The role of mycorrhizal associations in plant potassium nutrition

Garcia, Kevin; Zimmermann, Sabine D.

doi:10.3389/fpls.2014.00337

The role of mycorrhizal associations in plant potassium nutrition

Journal Article · Thu Jul 17 00:00:00 EDT 2014 · Frontiers in Plant Science

DOI:https://doi.org/10.3389/fpls.2014.00337· OSTI ID:1628258

Garcia, Kevin ^[1]; Zimmermann, Sabine D. ^[2]

Centre National de la Recherche Scientifique (CNRS), Montpellier (France). INRA/SupAgro/UM2. Biochimie et Physiologie Moleculaire des Plantes; DOE/OSTI
Centre National de la Recherche Scientifique (CNRS), Montpellier (France). INRA/SupAgro/UM2. Biochimie et Physiologie Moleculaire des Plantes

Potassium (K+) is one of the most abundant elements of soil composition but it’s very low availability limits plant growth and productivity of ecosystems. Because this cation participates in many biological processes, its constitutive uptake from soil solution is crucial for the plant cell machinery. Thus, the understanding of strategies responsible of K+ nutrition is a major issue in plant science. Mycorrhizal associations occurring between roots and hyphae of underground fungi improve hydro-mineral nutrition of the majority of terrestrial plants. The contribution of this mutualistic symbiosis to the enhancement of plant K+ nutrition is not well understood and poorly studied so far. This mini-review examines the current knowledge about the impact of both arbuscular mycorrhizal and ectomycorrhizal symbioses on the transfer of K+ from the soil to the plants. A model summarizing plant and fungal transport systems identified and hypothetically involved in K+ transport is proposed. In addition, some data related to benefits for plants provided by the improvement of K+ nutrition thanks to mycorrhizal symbioses are presented.

View Accepted Manuscript (DOE)

Research Organization:: Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)

Sponsoring Organization:: USDOE Office of Science (SC), Biological and Environmental Research (BER). Earth and Environmental Systems Science Division

Grant/Contract Number:: AC02-05CH11231

OSTI ID:: 1628258

Journal Information:: Frontiers in Plant Science, Journal Name: Frontiers in Plant Science Vol. 5; ISSN 1664-462X

Publisher:: Frontiers Research FoundationCopyright Statement

Country of Publication:: United States

Language:: English

References (90)

