed effects were related to the ionic but not osmotic component of salt stress. Pharmacological experiments have suggested that voltage‐gated K+‐permeable channels mediate K+ retention in leaf mesophyll upon elevated NaCl levels in the apoplast. It is concluded that MIFE measurements of NaCl‐induced K+ fluxes from leaf mesophyll may be used as an efficient screening tool for breeding in cereals for salinity tissue tolerance.
AbstractList This work investigated the importance of the ability of leaf mesophyll cells to control K(+) flux across the plasma membrane as a trait conferring tissue tolerance mechanism in plants grown under saline conditions. Four wheat (Triticum aestivum and Triticum turgidum) and four barley (Hordeum vulgare) genotypes contrasting in their salinity tolerance were grown under glasshouse conditions. Seven to 10-day-old leaves were excised, and net K(+) and H(+) fluxes were measured from either epidermal or mesophyll cells upon acute 100 mM treatment (mimicking plant failure to restrict Na(+) delivery to the shoot) using non-invasive microelectrode ion flux estimation (the MIFE) system. To enable net ion flux measurements from leaf epidermal cells, removal of epicuticular waxes was trialed with organic solvents. A series of methodological experiments was conducted to test the efficiency of different methods of wax removal, and the impact of experimental procedures on cell viability, in order to optimize the method. A strong positive correlation was found between plants' ability to retain K(+) in salt-treated leaves and their salinity tolerance, in both wheat and especially barley. The observed effects were related to the ionic but not osmotic component of salt stress. Pharmacological experiments have suggested that voltage-gated K(+) -permeable channels mediate K(+) retention in leaf mesophyll upon elevated NaCl levels in the apoplast. It is concluded that MIFE measurements of NaCl-induced K(+) fluxes from leaf mesophyll may be used as an efficient screening tool for breeding in cereals for salinity tissue tolerance.This work investigated the importance of the ability of leaf mesophyll cells to control K(+) flux across the plasma membrane as a trait conferring tissue tolerance mechanism in plants grown under saline conditions. Four wheat (Triticum aestivum and Triticum turgidum) and four barley (Hordeum vulgare) genotypes contrasting in their salinity tolerance were grown under glasshouse conditions. Seven to 10-day-old leaves were excised, and net K(+) and H(+) fluxes were measured from either epidermal or mesophyll cells upon acute 100 mM treatment (mimicking plant failure to restrict Na(+) delivery to the shoot) using non-invasive microelectrode ion flux estimation (the MIFE) system. To enable net ion flux measurements from leaf epidermal cells, removal of epicuticular waxes was trialed with organic solvents. A series of methodological experiments was conducted to test the efficiency of different methods of wax removal, and the impact of experimental procedures on cell viability, in order to optimize the method. A strong positive correlation was found between plants' ability to retain K(+) in salt-treated leaves and their salinity tolerance, in both wheat and especially barley. The observed effects were related to the ionic but not osmotic component of salt stress. Pharmacological experiments have suggested that voltage-gated K(+) -permeable channels mediate K(+) retention in leaf mesophyll upon elevated NaCl levels in the apoplast. It is concluded that MIFE measurements of NaCl-induced K(+) fluxes from leaf mesophyll may be used as an efficient screening tool for breeding in cereals for salinity tissue tolerance.
This work investigated the importance of the ability of leaf mesophyll cells to control K⁺ flux across the plasma membrane as a trait conferring tissue tolerance mechanism in plants grown under saline conditions. Four wheat (Triticum aestivum and Triticum turgidum) and four barley (Hordeum vulgare) genotypes contrasting in their salinity tolerance were grown under glasshouse conditions. Seven to 10‐day‐old leaves were excised, and net K⁺ and H⁺ fluxes were measured from either epidermal or mesophyll cells upon acute 100 mM treatment (mimicking plant failure to restrict Na⁺ delivery to the shoot) using non‐invasive microelectrode ion flux estimation (the MIFE) system. To enable net ion flux measurements from leaf epidermal cells, removal of epicuticular waxes was trialed with organic solvents. A series of methodological experiments was conducted to test the efficiency of different methods of wax removal, and the impact of experimental procedures on cell viability, in order to optimize the method. A strong positive correlation was found between plants' ability to retain K⁺ in salt‐treated leaves and their salinity tolerance, in both wheat and especially barley. The observed effects were related to the ionic but not osmotic component of salt stress. Pharmacological experiments have suggested that voltage‐gated K⁺‐permeable channels mediate K⁺ retention in leaf mesophyll upon elevated NaCl levels in the apoplast. It is concluded that MIFE measurements of NaCl‐induced K⁺ fluxes from leaf mesophyll may be used as an efficient screening tool for breeding in cereals for salinity tissue tolerance.
