Halophytes as a source of salt tolerance genes and mechanisms: a case study for the Salt Lake area, Turkey
Ceyda Ozfidan-Konakci A , Baris Uzilday B , Rengin Ozgur B , Evren Yildiztugay C , A. Hediye Sekmen B and Ismail Turkan B D
+ Author Affiliations
- Author Affiliations
A Department of Molecular Biology and Genetics, Faculty of Science, Necmettin Erbakan University, 42 090, Meram, Konya, Turkey.
B Department of Biology, Faculty of Science, Ege University, 35 100, Bornova, Izmir, Turkey.
C Department of Biology, Faculty of Science, Selcuk University, 42 250, Selcuklu, Konya, Turkey.
D Corresponding author. Email: ismail.turkan@ege.edu.tr
Functional Plant Biology 43(7) 575-589 https://doi.org/10.1071/FP15288
Submitted: 16 September 2015 Accepted: 22 February 2016 Published: 19 April 2016
Abstract
The worst case scenario of global climate change predicts both drought and salinity would be the first environmental factors restricting agriculture and natural ecosystems, causing decreased crop yields and plant growth that would directly affect human population in the next decades. Therefore, it is vital to understand the biology of plants that are already adapted to these extreme conditions. In this sense, extremophiles such as the halophytes offer valuable genetic information for understanding plant salinity tolerance and to improve the stress tolerance of crop plants. Turkey has ecological importance for its rich biodiversity with up to 3700 endemic plants. Salt Lake (Lake Tuz) in Central Anatolia, one of the largest hypersaline lakes in the world, is surrounded by salty marshes, with one of the most diverse floras in Turkey, where arid and semiarid areas have increased due to low rainfall and high evaporation during the summer season. Consequently, the Salt Lake region has a large number of halophytic, xerophytic and xero-halophytic plants. One good example is Eutrema parvulum (Schrenk) Al-Shehbaz & Warwick, which originates from the Salt Lake region, can tolerate up to 600 mM NaCl. In recent years, the full genome of E. parvulum was published and it has been accepted as a model halophyte due to its close relationship (sequence identity in range of 90%) with Arabidopsis thaliana (L. Heynh.). In this context, this review will focus on tolerance mechanisms involving hormone signalling, accumulation of compatible solutes, ion transporters, antioxidant defence systems, reactive oxygen species (ROS) signalling mechanism of some lesser-known extremophiles growing in the Salt Lake region. In addition, current progress on studies conducted with E. parvulum will be evaluated to shed a light on future prospects for improved crop tolerance.
Additional keywords: extremophiles, Eutrema parvulum, salinity, salt stress, Schrenkiella parvula.
References
Al-Karaki GN (2000) Growth, sodium, and potassium uptake and translocation in salt stressed tomato. Journal of Plant Nutrition 23, 369–379.| Growth, sodium, and potassium uptake and translocation in salt stressed tomato.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXhsVyju7s%3D&md5=1cd0475b6f20cfdb530bf1d345162371CAS |
Al-Shehbaz IA, O’Kane SL, Price RA (1999) Generic placement of species excluded from Arabidopsis (Brassicaceae). Novon 9, 296–307.
| Generic placement of species excluded from Arabidopsis (Brassicaceae).Crossref | GoogleScholarGoogle Scholar |
Ali Z, Park HC, Ali A, Oh DH, Aman R, Kropornicka A, Yun DJ (2012) TsHKT1; 2, a HKT1 homolog from the extremophile Arabidopsis relative Thellungiella salsuginea, shows K+ specificity in the presence of NaCl. Plant Physiology 158, 1463–1474.
| TsHKT1; 2, a HKT1 homolog from the extremophile Arabidopsis relative Thellungiella salsuginea, shows K+ specificity in the presence of NaCl.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XltVOktrk%3D&md5=7a84d4b6f87df1d168b2c9121b57247dCAS | 22238420PubMed |
Amtmann A (2009) Learning from evolution: Thellungiella generates new knowledge on essential and critical components of abiotic stress tolerance in plants. Molecular Plant 2, 3–12.
| Learning from evolution: Thellungiella generates new knowledge on essential and critical components of abiotic stress tolerance in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXovV2msbk%3D&md5=6354a9f76a7b8fcec89d707a16646ab0CAS | 19529830PubMed |
Arbona V, Argamasilla R, Gómez-Cadenas A (2010) Common and divergent physiological, hormonal and metabolic responses of Arabidopsis thaliana and Thellungiella halophila to water and salt stress. Journal of Plant Physiology 167, 1342–1350.
| Common and divergent physiological, hormonal and metabolic responses of Arabidopsis thaliana and Thellungiella halophila to water and salt stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXht1Wju7fI&md5=6135c9910e2e9ebe1593e4d4b197f8d4CAS | 20630614PubMed |
Asada K (2006) Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiology 141, 391–396.
| Production and scavenging of reactive oxygen species in chloroplasts and their functions.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xmt1aksbY%3D&md5=02aa399fad32027ca0622e210b7c849bCAS | 16760493PubMed |
Atia A, Smaoui A, Barhoumi Z, Abdelly C, Debez A (2011) Differential response to salinity and water deficit stress in Polypogon monspeliensis (L.) Desf. provenances during germination. Plant Biology 13, 541–545.
| Differential response to salinity and water deficit stress in Polypogon monspeliensis (L.) Desf. provenances during germination.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXlvFynsLs%3D&md5=2819fcf7bb6928d2b7fd63afe42f4f5fCAS | 21489106PubMed |
Balnokin YV, Myasoedov NA, Shamsutdinov ZS, Shamsutdinov NZ (2005) Significance of Na+ and K+ for sustained hydration of organ tissues in ecologically distinct halophytes of the family Chenopodiaceae. Russian Journal of Plant Physiology: a Comprehensive Russian Journal on Modern Phytophysiology 52, 779–787.
| Significance of Na+ and K+ for sustained hydration of organ tissues in ecologically distinct halophytes of the family Chenopodiaceae.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXht1enu7rL&md5=f0dc6932c89ccb243dfaaf72b325db2eCAS |
Barhoumi Z, Djebali W, Smaoui A, Chaïbi W, Abdelly C (2007) Contribution of NaCl excretion to salt resistance of Aeluropus littoralis (Willd) Parl. Journal of Plant Physiology 164, 842–850.
| Contribution of NaCl excretion to salt resistance of Aeluropus littoralis (Willd) Parl.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXoslSisbc%3D&md5=acc919c1df416626a44845df2a23ca66CAS | 16876911PubMed |
Bartels D, Dinakar C (2013) Balancing salinity stress responses in halophytes and non-halophytes: a comparison between Thellungiella and Arabidopsis thaliana. Functional Plant Biology 40, 819–831.