Nitrogen Transport in the Ectomycorrhiza Association: The Hebeloma cylindrosporom—Pinus pinaster Model Mueller, Tobias; Avolio, Meghan; Olivi, Martin ChemInform, Vol. 38, Issue 22 https://doi.org/10.1002/chin.200722270	journal	May 2007
A potassium transporter of the yeast Schwanniomyces occidentalis homologous to the Kup system of Escherichia coli has a high concentrative capacity. Bañuelos, M. A.; Klein, R. D.; Alexander-Bowman, S. J. The EMBO Journal, Vol. 14, Issue 13 https://doi.org/10.1002/j.1460-2075.1995.tb07304.x	journal	July 1995
Dispersed Polyphosphate in Fungal Vacuoles in Eucalyptus pilularis/Pisolithus tinctorius Ectomycorrhizas Ashford, Anne E.; Vesk, Peter A.; Orlovich, David A. Fungal Genetics and Biology, Vol. 28, Issue 1 https://doi.org/10.1006/fgbi.1999.1140	journal	October 1999
Potassium and sodium transport in non-animal cells: the Trk/Ktr/HKT transporter family Corratgé-Faillie, C.; Jabnoune, M.; Zimmermann, S. Cellular and Molecular Life Sciences, Vol. 67, Issue 15 https://doi.org/10.1007/s00018-010-0317-7	journal	March 2010
Arbuscular mycorrhizae: natural modulators of plant–nutrient relation and growth in stressful environments Thangavel, Palaniswamy; Anjum, Naser A.; Muthukumar, Thangavelu Archives of Microbiology, Vol. 204, Issue 5 https://doi.org/10.1007/s00203-022-02882-1	journal	April 2022
Improved Tolerance of Acacia nilotica to Salt Stress by Arbuscular Mycorrhiza, Glomus fasciculatum may be Partly Related to Elevated K/Na Ratios in Root and Shoot Tissues Giri, Bhoopander; Kapoor, Rupam; Mukerji, K. G. Microbial Ecology, Vol. 54, Issue 4 https://doi.org/10.1007/s00248-007-9239-9	journal	March 2007
Shaker-like potassium channels in Populus, regulated by the CBL–CIPK signal transduction pathway, increase tolerance to low-K+ stress Zhang, Hechen; Yin, Weilun; Xia, Xinli Plant Cell Reports, Vol. 29, Issue 9 https://doi.org/10.1007/s00299-010-0886-9	journal	June 2010
Phylogenetic distribution and evolution of mycorrhizas in land plants Wang, B.; Qiu, Y. -L. Mycorrhiza, Vol. 16, Issue 5 https://doi.org/10.1007/s00572-005-0033-6	journal	May 2006
Effect of arbuscular mycorrhizal colonization and two levels of compost supply on nutrient uptake and flowering of pelargonium plants Perner, Henrike; Schwarz, Dietmar; Bruns, Christian Mycorrhiza, Vol. 17, Issue 5 https://doi.org/10.1007/s00572-007-0116-7	journal	February 2007
Elemental composition of arbuscular mycorrhizal fungi at high salinity Hammer, Edith C.; Nasr, Hafedh; Pallon, Jan Mycorrhiza, Vol. 21, Issue 2 https://doi.org/10.1007/s00572-010-0316-4	journal	May 2010
Plant potassium content modifies the effects of arbuscular mycorrhizal symbiosis on root hydraulic properties in maize plants El-Mesbahi, Mohamed Najib; Azcón, Rosario; Ruiz-Lozano, Juan Manuel Mycorrhiza, Vol. 22, Issue 7 https://doi.org/10.1007/s00572-012-0433-3	journal	February 2012
Biotrophic transportome in mutualistic plant–fungal interactions Casieri, Leonardo; Ait Lahmidi, Nassima; Doidy, Joan Mycorrhiza, Vol. 23, Issue 8 https://doi.org/10.1007/s00572-013-0496-9	journal	April 2013
Benefit, cost and water-use efficiency of arbuscular mycorrhizal durum wheat grown under drought stress Al-Karaki, Ghazi N. Mycorrhiza, Vol. 8, Issue 1 https://doi.org/10.1007/s005720050209	journal	July 1998
Element distribution in mycorrhizal and nonmycorrhizal roots of the halophyte Aster tripolium determined by proton induced X-ray emission Scheloske, S.; Maetz, M.; Schneider, T. Protoplasma, Vol. 223, Issue 2-4 https://doi.org/10.1007/s00709-003-0027-1	journal	April 2004
The effect of Tuber melanosporum Vitt. mycorrhization on growth, nutrition, and water relations of Quercus petraea Liebl., Quercus faginea Lamk., and Pinus halepensis Mill. seedlings Domínguez Núñez, José Alfonso; Planelles González, Rosa; Rodríguez Barreal, José Antonio New Forests, Vol. 35, Issue 2 https://doi.org/10.1007/s11056-007-9069-0	journal	November 2007
