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Plant function and evolutionary biology
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The effect of hyper-osmotic salinity on protein pattern and enzyme activities of halophytes

Hans-Werner Koyro A , Christian Zörb B , Ahmed Debez C D and Bernhard Huchzermeyer C E
+ Author Affiliations
- Author Affiliations

A Institute of Plant Ecology, Justus-Liebig-University Giessen, Heinrich-Buff-Ring 26-32, D-35392 Giessen, Germany.

B Institute of Biology, Botany, University Leipzig, Johannisallee 21–23, D-04103 Leipzig, Germany.

C Institut of Botany, Leibniz Universitaet Hannover, Herrenhaeuser-Str. 2, D-30419 Hannover, Germany.

D Laboratoire des Plantes Extrêmophiles (LPE), Centre de Biotechnologie à la Technopole de Borj-Cedria (CBBC), BP 901, Hammam-Lif 2050, Tunisia.

E Corresponding author. Email: huchzermeyer@botanik.uni-hannover.de

This paper originates from a presentation at the COST WG2 MeetingPutting halophytes to workgenetics, biochemistry and physiologyHannover, Germany, 2831 August 2012.

Functional Plant Biology 40(9) 787-804 https://doi.org/10.1071/FP12387
Submitted: 20 December 2012  Accepted: 16 May 2013   Published: 26 June 2013

Abstract

Studies of the convergence of the expression of enzymes and the physiology of salt resistance are rare, and give the general impression of a jigsaw puzzle with many missing pieces. To date, only minor responses of plasma membrane and tonoplast proteins of halophytes have been reported. Mostly, subunits of the catalytic portions of ATPases were found to change. In succulent plants such as Salicornia europea the abundance of V-type ATPase subunits has been correlated with growth performance. This stresses the physiological strategy to sequester incoming salt into vacuoles, which may also benefit osmotic regulation and further promote growth. A considerable amount of information is available on the responses of proteins involved in photosynthesis and detoxification of reactive oxygen species (ROS) under saline conditions. Two aspects deserve special attention: (i) salt responsive multiple spot patterns of individual proteins (due to protein modification, phosphorylation, for instance); and (ii) correlations between salt-mediated protein abundance and plant performance. Relevant observations underline that there exists a tightly knit metabolic network underlying physiological observations. Although the exact functioning of control and signalling sequences remains elusive, another aspect becomes very obvious from the publications analysed: stress responses of halophytes are multi-variant and include not only an increase in abundance of enzymes, but also of chaperones and proteins controlling organisation of the cytoplasm.

Additional keywords: ATPase, compartmentation, compatible solutes, halophytes, ion selectivity, multi-variant stress response, proteomics, ROS, salt resistance, stress signalling, structural integrity.


References

Aghaei K, Ehsanpour AA, Komatsu S (2008) Proteome analysis of potato under salt stress. Journal of Proteome Research 7, 4858–4868.
Proteome analysis of potato under salt stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXht1CltbnF&md5=dd5cdfb3e14fe2991b531fa12c5c4023CAS | 18855355PubMed |

Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annual Review of Plant Biology 55, 373–399.
Reactive oxygen species: metabolism, oxidative stress, and signal transduction.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXlvFeisL0%3D&md5=bb62c10883f0f45b9778cbbe05a12a70CAS | 15377225PubMed |

Apse M, Blumwald E (2002) Engineering salt tolerance in plants. Current Opinion in Biotechnology 13, 146–150.
Engineering salt tolerance in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xis1CltL8%3D&md5=51a8027c374160a13b1a4715c0f5dcf9CAS | 11950567PubMed |

Apse MP, Sottosanto JB, Blumwald E (2003) Vacuolar cation/H+ exchange, ion homeostasis, and leaf development are altered in a T-DNA insertion mutant of AtNHX1, the Arabidopsis vacuolar Na+/H+ antiporter. The Plant Journal 36, 229–239.
Vacuolar cation/H+ exchange, ion homeostasis, and leaf development are altered in a T-DNA insertion mutant of AtNHX1, the Arabidopsis vacuolar Na+/H+ antiporter.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXpt1OgtLk%3D&md5=577998de8c12babbb465e36914674c1bCAS | 14535887PubMed |

Arenas-Huertero F, Arroyo A, Zhou L, Sheen J, León P (2000) Analysis of Arabidopsis glucose insensitive mutants, gin5 and gin6, reveals a central role of the plant hormone ABA in the regulation of plant vegetative development by sugar. Genes & Development 14, 2085–2096.

Askari H, Edqvist J, Hajheidari M, Kafi M, Salekdeh GH (2006) Effects of salinity levels on proteome of Sueda aegyptiaca leaves. Proteomics 6, 2542–2554.
Effects of salinity levels on proteome of Sueda aegyptiaca leaves.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XkslCgsbs%3D&md5=4f0f2d4a389775412cb0eb4b19c67ceeCAS | 16612795PubMed |

Barkla BJ, Vera-Estrella R, Maldonado-Gama M, Pantoja O (1999) Abscisic acid induction f vacuolar H+-ATPase activity in Mesembryanthemum crystallinum is developmental regulated. Plant Physiology 120, 811–820.
Abscisic acid induction f vacuolar H+-ATPase activity in Mesembryanthemum crystallinum is developmental regulated.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXks1amtbo%3D&md5=df80e63ff4e04f104c4b031c935f76f5CAS | 10398716PubMed |

