Potassium deficiency in plants: effects and signaling cascades

• Autorzy: Hafsi C. , Debez A. , Abdelly C.
• Języki publikacji: EN

Abstrakty

EN

Potassium (K⁺) is an important macronutrient for plant growth and productivity. It fulfills important functions and it is widely included in fertilization management strategies to increase crop production. Although K⁺ is one of the most abundant elements of the earth crust, its availability to plants is usually limited leading to severe reduction in plant growth and yield. In plants, K⁺ shortage induces several responses at different levels: morphological, physiological, biochemical, and molecular. Activation of signaling cascades including reactive oxygen species, phytohormones (ethylene, auxin, and jasmonic acid), Ca²⁺, and phosphatidic acid is also triggered. In this review, we summarize the main of these adaptive responses evolved by plants to cope with K⁺ deficiency in the rhizosphere.

• Wydawca: -
• Czasopismo: Acta Physiologiae Plantarum
• Rocznik: 2014
• Tom: 36
• Numer: 05
• Opis fizyczny: p.1055-1070,fig.,ref.

Twórcy

autor

Hafsi C.

• Laboratoire des Plantes Extremophiles, Centre de Biotechnologie a la Technopole de Borj Cedria, BP 901, Hammam-Lif 2050, Tunisie

autor

Debez A.

• Laboratoire des Plantes Extremophiles, Centre de Biotechnologie a la Technopole de Borj Cedria, BP 901, Hammam-Lif 2050, Tunisie

autor

Abdelly C.

• Laboratoire des Plantes Extremophiles, Centre de Biotechnologie a la Technopole de Borj Cedria, BP 901, Hammam-Lif 2050, Tunisie