Ben Saad R, Fabre D, Mieulet D, Meynard D, Dingkuhn M, Al‐Doos A, Hassairi A (2012) Expression of the Aeluropus littoralis AlSAP gene in rice confers broad tolerance to abiotic stresses through maintenance of photosynthesis. Plant, Cell & Environment 35, 626–643.
| Expression of the Aeluropus littoralis AlSAP gene in rice confers broad tolerance to abiotic stresses through maintenance of photosynthesis.Crossref | GoogleScholarGoogle Scholar |
Bertorello AM, Zhu JK (2009) SIK1/SOS2 networks: decoding sodium signals via calcium-responsive protein kinase pathways. Pflügers Archiv – European Journal of Physiology 458, 613–619.
| SIK1/SOS2 networks: decoding sodium signals via calcium-responsive protein kinase pathways.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXmvV2rtLo%3D&md5=1aa70dae8b00c656e984459636ad19b3CAS | 19247687PubMed |
Bose J, Rodrigo-Moreno A, Shabala S (2014) ROS homeostasis in halophytes in the context of salinity stress tolerance. Journal of Experimental Botany 65, 1241–1257.
| ROS homeostasis in halophytes in the context of salinity stress tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXks12htbY%3D&md5=75f259e49c111146271aa61a36df1a47CAS | 24368505PubMed |
Bressan R, Park HC, Orsini F, Oh D, Dassanayake M, Inan G, Yun G, Bohnert HJ, Maggio A (2013) Biotechnology for mechanisms that counteract salt stress in extremophile species: a genome-based view. Plant Biotechnology Reports 7, 27–37.
| Biotechnology for mechanisms that counteract salt stress in extremophile species: a genome-based view.Crossref | GoogleScholarGoogle Scholar |
Bromham L, Bennett TH (2014) Salt tolerance evolves more frequently in C4 grass lineages. Journal of Evolutionary Biology 27, 653–659.
| Salt tolerance evolves more frequently in C4 grass lineages.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXjt1Sku7c%3D&md5=80f0d4ccd6693af5a458152afc735486CAS | 24494637PubMed |
Chen G, Asada K (1989) Ascorbate peroxidase in tea leaves: occurrence of two isozymes and the differences in their enzymatic and molecular properties. Plant & Cell Physiology 30, 987–998.
Chen LIJ, Wang S, Huttermann A, Altman A (2001) Salt, nutrient uptake and transport and ABA of Populus euphratica, a hybrid in response to increasing soil NaCl. Trees – Structure and Function 15, 186–194.
| Salt, nutrient uptake and transport and ABA of Populus euphratica, a hybrid in response to increasing soil NaCl.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXosF2ku7g%3D&md5=7eed684e26ac7ddea7cb84b55c6f353eCAS |
Chen X, Han H, Jiang P, Nie L, Bao H, Fan P, Li Y (2011) Transformation of β-lycopene cyclase genes from Salicornia europaea and Arabidopsis conferred salt tolerance in Arabidopsis and tobacco. Plant & Cell Physiology 52, 909–921.
| Transformation of β-lycopene cyclase genes from Salicornia europaea and Arabidopsis conferred salt tolerance in Arabidopsis and tobacco.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXmtFymsrk%3D&md5=95bd40b24a83a97c997cc4d703552a21CAS |
Chen J, Lausser A, Dresselhaus T (2014) Hormonal responses during early embryogenesis in maize. Biochemical Society Transactions 42, 325–331.
| Hormonal responses during early embryogenesis in maize.Crossref | GoogleScholarGoogle Scholar | 24646239PubMed |
Cuin TA, Miller AJ, Laurie SA, Leigh RA (2003) Potassium activities in cell compartments of salt-grown barley leaves. Journal of Experimental Botany 54, 657–661.
| Potassium activities in cell compartments of salt-grown barley leaves.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXit1arurw%3D&md5=ae6201f14483561065098148737f8394CAS | 12554708PubMed |
Damon PM, Ma QF, Rengel Z (2011) Wheat genotypes differ in potassium accumulation and osmotic adjustment under drought stress. Crop and Pasture Science 62, 550–555.
| Wheat genotypes differ in potassium accumulation and osmotic adjustment under drought stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXpsFOgtLo%3D&md5=ff0710abf9b79823ec4157dca093522eCAS |
Dang ZH, Zheng LL, Wang J, Gao Z, Wu SB, Qi Z, Wang YC (2013) Transcriptomic profiling of the salt-stress response in the wild recretohalophyte Reaumuria trigyna. BMC Genomics 14, 29
| Transcriptomic profiling of the salt-stress response in the wild recretohalophyte Reaumuria trigyna.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXjsValsb4%3D&md5=4e42feb00409ed7ce0dabc85f7a454d9CAS | 23324106PubMed |
Dassanayake M, Oh D-H, Haas JS, Hernandez A, Hong H, Ali S, Yun D-J, Bressan RA, Zhu JK, Bohnert HJ, Cheeseman JM (2011) The genome of the extremophile crucifer Thellungiella parvula. Nature Genetics 43, 913–918.
| The genome of the extremophile crucifer Thellungiella parvula.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXpvVOltLo%3D&md5=a6282d3d7ef500750d3a756b799aa394CAS | 21822265PubMed |
Davis PH (1965) ‘Flora of Turkey and the east Aegean islands. Vol. 10.’ (Edinburgh University Press: Edinburgh)
Demidchik V, Tester M (2002) Sodium fluxes through nonselective cation channels in the plasma membrane of protoplasts from Arabidopsis roots. Plant Physiology 128, 379–387.
| Sodium fluxes through nonselective cation channels in the plasma membrane of protoplasts from Arabidopsis roots.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XhsVSrur0%3D&md5=11e09d6ebe769524238419600b74d0dbCAS | 11842142PubMed |
Dietz KJ, Jacob S, Oelze ML, Laxa M, Tognetti V, de Miranda SMN, Baier M, Finkemeier I (2006) The function of peroxiredoxins in plant organelle redox metabolism. Journal of Experimental Botany 57, 1697–1709.
Duarte B, Couto T, Freitas J, Valentim J, Silva H, Marques JC, Cacador I (2013) Abiotic modulation of Spartina maritima photobiology indifferent latitudinal populations. Estuarine, Coastal and Shelf Science 130, 127–137.
| Abiotic modulation of Spartina maritima photobiology indifferent latitudinal populations.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXktlCktL4%3D&md5=9d0cf07ce19abb8726fc15a7f5b7b974CAS |
Eken G, Magnin G (1999) A preliminary biodiversity atlas of the Konya Basin, Central Turkey. Biodiversity Programme Report No 13. Dogal Hayati Koruma Dernegi, Istanbul. [In Turkish].
Elstner EF (1987) Metabolism of activated oxygen species. In ‘Biochemistry of metabolism (the biochemistry of plants: a comprehensive treatise. Vol. 11)’. (Ed. DD Davies) pp. 253–315. (Academic Press: San Diego, CA, USA)
English JP, Colmer TD (2013) Tolerance of extreme salinity in two stem-succulent halophytes (Tecticornia species). Functional Plant Biology 40, 897–912.
Fan P, Feng J, Jiang P, Chen X, Bao H, Nie L, Li Y (2011) Coordination of carbon fixation and nitrogen metabolism in Salicornia europaea under salinity: comparative proteomic analysis on chloroplast proteins. Proteomics 11, 4346–4367.
| Coordination of carbon fixation and nitrogen metabolism in Salicornia europaea under salinity: comparative proteomic analysis on chloroplast proteins.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhsVSiu7bN&md5=2e0350ad8aa99582861859a94d3140f7CAS | 21905221PubMed |
FAO (2011) ‘The state of food and agriculture 2010–2011, women in agriculture: closing the gender gap for development.’ (FAO: Rome)
FAO (2012) ‘The state of food and agriculture: investing in agriculture for a better future.’ (FAO: Rome)
Flowers TJ, Colmer TD (2008) Salinity tolerance in halophytes. New Phytologist 179, 945–963.
| Salinity tolerance in halophytes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtFWqur%2FE&md5=ead9e0f52d5a777986f79fa03e42e1abCAS | 18565144PubMed |
Flowers TJ, Munns R, Colmer TD (2015) Sodium chloride toxicity and the cellular basis of salt tolerance in halophytes. Annals of Botany 115, 419–431.
| Sodium chloride toxicity and the cellular basis of salt tolerance in halophytes.Crossref | GoogleScholarGoogle Scholar | 25466549PubMed |
Furtana B, Duman H, Tipirdamaz R (2013) Seasonal changes of inorganic and organic osmolyte content in three endemic Limonium species of Lake Tuz (Turkey). Turkish Journal of Botany 37, 455–463.