Forms of nitrogen uptake, translocation, and transfer via arbuscular mycorrhizal fungi: A review Jin, HaiRu; Liu, Jie; Liu, Jing Science China Life Sciences, Vol. 55, Issue 6 https://doi.org/10.1007/s11427-012-4330-y	journal	June 2012
Poplar nutrition under drought as affected by ectomycorrhizal colonization Danielsen, Lara; Polle, Andrea Environmental and Experimental Botany, Vol. 108 https://doi.org/10.1016/j.envexpbot.2014.01.006	journal	December 2014
The influence of mycorrhization with Tuber melanosporum in the afforestation of a Mediterranean site with Quercus ilex and Quercus faginea Domínguez Núñez, José Alfonso; Serrano, Jesús Selva; Barreal, José Antonio Rodríguez Forest Ecology and Management, Vol. 231, Issue 1-3 https://doi.org/10.1016/j.foreco.2006.05.052	journal	August 2006
Elemental composition in vesicles of an arbuscular mycorrhizal fungus, as revealed by PIXE analysis Olsson, Pål Axel; Hammer, Edith C.; Pallon, Jan Fungal Biology, Vol. 115, Issue 7 https://doi.org/10.1016/j.funbio.2011.03.008	journal	July 2011
An overview of BORIS: Bioavailability of Radionuclides in Soils Tamponnet, C.; Martin-Garin, A.; Gonze, M. -A. Journal of Environmental Radioactivity, Vol. 99, Issue 5 https://doi.org/10.1016/j.jenvrad.2007.10.011	journal	May 2008
Mycorrhizal association of maritime pine, Pinus pinaster, with Rhizopogon roseolus has contrasting effects on the uptake from soil and root-to-shoot transfer of 137Cs, 85Sr and 95mTc Ladeyn, Ingrid; Plassard, Claude; Staunton, Siobhán Journal of Environmental Radioactivity, Vol. 99, Issue 5 https://doi.org/10.1016/j.jenvrad.2007.10.012	journal	May 2008
Effect of potassium and phosphorus on the transport of radiocesium by arbuscular mycorrhizal fungi Gyuricza, Veronika; Dupré de Boulois, Hervé; Declerck, Stéphane Journal of Environmental Radioactivity, Vol. 101, Issue 6 https://doi.org/10.1016/j.jenvrad.2008.04.002	journal	June 2010
Arbuscular mycorrhizal fungi decrease radiocesium accumulation in Medicago truncatula Gyuricza, Veronika; Declerck, Stéphane; Dupré de Boulois, Hervé Journal of Environmental Radioactivity, Vol. 101, Issue 8 https://doi.org/10.1016/j.jenvrad.2010.03.004	journal	August 2010
Arbuscular mycorrhizal fungi influence growth, osmotic adjustment and photosynthesis of citrus under well-watered and water stress conditions Wu, Qiang-Sheng; Xia, Ren-Xue Journal of Plant Physiology, Vol. 163, Issue 4 https://doi.org/10.1016/j.jplph.2005.04.024	journal	March 2006
Improved growth of salinity-stressed soybean after inoculation with salt pre-treated mycorrhizal fungi Sharifi, Mozafar; Ghorbanli, Mahlagha; Ebrahimzadeh, Hassan Journal of Plant Physiology, Vol. 164, Issue 9 https://doi.org/10.1016/j.jplph.2006.06.016	journal	September 2007
Arbuscular mycorrhizal fungi increased growth, nutrient uptake and tolerance to salinity in olive trees under nursery conditions Porras-Soriano, Andrés; Soriano-Martín, María Luisa; Porras-Piedra, Andrés Journal of Plant Physiology, Vol. 166, Issue 13 https://doi.org/10.1016/j.jplph.2009.02.010	journal	September 2009
K+ uptake in plant roots. The systems involved, their regulation and parallels in other organisms Nieves-Cordones, Manuel; Alemán, Fernando; Martínez, Vicente Journal of Plant Physiology, Vol. 171, Issue 9 https://doi.org/10.1016/j.jplph.2013.09.021	journal	May 2014
Ectomycorrhizal Pisolithus albus inoculation of Acacia spirorbis and Eucalyptus globulus grown in ultramafic topsoil enhances plant growth and mineral nutrition while limits metal uptake Jourand, Philippe; Hannibal, Laure; Majorel, Clarisse Journal of Plant Physiology, Vol. 171, Issue 2 https://doi.org/10.1016/j.jplph.2013.10.011	journal	January 2014
The twins K+ and Na+ in plants Benito, Begoña; Haro, Rosario; Amtmann, Anna Journal of Plant Physiology, Vol. 171, Issue 9 https://doi.org/10.1016/j.jplph.2013.10.014	journal	May 2014