Bibliografia

• Ahn SJ, Shin R, Schachtman DP (2004) Expression of KT/KUP genes in Arabidopsis and the role of root hairs in K⁺ uptake. Plant Physiol 134:1135–1145
• Alemán F, Nieves-Cordones M, Martínez V, Rubio F (2011) Root K⁺ acquisition in plants: the Arabidopsis thaliana model. Plant Cell Physiol 52(9):1603–1612
• Amtmann A, Armengaud P, Volvok V (2004) Potassium nutrition and salt stress. In: Blatt MR (ed) Membrane transport in plants. Blackwell Publishing, Oxford
• Andrews M, Sprent JI, Raven JA, Eady PE (1999) Relationships between shoot to root ratio, growth and leaf soluble protein concentration of Pisum sativum, Phaseolus vulgaris and Triticum aestivum under different nutrient deficiencies. Plant Cell Environ 22:949–958
• Arend M, Monshausen G, Wind C, Weisenseel MH, Fromm J (2004) Effect of potassium deficiency on the plasma membrane H⁺-ATPase of the wood ray parenchyma in poplar. Plant Cell Environ 27:1288–1296
• Armengaud P, Breitling R, Amtmann A (2004) The potassium dependent transcriptome of Arabidopsis reveals a prominent role of jasmonic acid in nutrient signaling. Plant Physiol 136:2556–2576
• Ashley MK, Grant M, Grabov A (2006) Plant responses to potassium deficiencies: a role for potassium transport proteins. J Exp Bot 57(2):425–436
• Askegaard M, Eriksen J, Olesen JE (2003) Exchangeable potassium and potassium balances in organic crop rotations on coarse sand. Soil Use Manag 19:96–103
• Bañuelos MA, Garciadeblas B, Cubero B, Rodríguez-Navarro A (2002) Inventory and functional characterization of the HAK potassium transporters of rice. Plant Physiol 130:784–795
• Bednarz CW, Oosterhuis DM, Evans RD (1998) Leaf photosynthesis and carbon isotope discrimination of cotton in response to potassium deficiency. Environ Exp Bot 39:131–139
• Benlloch M, Moreno I, Rodriguez-Navarro A (1989) Two modes of rubidium uptake in sunflower plants. Plant Physiol 90:939–942
• Bertsch PM, Thomas GW (1985) Potassium status of temperate region soils. In: Munson RD (ed) Potassium in agriculture. American Society of Agronomy, Madison, pp 131–162
• Bhandal IS, Malik CP (1988) Potassium estimation, uptake, and its role in the physiology and metabolism of flowering plants. Inter Rev Cytol 110:205–254
• Blaha G, Stelzl U, Spahn CMT, Agrawal RK, Frank J, Nierhaus KH (2000) Preparation of functional ribosomal complexes and effect of buffer conditions on tRNA positions observed by cryoelectron microscopy. Methods Enzymol 317:292–309
• Blevins DG, Barnett NM, Frost WB (1978) Role of potassium and malate in nitrate uptake and translocation by wheat seedlings. Plant Physiol 62:784–788
• Bottrill DE, Possingham JV, Kriedemann PE (1970) The effect of nutrient deficiencies on photosynthesis and respiration in spinach. Plant Soil 32:424–438
• Britto DT, Kronzucker HJ (2008) Cellular mechanisms of potassium transport in plants. Physiol Plant 133:637–650
• Brouder SM, Cassman KG (1990) Root development of two cotton cultivars in relation to potassium uptake and plant growth in a vermiculite soil. Field Crop Res 23:187–203
• Bruggemann LI, Pottosin II, Schonknecht G (1998) Cytoplasmic polyamines block the fast activating vacuolar cation channel. Plant J 16:101–105
• Buschmann PH, Vaidyanathan R, Gassmann W, Schroeder JI (2000) Enhancement of Na⁺ uptake currents, time-dependent inwardrectifying K⁺ channel currents, and K⁺ channel transcripts by K⁺ starvation in wheat root cells. Plant Physiol 122:1387–1397
• Cakmak I (2005) The role of potassium in alleviating detrimental effects of abiotic stresses in plants. J Plant Nutr Soil Sci 168:521–530
• Cakmak I, Hengeler C, Marschner H (1994) Partitioning of shoot and root dry matter and carbohydrates in bean plants suffering from phosphorus, potassium and magnesium deficiency. J Exp Bot 45:1245–1250
• Cao S, Su L, Fang Y (2006) Evidence for involvement of jasmonic acid in the induction of leaf senescence by potassium deficiency in Arabidopsis. Can J Bot 84:328–333
• Chen J, Gabelman WH (1995) Isolation of tomato strains varying in potassium acquisition using a sand-zeolite culture system. Plant Soil 176:65–70
• Chen J, Gabelman WH (2000) Morphological and physiological characteristics of tomato roots associated with potassium-acquisition efficiency. Sci Hortic 83:213–225
• Chen YF, Wang Y, Wu WH (2008) Membrane transporters for nitrogen, phosphate and potassium uptake in plants. J Integr Plant Biol 50:835–848
• Chérel I, Michard E, Platet N, Mouline K, Alcon C et al (2002) Physical and functional interaction of the Arabidopsis K⁺ channel AKT2 and phosphatase AtPP2CA. Plant Cell 14:1133–1146