Ghars MA, Parre E, Debez A, Bordenave M, Richard L, Leport L, Bouchereau A, Savoure A, Abdelly C (2008) Comparative salt tolerance analysis between Arabidopsis thaliana and Thellungiella halophila, with special emphasis on K+/Na+ selectivity and proline accumulation. Journal of Plant Physiology 165, 588–599.
| Comparative salt tolerance analysis between Arabidopsis thaliana and Thellungiella halophila, with special emphasis on K+/Na+ selectivity and proline accumulation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXls1Wgsr8%3D&md5=c5c47f20af49f487bf6513a5018b625fCAS | 17723252PubMed |
Ghars MA, Richard L, Lefebvre-De Vos D, Leprince AS, Parre E, Bordenave M, Savouré A (2012) Phospholipases C and D modulate proline accumulation in Thellungiella halophila/salsuginea differently according to the severity of salt or hyperosmotic stress. Plant & Cell Physiology 53, 183–192.
| Phospholipases C and D modulate proline accumulation in Thellungiella halophila/salsuginea differently according to the severity of salt or hyperosmotic stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XosFGgsg%3D%3D&md5=0330dbda49527ae2e17c7af3481641afCAS |
Gil R, Boscaiu M, Lull C, Bautista I, Lidón A, Vicente O (2013) Are soluble carbohydrates ecologically relevant for salt tolerance in halophytes? Functional Plant Biology 40, 805–818.
Guma IR, Padrón-Mederos MA, Santos-Guerra A, Reyes-Betancort JA (2010) Effect of temperature and salinity on germination of Salsola vermiculata L. (Chenopodiaceae) from Canary Islands. Journal of Arid Environments 74, 708–711.
| Effect of temperature and salinity on germination of Salsola vermiculata L. (Chenopodiaceae) from Canary Islands.Crossref | GoogleScholarGoogle Scholar |
Guner A, Ozhatay N, Ekim T, Baser KHC (2000) ‘Flora of Turkey and the East Aegean Islands (Suppl. 2). Vol. 11.’ (Edinburgh University Press: Edinburgh, UK)
Halliwell B, Gutteridge JMC (1985) ‘Free radicals in biology and medicine.’(Oxford University Press: Oxford)
Hamzaoğlu E, Aksoy A (2009) Phytosociological studies on the halophytic communities of Central Anatolia. Ekoloji 18, 1–14.
| Phytosociological studies on the halophytic communities of Central Anatolia.Crossref | GoogleScholarGoogle Scholar |
Han H, Li Y, Zhou S (2008) Overexpression of phytoene synthase gene from Salicornia europaea alters response to reactive oxygen species under salt stress in transgenic Arabidopsis. Biotechnology Letters 30, 1501–1507.
| Overexpression of phytoene synthase gene from Salicornia europaea alters response to reactive oxygen species under salt stress in transgenic Arabidopsis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXnsVCrsLc%3D&md5=84aa80ede32829431c4a60b34ceb838fCAS | 18414806PubMed |
Hasegawa PM, Bressan RA, Zhu JK, Bohnert HJ (2000) Plant cellular and molecular responses to high salinity. Annual Review of Plant Physiology and Plant Molecular Biology 51, 463–499.
| Plant cellular and molecular responses to high salinity.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXlsVymt7s%3D&md5=6d8ab79bcb839ec84ba41d6870cfc25eCAS | 15012199PubMed |
Hiraga S, Sasaki K, Ito H, Ohashi Y, Matsui H (2001) A large family of class III plant peroxidases. Plant & Cell Physiology 42, 462–468.
| A large family of class III plant peroxidases.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXktVWntrY%3D&md5=b11adfcfb62cb004ecc268c661ab4f29CAS |
Hogarth PJ (1999) ‘The biology of mangroves.’ (Oxford University Press: New York)
Hohmann S (2002) Osmotic stress signaling and osmoadaptation in yeasts. Microbiology and Molecular Biology Reviews 66, 300–372.
| Osmotic stress signaling and osmoadaptation in yeasts.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XltFSltrc%3D&md5=fb1f9b04ff13311409c83d5ca9211305CAS | 12040128PubMed |
Hosy E, Vavasseur A, Mouline K, Dreyer I, Gaymard F, Porée F, Simonneau T (2003) The Arabidopsis outward K+ channel GORK is involved in regulation of stomatal movements and plant transpiration. Proceedings of the National Academy of Sciences of the United States of America 100, 5549–5554.
| The Arabidopsis outward K+ channel GORK is involved in regulation of stomatal movements and plant transpiration.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXjs1yiu7w%3D&md5=7426f31b160d0cdde4837613dc31c3a0CAS | 12671068PubMed |
Hou Q, Bartels D (2015) Comparative study of the aldehyde dehydrogenase (ALDH) gene superfamily in the glycophyte Arabidopsis thaliana and Eutrema halophytes. Annals of Botany 115, 465–479.
| Comparative study of the aldehyde dehydrogenase (ALDH) gene superfamily in the glycophyte Arabidopsis thaliana and Eutrema halophytes.Crossref | GoogleScholarGoogle Scholar | 25085467PubMed |
Ingold A, Havill DC (1984) The influence of sulphide on the distribution of higher plants in salt marshes. Journal of Ecology 72, 1043–1054.
| The influence of sulphide on the distribution of higher plants in salt marshes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2MXksFSisw%3D%3D&md5=aeba85dce1074b8a1e6471563bce0340CAS |
IPCC (2014) ‘Climate change 2014: impacts, adaptation, and vulnerability: IPCC Working Group II Contribution to AR5.’ (Cambridge University Press, Cambridge, UK)
Islam S, Malik AI, Islam AKMR, Colmer TD (2007) Salt tolerance in a Hordeum marinum–Triticum aestivum amphiploid, and its parents. Journal of Experimental Botany 58, 1219–1229.
| Salt tolerance in a Hordeum marinum–Triticum aestivum amphiploid, and its parents.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXktlWjsbs%3D&md5=303d46f77d6973c0072a15236a9f664fCAS | 17283374PubMed |
Jensen A (1985) On the ecophysiology of Halimione portulacoides. In ‘Ecology of coastal vegetation. Advances in vegetation science. Vol. 6’. (Eds IWG Beeftink, JM Rozema, AHL Huiskes) pp. 231–240. (Springer: New York)
Kader MA, Lindberg S (2010) Cytosolic calcium and pH signaling in plants under salinity stress. Plant Signaling & Behavior 3, 1–7.