This work investigated the importance of the ability of leaf mesophyll cells to control K+ flux across the plasma membrane as a trait conferring tissue tolerance mechanism in plants grown under saline conditions. Four wheat (Triticum aestivum and Triticum turgidum) and four barley (Hordeum vulgare) genotypes contrasting in their salinity tolerance were grown under glasshouse conditions. Seven to 10-day-old leaves were excised, and net K+ and H+ fluxes were measured from either epidermal or mesophyll cells upon acute 100mM treatment (mimicking plant failure to restrict Na+ delivery to the shoot) using non-invasive microelectrode ion flux estimation (the MIFE) system. To enable net ion flux measurements from leaf epidermal cells, removal of epicuticular waxes was trialed with organic solvents. A series of methodological experiments was conducted to test the efficiency of different methods of wax removal, and the impact of experimental procedures on cell viability, in order to optimize the method. A strong positive correlation was found between plants' ability to retain K+ in salt-treated leaves and their salinity tolerance, in both wheat and especially barley. The observed effects were related to the ionic but not osmotic component of salt stress. Pharmacological experiments have suggested that voltage-gated K+-permeable channels mediate K+ retention in leaf mesophyll upon elevated NaCl levels in the apoplast. It is concluded that MIFE measurements of NaCl-induced K+ fluxes from leaf mesophyll may be used as an efficient screening tool for breeding in cereals for salinity tissue tolerance. [PUBLICATION ABSTRACT]
This work investigated the importance of the ability of leaf mesophyll cells to control K + flux across the plasma membrane as a trait conferring tissue tolerance mechanism in plants grown under saline conditions. Four wheat ( Triticum aestivum and Triticum turgidum ) and four barley ( Hordeum vulgare ) genotypes contrasting in their salinity tolerance were grown under glasshouse conditions. Seven to 10‐day‐old leaves were excised, and net K + and H + fluxes were measured from either epidermal or mesophyll cells upon acute 100  m M treatment (mimicking plant failure to restrict Na + delivery to the shoot) using non‐invasive microelectrode ion flux estimation (the MIFE ) system. To enable net ion flux measurements from leaf epidermal cells, removal of epicuticular waxes was trialed with organic solvents. A series of methodological experiments was conducted to test the efficiency of different methods of wax removal, and the impact of experimental procedures on cell viability, in order to optimize the method. A strong positive correlation was found between plants' ability to retain K + in salt‐treated leaves and their salinity tolerance, in both wheat and especially barley. The observed effects were related to the ionic but not osmotic component of salt stress. Pharmacological experiments have suggested that voltage‐gated K + ‐permeable channels mediate K + retention in leaf mesophyll upon elevated NaCl levels in the apoplast. It is concluded that MIFE measurements of NaCl ‐induced K + fluxes from leaf mesophyll may be used as an efficient screening tool for breeding in cereals for salinity tissue tolerance.
This work investigated the importance of the ability of leaf mesophyll cells to control K+ flux across the plasma membrane as a trait conferring tissue tolerance mechanism in plants grown under saline conditions. Four wheat (Triticum aestivum and Triticum turgidum) and four barley (Hordeum vulgare) genotypes contrasting in their salinity tolerance were grown under glasshouse conditions. Seven to 10‐day‐old leaves were excised, and net K+ and H+ fluxes were measured from either epidermal or mesophyll cells upon acute 100 mM treatment (mimicking plant failure to restrict Na+ delivery to the shoot) using non‐invasive microelectrode ion flux estimation (the MIFE) system. To enable net ion flux measurements from leaf epidermal cells, removal of epicuticular waxes was trialed with organic solvents. A series of methodological experiments was conducted to test the efficiency of different methods of wax removal, and the impact of experimental procedures on cell viability, in order to optimize the method. A strong positive correlation was found between plants' ability to retain K+ in salt‐treated leaves and their salinity tolerance, in both wheat and especially barley. The observed effects were related to the ionic but not osmotic component of salt stress. Pharmacological experiments have suggested that voltage‐gated K+‐permeable channels mediate K+ retention in leaf mesophyll upon elevated NaCl levels in the apoplast. It is concluded that MIFE measurements of NaCl‐induced K+ fluxes from leaf mesophyll may be used as an efficient screening tool for breeding in cereals for salinity tissue tolerance.