• Cochrane TT, Cochrane TA (2009) The vital role of potassium in the osmotic mechanism of stomata aperture modulation and its link with potassium deficiency. Plant Signal Behav 4(3):240–243
• Damon PM, Osborne LD, Rengel Z (2007) Canola genotypes differ in potassium efficiency during vegetative growth. Euphytica 156:387–397
• Deeken R, Sanders C, Ache P, Hedrich R (2000) Developmental and light dependent regulation of phloem-localised K⁺ channel of Arabidopsis thaliana. Plant J 23:285–290
• Degl’Innocenti E, Hafsi C, Guidi L, Navari-Izzo F (2009) The effect of salinity on photosynthetic activity in potassium-deficient barley species. J Plant Physiol 166:1968–1981
• Demidchik K, 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
• Diem B, Godbold DL (1993) Potassium, calcium and magnesium antagonism in clones of Populus trichocarpa. Plant Soil 155(156):411–414
• Dobrovinskaya OR, Muniz J, Pottosin II (1999) Inhibition of vacuolar ion channels by polyamines. Biophys J 167:127–140
• Drew MC (1975) Comparison of the effects of a localized supply of phosphate, nitrate, ammonium and potassium on the growth of the seminal root system, and the shoot in barley. New Phytol 75:490–749
• Duby G, Hosy E, Fizames C, Alcon A, Alcon C et al (2008) AtKC1, a conditionally targeted Shaker-type subunit, regulates the activity of plant K⁺ channels. Plant J 53:115–123
• Epstein E, Rains DW, Elzam OE (1963) Resolution of dual mechanisms of potassium absorption by barley roots. Proc Natl Acad Sci USA 49:684–692
• Evans NH (2003) Modulation of guard cell plasma membrane potassium currents by methyl jasmonate. Plant Physiol 131:8–11
• Evans HJ, Wildes RA (1971) Potassium and its role in enzyme activation. Potassium in biochemistry and physiology. International Potash Institute, Berne, pp 13–39
• Fageria NK, Baligar VC, Jones CA (1997) Growth and mineral nutrition of field crops, 2nd edn. Marcel Dekker, New York
• Fageria NK, Barbosa Filho MP, da Costa JGC (2001) Potassium-use efficiency in common bean genotypes. J Plant Nutr 24:1937–1945
• Fairbairn DJ, Liu W, Schachtman DP, Gomez-Gallego S, Day SR, Teasdale RD (2000) Characterisation of two distinct HKT1-like potassium transporters from Eucalyptus camaldulensis. Plant Mol Biol 43:515–525
• Feijó JA, Malhó R, Obermeyer G (1995) Ion dynamics and its possible role during in vitro pollen germination and tube growth. Protoplasma 187:155–167
• Fernando M, Kulpa J, Siddiqi YM, Glass ADM (1990) Potassium-dependent changes in the expression of membrane-associated proteins in barley roots. Plant Physiol 92(4):1128–1132
• Flowers TJ, Läuchli A (1983) Sodium versus potassium: substitution and compartmentation. In: Läuchli A, Pirson A (eds) Inorganic plant nutrition. Encyclopedia of plant physiology, vol. 15B. Springer, Berlin, pp 651–681
• Foreman J, Demidchik V, Bothwell JH, Mylona P, Miedema H, Torres MA, Linstead P, Costa S, Brownlee C, Jones JD et al (2003) Reactive oxygen species produced by NADPH oxidase regulate plant cell growth. Nature 422:442–446
• Gahoonia TS, Ali O, Sarker A, Nielsen NE, Rahman MM (2006) Genetic variation in root traits and nutrient acquisition of lentil genotypes. J Plant Nutr 29:643–655
• Gajdanowicz P, Michard E, Sandmann M, Rocha M, Correa LGG et al (2011) Potassium (K⁺) gradients serve as a mobile energy source in plant vascular tissues. Proc Natl Acad Sci USA 108:864–869
• Gambale F, Uozumi N (2006) Properties of Shaker-type potassium channels in higher plants. J Membr Biol 210:1–19
• Gaymard F, Pilot G, Lacombe B, Bouchez D, Bruneau D, Boucherez J, Michaux-Ferrière N, Thibaud JB, Sentenac H (1998). Identification and disruption of a plant Shaker-like outward channel involved in K⁺ release into the xylem sap. Cell 94:647–655
• Geiger D, Becker D, Vosloh D, Gambale F, Palme K et al (2009) Heteromeric AtKC1. AKT1channels in Arabidopsis roots facilitate growth under K⁺-limiting conditions. J Biol Chem 284:21288–21295
• Gerardeaux E, Saur E, Constantin J, Porté A, Jordan-Meille L (2009) Effect of carbon assimilation on dry weight production and partitioning during vegetative growth. Plant Soil 324:329–343
• Gerardeaux E, Jordan-Meille L, Constantin J, Pellerin S, Dingkuhn M (2010) Changes in plant morphology and dry matter partitioning caused by potassium deficiency in Gossypium hirsutum (L.). Environ Exp Bot 67:451–459
• Gierth M, Mäser P (2007) Potassium transporters in plants—involvement in K⁺ acquisition, redistribution and homeostasis. FEBS Lett 581:2348–2356