Barkla BJ, Vera-Estrella R, Hermández-Coronado M, Pantoja O (2009) Quantitative proteomics of the tonoplast reveals a role for glycolytic enzymes in salt tolerance. The Plant Cell 21, 4044–4058.
Quantitative proteomics of the tonoplast reveals a role for glycolytic enzymes in salt tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhvFSis7s%3D&md5=d1f5da6476b8909416333edfdcf56867CAS | 20028841PubMed |

Batelli G, Verslues PE, Agius F, Qiu Q, Fujii H, Pan SQ, Schumaker K, Grillo S, Zhu J-K (2007) SOS2 promotes salt tolerance in part by interacting with the vacuolar H+-ATPase and upregulating its transport activity. Molecular and Cellular Biology 27, 7781–7790.
SOS2 promotes salt tolerance in part by interacting with the vacuolar H+-ATPase and upregulating its transport activity.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtlWmsr3N&md5=3b7eb318a094ae42550542e796a1f26dCAS | 17875927PubMed |

Bohnert HJ, Nelson DE, Jensen RG (1995) Adaptations to environmental stresses. The Plant Cell 7, 1099–1111.

Borsani O, Valpuesta V, Botella MA (2003) Developing salt tolerant plants in a new century: a molecular biology approach. Plant Cell, Tissue and Organ Culture 73, 101–115.
Developing salt tolerant plants in a new century: a molecular biology approach.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXit1Kitrs%3D&md5=add5cb71cd16023b1a3f469a00bb4cb1CAS |

Chaves MM, Flexas J, Pinheiro C (2009) Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Annals of Botany 103, 551–560.
Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXktVGnu7s%3D&md5=c0a3d54246b0668e76fa3410ea5d90a2CAS | 18662937PubMed |

Cheeseman JM (1988) Mechanisms of salinity tolerance in plants. Plant Physiology 87, 547–550.
Mechanisms of salinity tolerance in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1cXltVOlt70%3D&md5=99b04d0af46e7d767cb00e6e9e7bbee3CAS | 16666181PubMed |

Cheeseman JM (2013) The integration of activity in saline environments: problems and perspectives. Functional Plant Biology 40,
The integration of activity in saline environments: problems and perspectives.Crossref | GoogleScholarGoogle Scholar |

Chen H-X, An S-Z, Li W-J, Gao H-Y, Zou Q (2004) Enhancement of the Mehler-peroxidase reaction in salt-stressed Rumex K-1 leaves. Acta Botanica Sinica 46, 811–818.

Chen S, Gollop N, Heuer B (2009) Proteomic analysis of salt-stressed tomato (Solanum lycopersicum) seedlings: effect of genotype and exogenous application of glycinebetaine. Journal of Experimental Botany 60, 2005–2019.
Proteomic analysis of salt-stressed tomato (Solanum lycopersicum) seedlings: effect of genotype and exogenous application of glycinebetaine.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXmtFSjur0%3D&md5=baa55808147cd2de88517b07e3a4e5dbCAS | 19336390PubMed |

Clark GB, Sessions A, Eastburn DJ, Roux SJ (2001) Differential expression of members of the annexin multigene family in Arabidopsis. Plant Physiology 126, 1072–1084.
Differential expression of members of the annexin multigene family in Arabidopsis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXlsVarur0%3D&md5=5b6864d806d6606f7387b25743bf4f9bCAS | 11457958PubMed |

Crowe JH, Hoekstra FA, Crowe LM (1992) Antibodies. Annual Review of Physiology 54, 579–599.

Dannelly HC, Cortay J-C, Cozzone AJ, Reeves HC (1989) Identification of phosphoserine in in vivo-labeled enolase from Escherichia coli. Current Microbiology 19, 237–240.
Identification of phosphoserine in in vivo-labeled enolase from Escherichia coli.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1MXlvFSht7s%3D&md5=08cb0da75c50cd1b01de24ab937ca875CAS |

Debez A, Braun H-P, Pich A, Taamalli W, Abdelly C, Huchzermeyer B (2012) Proteomic and physiological responses of the halophyte Cakile maritima to moderate NaCl-salinity at the germinative and vegetative stages. Journal of Proteomics 75, 5667–5694.
Proteomic and physiological responses of the halophyte Cakile maritima to moderate NaCl-salinity at the germinative and vegetative stages.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhsVOgsLnI&md5=745c805030a8926ab0e02e3f970c274fCAS | 22940175PubMed |

Delfine S, Alvino A, Villani MC, Loreto F (1999) Restrictions to carbon dioxide conductance and photosynthesis in spinach leaves recovering from salt stress. Plant Physiology 119, 1101–1106.
Restrictions to carbon dioxide conductance and photosynthesis in spinach leaves recovering from salt stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXhvFymu7w%3D&md5=281de0130557536a67e76f80ce15627fCAS | 10069849PubMed |

Dietz KJ, Tavakoli N, Kluge C, Mimura T, Sharma SS, Harris GC, Chardonnens AN, Golldack D (2001) Significance of the V-type ATPase for the adaptation to stressful growth conditions and its regulation on the molecular and biochemical level. Journal of Experimental Botany 52, 1969–1980.
Significance of the V-type ATPase for the adaptation to stressful growth conditions and its regulation on the molecular and biochemical level.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXns1Wktrc%3D&md5=e5a91b5d7b23d760913e695a6911424dCAS | 11559732PubMed |

Ducet G, Rosenberg AJ (1962) Leaf respiration. Annual Review of Plant Physiology 13, 171–200.
Leaf respiration.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaF3sXks1Cjtb4%3D&md5=477d486d50806fc860ede3b506aa1c8eCAS |

Elstner EF, Osswald W (1994) Mechanisms of oxygen activation during plant stress. Proceedings of the Royal Society of Edinburgh Section B 102, 131–154.