Kant S, Kant P, Raveh E, Barak S (2006) Evidence that differential gene expression between the halophyte, Thellungiella halophila, and Arabidopsis thaliana is responsible for higher levels of the compatible osmolyte proline and tight control of Na+ uptake in T. halophila. Plant, Cell & Environment 29, 1220–1234.
| Evidence that differential gene expression between the halophyte, Thellungiella halophila, and Arabidopsis thaliana is responsible for higher levels of the compatible osmolyte proline and tight control of Na+ uptake in T. halophila.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XnsVCqu7c%3D&md5=5615030e88ad1960d566657a4f54ddfcCAS |
Kant S, Bi YM, Weretilnyk E, Barak S, Rothstein SJ (2008) The Arabidopsis halophytic relative Thellungiella halophila tolerates nitrogen-limiting conditions by maintaining growth, nitrogen uptake, and assimilation. Plant Physiology 147, 1168–1180.
| The Arabidopsis halophytic relative Thellungiella halophila tolerates nitrogen-limiting conditions by maintaining growth, nitrogen uptake, and assimilation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXoslyis7g%3D&md5=dfd60c9f40fc43564046f4a7fd38609cCAS | 18467466PubMed |
Karimi G, Ghorbanli M, Heidari H, Khavarinejad RA, Assareh MH (2005) The effects of NaCl on growth, water relations, osmolytes and ion content in Kochia prostrate. Biologia Plantarum 49, 301–304.
| The effects of NaCl on growth, water relations, osmolytes and ion content in Kochia prostrate.Crossref | GoogleScholarGoogle Scholar |
Khan MA, Qaiser M (2006) Halophytes of Pakistan: characteristics, distribution and potential economic usages. In ‘Sabkha ecosystems. Vol. 2: West and Central Asia’. (Eds MA Khan, B Boer, GS Kust,H-J Barth) pp. 129–153. (Springer: Heidelberg, Germany)
Khan MA, Weber DJ (2006) ‘Ecophysiology of high salinity tolerant plants. (Springer: Dordrecht, The Netherlands)
Kirch HH, Bartels D, Wei Y, Schnable PS, Wood AJ (2004) The ALDH gene superfamily of Arabidopsis. Trends in Plant Science 9, 371–377.
| The ALDH gene superfamily of Arabidopsis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXmsVCqtb8%3D&md5=be147510b01e0b32bec7c8bacf6f9136CAS | 15358267PubMed |
Knight H, Trewavas AJ, Knight MR (1997) Calcium signalling in Arabidopsis thaliana responding to drought and salinity. The Plant Journal 12, 1067–1078.
| Calcium signalling in Arabidopsis thaliana responding to drought and salinity.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXktlegtw%3D%3D&md5=146a2c99028377b0525a35610f3afd67CAS | 9418048PubMed |
Kültür S (2007) Medicinal plants used in Kırklareli Province (Turkey). Journal of Ethnopharmacology 111, 341–364.
| Medicinal plants used in Kırklareli Province (Turkey).Crossref | GoogleScholarGoogle Scholar | 17257791PubMed |
Leach RP, Rogers J, Wheeler KP, Flowers TJ, Yeo AR (1990) Molecular markers for ion compartmentation in cells of higher plants. Journal of Experimental Botany 41, 1079–1087.
| Molecular markers for ion compartmentation in cells of higher plants.Crossref | GoogleScholarGoogle Scholar |
Lu JH, Li XY, Zhou LL, Wu L (2005) Characters of leaf epidermis and their systematic significance in Glycyrrhiza. Acta Botanica Yunnanica 27, 525–533.
Lv S, Jiang P, Chen X, Fan P, Wang X, Li Y (2012) Multiple compartmentalization of sodium conferred salt tolerance in Salicornia europaea. Plant Physiology and Biochemistry 51, 47–52.
| Multiple compartmentalization of sodium conferred salt tolerance in Salicornia europaea.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhs1Sgs77O&md5=ad303e83afe463a86e1b8710fe782b1bCAS | 22153239PubMed |
M’rah S, Ouerghi Z, Berthomieu C, Havaux M, Jungas C, Hajji M, Lachaâl M (2006) Effects of NaCl on the growth, ion accumulation and photosynthetic parameters of Thellungiella halophila. Journal of Plant Physiology 163, 1022–1031.
| Effects of NaCl on the growth, ion accumulation and photosynthetic parameters of Thellungiella halophila.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtFajsr7I&md5=420521fd54622fe1d3d6f4f321e3260bCAS | 16971214PubMed |
M’rah S, Ouerghi Z, Eymery F, Rey P, Hajji M, Grignon C, Lachaal M (2007) Efficiency of biochemical protection against toxic effects of accumulated salt differentiates Thellungiella halophila from Arabidopsis thaliana. Journal of Plant Physiology 164, 375–384.
| Efficiency of biochemical protection against toxic effects of accumulated salt differentiates Thellungiella halophila from Arabidopsis thaliana.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXkvFSqtrk%3D&md5=029e730e76943dabecc3d38233780f41CAS | 17074409PubMed |
Ma J, Zhang M, Xiao X, You J, Wang J, Wang T, Tian C (2013) Global transcriptome profiling of Salicornia europaea L. shoots under NaCl treatment. PLOS ONE
Maathuis FJM, Flowers TJ, Yeo AR (1992) Sodium chloride compartmentation in leaf vacuoles of the halophyte Suaeda maritima (L.) Dum. and its relation to tonoplast permeability. Journal of Experimental Botany 43, 1219–1223.
| Sodium chloride compartmentation in leaf vacuoles of the halophyte Suaeda maritima (L.) Dum. and its relation to tonoplast permeability.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3sXnsFCktg%3D%3D&md5=e1f5719cedb22da406dda3193cb7fd43CAS |
Mahajan S, Tuteja N (2005) Cold, salinity and drought stresses: an overview. Archives of Biochemistry and Biophysics 444, 139–158.
| Cold, salinity and drought stresses: an overview.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXht1Olt7fI&md5=a00ca133fe7ac00a857c39a454965f12CAS | 16309626PubMed |
Missihoun TD, Hou Q, Mertens D, Bartels D (2014) Sequence and functional analyses of the aldehyde dehydrogenase 7B4 gene promoter in Arabidopsis thaliana and selected Brassicaceae: regulation patterns in response to wounding and osmotic stress. Planta 239, 1281–1298.
| Sequence and functional analyses of the aldehyde dehydrogenase 7B4 gene promoter in Arabidopsis thaliana and selected Brassicaceae: regulation patterns in response to wounding and osmotic stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXktVWhsrs%3D&md5=accfa5f15334ad54ac565b7a51dd1f7cCAS | 24619504PubMed |
Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends in Plant Science 7, 405–410.
| Oxidative stress, antioxidants and stress tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XntVWnu7Y%3D&md5=a9c33b8f88b87c4f315a8314d742a6d9CAS | 12234732PubMed |
Modarresi M, Nematzadeh GA, Moradian F, Alavi SM (2012) Identification and cloning of the Cu/Zn superoxide dismutase gene from halophyte plant Aeluropus littoralis. Russian Journal of Genetics 48, 118–122.
| Identification and cloning of the Cu/Zn superoxide dismutase gene from halophyte plant Aeluropus littoralis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xjsl2ktA%3D%3D&md5=1092b87fc28a7340588598dcd6a03359CAS |
Modarresi M, Nematzadeh GA, Moradian F (2013) Salinity response pattern and isolation of catalase gene from halophyte plant Aeluropus littoralis. Photosynthetica 51, 621–629.