• Gierth M, Maser P, Schroeder JI (2005) The potassium transporter AtHAK5 functions in K⁺ deprivation-induced high-affinity K⁺ uptake and AKT1 K⁺ channel contribution to K⁺ uptake kinetics in Arabidopsis roots. Plant Physiol 137:1105–1114
• Glass ADM, Dunlop J (1978) The influence of potassium content on the kinetics of potassium influx into excised ryegrass and barley roots. Planta 141(1):117–119
• Grattan SR, Grieve CM (1992) Mineral element acquisition and growth response of plants grown in saline environments. Agric Ecosyst Environ 38:275–300 (Elsevier Science Publishers B.V., Amsterdam)
• Gruber BD, Giehl RFH, Friedel S, von Wirén N (2013) Plasticity of the Arabidopsis root system under nutrient deficiencies. Plant Physiol 163:161–179
• Guo ZK, Yang Q, Wan XQ, Yan PQ (2008) Functional characterization of a potassium transporter gene NrHAK1 in Nicotiana rustica. J Zhejiang Univ Sci 9(12):944–952
• Guoping Z, Jingxing C, Tirore EA (1999) Genotypic variation for potassium uptake and utilization efficiency in wheat. Nutr Cycl Agroecosyst 54:41–48
• Hafsi C, Russo MA, Sgherri C, Izzo R, Abdelly C, Navari-Izzo F (2008) Has glyceraldehyde-3-phosphate dehydrogenase a role in the early response of Hordeum maritimum L. to potassium deprivation? Agrochimica 2(4):253–262
• Hafsi C, Russo MA, Sgherri C, Izzo R, Navari-Izzo F, Abdelly C (2009) Implication of phospholipase D in response of Hordeum vulgare root to short-term potassium deprivation. J Plant Physiol 166:499–506
• Hafsi C, Atia A, Lakhdar A, Debez A, Abdelly C (2011) Differential responses in potassium absorption and use efficiencies in the halophytes Catapodium rigidum and Hordeum maritimum to various potassium concentrations in the medium. Plant Prod Sci 14(2):135–140
• Hammond JP, Broadley MR, White PJ (2004) Genetic responses to phosphorus deficiency. Ann Bot 94:323–332
• Hampton CR, Bowen HC, Broadley MR, Hammond JP, Mead A, Payne KA, Pritchard J, White PJ (2004) Cesium toxicity in Arabidopsis. Plant Physiol 136:3824–3837
• Han-Bai H, Zhao-Hu L, Xiao-Li T (2009) Mechanism of tolerance to potassium deficiency between Liaomian 18 and NuCOTN99B at seedling stage. Acta Agric Sinica 35(3):475–482
• Havlin JL, Beaton JD, Tisdale SL, Nelson WL (2005) Soil fertility and fertilizers: an introduction to nutrient management, 7th edn. Prentice Hall, Upper Saddle River
• Hernandez M, Fernandez-Garcia N, Garcia-Garma J, Rubio-Asensio JS, Rubio F, Olmos E (2012) Potassium starvation induces oxidative stress in Solanum lypersicum L. roots. J Plant Physiol 169:1366–1374
• Hewitt EJ (1963) Essential nutrient elements for plants: requirement and interaction in plants. In: Steward FC (ed) Plant physiol, vol III. Academic Press Inc., New York, pp 137–360
• Hirsch RE, Lewis BD, Spalding EP, Sussman MR (1998) A role for the AKT1 potassium channel in plant nutrition. Science 280:918–921
• Høgh-Jensen H (2003) The effect of potassium deficiency on growth and N2-fixation in Trifolium repens. Physiol Plant 119:440–449
• Hong Y, Devaiah SP, Bahn SC, Thamasandra BN, Li M, Welti R, Wang X (2009) Phospholipase Dɛ and phosphatidic acid enhance Arabidopsis nitrogen signaling and growth. Plant J 58:376–387
• Hong JP, Takeshi Y, Kondou Y, Schachtman DP, Matsui M, Shin R (2013) Identification and characterization of transcription factors regulating Arabidopsis HAK5. Plant Cell Physiol 54(9):1478–1490
• Honsbein A, Sokolovski S, Grefen C, Campanoni P, Pratelli R et al (2009) A tripartite SNARE-K⁺ channel complex mediates in channel-dependent K⁺ nutrition in Arabidopsis. Plant Cell 21:2859–2877
• Hosy E, Vavasseur A, Mouline K, Dreyer I, Gaymard F et al (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
• Howe GA, Schilmiller AL (2002) Oxylipin metabolism in response to stress. Curr Opin Plant Biol 5:230–236
• Jeanguenin L, Alcon C, Duby G, Boeglin M, Cherel I et al (2011) AtKC1 is a general modulator of Arabidopsis inward Shaker channel activity. Plant J 67:570–582
• Johnston AE (2005) Understanding potassium and its use in agriculture. EFMA, Brussels
• Jordan-Meille L, Pellerin S (2004) Leaf area establishment of a maize (Zea Mays L.) field crop under potassium deficiency. Plant Soil 265:75–92
• Jordan-Meille L, Pellerin S (2008) Shoot and root growth of hydroponic maize (Zea mays L.) as influence by K deficiency. Plant Soil 304:157–168
• Jung JY, Shin R, Schachtman DP (2009) Ethylene mediates response and tolerance to potassium deprivation in Arabidopsis. Plant Cell 21:607–621