Erhardt M, Adamska I, Franco OL (2010) Plant nuclear proteomics – inside the cell maestro. FEBS Journal 277, 3295–3307.
Plant nuclear proteomics – inside the cell maestro.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtVOht77K&md5=12c4f528f30692dea0cc61db20d69379CAS | 20629746PubMed |

Flowers TJ (2004) Improving crop salt tolerance. Journal of Experimental Botany 55, 307–319.
Improving crop salt tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXms1egtQ%3D%3D&md5=ba62fd0b22f1d3b5393d8ae4f78ee465CAS | 14718494PubMed |

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=06dcabcbf1411c34a35d7aed78f04afbCAS | 18565144PubMed |

Flowers TJ, Troke PF, Yeo AR (1977) The mechanism of salt tolerance in halophytes. Annual Review of Plant Physiology 28, 89–121.
The mechanism of salt tolerance in halophytes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE2sXksFSisb8%3D&md5=ab0a16957d0ffbee896436c71cd4eb84CAS |

Forsthoefel N, Cushman M, Cushman J (1995) Posttranscriptional and posttranslational control of enolase expression in the facultative Crassulacean acid metabolism plant Mesebryanthemum crystallinum L. Plant Physiology 108, 1185–1195.
Posttranscriptional and posttranslational control of enolase expression in the facultative Crassulacean acid metabolism plant Mesebryanthemum crystallinum L.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXmvFGmurs%3D&md5=1c70751d60e70d515989327026b61927CAS | 7630941PubMed |

Geilfus CM, Zörb C, Neuhaus C, Hansen T, Lüthen H, Mühling KH (2011) Differential transcript expression of wall-loosening candidates in leaves of maize cultivars differing in salt resistance. Journal of Plant Growth Regulation 30, 387–395.
Differential transcript expression of wall-loosening candidates in leaves of maize cultivars differing in salt resistance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhtlyqtL3E&md5=f120df327195d0aae6cd9b376d01db33CAS |

Geissler N, Hussin S, Koyro H-W (2010) Elevated atmospheric CO2 concentration enhances salinity tolerance in Aster tripolium. Planta 231, 583–594.
Elevated atmospheric CO2 concentration enhances salinity tolerance in Aster tripolium.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXlslWnuw%3D%3D&md5=81a25973d9ec2aece58708076665a677CAS | 20072826PubMed |

Gong Q, Li P, Ma S, Rupassara SI, Bohnert HJ (2005) Salinity stress adaptation competence in the extremophile Thellungiella halophila in comparison with its relative Arabidopsis thaliana. The Plant Journal 44, 826–839.
Salinity stress adaptation competence in the extremophile Thellungiella halophila in comparison with its relative Arabidopsis thaliana.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtlWltrbN&md5=620030b0bcdb8cf64087da8a830c4207CAS | 16297073PubMed |

Grattan SR, Grieve CM (1998) Salinity-mineral nutrient relations in horticultural crops. Scientia Horticulturae 78, 127–157.
Salinity-mineral nutrient relations in horticultural crops.Crossref | GoogleScholarGoogle Scholar |

Greenway H, Munns R (1980) Mechanisms of salt tolerance in nonhalophytes. Annual Review of Plant Physiology 31, 149–190.
Mechanisms of salt tolerance in nonhalophytes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3cXksVWntb4%3D&md5=03b2e3789f9318b2329214779e4586beCAS |

Hajibagheri MA, Flowers TJ (1985) Salt tolerance in the halophyte Sueda maritima (L.) Dum. The influence of salinity of the culture solution on leaf starch and phosphate content. Plant, Cell & Environment 8, 261–267.

Halliwell B, Gutteridge JM (1990) Role of free radicals and catalytic metal ions in human disease: an overview. Methods in Enzymology 186, 1–85.
Role of free radicals and catalytic metal ions in human disease: an overview.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXksVKrt7Y%3D&md5=e15cfcdf216d3dd55dde4d14fc00216fCAS | 2172697PubMed |

Han KH, Hwang CH (2003) Salt tolerance enhanced by transformation of a P5CS gene in carrot. Journal of Plant Biotechnology 5, 149–153.

Hare PD, Cress WA, van Staden J (1999) Proline synthesis and degradation: a model system for elucidating stress-related signal transduction. Journal of Experimental Botany 50, 413–434.

Hasegawa PM, Bressan RA, Zhu J-K, 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=c67a7b95a8761aa0d533df99ebe4cd38CAS | 15012199PubMed |

Hauser F, Horie T (2010) A conserved primary salt tolerance mechanism mediated by HKT transporters: a mechanism for sodium exclusion and maintenance of high K+/Na+ ratio in leaves during salinity stress. Plant, Cell & Environment 33, 552–565.
A conserved primary salt tolerance mechanism mediated by HKT transporters: a mechanism for sodium exclusion and maintenance of high K+/Na+ ratio in leaves during salinity stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXltV2hurY%3D&md5=e7bc4692a047ea912227632c254a539fCAS |

Havaux M, Dall’Osto L, Cuine S, Giuliano G, Bassi R (2004) The effect of zeaxanthin as the only xanthophyll on the structure and function of the photosynthetic apparatus in Arabidopsis thaliana. Journal of Biological Chemistry 279, 13878–13888.
The effect of zeaxanthin as the only xanthophyll on the structure and function of the photosynthetic apparatus in Arabidopsis thaliana.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXis1elsbs%3D&md5=32f6e3a45b03b0e7445ad14933e0f00dCAS | 14722117PubMed |