Going beyond nutrition: Regulation of potassium homoeostasis as a common denominator of plant adaptive responses to environment Anschütz, Uta; Becker, Dirk; Shabala, Sergey Journal of Plant Physiology, Vol. 171, Issue 9 https://doi.org/10.1016/j.jplph.2014.01.009	journal	May 2014
Symbiotic fungi that are essential for plant nutrient uptake investigated with NMP Pallon, J.; Wallander, H.; Hammer, E. Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms, Vol. 260, Issue 1 https://doi.org/10.1016/j.nimb.2007.02.018	journal	July 2007
The arbuscular mycorrhizal symbiosis can overcome reductions in yield and nutritional quality in greenhouse-lettuces cultivated at inappropriate growing seasons Baslam, Marouane; Garmendia, Idoia; Goicoechea, Nieves Scientia Horticulturae, Vol. 164 https://doi.org/10.1016/j.scienta.2013.09.021	journal	December 2013
Elemental composition and function of polyphosphates in ectomycorrhizal fungi — an X-ray microanalytical study Bücking, H.; Heyser, W. Mycological Research, Vol. 103, Issue 1 https://doi.org/10.1017/s0953756298006935	journal	January 1999
A new family of outwardly rectifying potassium channel proteins with two pore domains in tandem Ketchum, Karen A.; Joiner, William J.; Sellers, Andrew J. Nature, Vol. 376, Issue 6542 https://doi.org/10.1038/376690a0	journal	August 1995
The genome of Laccaria bicolor provides insights into mycorrhizal symbiosis Martin, F.; Aerts, A.; Ahrén, D. Nature, Vol. 452, Issue 7183 https://doi.org/10.1038/nature06556	journal	March 2008
Périgord black truffle genome uncovers evolutionary origins and mechanisms of symbiosis Martin, Francis; Kohler, Annegret; Murat, Claude Nature, Vol. 464, Issue 7291 https://doi.org/10.1038/nature08867	journal	March 2010
Interdependence of phosphorus, nitrogen, potassium and magnesium translocation by the ectomycorrhizal fungus Paxillus involutus Jentschke, Georg; Brandes, Bettina; Kuhn, Arnd J. New Phytologist, Vol. 149, Issue 2 https://doi.org/10.1046/j.1469-8137.2001.00014.x	journal	February 2001
Polyphosphate (phytate) formation in Quercus acutissima - Scleroderma verrucosum ectomycorrhizae supplied with phosphate Jung, Nam Chul; Tamai, Yutaka Journal of Plant Interactions, Vol. 8, Issue 4 https://doi.org/10.1080/17429145.2013.816789	journal	December 2013
Plant KT/KUP/HAK Potassium Transporters: Single Family - Multiple Functions Grabov, A. Annals of Botany, Vol. 99, Issue 6 https://doi.org/10.1093/aob/mcm066	journal	January 2007
Arbuscular mycorrhizal influence on leaf water potential, solute accumulation, and oxidative stress in soybean plants subjected to drought stress Porcel, R. Journal of Experimental Botany, Vol. 55, Issue 403 https://doi.org/10.1093/jxb/erh188	journal	July 2004
Growth and nutrition of nonmycorrhizal and mycorrhizal pitch pine (Pinus rigida) seedlings under phosphorus limitation Cumming, J. R. Tree Physiology, Vol. 13, Issue 2 https://doi.org/10.1093/treephys/13.2.173	journal	September 1993
Influence of ectomycorrhization and cesium/potassium ratio on uptake and localization of cesium in Norway spruce seedlings Brunner, I.; Frey, B.; Riesen, T. K. Tree Physiology, Vol. 16, Issue 8 https://doi.org/10.1093/treephys/16.8.705	journal	August 1996
Carbon dioxide concentration and nitrogen input affect the C and N storage pools in Amanita muscaria-Picea abies mycorrhizae Tarnau, K.; Berger, A.; Loewe, A. Tree Physiology, Vol. 21, Issue 2-3 https://doi.org/10.1093/treephys/21.2-3.93	journal	February 2001
Growth and Potassium Content of Plants in Solution Cultures Maintained at Constant Potassium Concentrations Asher, C. J.; Ozanne, P. G. Soil Science, Vol. 103, Issue 3 https://doi.org/10.1097/00010694-196703000-00002	journal	January 1967
Structure and Expression Profile of the Phosphate Pht1 Transporter Gene Family in Mycorrhizal Populus trichocarpa Loth-Pereda, Verónica; Orsini, Elena; Courty, Pierre-Emmanuel Plant Physiology, Vol. 156, Issue 4 https://doi.org/10.1104/pp.111.180646	journal	June 2011