• Kanai S, Ohkura K, Adu-Gyamfi JJ, Mohapatra PK, Nguyen NT, Saneoka H, Fujita K (2007) Depression of sink activity precedes the inhibition of biomass production in tomato plants subjected to potassium deficiency stress. J Exp Bot 58(11):2917–2928
• Kanai S, Moghaieb RE, El-Shemy HA, Panigrahi R, Mohapatra PK, Ito J, Nguyen NT, Saneoka H, Fujita K (2011) Potassium deficiency affects water status and photosynthetic rate of the vegetative sink in green house tomato prior to its effects on source activity. Plant Sci 180:368–374
• Kang Y, Outlaw WH, Andersen PC, Fiore GB (2007) Guard-cell apoplastic sucrose concentration–a link between leaf photosynthesis and stomatal aperture size in the apoplastic phloem loader Vicia faba L. Plant Cell Environ 30:551–558
• Kellermeier F, Chardon F, Amtmann A (2013) Natural variation of Arabidopsis root architecture reveals complementing adaptive strategies to potassium starvation. Plant Physiol 161:1421–1432
• Kim MJ, Ruzicka D, Shin R, Schachtman DP (2012) The Arabidopsis AP2/ERF transcription factor RAP2.11 modulates plant response to low-potassium conditions. Mol Plant 5(5):1042–1057
• Kramell R, Miersch O, Atzorn R, Parthier B, Wasternack C (2000) Octadecanoid-derived alteration of gene expression and the oxylipin signature in stressed barley leaves—implications for different signalling pathways. Plant Physiol 123:177–186
• Kudla J, Batistič O, Hashimoto K (2010) Calcium signals: the lead currency of plant information processing. Plant Cell 22:541–563
• Lacombe B, Pilot G, Michard E, Gaymard F, Sentenac H, Thibaud JB (2000) A shaker-like K⁺ channel with weak rectification is expressed in both source and sink phloem tissues of Arabidopsis. Plant Cell 12:837–851
• Lan WZ, Lee SC, Chec YF, Jiang YQ, Luan S (2011) Mechanistic analysis of AKT1 regulation by the CBL–CIPK–PP2CA interactions. Mol Plant 4:527–536
• Lee SC, Lan WZ, Kim BG, Li L, Cheong YH, Pandey GK, Lu G, Buchanan BB, Luan SA (2007) Protein phosphorylation/dephosphorylation network regulates a plant potassium channel. Proc Natl Acad Sci USA 104(40):15959–15964
• Leigh RA, Wyn Jones RG (1984) A hypothesis relating critical potassium concentrations for growth to the distribution and functions of this ion in the plant cell. New Phytol 97:1–13
• Li L, Kim BG, Cheong YH, Pandey GK, Luan S (2006) A Ca²⁺ signaling pathway regulates a K⁺ channel for low-K response in Arabidopsis. Proc Natl Acad Sci USA 103(33):12625–12630
• Liu K, Fu HH, Bei QX, Luan S (2000) Inward potassium channel in guard cells as a target for polyamine regulation of stomatal movements. Plant Physiol 124:1315–1325
• Liu LL, Ren HM, Chen LQ, Wang Y, Wu WH (2013) A protein kinase CIPK9 interacts with calcium sensor CBL3 and regulates K⁺ homeostasis under low-K⁺ stress in Arabidopsis. Plant Physiol 161:266–277
• Ma TL, Wu WH, Wang Y (2012) Transcriptome analysis of rice root responses to potassium deficiency. BMC Plant Biol 12:161
• Maathuis FJM, Sanders D (1994) Mechanism of high affinity potassium uptake in roots of Arabidopsis thaliana. Proc Natl Acad Sci USA 91:9272–9276
• Maathuis FJM, Sanders D (1995) Contrasting roles in ion transport of two K⁺-channel types in root cells of Arabidopsis thaliana. Planta 197:456–464
• Maathuis FJM, Sanders D (1996) Mechanisms of potassium absorption by higher plant roots. Physiol Plant 96:158–168
• Maathuis FJM, Filatov V, Herzyk P et al (2003) Transcriptome analysis of root transporters reveals participation of multiple gene families in the response to cation stress. Plant J 35:675–692
• Mahmood T, GILL MA, Ranjha AM, Ahmad Z, Rehman H (2001) Potassium deficiency-stress tolerance in wheat genotypes I: sand culture study. Inter J Agric Biol 3(1):113–116
• Marschner H (1986) Mineral nutrition of higher plants. Acad Press, London
• Marschner H (1995) Mineral nutrition of higher plants. Springer, New York
• Marschner H, Römheld V (1994) Strategies of plant acquisition of iron. Plant Soil 165:261–274
• 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
• Martínez-Cordero MA, Martínez V, Rubio F (2004) Cloning and functional characterization of the high-affinity K⁺ transporter HAK1 of pepper. Plant Mol Biol 56:413–421
• Meijer HJ, Munnik T (2003) Phospholipase based signalling in plants. Ann Rev Plant Biol 54:265–306
• Memon AR, Siddiqi MY, Glass ADM (1985) Efficiency of K⁺ utilization by barley varieties: activation of pyruvate kinase. J Exp Bot 36:79–90