Hebbelmann I, Selinski J, Wehmeyer C, Goss T, Voss I, Mulo P, Kangasjärvi S, Aro E-M, Oelze M-L, Dietz K-J, Nunes-Nesi A, Do PT, Fernie AR, Talla SK, Raghavendra AS, Linke V, Scheibe R (2012) Multiple strategies to prevent oxidative stress in Arabidopsis plants lacking the malate valve enzyme NADP-malate dehydrogenase. Journal of Experimental Botany 63, 1445–1459.
Multiple strategies to prevent oxidative stress in Arabidopsis plants lacking the malate valve enzyme NADP-malate dehydrogenase.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xit1Olt70%3D&md5=e251899eafbff4c875ce1b9b7053656fCAS | 22140244PubMed |

Heineke D, Kruse A, Flügge U-I, Frommer WB, Riesmeier JW, Willmitzer L, Heldt HW (1994) Effect of antisense repression of the chloroplast triose-phosphate translocator on photosynthetic metabolism in transgenic potato plants. Planta 193, 174–180.
Effect of antisense repression of the chloroplast triose-phosphate translocator on photosynthetic metabolism in transgenic potato plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2cXisVSnt7o%3D&md5=59c2f80eee5ac586625ef9b85300859bCAS |

Homeyer U, Litek K, Huchzermeyer B, Schultz G (1989) Uptake of phenylalanine into isolated barley vacuoles is driven by both, tonoplast adenosine triphosphatase and pyrophosphatase. Plant Physiology 89, 1388–1393.
Uptake of phenylalanine into isolated barley vacuoles is driven by both, tonoplast adenosine triphosphatase and pyrophosphatase.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1MXitVOqtbw%3D&md5=54ae15e2dc16e8c08341e6aa98f5d1c2CAS | 16666714PubMed |

Horton P (2000) Prospects for crop improvement through the genetic manipulation of photosynthesis: morphological and biochemical aspects of light capture. Journal of Experimental Botany 51, 475–485.
Prospects for crop improvement through the genetic manipulation of photosynthesis: morphological and biochemical aspects of light capture.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXhsVOjsro%3D&md5=f5d8f4126e5de0aafcab06b8d4f4d63fCAS | 10938855PubMed |

Huchzermeyer B (1988) Nucleotide binding and ATPase activity of membrane bound chloroplast coupling factor (CF1). Zeitschrift für Naturforschung 43c, 133–139.

Huchzermeyer B, Koyro H-W (2005) Salt and drought stress effects on photosynthesis. Enzyme cohesion and high turn-over metabolite shuttling, essential for functioning of pathways, is impaired by changes in cytosolic water potential. In ‘Handbook of photosynthesis’. 2nd edn. (Ed. M Pessarakli) pp. 751–777. (Taylor & Francis: Boca Raton, FL)

Huchzermeyer B, Strotmann H (1977) Acid/base-induced exchange of adenine nucleotides on chloroplast coupling factor (CF1). Zeitschrift für Naturforschung 32c, 803–809.

Huchzermeyer B, Löhr A, Willms I (1986) A direct interaction between photosystem I and the chloroplast coupling factor. Biochemical Journal 234, 217–220.

Huchzermeyer B, Hausmann N, Paqet-Durant F, Koyro H-W (2004) Biochemical and physiological mechanisms leading to salt tolerance. Tropical Ecology 45, 141–150.

Jithesh MN, Prashanth SR, Sivaprakash KR, Parida AK (2006) Antioxidative response mechanisms in halophytes: their role in stress defence. Journal of Genetics 85, 237–254.
Antioxidative response mechanisms in halophytes: their role in stress defence.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXlsVCmtLc%3D&md5=8908bfb0fdcca87b70055646c8b649e5CAS | 17406103PubMed |

Kant S, Kant P, Raveh E, Barak S (2006) Evidence that differential gene expression between the halophyte, Tehellugiella 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, Tehellugiella 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=24219944b87a28842a228b43fab0c045CAS |

Kishor KPB, Hong Z, Miao G-H, Hu C-AA, Verma DPS (1995) Overexpression of Δ1-pyrroline-5-carboxylate synthetase increases proline production and confers osmotolerance in transgenic plants. Plant Physiology 108, 1387–1394.

Kishor KPB, Sangam S, Amrutha RN, Sri Laxmi P, Naidu KR, Rao KRSS, Rao S, Reddy KJ, Theriappan P, Sreenivasulu N (2005) Regulation of proline biosynthesis, degradation, uptake and transport in higher plants: its implications in plant growth and abiotic stress tolerance. Current Science 88, 424–438.