Mycorrhizal Effects on Potassium Fluxes by Northwest Coniferous Seedlings Rygiewicz, Paul T.; Bledsoe, Caroline S. Plant Physiology, Vol. 76, Issue 4 https://doi.org/10.1104/pp.76.4.918	journal	December 1984
Phosphate in the arbuscular mycorrhizal symbiosis: transport properties and regulatory roles: Phosphate transport in the AM symbiosis Javot, HÉLÈNe; Pumplin, Nathan; Harrison, Maria J. Plant, Cell & Environment, Vol. 30, Issue 3 https://doi.org/10.1111/j.1365-3040.2006.01617.x	journal	December 2006
Kinetics of NH4+ and K+ uptake by ectomycorrhizal fungi. Effect of NH4+ on K+ uptake Jongbloed, R. H.; Clement, J. M. A. M.; Borst-Pauwels, G. W. F. H. Physiologia Plantarum, Vol. 83, Issue 3 https://doi.org/10.1111/j.1399-3054.1991.tb00116.x	journal	November 1991
A Hypothesis Relating Critical Potassium Concentrations for Growth to the Distribution and Functions of this ion in the Plant cell Leigh, R. A.; Wyn Jones, R. G. New Phytologist, Vol. 97, Issue 1 https://doi.org/10.1111/j.1469-8137.1984.tb04103.x	journal	May 1984
Large-scale identification of genes in the fungus Hebeloma cylindrosporum paves the way to molecular analyses of ectomycorrhizal symbiosis Lambilliotte, Raphaël; Cooke, Richard; Samson, Delphine New Phytologist, Vol. 164, Issue 3 https://doi.org/10.1111/j.1469-8137.2004.01185.x	journal	September 2004
The sugar porter gene family of Laccaria bicolor : function in ectomycorrhizal symbiosis and soil-growing hyphae Fajardo López, Mónica; Dietz, Sandra; Grunze, Nina New Phytologist, Vol. 180, Issue 2 https://doi.org/10.1111/j.1469-8137.2008.02539.x	journal	October 2008
Genome-wide reprogramming of regulatory networks, transport, cell wall and membrane biogenesis during arbuscular mycorrhizal symbiosis in Lotus japonicus Guether, Mike; Balestrini, Raffaella; Hannah, Matthew New Phytologist, Vol. 182, Issue 1 https://doi.org/10.1111/j.1469-8137.2008.02725.x	journal	January 2009
PIXE analysis to estimate the elemental composition of ectomycorrhizal rhizomorphs grown in contact with different minerals in forest soil Wallander, HÃ¥kan; Johansson, Leif; Pallon, Jan FEMS Microbiology Ecology, Vol. 39, Issue 2 https://doi.org/10.1111/j.1574-6941.2002.tb00916.x	journal	February 2002
Elemental composition of ectomycorrhizal mycelia identified by PCRâRFLP analysis and grown in contact with apatite or wood ash in forest soil Wallander, HÃ¥kan; Mahmood, Shahid; Hagerberg, David FEMS Microbiology Ecology, Vol. 44, Issue 1 https://doi.org/10.1111/j.1574-6941.2003.tb01090.x	journal	May 2003
Tit for tat? A mycorrhizal fungus accumulates phosphorus under low plant carbon availability: P accumulation in an AMF under low plant C status Hammer, Edith C.; Pallon, Jan; Wallander, Håkan FEMS Microbiology Ecology, Vol. 76, Issue 2 https://doi.org/10.1111/j.1574-6941.2011.01043.x	journal	February 2011
Potassium channels in plant cells: Potassium channels in plants Dreyer, Ingo; Uozumi, Nobuyuki FEBS Journal, Vol. 278, Issue 22 https://doi.org/10.1111/j.1742-4658.2011.08371.x	journal	October 2011
Unravelling potassium nutrition in ectomycorrhizal associations Benito, Begoña; González-Guerrero, Manuel New Phytologist, Vol. 201, Issue 3 https://doi.org/10.1111/nph.12659	journal	January 2014
Arbuscular mycorrhizal fungi native from a Mediterranean saline area enhance maize tolerance to salinity through improved ion homeostasis: Improved ion homeostasis in maize plants by salt-adapted AMF Estrada, Beatriz; Aroca, Ricardo; Maathuis, Frans J. M. Plant, Cell & Environment, Vol. 36, Issue 10 https://doi.org/10.1111/pce.12082	journal	March 2013
Regulation of potassium transport in plants under hostile conditions: implications for abiotic and biotic stress tolerance Shabala, Sergey; Pottosin, Igor Physiologia Plantarum, Vol. 151, Issue 3 https://doi.org/10.1111/ppl.12165	journal	March 2014