• Meng TC, Fukada T, Tonks NK (2002) Reversible oxidation and inactivation of protein tyrosine phosphatases in vivo. Mol Cell 9:387–399
• Mengel K, Kirkby EA (1982) Potassium. In: Mengel K, Kirkby EA (eds) Principles of plant nutrition. International Potash Institute, Worblaufeu-Bern, pp 335–368
• Mengel K, Haghparast MR, Koch K (1974) The effect of potassium on the fixation of molecular nitrogen by root nodules of Vicia faba. Plant Physiol 54:535–538
• Minjian C, Haiqiu Y, Hongkui Y, Chunji J (2007) Difference in tolerance to potassium deficiency between two maize inbred lines. Plant Biosyst 134(3):333–339
• Mouline K, Véry AA, Gaymard F, Boucherez J, Pilot G et al (2002) Pollen tube development and competitive ability are impaired by disruption of a Shaker K⁺ channel in Arabidopsis. Genes Dev 16:339–350
• Munnik T, Meijer HJG, Ter Riet B, Hirt H, Frank W, Bartels D, Musgrave A (2000) Hyperosmotic stress stimulates phospholipase D activity and elevates the levels of phosphatidic acid and diacylglycerol pyrophosphate. Plant J 22:147–154
• Navari-Izzo F, Cestone B, Cavallini A, Natali L, Giordani T, Quartacci MF (2006) Copper excess triggers phospholipase D activity in wheat roots. Phytochemistry 67:1232–1242
• Neill S, Desikan R, Hancock J (2002) Hydrogen peroxide signaling. Curr Opin Plant Biol 5:388–395
• Ni DA (2012) Role of vacuolar invertase in regulating Arabidopsis stomatal opening. Acta Physiol Plant 34:2449–2452
• Nieves-Cordones M, Miller A, Alemán F, Martínez V, Rubio F (2008) A putative role for the plasma membrane potential in the control of the expression of the gene encoding the tomato high-affinity potassium transporter HAK5. Plant Mol Biol 68:521–532
• Obermeyer G, Blatt MR (1995) Electrical properties of intact pollen germination of Lilium longiflorum: characteristics of the non-germinating pollen grains. J Exp Bot 46:803–813
• Ottow EA, Brinker M, Teichmann T, Fritz E, Kaiser W, Brosché M, Kangasjärvi J, Jiang X, Polle A (2005) Populus euphratica displays apoplastic sodium accumulation, osmotic adjustment by decreases in calcium and soluble carbohydrates, and develops leaf succulence under salt stress. Plant Physiol 139:1762–1772
• Pandey GK, Cheong YH, Kim BG, Grant JJ, Li L et al (2007) CIPK9: a calcium sensor-interacting protein kinase required for low-potassium tolerance in Arabidopsis. Cell Res 17:411–421
• Pettigrew WT (2008) Potassium influences on yield and quality production for maize, wheat, soybean and cotton. Physiol Plant 133:670–681
• Philippar K, Fuchs I, Luthen H, Hoth S, Bauer CS et al (1999) Auxin-induced K⁺ channel expression represents an essential step in coleoptile growth and gravitropism. Proc Natl Acad Sci USA 96:12186–12191
• Pilot G, Lacombe B, Gaymard F, Chérel I, Boucherez J et al (2001) Guard cell inward K⁺ channel activity in Arabidopsis involves expression of the twin channel subunits KAT1 and KAT2. J Biol Chem 276:3215–3221
• Pilot G, Gaymard F, Mouline K, Chérel I, Sentenac H (2003) Regulated expression of Arabidopsis shaker K⁺ channel genes involved in K⁺ uptake and distribution in the plant. Plant Mol Biol 51:773–787
• Pottosin II, Estévez M (2003) Regulation of the fast vacuolar channel by cytosolic and vacuolar potassium. Biophys J 84:977–986
• Pujos A, Morard P (1997) Effects of potassium deficiency on tomato growth and mineral nutrition at the early production stage. Plant Soil 189:189–196
• Pyo Y, Gierth M, Schroeder JI, Cho MH (2010) High-affinity K⁺ transport in Arabidopsis: AtHAK5 and AKT1 are vital for seedling establishment and postgermination growth under low K⁺ conditions. Plant Physiol 153:863–875
• Qi Z, Hampton CR, Shin R, Barkla BJ, White PJ, Schachtman DP (2008) The high affinity K⁺ transporter AtHAK5 plays a physiological role in planta at very low K⁺ concentrations and provides a caesium uptake pathway in Arabidopsis. J Exp Bot 59:595–607
• Qin C, Wang X (2002) The Arabidopsis phospholipase D family. Characterization of a calcium-independent and phosphatidylcholine-selective PLDf1 with distinct regulatory domains. Plant Physiol 128:1057–1068
• Qu C, Liu C, Ze Y, Gong X, Hong M, Wang L, Hong F (2011) Inhibition of nitrogen and photosynthetic carbon assimilation of maize seedlings by exposure to a combination of salt stress and potassium-deficient stress. Biol Trace Elem Res 144:1159–1174
• Raven PH, Evert RF, Curtis H (1976) Biology of plants. Worth Publishers, New York
• Reintanz B, Szyroki A, Ache P, Ivashikina N, Godde M et al (2002) AtKC1, a silent Arabidopsis potassium channel α-subunit modulates root hair K⁺ influx. Proc Natl Acad Sci USA 99:4079–4084