Koch K (2004) Sugar metabolism: regulatory mechanisms and pivotal roles in sugar sensing and plant development. Current Opinion in Plant Biology 7, 235–246.
Sugar metabolism: regulatory mechanisms and pivotal roles in sugar sensing and plant development.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXjvVams7s%3D&md5=562d10f2c2b1f02a20ba9d5370c982beCAS | 15134743PubMed |

Koiwa H, Li F, McCully MG, Mendoza I, Koizumi N, Manabe Y, Nakagawa Y, Zhu J, Rus A, Pardo JM, Bressan RA, Hasegawa PM (2003) The STT3a subunit isoform of the Arabidopsis oligosaccharyltransferase controls adaptive responses to salt/osmotic stress. The Plant Cell 15, 2273–2284.
The STT3a subunit isoform of the Arabidopsis oligosaccharyltransferase controls adaptive responses to salt/osmotic stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXotlGmtL4%3D&md5=c0bc41abbad3d1b665cbd3107ebcb88cCAS | 12972670PubMed |

Kosová K, Vítámvás P, Urban MO, Prášil IT (2013) Plant proteome responses to salinity stress - comparison of glycophytes and halophytes. Functional Plant Biology

Koyro H-W, Geißler N, Hussin S, Huchzermeyer B (2008) Strategies of halophytes to survive in a salty environment. In ‘Abiotic stress and plant responses’. (Eds NA Khan, S Singh) pp. 83–104. (IK International: New Delhi)

Koyro H-W, Huchzermeyer B (2004) Ecophysiological mechanisms leading to salinity tolerance – screening of cash-crop halophytes. Plant Science 1, 187–207.

Koyro H-W, Huchzermeyer B (2005) Breeding for abiotic stress tolerance in maize. In ‘Abiotic stress. Plant resistance through breeding and molecular approaches’. (Eds M Ashraf, PJC Harris) pp. 545–576. (The Haworth Press: New York)

Koyro H-W, Stelzer R, Huchzermeyer B (1993) ATPase activities and membrane fine structures of rhizodermal cells from Sorghum and Spartina roots grown under mild salt stress. Botanica Acta 106, 110–119.

Koyro H-W, Huchzermeyer B, Harrouni MC (2001) Comparison of strategies of halophytes from different plant families to avoid salt injury. In ‘Plant nutrition. Food security and sustainability of agro-ecosystems through basic and applied research’. (Eds WJ Horst, MK Schenk, A Bürkert, N Claasen, H Flessa, WB Frommer, H Goldbach, H-W Olfs, V Römheld, B Sattelmacher, U Schmidhalter, S Schubert, NV Wirén, L Wittenmayer) pp. 414–415. (Kluwer Academic Publishers: Dordrecht, The Netherlands)

Koyro H-W, Geissler N, Seenivasan R, Huchzermeyer B (2011) Plant stress physiology: physiological and biochemical strategies allowing plants/crops to thrive under ionic stress’. In ‘Handbook of plant and crop stress’. 3rd edn. (Ed. M Pessarakli) pp. 1051–1093. (Taylor & Francis Group: Boca Raton, FL, USA)

Koyro H-W, Geissler N, Ahmad P, Geissler N (2012) Abiotic stress responses in plants: an overview. In ‘Environmental adaptations and stress tolerance of plants in the era of climate change’. (Eds P Ahmad, MNV Prasad) (Springer Science Business Media, LLC: New York)

Krisch R, Rakowski K, Ratajczak R (2000) Processing of V-ATPase subunit B of Mesembryanthemum crystallinum L. is mediated in vitro by a protease and/or reactive oxygen species. Biological Chemistry 381, 583–592.
Processing of V-ATPase subunit B of Mesembryanthemum crystallinum L. is mediated in vitro by a protease and/or reactive oxygen species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXmvFShs7Y%3D&md5=a403445a7d5e59f5a18877a6dcf9dbb5CAS | 10987365PubMed |

Lee S, Lee EJ, Yang EJ, Lee JE, Park AR, Song WH, Park OK (2004) Proteomic identification of annexins, calcium-dependent membrane binding proteins that mediate osmotic stress and abscisic acid signal transduction in Arabidopsis. The Plant Cell 16, 1378–1391.
Proteomic identification of annexins, calcium-dependent membrane binding proteins that mediate osmotic stress and abscisic acid signal transduction in Arabidopsis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXlsFWlsL4%3D&md5=1942addf6779d68a43c23b07ff9a6821CAS | 15161963PubMed |

Li W, Zhang C, Lu Q, Wen X, Lu C (2011) The combined effect of salt stress and heat shock on proteome profiling in Sueda salsa. Journal of Plant Physiology 168, 1743–1752.
The combined effect of salt stress and heat shock on proteome profiling in Sueda salsa.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXpvFGiu78%3D&md5=49f7daaff3d85c068ec7721faf82efadCAS | 21663998PubMed |

Liu J, Ishitani M, Halfter U, Kim C, Zhu J-K (2000) The Arabidopsis thaliana SOS2 gene encodes a protein kinase that is required for salt tolerance. Proceedings of the National Academy of Sciences of the United States of America 97, 3730–3734.
The Arabidopsis thaliana SOS2 gene encodes a protein kinase that is required for salt tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXitlajsrs%3D&md5=7f45bc9d5ba0e2a6be8d93874ca2fe57CAS | 10725382PubMed |

Löw R, Rockel B, Kirsch M, Ratajczak R, Hörtensteiner S, Martinoia E, Lüttge U, Rausch T (1996) Early salt stress effects on the differential expression of vacuolar H+-ATPase genes in roots and leaves of Mesembryanthemum crystallinum. Plant Physiology 110, 259–265.
Early salt stress effects on the differential expression of vacuolar H+-ATPase genes in roots and leaves of Mesembryanthemum crystallinum.Crossref | GoogleScholarGoogle Scholar | 8587987PubMed |

Mehler AH, Brown AH (1952) Studies on reactions of illuminated chloroplasts. III. Simultaneous photoproduction and consumption of oxygen studied with oxygen isotopes. Archives of Biochemistry and Biophysics 38, 365–370.
Studies on reactions of illuminated chloroplasts. III. Simultaneous photoproduction and consumption of oxygen studied with oxygen isotopes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaG3sXjvFGj&md5=bcb3c3c59661fd0e02c4e7dcb190fd62CAS | 12997112PubMed |