The physiology of channel-mediated K ⁺ acquisition in roots of higher plants Coskun, Devrim; Britto, Dev T.; Kronzucker, Herbert J. Physiologia Plantarum, Vol. 151, Issue 3 https://doi.org/10.1111/ppl.12174	journal	March 2014
Cloning of genomic and complementary DNA from Shaker, a putative potassium channel gene from Drosophila Papazian, D.; Schwarz, T.; Tempel, B. Science, Vol. 237, Issue 4816 https://doi.org/10.1126/science.2441470	journal	August 1987
A Role for the AKT1 Potassium Channel in Plant Nutrition Hirsch, R. E. Science, Vol. 280, Issue 5365 https://doi.org/10.1126/science.280.5365.918	journal	May 1998
Phosphorus Availability Influences Elemental Uptake in the Mycorrhizal Fungus Glomus intraradices, as Revealed by Particle-Induced X-Ray Emission Analysis Olsson, Pål Axel; Hammer, Edith C.; Wallander, Håkan Applied and Environmental Microbiology, Vol. 74, Issue 13 https://doi.org/10.1128/aem.00376-08	journal	May 2008
No Significant Contribution of Arbuscular Mycorrhizal Fungi to Transfer of Radiocesium from Soil to Plants Joner, E. J.; Roos, P.; Jansa, J. Applied and Environmental Microbiology, Vol. 70, Issue 11 https://doi.org/10.1128/aem.70.11.6512-6517.2004	journal	November 2004
Specific cesium transport via the Escherichia coli Kup (TrkD) K+ uptake system. Bossemeyer, D.; Schlösser, A.; Bakker, E. P. Journal of Bacteriology, Vol. 171, Issue 4 https://doi.org/10.1128/jb.171.4.2219-2221.1989	journal	January 1989
TRK1 and TRK2 encode structurally related K+ transporters in Saccharomyces cerevisiae Ko, C. H.; Gaber, R. F. Molecular and Cellular Biology, Vol. 11, Issue 8 https://doi.org/10.1128/mcb.11.8.4266-4273.1991	journal	August 1991
Cloned Potassium Channels from Eukaryotes and Prokaryotes Jan, Lily Yeh; Jan, Yuh Nung Annual Review of Neuroscience, Vol. 20, Issue 1 https://doi.org/10.1146/annurev.neuro.20.1.91	journal	March 1997
Influence of Mycorrhizal Fungi on the Mineral Nutrition and Yield of Onion in Saline Soil ¹ Ojala, J. C.; Jarrell, W. M.; Menge, J. A. Agronomy Journal, Vol. 75, Issue 2 https://doi.org/10.2134/agronj1983.00021962007500020023x	journal	March 1983
Lateral root function and root overlap among mycorrhizal and nonmycorrhizal herbs in a Florida shrubland, measured using rubidium as a nutrient analog Hawkes, C. V.; Casper, B. B. American Journal of Botany, Vol. 89, Issue 8 https://doi.org/10.3732/ajb.89.8.1289	journal	August 2002
Temporal changes in the elemental composition of Rhizopogon rhizomorphs during colonization of patches with fresh organic matter or acid-washed sand Wallander, H.; Pallon, J. Mycologia, Vol. 97, Issue 2 https://doi.org/10.3852/mycologia.97.2.295	journal	March 2005
The supply of nutrient ions by diffusion to plant roots in soil: II. The effect of root hairs on the uptake of potassium by roots of rye grass (Lolium multiflorum) Drew, M. C.; Nye, P. H. Plant and Soil, Vol. 31, Issue 3 https://doi.org/10.1007/BF01373813	journal	December 1969
Polyphosphate granules are an artefact of specimen preparation in the ectomycorrhizal fungusPisolithus tinctorius Orlovich, D. A.; Ashford, A. E. Protoplasma, Vol. 173, Issue 3-4 https://doi.org/10.1007/BF01378998	journal	September 1993
Effects of endomycorrhizal infection on phosphate and cation uptake byTrifolium subterraneum Smith, Sarah E.; Smith, F. Andrew; Nicholas, D. J. Donald Plant and Soil, Vol. 63, Issue 1 https://doi.org/10.1007/BF02374257	journal	February 1981
The supply of nutrient ions by diffusion to plant roots in soil: IV. Direct measurement of changes in labile phosphate content in soil near absorbing roots Farr, E.; Vaidyanathan, L. V. Plant and Soil, Vol. 37, Issue 3 https://doi.org/10.1007/bf01348518	journal	March 1972