• Rengel Z, Damon PM (2008) Crops and genotypes differ in efficiency of potassium uptake and use. Physiol Plant 133:624–636
• Rodríguez-Navarro A (2000) Potassium transport in fungi and plants. Biochim Biophys Acta 1469:1–30
• Römheld V (1987) Different strategies for iron acquisition in higher plants. Physiol Plant 70:231–234
• Rubio F, Nieves-Cordones M, Alemàn F, Martinez V (2008) Relative contribution of AtHAK5 and AtAKT1 to K⁺ uptake in the high-affinity range of concentrations. Physiol Plant 134:598–608
• Russo MA, Quartacci MF, Izzo R, Belligno A, Navari-Izzo F (2007) Long- and short-term phosphate deprivation in bean roots: plasma membrane lipid alterations and transient stimulation of phospholipases. Phytochemistry 68:1564–1571
• Sakaguchi T, Nishizawa NK, Nakanishi H, Yoshimura E, Mori S (1999) The role of potassium in the secretion of mugineic acids family phytosiderophores from iron-deficient barley roots. Plant Soil 215:221–227
• Samal D, Kovar JL, Steingrobe B, Sadana US, Bhadoria PS, Claassen N (2010) Potassium uptake efficiency and dynamics in the rhizosphere of maize (Zea mays L.), wheat (Triticum aestivum L.), and sugar beet (Beta vulgaris L.) evaluated with a mechanistic model. Plant Soil 332:105–121
• Sattelmacher B, Horst WJ, Becher HC (1994) Factors that contribute to genetic variation for nutrient efficiency of crop plants. Z Pflanzenernahr Bodenkd 157:215–224
• Sauerbeck DC, Helal HM (1990) Factors affecting the nutrient efficiency of plants. In: El Bassam N (ed) Genetic aspects of plant mineral nutrition. Martinus Nijhoff, Dordrecht, pp 11–17
• Schachtman DP, Schroeder JI (1994) Structure and transport mechanism of a high-affinity potassium uptake transporter from higher plants. Nature 370:655–658
• Schachtman DP, Shin R (2007) Nutrient sensing and signaling: nPKS. Ann Rev Plant Biol 58:47–69
• Schachtman DP, Schroeder JI, Lucas WJ, Anderson JA, Gaber RF (1992) Expression of an inward rectifying potassium channel by the Arabidopsis KAT1 cDNA. Science 258:1654–1658
• Schuppe-Koistinen I, Moldeus P, Bergman T, Cotgreave IA (1994) S-thiolation of human endothelial cell glyceraldehyde-3-phosphate dehydrogenase after hydrogen peroxide treatment. Eur J Biochem 221:1033–1037
• Sentenac H, Bonneaud N, Minet M, Lacroute F, Salmon JM, Gaymard F, Grignon C (1992) Cloning and expression in yeast of a plant potassium ion transport. Science 256:663–665
• Shin R, Schachtman DP (2004) Hydrogen peroxide mediates plant root cell response to nutrient deprivation. Proc Natl Acad Sci USA 101(23):8827–8832
• Shin R, Berg RH, Schachtman DP (2005) Reactive oxygen species and root hairs in Arabidopsis response to nitrogen, phosphorus and potassium deficiency. Plant Cell Physiol 46(8):1350–1357
• Singh P, Blanke MM (2000) Deficiency of potassium but not phosphorus enhances root respiration. Plant Growth Regul 32:77–81
• Spalding EP, Hirsch RE, Lewis DR, Qi Z, Sussman MR, Lewis BD (1999) Potassium uptake supporting plant growth in the absence of AKT1 channel activity. J Gen Physiol 113:909–918
• Sparks DL (1987) Potassium dynamics in soil. In: Stewart BA (ed) Advances in soil science. Springer, New York, pp 1–63
• Sparks DL, Huang PM (1985) Physical chemistry of soil potassium. In: Munson RD (ed) Potassium in agriculture. American Society of Agronomy, Madison, pp 201–276
• Stintzi A, Weber H, Reymond P, Browse J, Farmer EE (2001) Plant defense in the absence of jasmonic acid: the role of cyclopentenones. Proc Natl Acad Sci USA 98:12837–12842
• Talbott LD, Zeiger E (1996) Central roles for potassium and sucrose in guard-cell osmoregulation. Plant Physiol 111:1051–1057
• Taylor LP, Hepler PK (1997) Pollen germination and tube growth. Ann Rev Plant Physiol Plant Mol Biol 48:461–491
• Tester M, Blatt MR (1989) Direct measurement of K⁺ channels in thylakoid membranes by incorporation of vesicles planar lipid bilayer. Plant Physiol 91:249–252
• Tewari RK, Kumar P, Tewari N, Srivastava S, Sharma PN (2004) Macronutrient deficiencies and differential antioxidant responses-influence on the activity and expression of superoxide dismutase in maize. Plant Sci 166:687–694
• Tewari RK, Kumar P, Sharma PN (2007) Oxidative stress and antioxidant responses in young leaves of mulberry plants under nitrogen, phosphorus or potassium deficiency. J Integr Plant Biol 49(3):313–332
• Thaler P, Pages L (1998) Modeling the influence of assimilates availability on root growth and architecture. Plant Soil 201:307–320