Author Shabala, Sergey
Zhou, Meixue
Barry, Karen
Shabala, Lana
Wu, Honghong
Author_xml – sequence: 1
  givenname: Honghong
  surname: Wu
  fullname: Wu, Honghong
  organization: School of Agricultural Science and Tasmanian Institute of Agriculture, University of Tasmania, Tasmania, 7001, Hobart, Australia
– sequence: 2
  givenname: Lana
  surname: Shabala
  fullname: Shabala, Lana
  organization: School of Agricultural Science and Tasmanian Institute of Agriculture, University of Tasmania, Tasmania, 7001, Hobart, Australia
– sequence: 3
  givenname: Karen
  surname: Barry
  fullname: Barry, Karen
  organization: School of Agricultural Science and Tasmanian Institute of Agriculture, University of Tasmania, Tasmania, 7001, Hobart, Australia
– sequence: 4
  givenname: Meixue
  surname: Zhou
  fullname: Zhou, Meixue
  organization: School of Agricultural Science and Tasmanian Institute of Agriculture, University of Tasmania, Tasmania, 7001, Hobart, Australia
– sequence: 5
  givenname: Sergey
  surname: Shabala
  fullname: Shabala, Sergey
  email: Sergey.Shabala@utas.edu.au
  organization: School of Agricultural Science and Tasmanian Institute of Agriculture, University of Tasmania, Tasmania, 7001, Hobart, Australia
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IsPeerReviewed true
IsScholarly true
Issue 4
Keywords Ability
Halotolerance
Monocotyledones
Hordeum vulgare
Plant leaf
Cereal crop
Salinity
Triticum
Mesophyll
Plant physiology
Gramineae
Angiospermae
Spermatophyta
Potassium
Language English
License CC BY 4.0
2013 Scandinavian Plant Physiology Society.
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PublicationDate December 2013
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PublicationTitle Physiologia plantarum
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PublicationYear 2013
Publisher Blackwell Publishing Ltd
Blackwell
Wiley Subscription Services, Inc
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References Cuin TA, Zhou M, Parsons D, Shabala S (2012) Genetic behaviour of physiological traits conferring K+/Na+ homeostasis in wheat. Plant Biol 14: 438-446
Demidchik V, Shabala SN, Davies JM (2007) Spatial variation in H2O2 response of Arabidopsis thaliana root epidermal Ca2+ flux and plasma membrane Ca2+ channels. Plant J 49: 377-386
Agrawal PB, Nierstrasz VA, Klug-Santner BG, Gübitz GM, Lenting HBM, Warmoeskerken MMCG (2007) Wax removal for accelerated cotton scouring with alkaline pectinase. Biotechnol J 2: 306-315
Shabala S (2003) Regulation of potassium transport in leaves: from molecular to tissue level. Ann Bot 92: 627-634
Suelter CH (1970) Enzymes activated by monovalent cations. Science 168: 789-795
Shabala S, Cuin TA (2008) Potassium transport and plant salt tolerance. Physiol Plant 133: 651-669
Fang Z, Mi F, Berkowitz GA (1995) Molecular and physiological analysis of a thylakoid K+ channel protein. Plant Physiol 108: 1725-1734
Maathuis F, Amtmann A (1999) K+ nutrition and Na+ toxicity: the basis of cellular K+/Na+ ratios. Ann Bot 84: 123-133
Horie T, Schroeder JI (2004) Sodium transporters in plants. Diverse genes and physiological functions. Plant Physiol 136: 2457-2462
Bewick TA, Shilling DG, Querns R (1993) Evaluation of epicuticular wax removal from whole leaves with chloroform. Weed Technol 7: 706-716
Chen Z, Pottosin II, Cuin TA, Fuglsang AT, Tester M, Jha D, Zepeda-Jazo I, Zhou MX, Palmgren MG, Newman IA, Shabala S (2007b) Root plasma membrane transporters controlling K+/Na+ homeostasis in salt-stressed barley. Plant Physiol 145: 1714-1725
Demidchik V, Shabala SN, Coutts KB, Tester MA, Davies JM (2003) Free oxygen radicals regulate plasma membrane Ca2+- and K+-permeable channels in plant root cells. J Cell Sci 116: 81-88
Talbott LD, Zeiger E (1996) Central roles for potassium and sucrose in guard-cell osmoregulation. Plant Physiol 111: 1051-1057
Shabala S, Shabala L (2002) Kinetics of net H+, Ca2+, K+, Na+, NH4+, and Cl- fluxes associated with post-chilling recovery of plasma membrane transporters in Zea mays leaf and root tissues. Physiol Plant 114: 47-56