Mou Z, Wang X, Fu Z, Dai Y, Han C, Ouyang J, Bao F, Hu Y, Li J (2002) Silencing of phosphoethanolamine N-methyltransferase results in temperature-sensitive male sterility and salt hypersensitivity in Arabidopsis. The Plant Cell 14, 2031–2043.
Silencing of phosphoethanolamine N-methyltransferase results in temperature-sensitive male sterility and salt hypersensitivity in Arabidopsis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XnsFemtb8%3D&md5=2dc58764692efd9823d2f425b22c77bcCAS | 12215503PubMed |

Munns R, James RA, Xu B, Athman A, Conn SJ, Lordans C, Byrt CS, Hare RA, Tyerman SD, Tester M, Plett D, Gilliham M (2012) Wheat grain yield on saline soils is improved by an ancestral Na+ transporter gene. Nature Biotechnology 30, 360–364.
Wheat grain yield on saline soils is improved by an ancestral Na+ transporter gene.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XjtlOgu7w%3D&md5=7c1aaac749903736cdb6d4cad7aba404CAS | 22407351PubMed |

Niu X, Zhu JK, Narasimhan ML, Bressan RA, Hasegawa PM (1993) Plasma-membrane H+-ATPase gene expression is regulated by NaCl in cells of the halophyte Atriplex nummularia L. Planta 190, 433–438.
Plasma-membrane H+-ATPase gene expression is regulated by NaCl in cells of the halophyte Atriplex nummularia L.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3sXltlGks7s%3D&md5=315271fa7da6ce75aa8bcec6e5d94e14CAS | 7763822PubMed |

Oh D-H, Dassanayake M, Haas JS, Kropornika A, Wright C, Paino d’Urzo M, Hong H, Ali S, Hernandez A, Lambert GM, Inan G, Galbraith DW, Bressan RA, Yun D-J, Zhu J-K, Cheeseman JM, Bohnert HJ (2010) Genome structures and halophyte-specific gene expression of the extremophile Thellungiella parvula in comparison with Thelungiella 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 Thelungiella salsuginea (Thellungiella halophila) and Arabidopsis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhsV2nsbfP&md5=87279db9296b926d0fb9d036cc19ccbeCAS | 20833729PubMed |

Ohta H (2002) Introduction of a Na+/H+ antiporter gene from Atriplex gmelini confers salt tolerance to rice. FEBS Letters 532, 279–282.
Introduction of a Na+/H+ antiporter gene from Atriplex gmelini confers salt tolerance to rice.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XptlCqt7g%3D&md5=ce16824df7c03af74de7a3bd6a272281CAS |

Oono Y, Seki M, Nanjo T, Narusaka M, Fujita M, Satoh R, Satou M, Sakurai T, Ishida J, Akiyama K, Iida K, Maruyama K, Satoh S, Yamaguchi-Shinozaki K, Shinozaki K (2003) Monitoring expression profiles of Arabidopsis gene expression during re-hydration process after dehydration using ca. 7000 full length microarray. The Plant Journal 34, 868–887.
Monitoring expression profiles of Arabidopsis gene expression during re-hydration process after dehydration using ca. 7000 full length microarray.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXlvFajsbo%3D&md5=a4ab0622828edeb79f824a425ec51154CAS | 12795706PubMed |

Ozgur R, Uzilday B, Sekmen AH, Turkan I (2013) ROS regulation and antioxidant defense in halophytes. Functional Plant Biology
ROS regulation and antioxidant defense in halophytes.Crossref | GoogleScholarGoogle Scholar |

Padmanaban S, Lin X, Perera I, Kawamura Y, Sze H (2004) Differential expression of vacuolar H+-ATPase subunit c genes in tissues active in membrane trafficking and their roles in plant growth as revealed by RNAi. Plant Physiology 134, 1514–1526.
Differential expression of vacuolar H+-ATPase subunit c genes in tissues active in membrane trafficking and their roles in plant growth as revealed by RNAi.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXjsFKmsL4%3D&md5=6feab94c91783212511cd95d54a9ae2dCAS | 15051861PubMed |

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=acb43941c8b68676f0da9f5da4a2b77dCAS | 20377188PubMed |

Pardo JM (2010) Biotechnology of water and salinity stress tolerance. Current Opinion in Biotechnology 21, 185–196.
Biotechnology of water and salinity stress tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXlvVehtrY%3D&md5=5d1842097dc33b30dcb7c42539174935CAS | 20189794PubMed |

Parker R, Flowers TJ, Moore AL, Harpham NVJ (2006) An accurate and reproducible method for proteome profiling of the effects of salt stress in the rice leaf lamina. Journal of Experimental Botany 57, 1109–1118.
An accurate and reproducible method for proteome profiling of the effects of salt stress in the rice leaf lamina.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xis1Gls7k%3D&md5=0f3bc9dd80e6fa19c5e65721741b9053CAS | 16513811PubMed |

Portis AR (2003) Rubisco activase – Rubisco’s catalytic chaperone. Photosynthesis Research 75, 11–27.
Rubisco activase – Rubisco’s catalytic chaperone.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXht1Krurk%3D&md5=ad98dc91e8c13bfa07b8e0c8b4086c8aCAS | 16245090PubMed |