Selective Element Deposits in Maize Colonized by a Heavy Metal Tolerance Conferring Arbuscular Mycorrhizal Fungus Kaldorf, M.; Kuhn, A. J.; Schröder, W. H. Journal of Plant Physiology, Vol. 154, Issue 5-6 https://doi.org/10.1016/S0176-1617(99)80250-8	journal	May 1999
Potassium in agriculture – Status and perspectives Zörb, Christian; Senbayram, Mehmet; Peiter, Edgar Journal of Plant Physiology, Vol. 171, Issue 9 https://doi.org/10.1016/j.jplph.2013.08.008	journal	May 2014
Nitrogen transport in the ectomycorrhiza association: The Hebeloma cylindrosporum–Pinus pinaster model Müller, Tobias; Avolio, Meghan; Olivi, Martin Phytochemistry, Vol. 68, Issue 1 https://doi.org/10.1016/j.phytochem.2006.09.021	journal	January 2007
Elemental composition and function of polyphosphates in ectomycorrhizal fungi — an X-ray microanalytical study Bücking, H.; Heyser, W. Mycological Research, Vol. 103, Issue 1 https://doi.org/10.1017/S0953756298006935	journal	January 1999
Kinetics of NH4+ and K+ uptake by ectomycorrhizal fungi. Effect of NH4+ on K+ uptake Jongbloed, R. H.; Clement, J. M. A. M.; Borst-Pauwels, G. W. F. H. Physiologia Plantarum, Vol. 83, Issue 3 https://doi.org/10.1034/j.1399-3054.1991.830315.x	journal	November 1991
Molecular and Functional Characterization of a Na+-K+ Transporter from the Trk Family in the Ectomycorrhizal Fungus Hebeloma cylindrosporum Corratgé, Claire; Zimmermann, Sabine; Lambilliotte, Raphaël Journal of Biological Chemistry, Vol. 282, Issue 36 https://doi.org/10.1074/jbc.M611613200	journal	September 2007
Effects of Mycorrhizal Colonization and Fertilization on Growth and Photosynthesis of Sweet Basil Under Salt Stress Zuccarini, Paolo; Okurowska, Paulina Journal of Plant Nutrition, Vol. 31, Issue 3 https://doi.org/10.1080/01904160801895027	journal	February 2008
Root K+ Acquisition in Plants: The Arabidopsis thaliana Model Aleman, F.; Nieves-Cordones, M.; Martinez, V. Plant and Cell Physiology, Vol. 52, Issue 9 https://doi.org/10.1093/pcp/pcr096	journal	July 2011
Phosphorus nutrition of mycorrhizal trees Plassard, C.; Dell, B. Tree Physiology, Vol. 30, Issue 9 https://doi.org/10.1093/treephys/tpq063	journal	July 2010
Transport, signaling, and homeostasis of potassium and sodium in plants: K ⁺ and Na ⁺ transport and signaling Adams, Eri; Shin, Ryoung Journal of Integrative Plant Biology, Vol. 56, Issue 3 https://doi.org/10.1111/jipb.12159	journal	March 2014
Potassium nutrition of ectomycorrhizal Pinus pinaster : overexpression of the Hebeloma cylindrosporum Hc Trk1 transporter affects the translocation of both K ⁺ and phosphorus in the host plant Garcia, Kevin; Delteil, Amandine; Conéjéro, Geneviève New Phytologist, Vol. 201, Issue 3 https://doi.org/10.1111/nph.12603	journal	November 2013
Phosphorus Availability Influences Elemental Uptake in the Mycorrhizal Fungus Glomus intraradices, as Revealed by Particle-Induced X-Ray Emission Analysis Olsson, Pål Axel; Hammer, Edith C.; Wallander, Håkan Applied and Environmental Microbiology, Vol. 74, Issue 13 https://doi.org/10.1128/AEM.00376-08	journal	May 2008
No Significant Contribution of Arbuscular Mycorrhizal Fungi to Transfer of Radiocesium from Soil to Plants Joner, E. J.; Roos, P.; Jansa, J. Applied and Environmental Microbiology, Vol. 70, Issue 11 https://doi.org/10.1128/AEM.70.11.6512-6517.2004	journal	November 2004
TRK1 and TRK2 encode structurally related K+ transporters in Saccharomyces cerevisiae. Ko, C. H.; Gaber, R. F. Molecular and Cellular Biology, Vol. 11, Issue 8 https://doi.org/10.1128/MCB.11.8.4266	journal	August 1991
Potassium Transport and Signaling in Higher Plants Wang, Yi; Wu, Wei-Hua Annual Review of Plant Biology, Vol. 64, Issue 1 https://doi.org/10.1146/annurev-arplant-050312-120153	journal	April 2013
Improved Growth of Onion and Bell Pepper in Saline Soils by Two Vesicular-Arbuscular Mycorrhizal Fungi Hirrel, Marc C.; Gerdemann, J. W. Soil Science Society of America Journal, Vol. 44, Issue 3 https://doi.org/10.2136/sssaj1980.03615995004400030046x	journal	May 1980