Munns R, James RA, Läuchli A (2006) Approaches to increasing the salt tolerance of wheat and other cereals. J Exp Bot 57: 1025-1043
Koch K, Barthlott W, Koch S, Hommes A, Wandelt K, Mamdouh W, De-Feyter S, Broekmann P (2006) Structural analysis of wheat wax (Triticum aestivum, c.v. 'Naturastar' L.): from the molecular level to three dimensional crystals. Planta 223: 258-270
Shabala S (2000) Ionic and osmotic components of salt stress specifically modulate net ion fluxes from bean mesophyll. Plant Cell Environ 23: 825-837
Hedrich R, Schroeder JI (1989) The physiology of ion channels and electrogenic pumps in higher plants. Annu Rev Plant Physiol 40: 539-569
Osaki M, Shinano T, Tadano T (1993) Effect of nitrogen, phosphorus, or potassium deficiency on the accumulation of ribulose-1,5-bisphosphate carboxylase/oxygenase and chlorophyll in several field crops. Soil Sci Plant Nutr 39: 417-425
Rengasamy P (2010) Soil processes affecting crop production in salt-affected soils. Funct Plant Biol 37: 613-620
Rhee Y, Hlousek-Radojcic A, Ponsamuel J, Liu D, Post-Beittenmiller D (1998) Epicuticular wax accumulation and fatty acid elongation activities are induced during leaf development of leeks. Plant Physiol 116: 901-911
Demidchik V, Cuin TA, Svistunenko D, Smith SJ, Miller AJ, Shabala S, Sokolik A, Yurin V (2010) Arabidopsis root K+-efflux conductance activated by hydroxyl radicals: signal-channel properties, genetic basis and involvement in stress-induced cell death. J Cell Sci 123: 1468-1479
Hughes FM, Cidlowski JA (1999) Potassium is a critical regulator of apoptotic enzymes in vitro and in vivo. Adv Enzyme Regul 39: 157-171
Shabala S, Newman I (1999) Light-induced changes in hydrogen, calcium, potassium, and chloride ion fluxes and concentrations from mesophyll and epidermal tissues of bean leaves. Understanding the ionic basis of light-induced bioelectrogenesis. Plant Physiol 119: 1115-1124
Chen Z, Cuin TA, Zhou M, Twomey A, Naidu BP, Shabala S (2007a) Compatible solute accumulation and stress-mitigating effects in barley genotype contrasting in their genotype. J Exp Bot 58: 4245-4255
Chen Z, Newman I, Zhou M, Mendham N, Zhang G, Shabala S (2005) Screening plants for salt tolerance by measuring K+ flux: a case study for barley. Plant Cell Environ 28: 1230-1246
Plett D, Safwat G, Gilliham M, Møller IS, Roy S, Shirley N, Jacobs A, Johnson A, Tester M (2010) Improved salinity tolerance of rice through cell type-specific expression of AtHKT1;1. PLoS One 5: e12571
Greenway H, Munns R (1980) Mechanisms of salt tolerance in nonhalophytes. Annu Rev Plant Physiol 31: 149-190
Shabala S, Demidchik V, Shabala L, Cuin TA, Smith SJ, Miller AJ, Davies JM, Newman IA (2006) Extracellular Ca2+ ameliorate NaCl induced K+ loss from Arabidopsis root and leaf cells by controlling plasma membrane K+-permeable channels. Plant Physiol 141: 1653-1665
Mäser P, Thomine S, Schroeder JI, Ward JM, Hirschi K, Sze H, Talke IN, Amtmann A, Maathuis FJM, Sanders D, Harper JF, Tchieu J, Gribskov M, Persans MW, Salt DE, Kim SA, Guerinot ML (2001) Phylogenetic relationships within cation transporter families of Arabidopsis. Plant Physiol 126: 1646-1667
Davies MJ, Poole RJ, Rea PA, Sanders D (1992) Potassium transport into plant vacuoles energized directly by a proton-pumping inorganic pyrophosphatase. Proc Natl Acad Sci USA 89: 11701-11705
Hosy E, Vavasseur A, Mouline K, Dreyer I, Gaymard F, Porée F, Boucherez J, Lebaudy A, Bouchez D, Véry A, Simonneau T, Thibaud J, Sentenac H (2003) The Arabidopsis outward K+ channel GORK is involved in regulation of stomatal movements and plant transpiration. Proc Natl Acad Sci USA 100: 5549-5554
Marschner H, Kirkby EA, Cakmak I (1996) Effect of mineral nutritional status on shoot-root partitioning of photoassimilates and cycling of mineral nutrients. J Exp Bot 47: 1255-1263
Cavalcanti FR, Lima JPMS, Ferreira-Silva SL, Viégas RA, Silveria JAG (2007) Roots and leaves display contrasting oxidative response during salt stress and recovery in cowpea. J Plant Physiol 164: 591-600