• Trehan SP, Sharma RC (2002) Potassium uptake efficiency of young plants of three potato cultivars as related to root and shoot parameters. Commun Soil Sci Plant Anal 33:1813–1823
• Troufflard S, Mullen W, Larson T, Graham I, Crozier A, Amtmann A (2010) Potassium deficiency induces the biosynthesis of oxylipins and glucosinolates in Arabidopsis thaliana. BMC Plant Biol 10:172–184
• Tuteja N, Mahaja S (2007) Calcium signaling network in plants. Plant Signal Behav 2(2):79–85
• Véry AA, Sentenac H (2003) Molecular mechanisms and regulation of K⁺ transport in higher plants. Ann Rev Plant Biol 54:575–603
• Vicente-Agullo F, Rigas S, Desbrosses G, Dolan L, Hatzopoulos P, Grabov A (2004) Potassium carrier TRH1 is required for auxin transport in Arabidopsis roots. Plant J 40:523–535
• Vigliocco A, Bonamico B, Alemano S, Miersch O, Abdala G (2002) Stimulation of jasmonic acid production in Zea mays L. infected by the maize rough dwarf virus—Río Cuarto. Reversion of symptoms by salicylic acid. Biocell 26(3):369–374
• Walker DJ, Leigh RA, Miller AJ (1996) Potassium homeostasis in vacuolate plant cells. Proc Natl Acad Sci USA 93:10510–10514
• Wang X (2000) Multiple forms of phospholipase D in plants: the gene family, catalytic and regulatory properties, and cellular functions. Prog Lipid Res 39:109–149
• Wang Y, Wu WH (2010) Plant sensing and signaling in response to K⁺-deficiency. Mol Plant 3:280–287
• Wang Y, Wu WH (2013) Potassium transport and signaling in higher plants. Annu Rev Plant Biol 64:451–476
• Wang TB, Gassmann W, Rubio F, Schroeder JI, Glass ADM (1998) Rapid up-regulation of HKT1, a high-affiniy potassium transporter gene, in roots of barley and wheat following withdrawal of potassium. Plant Physiol 118:651–659
• Wang Y, He L, Li HD, Xu J, Wu WH (2010) Potassium channel α-subunit AtKC1 negatively regulates AKT1-mediated K⁺ uptake in Arabidopsis roots under low-K⁺ stress. Cell Res 20:826–837
• Wang N, Hua H, Eneji AE, Li Z, Duan L, Tian X (2012) Genotypic variations in photosynthetic and physiological adjustment to potassium deficiency in cotton (Gossypium hirsutum). J Photochem Photobiol B: Biol 110:1–8
• White PJ, Karley AJ (2010) Potassium. In: Hell R, Mendel R–R (eds) Cell biology of metals and nutrients. Springer, Heidelberg, pp 199–224
• Williamson LC, Ribrioux SPCP, Fitter AH, Leyser HMO (2001) Phosphate availability regulates root system architecture in Arabidopsis. Plant Physiol 126:875–882
• Woodend JJ, Glass AMD (1993) Genotype-environment interaction and correlation between vegetative and grain production measures of potassium use-efficiency in wheat (T. aestivum L.) grown under potassium stress. Plant Soil 151:39–44
• Xiao-Lei W, Hai-Qiu Y, Ning L, Bing YI, Jing W, Xing-Tao L, Xin-Hua Z, Min-Jian C (2012) Some physiological characteristics in maize (Zea mays L.) inbred lines tolerant to low potassium from grain filling to maturity. Afr J Agric Res 7(11):1761–1771
• Xiao-Li T, Gang-Wei W, Rui Z, Pei-Zhu Y, Liu-Sheng D, Zhao-Hu L (2008) Conditions and indicators for screening cotton (Gossypium hirsutum L.) varieties tolerant to low potassium. Acta Agric Sinica 34(8):1435–1443
• Xu J, Li HD, Chen LQ, Wang Y, Liu LL, He L, Wu WH (2006) A protein kinase, interacting with two calcineurin B-like proteins, regulates K⁺ transporter AKT1 in Arabidopsis. Cell 125:1347–1360
• Yamaguchi T, Tanabe S, Minami E, Shibuya N (2004) Activation of phospholipase D induced by hydrogen peroxide in suspension cultured rice cells. Plant Cell Physiol 45(9):1261–1270
• Yang T, Poovaiah BW (2002) Hydrogen peroxide homeostasis: activation of plant catalase by calcium/calmodulin. Proc Natl Acad Sci USA 99:4097–4102
• Yang XE, Liu JX, Wang WM, Li H, Luo AC, Ye ZQ, Yang YA (2003) Genotypic differences and some associated plant traits in potassium internal use efficiency of lowland rice (Oryza sativa L.). Nutr Cycl Agroecosyst 67(3):273–282
• Yawson DO, Kwakye PK, Armah FA, Frimpong KA (2011) The dynamics of potassium (K) in representative soil series of Ghana. J Agric Biol Sci 6(1):48–55
• Zhang W, Wang C, Qin C, Wood T, Olafsdottir G, Welti R, Wang X (2003) The oleate stimulated phospholipase D, PLDδ, and phosphatidic acid decrease H₂O₂-induced cell death in Arabidopsis. Plant Cell 15:2285–2295
• Zhao D, Oosterhuis DM, Bednarz CW (2001) Influence of potassium deficiency on photosynthesis, chlorophyll content, and chloroplast ultrastructure of cotton plants. Photosynthetica 39(1):103–109

Identyfikatory

DOI

10.1007/s11738-014-1491-2