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Arbuscular Mycorrhizal Fungi as Natural Biofertilizers: Let's Benefit from Past Successes Berruti, Andrea; Lumini, Erica; Balestrini, Raffaella Frontiers in Microbiology, Vol. 6 https://doi.org/10.3389/fmicb.2015.01559	journal	January 2016
The Potential Role of Arbuscular Mycorrhizal Fungi in the Restoration of Degraded Lands Asmelash, Fisseha; Bekele, Tamrat; Birhane, Emiru Frontiers in Microbiology, Vol. 7 https://doi.org/10.3389/fmicb.2016.01095	journal	July 2016
Arbuscular mycorrhizal symbiosis and osmotic adjustment in response to NaCl stress: a meta-analysis AugÃ©, Robert M.; Toler, Heather D.; Saxton, Arnold M. Frontiers in Plant Science, Vol. 5 https://doi.org/10.3389/fpls.2014.00562	journal	October 2014
Molecular Cloning and Functional Analysis of a Na+-Insensitive K+ Transporter of Capsicum chinense Jacq Ruiz-Lau, Nancy; Bojórquez-Quintal, Emanuel; Benito, Begoña Frontiers in Plant Science, Vol. 7 https://doi.org/10.3389/fpls.2016.01980	journal	December 2016
Arbuscular Mycorrhizal Fungus Rhizophagus irregularis Increased Potassium Content and Expression of Genes Encoding Potassium Channels in Lycium barbarum Zhang, Haoqiang; Wei, Suzhen; Hu, Wentao Frontiers in Plant Science, Vol. 8 https://doi.org/10.3389/fpls.2017.00440	journal	March 2017
The Role of Soil Fungi in K+ Plant Nutrition Haro, Rosario; Benito, Begoña International Journal of Molecular Sciences, Vol. 20, Issue 13 https://doi.org/10.3390/ijms20133169	journal	June 2019
The Protective Role of 28-Homobrassinolide and Glomus versiforme in Cucumber to Withstand Saline Stress Ahmad, Husain; Hayat, Sikandar; Ali, Muhammad Plants, Vol. 9, Issue 1 https://doi.org/10.3390/plants9010042	journal	December 2019
Distributions of ectomycorrhizal and foliar endophytic fungal communities associated with Pinus ponderosa along a spatially constrained elevation gradient Bowman, Elizabeth A.; Arnold, A. Elizabeth American Journal of Botany, Vol. 105, Issue 4 https://doi.org/10.1002/ajb2.1072	journal	April 2018
The combination of arbuscular mycorrhizal fungi inoculation (Glomus versiforme) and 28-homobrassinolide spraying intervals improves growth by enhancing photosynthesis, nutrient absorption, and antioxidant system in cucumber (Cucumis sativus L.) under sali Ahmad, Husain; Hayat, Sikandar; Ali, Muhammad Ecology and Evolution, Vol. 8, Issue 11 https://doi.org/10.1002/ece3.4112	journal	May 2018
Ectomycorrhizal symbiosis helps plants to challenge salt stress conditions Guerrero-Galán, Carmen; Calvo-Polanco, Monica; Zimmermann, Sabine Dagmar Mycorrhiza, Vol. 29, Issue 4 https://doi.org/10.1007/s00572-019-00894-2	journal	April 2019
Estimating the contribution of arbuscular mycorrhizal fungi to drought tolerance of potted olive trees (Olea europaea) Ouledali, Sarra; Ennajeh, Mustapha; Zrig, Ahlem Acta Physiologiae Plantarum, Vol. 40, Issue 5 https://doi.org/10.1007/s11738-018-2656-1	journal	April 2018
Abiotic soil attributes and their relation to morphological root characteristics and mycorrhizal colonization of grasses de Cesaro Krzyzanski, Heloisa; Carrenho, Rosilaine; Araujo, Marcelo Alessandro Brazilian Journal of Botany, Vol. 41, Issue 3 https://doi.org/10.1007/s40415-018-0481-9	journal	July 2018
Unearthing the roots of ectomycorrhizal symbioses Martin, Francis; Kohler, Annegret; Murat, Claude Nature Reviews Microbiology, Vol. 14, Issue 12 https://doi.org/10.1038/nrmicro.2016.149	journal	October 2016
Effects of endophytic and ectomycorrhizal basidiomycetes on Quercus virginiana seedling growth and nutrient absorption Jin, Wei; Peng, Long; Zhang, Xiaoguo Journal of Sustainable Forestry, Vol. 38, Issue 5 https://doi.org/10.1080/10549811.2019.1570467	journal	January 2019
Plant potassium nutrition in ectomycorrhizal symbiosis: properties and roles of the three fungal TOK potassium channels in Hebeloma cylindrosporum: TOK potassium channels of an ectomycorrhizal fungus Guerrero-Galán, Carmen; Delteil, Amandine; Garcia, Kevin Environmental Microbiology, Vol. 20, Issue 5 https://doi.org/10.1111/1462-2920.14122	journal	April 2018
Biological mobilization of potassium from soil by thirteen Suillus species and ectomycorrhizal Pinus massoniana Lamb. seedlings Peng, Liyuan; Huang, Jianguo; Yuan, Ling European Journal of Soil Science, Vol. 71, Issue 4 https://doi.org/10.1111/ejss.12898	journal	November 2019
Transcriptome Analysis Provides Novel Insights into the Capacity of the Ectomycorrhizal Fungus Amanita pantherina To Weather K-Containing Feldspar and Apatite Sun, Qibiao; Fu, Ziyu; Finlay, Roger Applied and Environmental Microbiology, Vol. 85, Issue 15 https://doi.org/10.1128/aem.00719-19	journal	May 2019
To trade in the field: the molecular determinants of arbuscular mycorrhiza nutrient exchange Salvioli di Fossalunga, Alessandra; Novero, Mara Chemical and Biological Technologies in Agriculture, Vol. 6, Issue 1 https://doi.org/10.1186/s40538-019-0150-7	journal	June 2019
Soil Physicochemical Properties and the Rhizosphere Soil Fungal Community in a Mulberry (Morus alba L.)/Alfalfa (Medicago sativa L.) Intercropping System Zhang, Mengmeng; Wang, Ning; Zhang, Jingyun Forests, Vol. 10, Issue 2 https://doi.org/10.3390/f10020167	journal	February 2019
Diversity and Enzyme Activity of Ectomycorrhizal Fungal Communities Following Nitrogen Fertilization in an Urban-Adjacent Pine Plantation Ning, Chen; Mueller, Gregory; Egerton-Warburton, Louise Forests, Vol. 9, Issue 3 https://doi.org/10.3390/f9030099	journal	February 2018
Exodermis and Endodermis Respond to Nutrient Deficiency in Nutrient-Specific and Localized Manner Namyslov, Jiří; Bauriedlová, Zuzana; Janoušková, Jana Plants, Vol. 9, Issue 2 https://doi.org/10.3390/plants9020201	journal	February 2020

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54 ENVIRONMENTAL SCIENCES
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arbuscular mycorrhizal symbiosis
ectomycorrhizal symbiosis
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transport systems

The role of mycorrhizal associations in plant potassium nutrition

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