Zhou G, Johnson P, Ryan PR, Delhaize E, Zhou M (2012) Quantitative trait loci for salinity tolerance in barley (Hordeum vulgare L.). Mol Breed 29: 427-436
Cuin TA, Betts SA, Chalmandrier R, Shabala S (2008) A root's ability to retain K+ correlates with salt tolerance in wheat. J Exp Bot 59: 2697-2706
Eleuch L, Jilal A, Grando S, Ceccarelli S, von Korff SM, Tsujimoto H, Hajer A, Daaloul A, Baum M (2008) Genetic diversity and association analysis for salinity tolerance, heading date and plant height of barley germplasm using simple sequence repeat markers. J Integr Plant Biol 50: 1004-1014
Demidchik V, Davenport RJ, Tester M (2002) Nonselective cation channels in plants. Annu Rev Plant Biol 53: 67-107
Véry A, Sentenac H (2003) Molecular mechanisms and regulation of K+ transport in higher plants. Annu Rev Plant Biol 54: 575-603
Blumwald E, Aharon GS, Apse MP (2000) Sodium transport in plant cells. Biochim Biophys Acta 1465: 140-151
Cuin TA, Bose J, Stefano G, Jha D, Tester M, Mancuso S, Shabala S (2011) Assessing of root plasma membrane and tonoplast Na+/H+ exchangers in salinity tolerance in wheat: in planta quantification methods. Plant Cell Environ 34: 947-961
Shabala S, Cuin TA, Prismall L, Nemchinov LG (2007) Expression of animal CED-9 anti-apoptotic gene in tobacco modifies plasma membrane ion fluxes in response to salinity and oxidative stress. Planta 227: 189-197
Sze H, Li X, Palmgren MG (1999) Energization of plant cell membranes by H+-pumping ATPase: regulation and biosynthesis. Plant Cell 11: 677-689
Xu R, Wang J, Li C, Johnson P, Lu C, Zhou M (2012) A single locus is responsible for salinity tolerance in a Chinese landrace barley (Hordeum vulgare L.). PLoS One 7: e43079
Shabala S, Lew RR (2002) Turgor regulation in osmotically stressed Arabidopsis epidermal root cells. Direct support for the role of inorganic ion uptake as revealed by concurrent flux and cell turgor measurements. Plant Physiol 129: 290-299
Živanović BD, Pang J, Shabala S (2005) Light-induced transient ion flux response from maize leaves and their association with leaf growth and photosynthesis. Plant Cell Environ 28: 340-352
James RA, Rivelli AR, Munns R, von Caemmerer S (2002) Factors affecting CO2 assimilation, leaf injury and growth in salt-stressed durum wheat. Funct Plant Biol 29: 1393-1403
Tegg R, Melian L, Wilson CR, Shabala S (2005) Plant cell growth and ion flux responses to the streptomycete phytotoxin thaxtomin A: calcium and hydrogen flux patterns revealed by the non-invasive MIFE technique. Plant Cell Physiol 46: 638-648
Dreyer I, Uozum N (2011) Potassium channels in plant cells. FEBS J 278: 4293-4303
Demidchik V, Maathuis JM (2007) Physiological roles of nonselective cation channels in plant: from salt stress to signalling and development. New Phytol 175: 387-404
Chen Z, Zhou M, Newman IA, Mendham NJ, Zhang GP, Shabala S (2007c) Potassium and sodium relations in salinised barley tissues as a basis of differential salt tolerance. Funct Plant Biol 34: 150-162
Mano Y, Takeda K (1997) Mapping quantitative trait loci for salt tolerance at germination and the seedling stage in barley (Hordeum vulgare L.). Euphytica 94: 263-272
Newman IA (2001) Ion transport in plants: measurement of fluxes using ion-selective microelectrodes to characterize transporter function. Plant Cell Environ 24: 1-14
Smethurst CF, Shabala S (2003) Screening methods for waterlogging tolerance in lucerne: comparative analysis of waterlogging effects on chlorophyll fluorescence, photosynthesis, biomass and chlorophyll content. Funct Plant Biol 30: 335-343
Evans HJ, Sorger GJ (1966) Role of mineral elements with emphasis on the univalent cations. Annu Rev Plant Physiol 17: 47-76
Cuin TA, Tian Y, Betts SA, Chalmandrier R, Shabala S (2009) Ionic relations and osmotic adjustment in durum and bread wheat under saline conditions. Funct Plant Biol 36: 1110-1119
Flowers TJ (2004) Improving cro
1993; 7