Qiu Q-S, Guo F, Quintero FJ, Pardo JM, Schumaker KS, Zhu J-K (2004) Regulation of vacuolar Na+/H+ exchange in Arabidopsis thaliana by the salt-overly-sensitive (SOS) pathway. Journal of Biological Chemistry 279, 207–215.
Regulation of vacuolar Na+/H+ exchange in Arabidopsis thaliana by the salt-overly-sensitive (SOS) pathway.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXhtVSqtrvM&md5=a8959679841c73685164bb7c40815039CAS | 14570921PubMed |

Reddy VS, Reddy ASN (2004) Proteomics of calcium-signaling components in plants. Phytochemistry 65, 1745–1776.
Proteomics of calcium-signaling components in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXmtVequrk%3D&md5=41238a880a2910ba04b611d18b2ae8deCAS | 15276435PubMed |

Riechmann JL, Ratcliffe OJ (2000) A genomic perspective on plant transcription factors. Current Opinion in Plant Biology 3, 423–434.
A genomic perspective on plant transcription factors.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXntV2jsrw%3D&md5=0687251a6762d62b6b98b6082ec5d1caCAS | 11019812PubMed |

Rokka A, Zhang L, Aro E-M (2001) Rubisco activase: an enzyme with a temperature-dependent dual function? The Plant Journal 25, 463–471.
Rubisco activase: an enzyme with a temperature-dependent dual function?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXislymt7c%3D&md5=61f1d98f2aa97a8f40b3135a83087476CAS | 11260502PubMed |

Rolland F, Moore B, Sheen J (2002) Sugar sensing and signaling in plants. The Plant Cell 14, 185–205.

Sahu BB, Shaw BP (2009) Isolation, identification and expression analysis of salt-induced genes in Sueda maritima, a natural halophyte, using PCR-based suppression substractive hybridization. BMC Plant Biology 9, 69
Isolation, identification and expression analysis of salt-induced genes in Sueda maritima, a natural halophyte, using PCR-based suppression substractive hybridization.Crossref | GoogleScholarGoogle Scholar | 19497134PubMed |

Satoh R, Nakashima K, Seki M, Shinozaki K, Yamaguchi-Shinozaki K (2002) ACTCAT, a novel cis-acting element for proline- and hypo-osmolarity-responsive expression of the ProDH gene encoding proline dehydrogenase in Arabidopsis. Plant Physiology 130, 709–719.
ACTCAT, a novel cis-acting element for proline- and hypo-osmolarity-responsive expression of the ProDH gene encoding proline dehydrogenase in Arabidopsis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XotVKntL8%3D&md5=5f84f864927de7abe0201e63444b9ea7CAS | 12376638PubMed |

Scheibe R (2004) Malate valves to balance cellular energy supply. Physiologia Plantarum 120, 21–26.
Malate valves to balance cellular energy supply.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXpvFSltw%3D%3D&md5=4cadaf738c69c6b64bd7aa982005199dCAS | 15032873PubMed |

Seki M, Kamei A, Yamaguchi-Shinozaki K, Shinozaki K (2003) Molecular responses to drought, salinity and frost: common and different paths for plant protection. Current Opinion in Plant Biology 14, 194–199.

Sengupta S, Majumder AL (2009) Insight into the salt tolerance factors of a wild halophytic rice, Porteresia coarctata: a physiological and proteomic approach. Planta 229, 911–929.
Insight into the salt tolerance factors of a wild halophytic rice, Porteresia coarctata: a physiological and proteomic approach.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXit1agsb0%3D&md5=323df2e9e2fa6e7e9038e49195f591cbCAS | 19130079PubMed |

Shi H, Ishitani M, Kim C, Zhu J-K (2000) The Arabidopsis thaliana salt tolerance gene SOS1 encodes a putative Na+/H+ antiporter. Proceedings of the National Academy of Sciences of the United States of America 97, 6896–6901.
The Arabidopsis thaliana salt tolerance gene SOS1 encodes a putative Na+/H+ antiporter.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXktFahtrs%3D&md5=55efc6e21ef49d2fa4b8ba59e5aa88d8CAS | 10823923PubMed |

Smeekens S (1998) Sugar regulation of gene expression in plants. Current Opinion in Plant Biology 1, 230–234.
Sugar regulation of gene expression in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXktFaku70%3D&md5=12957f5465aff4438dc8727ac862d87dCAS | 10066585PubMed |

Sobhanian H, Motamed N, Jazii FR, Nakamura T, Komatsu S (2010) Salt stress induced differential proteome and metabolome response in the shoots of Aeluropus lagopoides (Poaceae), a halophyte C4 plant. Journal of Proteome Research 9, 2882–2897.
Salt stress induced differential proteome and metabolome response in the shoots of Aeluropus lagopoides (Poaceae), a halophyte C4 plant.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXlt1OntrY%3D&md5=72afeae0c6265534bb6080c7cc469439CAS | 20397718PubMed |

Sudhir P, Murthy SDS (2004) Effects of salt stress on basic processes of photosynthesis. Photosynthetica 42, 481–486.
Effects of salt stress on basic processes of photosynthesis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhsVOmtbw%3D&md5=0aae7954e99014a17364cc00554604b5CAS |

Süss KH, Arkona C, Manteuffel R, Adler K (1993) Calvin cycle multienzyme complexes are bound to chloroplast thylakoid membranes of higher plants in situ. Proceedings of the National Academy of Sciences of the United States of America 90, 5514–5518.
Calvin cycle multienzyme complexes are bound to chloroplast thylakoid membranes of higher plants in situ.Crossref | GoogleScholarGoogle Scholar | 11607406PubMed |

Szabados L, Savoré 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=6ef05c7dd8725df8b7e99ff345554897CAS | 20036181PubMed |