| Salinity response pattern and isolation of catalase gene from halophyte plant Aeluropus littoralis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXhvVGmsrzK&md5=6a3ff8f3cbdc33141a210056c056b41dCAS |
Moghaieb RE, Saneoka H, Fujita K (2004) Effect of salinity on osmotic adjustment, glycinebetaine accumulation and the betaine aldehyde dehydrogenase gene expression in two halophytic plants, Salicornia europaea and Suaeda maritima. Plant Science 166, 1345–1349.
| Effect of salinity on osmotic adjustment, glycinebetaine accumulation and the betaine aldehyde dehydrogenase gene expression in two halophytic plants, Salicornia europaea and Suaeda maritima.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXivVWls7s%3D&md5=74c671ca0f83131bc2fe38dec7c860ccCAS |
Munns R, Tester M (2008) Mechanisms of salinity tolerance. Annual Review of Plant Biology 59, 651–681.
| Mechanisms of salinity tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXntFaqtrw%3D&md5=dd68a82a6d2c6414e1266213f98edac3CAS | 18444910PubMed |
Nilhan TG, Emre YA, Osman K (2008) Soil determinants for distribution of Halocnemum strobilaceum Bieb. (Chenopodiaceae) around Lake Tuz, Turkey. Pakistan Journal of Biological Sciences 11, 565–570.
| Soil determinants for distribution of Halocnemum strobilaceum Bieb. (Chenopodiaceae) around Lake Tuz, Turkey.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXovFSitbg%3D&md5=548267d68c0b6628ba23ca06e6197da5CAS | 18817127PubMed |
Niu X, Bressan RA, Hasegawa PM, Pardo JM (1995) Ion homeostasis in NaCl stress environments. Plant Physiology 109, 735–742.
Noctor G, Foyer CH (1998) Ascorbate and glutathione: keeping active oxygen under control. Annual Review of Plant Physiology and Plant Molecular Biology 49, 249–279.
| Ascorbate and glutathione: keeping active oxygen under control.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXjvVShtrc%3D&md5=87d91a87e031b21640ffe872c6ca679dCAS | 15012235PubMed |
Noctor G, Veljovic‐Jovanovic S, Driscoll S, Novitskaya L, Foyer CH (2002) Drought and oxidative load in the leaves of C3 plants: a predominant role for photorespiration? Annals of Botany 89, 841–850.
| Drought and oxidative load in the leaves of C3 plants: a predominant role for photorespiration?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XlsVeitLs%3D&md5=ac0924bb5ce0463a21c959f742a2f363CAS | 12102510PubMed |
Noctor G, De Paepe R, Foyer CH (2007) Mitochondrial redox biology and homeostasis in plants. Trends in Plant Science 12, 125–134.
| Mitochondrial redox biology and homeostasis in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXivVShtr8%3D&md5=5ce85e2184bbfa944595f78b363b0c24CAS | 17293156PubMed |
Oh DH, Dassanayake M, Haas JS, Kropornika A, Wright C, d’Urzo MP, Bohnert HJ (2010) Genome structures and halophyte-specific gene expression of the extremophile Thellungiella parvula in comparison with Thellungiella salsuginea (Thellungiella halophila) and Arabidopsis. Plant Physiology 154, 1040–1052.
| Genome structures and halophyte-specific gene expression of the extremophile Thellungiella parvula in comparison with Thellungiella salsuginea (Thellungiella halophila) and Arabidopsis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhsV2nsbfP&md5=4f97a973452c1f5e7f9c6f3e72af75c4CAS | 20833729PubMed |
Orsini F, D’Urzo MP, Inan G, Serra S, Oh DH, Mickelbart MV, Consiglio F, Li X, Jeong JC, Yun DJ, Bohnert HJ, Bressan RA, Maggio A (2010) A comparative study of salt tolerance parameters in 11 wild relatives of Arabidopsis thaliana. Journal of Experimental Botany 61, 3787–3798.
| A comparative study of salt tolerance parameters in 11 wild relatives of Arabidopsis thaliana.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtVert7jO&md5=725ed91138abd6e86295c684a52a7fb6CAS | 20595237PubMed |
Ozgur R, Uzilday B, Sekmen AH, Turkan I (2013) Reactive oxygen species regulation and antioxidant defence in halophytes. Functional Plant Biology 40, 832–847.
Pang Q, Chen S, Dai S, Chen Y, Wang Y, Yan X (2010) Comparative proteomics of salt tolerance in Arabidopsis thaliana and Thellungiella halophila. Journal of Proteome Research 9, 2584–2599.
| Comparative proteomics of salt tolerance in Arabidopsis thaliana and Thellungiella halophila.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXkvVKrur8%3D&md5=1f10d4c02c7db9cf541ff69541c6c33aCAS | 20377188PubMed |
Panta S, Flowers T, Lane P, Doyle R, Haros G, Shabala S (2014) Halophyte agriculture: Success stories. Environmental and Experimental Botany 107, 71–83.
| Halophyte agriculture: Success stories.Crossref | GoogleScholarGoogle Scholar |
Parida AK, Das AB (2005) Salt tolerance and salinity effects on plants: a review. Ecotoxicology and Environmental Safety 60, 324–349.
| Salt tolerance and salinity effects on plants: a review.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXhtVKlt7nN&md5=9d55e0ad2b8888272c2ab5e3fe9be232CAS | 15590011PubMed |
Pearson J, Havill DC (1988) The effect of hypoxia and sulphide on culture-grown wetland and non-wetland plants. Journal of Experimental Botany 39, 431–439.
| The effect of hypoxia and sulphide on culture-grown wetland and non-wetland plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1cXktlegurg%3D&md5=268f079f256da2511c533b6eb0b951c2CAS |
Qu XX, Huang ZY, Baskin JM, Baskin CC (2008) Effect of temperature, light and salinity on seed germination and radicle growth of the geographically widespread halophyte shrub Halocnemum strobilaceum. Annals of Botany 101, 293–299.
| Effect of temperature, light and salinity on seed germination and radicle growth of the geographically widespread halophyte shrub Halocnemum strobilaceum.Crossref | GoogleScholarGoogle Scholar | 17428834PubMed |
Reboreda R, Caçador I (2007) Halophyte vegetation influences in salt marsh retention capacity for heavy metals. Environmental Pollution 146, 147–154.
| Halophyte vegetation influences in salt marsh retention capacity for heavy metals.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtlartro%3D&md5=4645041ba51092e4b618ed1b01ff3566CAS | 16996176PubMed |
Redondo-Gómez S, Mateos-Naranjo E, Davy AJ, Fernández-Muñoz F, Castellanos EM, Luque T, Figueroa ME (2007) Growth and photosynthetic responses to salinity of the salt-marsh shrub Atriplex portulacoides. Annals of Botany 100, 555–563.
| Growth and photosynthetic responses to salinity of the salt-marsh shrub Atriplex portulacoides.Crossref | GoogleScholarGoogle Scholar | 17684026PubMed |
Robinson MF, Very AA, Sanders D, Mansfield TA (1997) How can stomata contribute to salt tolerance? Annals of Botany 80, 387–393.
| How can stomata contribute to salt tolerance?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2sXmvFGktrk%3D&md5=45bed625b1f9ddcf5fb5c9928b999ccaCAS |
Roshandel P, Flowers T (2009) The ionic effects of NaCl on physiology and gene expression in rice genotypes differing in salt tolerance. Plant and Soil 315, 135–147.