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References_xml – reference: Demidchik V, Cuin TA, Svistunenko D, Smith SJ, Miller AJ, Shabala S, Sokolik A, Yurin V (2010) Arabidopsis root K+-efflux conductance activated by hydroxyl radicals: signal-channel properties, genetic basis and involvement in stress-induced cell death. J Cell Sci 123: 1468-1479
– reference: Chen Z, Cuin TA, Zhou M, Twomey A, Naidu BP, Shabala S (2007a) Compatible solute accumulation and stress-mitigating effects in barley genotype contrasting in their genotype. J Exp Bot 58: 4245-4255
– reference: Shabala S (2003) Regulation of potassium transport in leaves: from molecular to tissue level. Ann Bot 92: 627-634
– reference: Cuin TA, Zhou M, Parsons D, Shabala S (2012) Genetic behaviour of physiological traits conferring K+/Na+ homeostasis in wheat. Plant Biol 14: 438-446
– reference: Eleuch L, Jilal A, Grando S, Ceccarelli S, von Korff SM, Tsujimoto H, Hajer A, Daaloul A, Baum M (2008) Genetic diversity and association analysis for salinity tolerance, heading date and plant height of barley germplasm using simple sequence repeat markers. J Integr Plant Biol 50: 1004-1014
– reference: Bewick TA, Shilling DG, Querns R (1993) Evaluation of epicuticular wax removal from whole leaves with chloroform. Weed Technol 7: 706-716
– reference: Hedrich R, Schroeder JI (1989) The physiology of ion channels and electrogenic pumps in higher plants. Annu Rev Plant Physiol 40: 539-569
– reference: Shabala S, Demidchik V, Shabala L, Cuin TA, Smith SJ, Miller AJ, Davies JM, Newman IA (2006) Extracellular Ca2+ ameliorate NaCl induced K+ loss from Arabidopsis root and leaf cells by controlling plasma membrane K+-permeable channels. Plant Physiol 141: 1653-1665
– reference: Véry A, Sentenac H (2003) Molecular mechanisms and regulation of K+ transport in higher plants. Annu Rev Plant Biol 54: 575-603
– reference: Fang Z, Mi F, Berkowitz GA (1995) Molecular and physiological analysis of a thylakoid K+ channel protein. Plant Physiol 108: 1725-1734
– reference: Demidchik V, Maathuis JM (2007) Physiological roles of nonselective cation channels in plant: from salt stress to signalling and development. New Phytol 175: 387-404
– reference: Plett D, Safwat G, Gilliham M, Møller IS, Roy S, Shirley N, Jacobs A, Johnson A, Tester M (2010) Improved salinity tolerance of rice through cell type-specific expression of AtHKT1;1. PLoS One 5: e12571
– reference: Munns R, James RA, Läuchli A (2006) Approaches to increasing the salt tolerance of wheat and other cereals. J Exp Bot 57: 1025-1043
– reference: Shabala S, Cuin TA (2008) Potassium transport and plant salt tolerance. Physiol Plant 133: 651-669
– reference: Demidchik V, Davenport RJ, Tester M (2002) Nonselective cation channels in plants. Annu Rev Plant Biol 53: 67-107
– reference: Chen Z, Zhou M, Newman IA, Mendham NJ, Zhang GP, Shabala S (2007c) Potassium and sodium relations in salinised barley tissues as a basis of differential salt tolerance. Funct Plant Biol 34: 150-162
– reference: Talbott LD, Zeiger E (1996) Central roles for potassium and sucrose in guard-cell osmoregulation. Plant Physiol 111: 1051-1057
– reference: Xu R, Wang J, Li C, Johnson P, Lu C, Zhou M (2012) A single locus is responsible for salinity tolerance in a Chinese landrace barley (Hordeum vulgare L.). PLoS One 7: e43079
– reference: Shabala S (2000) Ionic and osmotic components of salt stress specifically modulate net ion fluxes from bean mesophyll. Plant Cell Environ 23: 825-837
– reference: Evans HJ, Sorger GJ (1966) Role of mineral elements with emphasis on the univalent cations. Annu Rev Plant Physiol 17: 47-76
– reference: Shabala S, Shabala L (2002) Kinetics of net H+, Ca2+, K+, Na+, NH4+, and Cl- fluxes associated with post-chilling recovery of plasma membrane transporters in Zea mays leaf and root tissues. Physiol Plant 114: 47-56
– reference: Koch K, Barthlott W, Koch S, Hommes A, Wandelt K, Mamdouh W, De-Feyter S, Broekmann P (2006) Structural analysis of wheat wax (Triticum aestivum, c.v. 'Naturastar' L.): from the molecular level to three dimensional crystals. Planta 223: 258-270
– reference: Rengasamy P (2010) Soil processes affecting crop production in salt-affected soils. Funct Plant Biol 37: 613-620
– reference: Suelter CH (1970) Enzymes activated by monovalent cations. Science 168: 789-795
– reference: Sze H, Li X, Palmgren MG (1999) Energization of plant cell membranes by H+-pumping ATPase: regulation and biosynthesis. Plant Cell 11: 677-689
– reference: Tegg R, Melian L, Wilson CR, Shabala S (2005) Plant cell growth and ion flux responses to the streptomycete phytotoxin thaxtomin A: calcium and hydrogen flux patterns revealed by the non-invasive MIFE technique. Plant Cell Physiol 46: 638-648
– reference: Flowers TJ (2004) Improving crop salt tolerance. J Exp Bot 55: 307-319
– reference: Chen Z, Newman I, Zhou M, Mendham N, Zhang G, Shabala S (2005) Screening plants for salt tolerance by measuring K+ flux: a case study for barley. Plant Cell Environ 28: 1230-1246
– reference: Newman IA (2001) Ion transport in plants: measurement of fluxes using ion-selective microelectrodes to characterize transporter function. Plant Cell Environ 24: 1-14
– reference: Shabala S, Lew RR (2002) Turgor regulation in osmotically stressed Arabidopsis epidermal root cells. Direct support for the role of inorganic ion uptake as revealed by concurrent flux and cell turgor measurements. Plant Physiol 129: 290-299
– reference: Cavalcanti FR, Lima JPMS, Ferreira-Silva SL, Viégas RA, Silveria JAG (2007) Roots and leaves display contrasting oxidative response during salt stress and recovery in cowpea. J Plant Physiol 164: 591-600
– reference: Davies MJ, Poole RJ, Rea PA, Sanders D (1992) Potassium transport into plant vacuoles energized directly by a proton-pumping inorganic pyrophosphatase. Proc Natl Acad Sci USA 89: 11701-11705
– reference: Hughes FM, Cidlowski JA (1999) Potassium is a critical regulator of apoptotic enzymes in vitro and in vivo. Adv Enzyme Regul 39: 157-171
– reference: Osaki M, Shinano T, Tadano T (1993) Effect of nitrogen, phosphorus, or potassium deficiency on the accumulation of ribulose-1,5-bisphosphate carboxylase/oxygenase and chlorophyll in several field crops. Soil Sci Plant Nutr 39: 417-425
– reference: Zhou G, Johnson P, Ryan PR, Delhaize E, Zhou M (2012) Quantitative trait loci for salinity tolerance in barley (Hordeum vulgare L.). Mol Breed 29: 427-436
– reference: Blumwald E, Aharon GS, Apse MP (2000) Sodium transport in plant cells. Biochim Biophys Acta 1465: 140-151
– reference: Munns R, Tester M (2008) Mechanism of salinity tolerance. Annu Rev Plant Biol 59: 651-681
– reference: Chen Z, Pottosin II, Cuin TA, Fuglsang AT, Tester M, Jha D, Zepeda-Jazo I, Zhou MX, Palmgren MG, Newman IA, Shabala S (2007b) Root plasma membrane transporters controlling K+/Na+ homeostasis in salt-stressed barley. Plant Physiol 145: 1714-1725
– reference: Maathuis F, Amtmann A (1999) K+ nutrition and Na+ toxicity: the basis of cellular K+/Na+ ratios. Ann Bot 84: 123-133
– reference: Shabala S, Cuin TA, Prismall L, Nemchinov LG (2007) Expression of animal CED-9 anti-apoptotic gene in tobacco modifies plasma membrane ion fluxes in response to salinity and oxidative stress. Planta 227: 189-197
– reference: Cuin TA, Betts SA, Chalmandrier R, Shabala S (2008) A root's ability to retain K+ correlates with salt tolerance in wheat. J Exp Bot 59: 2697-2706
– reference: Smethurst CF, Shabala S (2003) Screening methods for waterlogging tolerance in lucerne: comparative analysis of waterlogging effects on chlorophyll fluorescence, photosynthesis, biomass and chlorophyll content. Funct Plant Biol 30: 335-343
– reference: Dreyer I, Uozum N (2011) Potassium channels in plant cells. FEBS J 278: 4293-4303
– reference: Mäser P, Thomine S, Schroeder JI, Ward JM, Hirschi K, Sze H, Talke IN, Amtmann A, Maathuis FJM, Sanders D, Harper JF, Tchieu J, Gribskov M, Persans MW, Salt DE, Kim SA, Guerinot ML (2001) Phylogenetic relationships within cation transporter families of Arabidopsis. Plant Physiol 126: 1646-1667