| The ionic effects of NaCl on physiology and gene expression in rice genotypes differing in salt tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXjvFersw%3D%3D&md5=a2c5bf4ad240dd25e8651bed6575f29dCAS |
Rozema J, Gude H, Pollack G (1981) An ecophysical study of the salt secretion of four halophytes. New Phytologist 89, 201–217.
| An ecophysical study of the salt secretion of four halophytes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL38XhslChtQ%3D%3D&md5=3d2a46be1280022fd0690ed68c5645abCAS |
Sage RF, Sage TL, Kocacinar F (2012) Photorespiration and the evolution of C4 photosynthesis. Annual Review of Plant Biology 63, 19–47.
| Photorespiration and the evolution of C4 photosynthesis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xos1amsro%3D&md5=58b8b662228fcf585d3c8438b5de6570CAS | 22404472PubMed |
Sekmen AH, Ozdemir F, Turkan I (2004) Effects of salinity, light, and temperature on seed germination in a Turkish endangered halophyte, Kalidiopsis wagenitzii (Chenopodiaceae). Israel Journal of Plant Sciences 52, 21–30.
| Effects of salinity, light, and temperature on seed germination in a Turkish endangered halophyte, Kalidiopsis wagenitzii (Chenopodiaceae).Crossref | GoogleScholarGoogle Scholar |
Sekmen AH, Turkan I, Takio S (2007) Differential responses of antioxidative enzymes and lipid peroxidation to salt stress in salt-tolerant Plantago maritima and salt-sensitive Plantago media. Physiologia Plantarum 131, 399–411.
| Differential responses of antioxidative enzymes and lipid peroxidation to salt stress in salt-tolerant Plantago maritima and salt-sensitive Plantago media.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXht1KqsrvM&md5=5be2c16cbe992fabfc985fbf39067f0fCAS | 18251879PubMed |
Sekmen AH, Turkan I, Tanyolac ZO, Ozfidan C, Dinc A (2012) Different antioxidant defense responses to salt stress during germination and vegetative stages of endemic halophyte Gypsophila oblanceolata BARK. Environmental and Experimental Botany 77, 63–76.
| Different antioxidant defense responses to salt stress during germination and vegetative stages of endemic halophyte Gypsophila oblanceolata BARK.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xht1Onurc%3D&md5=e0d7960b3688e7a503b7b2f8807cd065CAS |
Shabala S (2013) Learning from halophytes: physiological basis and strategies to improve abiotic stress tolerance in crops. Annals of Botany 112, 1209–1221.
| Learning from halophytes: physiological basis and strategies to improve abiotic stress tolerance in crops.Crossref | GoogleScholarGoogle Scholar | 24085482PubMed |
Shabala S, Cuin TA (2008) Potassium transport and plant salt tolerance. Physiologia Plantarum 133, 651–669.
| Potassium transport and plant salt tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXps1Oit70%3D&md5=e3b7086a1c0639a11d71b2068d781bd9CAS | 18724408PubMed |
Shabala S, Mackay AS (2011) Ion transport in halophytes. Advances in Botanical Research 57, 151–199.
| Ion transport in halophytes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXps1Sit74%3D&md5=0be98b691971716a3ef0e5235d525e71CAS |
Shabala S, Demidchik V, Shabala L, Cuin TA, Smith SJ, Miller AJ, Davies JM, Newman IA (2006) Extracellular Ca2+ ameliorates NaCl-induced K+ loss from Arabidopsis root and leaf cells by controlling plasma membrane K+-permeable channels. Plant Physiology 141, 1653–1665.
| Extracellular Ca2+ ameliorates NaCl-induced K+ loss from Arabidopsis root and leaf cells by controlling plasma membrane K+-permeable channels.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XosVKitbo%3D&md5=6c9da843f45a66bc80097588e3964869CAS | 16798942PubMed |
Shabala S, Bose J, Hedrich R (2014) Salt bladders: do they matter? Trends in Plant Science 19, 687–691.
| Salt bladders: do they matter?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXhvVart73M&md5=d9ff5e40cfcebf189aa8e9abb0f282c1CAS | 25361704PubMed |
Shinozaki K, Yamaguchi-Shinozaki K, Seki M (2003) Regulatory network of gene expression in the drought and cold stress responses. Current Opinion in Plant Biology 6, 410–417.
| Regulatory network of gene expression in the drought and cold stress responses.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXntVKhsb8%3D&md5=b9e04fd98f931904dc802bbcd6ee5b7eCAS | 12972040PubMed |
Singh D, Jha B (2014) The isolation and identification of salt-responsive novel microRNAs from Salicornia brachiata, an extreme halophyte. Plant Biotechnology Reports 8, 325–336.
| The isolation and identification of salt-responsive novel microRNAs from Salicornia brachiata, an extreme halophyte.Crossref | GoogleScholarGoogle Scholar |
Singh DK, Sale PW, Pallaghy CK, Singh V (2000) Role of proline and leaf expansion rate in the recovery of stressed white clover leaves with increased phosphorus concentration. New Phytologist 146, 261–269.
| Role of proline and leaf expansion rate in the recovery of stressed white clover leaves with increased phosphorus concentration.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXktlGlsLs%3D&md5=a5503cdade62d2d906bb4a0bc41d2448CAS |
Singh D, Buhmann AK, Flowers TJ, Seal CE, Papenbrock J (2014a) Salicornia as a crop plant in temperate regions: selection of genetically characterized ecotypes and optimization of their cultivation conditions. AoB Plants 6, plu071
| Salicornia as a crop plant in temperate regions: selection of genetically characterized ecotypes and optimization of their cultivation conditions.Crossref | GoogleScholarGoogle Scholar | 25387752PubMed |
Slama I, Abdelly C, Bouchereau A, Flowers T, Savouré A (2015) Diversity, distribution and roles of osmoprotective compounds accumulated in halophytes under abiotic stress. Annals of Botany 115, 433–447.
| Diversity, distribution and roles of osmoprotective compounds accumulated in halophytes under abiotic stress.Crossref | GoogleScholarGoogle Scholar | 25564467PubMed |
Song J, Feng G, Zhang F (2006) Salinity and temperature effects on germination for three salt-resistant euhalophytes, Halostachys caspica, Kalidium foliatum and Halocnemum strobilaceum. Plant and Soil 279, 201–207.
| Salinity and temperature effects on germination for three salt-resistant euhalophytes, Halostachys caspica, Kalidium foliatum and Halocnemum strobilaceum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhsVaru7w%3D&md5=3b570e8e7c7a87cec3984a42d0c8d8b1CAS |
Sousa AI, Caçador I, Lillebø AI, Pardal MA (2008) Heavy metal accumulation in Halimione portulacoides: intra-and extra-cellular metal binding sites. Chemosphere 70, 850–857.
| Heavy metal accumulation in Halimione portulacoides: intra-and extra-cellular metal binding sites.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtlGhsbrO&md5=55b110498088cb77b21fd3139ce32085CAS | 17764720PubMed |
Steinhorst L, Kudla J (2013) Calcium and reactive oxygen species rule the waves of signaling. Plant Physiology 163, 471–485.