– reference: James RA, Rivelli AR, Munns R, von Caemmerer S (2002) Factors affecting CO2 assimilation, leaf injury and growth in salt-stressed durum wheat. Funct Plant Biol 29: 1393-1403
– reference: Demidchik V, Shabala SN, Coutts KB, Tester MA, Davies JM (2003) Free oxygen radicals regulate plasma membrane Ca2+- and K+-permeable channels in plant root cells. J Cell Sci 116: 81-88
– reference: Shabala S, Newman I (1999) Light-induced changes in hydrogen, calcium, potassium, and chloride ion fluxes and concentrations from mesophyll and epidermal tissues of bean leaves. Understanding the ionic basis of light-induced bioelectrogenesis. Plant Physiol 119: 1115-1124
– reference: Hosy E, Vavasseur A, Mouline K, Dreyer I, Gaymard F, Porée F, Boucherez J, Lebaudy A, Bouchez D, Véry A, Simonneau T, Thibaud J, Sentenac H (2003) The Arabidopsis outward K+ channel GORK is involved in regulation of stomatal movements and plant transpiration. Proc Natl Acad Sci USA 100: 5549-5554
– reference: Živanović BD, Pang J, Shabala S (2005) Light-induced transient ion flux response from maize leaves and their association with leaf growth and photosynthesis. Plant Cell Environ 28: 340-352
– reference: Marschner H, Kirkby EA, Cakmak I (1996) Effect of mineral nutritional status on shoot-root partitioning of photoassimilates and cycling of mineral nutrients. J Exp Bot 47: 1255-1263
– reference: Agrawal PB, Nierstrasz VA, Klug-Santner BG, Gübitz GM, Lenting HBM, Warmoeskerken MMCG (2007) Wax removal for accelerated cotton scouring with alkaline pectinase. Biotechnol J 2: 306-315
– reference: Demidchik V, Shabala SN, Davies JM (2007) Spatial variation in H2O2 response of Arabidopsis thaliana root epidermal Ca2+ flux and plasma membrane Ca2+ channels. Plant J 49: 377-386
– reference: Cuin TA, Tian Y, Betts SA, Chalmandrier R, Shabala S (2009) Ionic relations and osmotic adjustment in durum and bread wheat under saline conditions. Funct Plant Biol 36: 1110-1119
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Snippet This work investigated the importance of the ability of leaf mesophyll cells to control K+ flux across the plasma membrane as a trait conferring tissue...
This work investigated the importance of the ability of leaf mesophyll cells to control K + flux across the plasma membrane as a trait conferring tissue...
This work investigated the importance of the ability of leaf mesophyll cells to control K(+) flux across the plasma membrane as a trait conferring tissue...
This work investigated the importance of the ability of leaf mesophyll cells to control K⁺ flux across the plasma membrane as a trait conferring tissue...
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StartPage 515
SubjectTerms apoplast
Barley
Biological and medical sciences
breeding
cell viability
correlation
epicuticular wax
epidermis (plant)
Fluctuations
Fundamental and applied biological sciences. Psychology
Genotype
Genotypes
greenhouse experimentation
Hordeum - drug effects
Hordeum - genetics
Hordeum - physiology
Hordeum vulgare
hydrogen ions
ion transport
Leaves
mesophyll
Mesophyll Cells - metabolism
Organic solvents
osmosis
pharmacology
Phenotype
Plant Leaves - drug effects
Plant Leaves - genetics
Plant Leaves - physiology
Plant physiology and development
plasma membrane
potassium
Potassium - metabolism
potassium channels
Salinity
Salinity tolerance
salt stress
Salt-Tolerance
screening
shoots
sodium
Sodium - metabolism
Sodium chloride
Sodium Chloride - pharmacology
solvents
Triticum - drug effects
Triticum - genetics
Triticum - physiology
Triticum aestivum
Triticum turgidum
waxes
Wheat
Title Ability of leaf mesophyll to retain potassium correlates with salinity tolerance in wheat and barley
URI https://api.istex.fr/ark:/67375/WNG-9PF8GSQ9-8/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fppl.12056
https://www.ncbi.nlm.nih.gov/pubmed/23611560
https://www.proquest.com/docview/1458568731
https://www.proquest.com/docview/1501357612
https://www.proquest.com/docview/1812889482
Volume 149
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