| Calcium and reactive oxygen species rule the waves of signaling.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXhs1Ojs7nP&md5=8934afdb1ea6c1709fa7fa8614fa3ed9CAS | 23898042PubMed |
Stepien P, Johnson GN (2009) Contrasting responses of photosynthesis to salt stress in the glycophyte Arabidopsis and the halophyte Thellungiella: role of the plastid terminal oxidase as an alternative electron sink. Plant Physiology 149, 1154–1165.
| Contrasting responses of photosynthesis to salt stress in the glycophyte Arabidopsis and the halophyte Thellungiella: role of the plastid terminal oxidase as an alternative electron sink.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXjt1ajs7c%3D&md5=4c938cb873adc8a5aee413cc8b7a565dCAS | 19052149PubMed |
Subbarao GV, Wheeler RM, Levine LH, Stutte GW (2001) Glycine betaine accumulation, ionic and water relations of red-beet at contrasting levels of sodium supply. Journal of Plant Physiology 158, 767–776.
| Glycine betaine accumulation, ionic and water relations of red-beet at contrasting levels of sodium supply.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXlslShtrY%3D&md5=42e7e3d6581e07612c8fe4a2bb4bfee7CAS | 12033231PubMed |
Szabados L, Savouré A (2010) Proline: a multifunctional amino acid. Trends in Plant Science 15, 89–97.
| Proline: a multifunctional amino acid.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhs1yit7s%3D&md5=512f9924f05362a33990e97c402adf34CAS | 20036181PubMed |
Tester M, Bacic A (2005) Abiotic stress tolerance in grasses – from model plants to crop plants. Plant Physiology 137, 791–793.
| Abiotic stress tolerance in grasses – from model plants to crop plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXislOrurw%3D&md5=7008269eadb15eebcfed98b44396f5a7CAS | 15761207PubMed |
Tester M, Davenport R (2003) Na+ tolerance and Na+ transport in higher plants. Annals of Botany 91, 503–527.
| Na+ tolerance and Na+ transport in higher plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXjsVyisbk%3D&md5=6932d667a0e2151e78f7fd397864abacCAS | 12646496PubMed |
Tester M, Langridge P (2010) Breeding technologies to increase crop production in a changing world. Science 327, 818–822.
| Breeding technologies to increase crop production in a changing world.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhslWisLg%3D&md5=b2caf8a1006ace209e819db8aed0f155CAS | 20150489PubMed |
Thomson WW, Faraday CD, Oross JW (1988) Salt glands. In ‘Solute transport in plant cells and tissues’. (Eds DA Baker, JL Hall) pp. 498–537. (Longman Scientific and Technical: Harlow, UK)
Tipirdamaz R, Gagneul D, Duhazé C, Aïnouche A, Monnier C, Ozkum D, Larher FR (2006) Clustering of halophytes from an inland salt marsh in Turkey according to their ability to accumulate sodium and nitrogenous osmolytes. Environmental and Experimental Botany 57, 139–153.
| Clustering of halophytes from an inland salt marsh in Turkey according to their ability to accumulate sodium and nitrogenous osmolytes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XkslSksr0%3D&md5=915cd5fd3304069dba2a256b8e79dc5dCAS |
Ueda A, Kanechi M, Uno Y, Inagaki N (2003) Photosynthetic limitations of a halophyte sea aster (Aster tripolium L) under water stress and NaCl stress. Journal of Plant Research 116, 63–68.
Ushakova SA, Kovaleva NP, Gribovskaya IV, Dolgushev VA, Tikhomirova NA (2005) Effect of NaCl concentration on productivity and mineral composition of Salicornia europaea as a potential crop for utilization NaCl in LSS. Advances in Space Research 36, 1349–1353.
| Effect of NaCl concentration on productivity and mineral composition of Salicornia europaea as a potential crop for utilization NaCl in LSS.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXht1alurrK&md5=432b45aa9b3a626b3d1892af1d66848bCAS |
Uzilday B, Turkan I, Ozgur R, Sekmen AH (2014) Strategies of ROS regulation and antioxidant defense during transition from C3 to C4 photosynthesis in the genus Flaveria under PEG-induced osmotic stress. Journal of Plant Physiology 171, 65–75.
| Strategies of ROS regulation and antioxidant defense during transition from C3 to C4 photosynthesis in the genus Flaveria under PEG-induced osmotic stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXht1WrsLrL&md5=804445cdd83d1b46e497491b8f1f1a81CAS | 23920414PubMed |
Uzilday B, Ozgur R, Sekmen AH, Yildiztugay E, Turkan I (2015) Changes in the alternative electron sinks and antioxidant defence in chloroplasts of the extreme halophyte Eutrema parvulum (Thellungiella parvula) under salinity. Annals of Botany 115, 449–463.
| Changes in the alternative electron sinks and antioxidant defence in chloroplasts of the extreme halophyte Eutrema parvulum (Thellungiella parvula) under salinity.Crossref | GoogleScholarGoogle Scholar | 25231894PubMed |
Vakhmistrov DB, Tikhaya NI, Mishustina NE (1982) Characterization and comparison of membrane-bound Na, K, Mg-ATPase from tissues of Hordeum vulgare L. and Halocnemum strobilaceum L. Physiologia Plantarum 55, 155–160.
| Characterization and comparison of membrane-bound Na, K, Mg-ATPase from tissues of Hordeum vulgare L. and Halocnemum strobilaceum L.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL38XksFWls7w%3D&md5=28c27adfcda10021ee4554bf14caa622CAS |
Van Camp W (2005) Yield enhancement genes: seeds for growth. Current Opinion in Biotechnology 16, 147–153.
| Yield enhancement genes: seeds for growth.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXjtlamu7g%3D&md5=7fa7879ac827856774e1a65aa121fc4bCAS | 15831379PubMed |
Vicente O, Boscaiu M, Naranjo MA, Estrelles E, Bellés JM, Soriano P (2004) Responses to salt stress in the halophyte Plantago crassifolia (Plantaginaceae). Journal of Arid Environments 58, 463–481.
| Responses to salt stress in the halophyte Plantago crassifolia (Plantaginaceae).Crossref | GoogleScholarGoogle Scholar |
Volkov V, Wang B, Dominy PJ, Fricke W, Amtmann A (2004) Thellungiella halophila, a salt‐tolerant relative of Arabidopsis thaliana, possesses effective mechanisms to discriminate between potassium and sodium. Plant, Cell & Environment 27, 1–14.
| Thellungiella halophila, a salt‐tolerant relative of Arabidopsis thaliana, possesses effective mechanisms to discriminate between potassium and sodium.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXhs1emtLo%3D&md5=7e045709e3fc013e47a72181f5dcfc53CAS |
Vural M, Duman H, Aytaç Z, Adıgüzel Z (2012) A new genus and three new species from Central Anatolia, Turkey. Turkish Journal of Botany 36, 427–433.
Wang W, Vinocur B, Altman A (2003) Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance. Planta 218, 1–14.
| Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXovV2ltbo%3D&md5=672213265881cc71567e5478f7f0c669CAS | 14513379PubMed |
Wang X, Fan P, Song H, Chen X, Li X, Li Y (2009) Comparative proteomic analysis of differentially expressed proteins in shoots of Salicornia europaea under different salinity. Journal of Proteome Research 8, 3331–3345.
| Comparative proteomic analysis of differentially expressed proteins in shoots of Salicornia europaea under different salinity.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXmvFOitLY%3D&md5=bd2c1c90d3555fb7438af2b2bb7f6804CAS | 19445527PubMed |
Wang X, Chang L, Wang B, Wang D, Li P, Wang L, Guo A (2013) Comparative proteomics of Thellungiella halophila leaves from plants subjected to salinity reveals the importance of chloroplastic starch and soluble sugars in halophyte salt tolerance. Molecular & Cellular Proteomics 12, 2174–2195.
| Comparative proteomics of Thellungiella halophila leaves from plants subjected to salinity reveals the importance of chloroplastic starch and soluble sugars in halophyte salt tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXht1Sht73J&md5=a5218aef70342dc1a7e1e4d237ff10e5CAS |
Ward JM, Hirschi KD, Sze H (2003) Plants pass the salt. Trends in Plant Science 8, 200–201.
| Plants pass the salt.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXjvFWls7Y%3D&md5=c2f0762c70635084fe5f6b2e6c2209ebCAS | 12758034PubMed |
Willekens H, Chamnongpol S, Davey M, Schraudner M, Langebartels C, Van Montagu M, Inze D, Van Camp W (1997) Catalase is a sink for H2O2 and is indispensable for stress defence in C3 plants. EMBO Journal 16, 4806–4816.
| Catalase is a sink for H2O2 and is indispensable for stress defence in C3 plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2sXlslOhs7c%3D&md5=e6ef3f153eca326101e3d9af4df006c4CAS | 9305623PubMed |
Wu HJ, Zhang Z, Wang JY, Oh DH, Dassanayake M, Liu B, Xie Q (2012) Insights into salt tolerance from the genome of Thellungiella salsuginea. Proceedings of the National Academy of Sciences of the United States of America 109, 12219–12224.
| Insights into salt tolerance from the genome of Thellungiella salsuginea.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xht1GktbvN&md5=da4aecca5b823e8156d26ab67f92c2d9CAS | 22778405PubMed |
Xing W, Rajashekar CB (2001) Glycine betaine involvement in freezing tolerance and water stress in Arabidopsis thaliana. Environmental and Experimental Botany 46, 21–28.
| Glycine betaine involvement in freezing tolerance and water stress in Arabidopsis thaliana.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXjvV2gtLc%3D&md5=2ad54a2283d6f638db61ff7bc8cdd261CAS | 11378169PubMed |
Yang CY, Liu SJ, Zhou SW, Wu HF, Yu JB, Xia CH (2011) Allelochemical ethyl 2-methyl acetoacetate (EMA) induces oxidative damage and antioxidant responses in Phaeodactylum tricornutum. Pesticide Biochemistry and Physiology 100, 93–103.
| Allelochemical ethyl 2-methyl acetoacetate (EMA) induces oxidative damage and antioxidant responses in Phaeodactylum tricornutum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXktF2lsLk%3D&md5=fe6026716be764bee4b0facdc02a8a52CAS |
Yıldıztugay E, Sekmen AH, Turkan I, Kucukoduk M (2011) Elucidation of physiological and biochemical mechanisms of an endemic halophyte Centaurea tuzgoluensis under salt stress. Plant Physiology and Biochemistry 49, 816–824.
| Elucidation of physiological and biochemical mechanisms of an endemic halophyte Centaurea tuzgoluensis under salt stress.Crossref | GoogleScholarGoogle Scholar | 21605980PubMed |
Yildiztugay E, Ozfidan-Konakci C, Kucukoduk M (2014) The role of antioxidant responses on the tolerance range of extreme halophyte Salsola crassa grown under toxic salt concentrations. Ecotoxicology and Environmental Safety 110, 21–30.
| The role of antioxidant responses on the tolerance range of extreme halophyte Salsola crassa grown under toxic salt concentrations.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXhsVOnu73K&md5=ebb678e69e5e22e8c61ff72f1121ab19CAS | 25193881PubMed |
Yuan HJ, Ma Q, Wu GQ, Wang P, Hu J, Wang SM (2015) ZxNHX controls Na+ and K+ homeostasis at the whole-plant level in Zygophyllum xanthoxylum through feedback regulation of the expression of genes involved in their transport. Annals of Botany 115, 495–507.
| ZxNHX controls Na+ and K+ homeostasis at the whole-plant level in Zygophyllum xanthoxylum through feedback regulation of the expression of genes involved in their transport.Crossref | GoogleScholarGoogle Scholar | 25252687PubMed |
Zhang HX, Hodson JN, Williams JP, Blumwald E (2001) Engineering salt-tolerant Brassica plants: characterization of yield and seed oil quality in transgenic plants with increased vacuolar sodium accumulation. Proceedings of the National Academy of Sciences of the United States of America 98, 12832–12836.
| Engineering salt-tolerant Brassica plants: characterization of yield and seed oil quality in transgenic plants with increased vacuolar sodium accumulation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXotFahsLs%3D&md5=84208cecc441898509facdb5873fca2eCAS | 11606781PubMed |
Zhang LQ, Niu YD, Huridu H, Hao JF, Qi Z, Hasi A (2014) Salicornia europaea L. Na+/H+ antiporter gene improves salt tolerance in transgenic alfalfa (Medicago sativa L.). Genetics and Molecular Research 13, 5350–5360.
| Salicornia europaea L. Na+/H+ antiporter gene improves salt tolerance in transgenic alfalfa (Medicago sativa L.).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXhslait73I&md5=17c6dc67d2cf2d7f008ede8bc5bbe448CAS | 25078591PubMed |
Zhifang G, Loescher WH (2003) Expression of a celery mannose 6-phosphate reductase in Arabidopsis thaliana enhances salt tolerance and induces biosynthesis of both mannitol and a glucosyl-mannitol dimmer. Plant, Cell & Environment 26, 275–283.
| Expression of a celery mannose 6-phosphate reductase in Arabidopsis thaliana enhances salt tolerance and induces biosynthesis of both mannitol and a glucosyl-mannitol dimmer.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXhslOgurw%3D&md5=ee78a19d1adde1d67b2b6aa4bdac9b32CAS |
Zhou Y, Gao F, Li X, Zhang J, Zhang G (2010) Alterations in phosphoproteome under salt stress in Thellungiella roots. Chinese Science Bulletin 55, 3673–3679.
| Alterations in phosphoproteome under salt stress in Thellungiella roots.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhsFWjurzK&md5=711af339b69a20b1f3a59d31997859d9CAS |
Zhu JK (2000) Genetic analysis of plant salt tolerance using Arabidopsis. Plant Physiology 124, 941–948.
| Genetic analysis of plant salt tolerance using Arabidopsis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXotlWrurw%3D&md5=0ff0e952e4c0157cd68dac03e6e337aaCAS | 11080272PubMed |
Zhu JK (2001) Plant salt tolerance. Trends in Plant Science 6, 66–71.
| Plant salt tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXlsFyjtLs%3D&md5=1e14ced429b923e751d9f157947218dbCAS | 11173290PubMed |
Zouari N, Saad RB, Legavre T, Azaza J, Sabau X, Jaoua M, Masmoudi K, Hassairi A (2007) Identification and sequencing of ESTs from the halophyte grass Aeluropus littoralis. Gene 404, 61–69.
| Identification and sequencing of ESTs from the halophyte grass Aeluropus littoralis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtFyku7nE&md5=78a059101c56f8e339e1356bbd4d3394CAS | 17916418PubMed |