Szabados L, Kovács H, Zilberstein A, Bouchereau A (2011) Plants in extreme environments: importance of protective compounds in stress tolerance. Advances in Botanical Research 57, 105–150.
Plants in extreme environments: importance of protective compounds in stress tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXps1Sitrg%3D&md5=538ed36536f4068111347a76629484e6CAS |

Székely G, Ábrahám E, Csépló A, Rigó G, Zsigmond L, Csiszár J, Ayaydin F, Strizhov N, Jásik J, Schmelzer E, Koncz C, Sabados L (2008) Duplicated P5CS genes of Arabidopsis play distinct roles in stress regulation and developmental control of proline biosynthesis. The Plant Journal 53, 11–28.
Duplicated P5CS genes of Arabidopsis play distinct roles in stress regulation and developmental control of proline biosynthesis.Crossref | GoogleScholarGoogle Scholar | 17971042PubMed |

Teige M, Huchzermeyer B, Schultz G (1990) Inhibition of chloroplast ATP synthase/ATPase is a primary effect of heavy metal toxicity in spinach plants. Biochemie und Physiologie der Pflanzen 186, 165–168.

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=88eb811f9dc3f2cd8aa877eaee28c69dCAS | 12646496PubMed |

Tsiantis MS, Bartholomew DM, Smith JAC (1996) Salt regulation of transcript levels for the c subunit of a leaf vacuolar H+-ATPase in the halophyte Mesembryanthemum crystallinum. The Plant Journal 9, 729–736.
Salt regulation of transcript levels for the c subunit of a leaf vacuolar H+-ATPase in the halophyte Mesembryanthemum crystallinum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XjvVSlsrw%3D&md5=1fa5e73a02956d9a8a196c4da3ed0559CAS | 8653119PubMed |

Veeranagamallaiah G, Jyothsnakumari G, Thippeswamy M, Reddy CO, Surabhi GK, Siranganayakulu G, Mahesh Y, Rajasekhar B, Madhurrarekha CH (2008) Proteomic analysis of salt stress responses in foxtail millet (Setaria italica L. cv. Prasad) seedlings. Plant Science 175, 631–641.
Proteomic analysis of salt stress responses in foxtail millet (Setaria italica L. cv. Prasad) seedlings.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtFCktr%2FM&md5=4b6412e278b95c88909b30f37b59b192CAS |

Vera-Estrella R, Barkla BJ, García-Ramírez L, Pantoja O (2004) Novel regulation of aquaporins during osmotic stress. Plant Physiology 135, 2318–2329.
Novel regulation of aquaporins during osmotic stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXnt1Ggsb8%3D&md5=2718778e3ba12159f1ccd616e52491f5CAS | 15299122PubMed |

Verbruggen N, Hermans C (2008) Proline accumulation in plants: a review. Amino Acids 35, 753–759.
Proline accumulation in plants: a review.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXht1aisrfP&md5=0ee3f762d1e8f9f2650e618694cca205CAS | 18379856PubMed |

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=51fae0c6c8b2c2ca68b113b8ac590f0aCAS | 19445527PubMed |

Wetson AM, Zörb C, John EA, Flowers TJ (2012) High phenotypic plasticity of Suaeda maritima observed under hypoxic conditions in relation to its physiological basis. Annals of Botany 109, 1027–1036.
High phenotypic plasticity of Suaeda maritima observed under hypoxic conditions in relation to its physiological basis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XkvVSltbc%3D&md5=523af1206af06039232f8be31b2d6831CAS | 22316572PubMed |

Wyn Jones RG, Gorham J (2002) Intra- and inter-cellular compartmentation of ions. In ‘Salinity: environment – plants – molecules’. (Eds A Läuchli, U Lüttge) pp. 159–180. (Kluwer Academic Publishers: Dordrecht, The Netherlands)

Xu C, Sibicky T, Huang B (2010) Protein profile analysis of salt-responsive proteins in leaves and roots in two cultivars of creeping bentgrass differing in salinity tolerance. Plant Cell Reports 29, 595–615.
Protein profile analysis of salt-responsive proteins in leaves and roots in two cultivars of creeping bentgrass differing in salinity tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXmtV2jtbk%3D&md5=fb39d2b5c4c5d5487c327230c2e31f45CAS | 20361191PubMed |

Yan S, Tang Z, Su W, Sun W (2005) Proteomic analysis of salt stress responsive proteins in rice root. Proteomics 5, 235–244.
Proteomic analysis of salt stress responsive proteins in rice root.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtleisL8%3D&md5=d76ef064f59b987ffc47a11058ad33a3CAS | 15672456PubMed |

Yancey P, Clark ME, Had SC, Bowlus RD, Somero GN (1982) Living with the water stress: evolution of osmolyte system. Science 217, 1214–1222.
Living with the water stress: evolution of osmolyte system.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL38XlsFyisbw%3D&md5=bf1709a0f97fc216b83a6dd8ae279ad6CAS | 7112124PubMed |

Yao R, Fang S (2009) Cytochemical localization of H+-ATPase and sub-cellular variation in mesophyll cells of salt-treated Cyclocarya paliurus seedlings. Frontiers of Forestry in China 4, 494–500.
Cytochemical localization of H+-ATPase and sub-cellular variation in mesophyll cells of salt-treated Cyclocarya paliurus seedlings.Crossref | GoogleScholarGoogle Scholar |

Yokoi S, Quintero FJ, Cubero B, Ruiz T, Bressan RA, Hasegawa PM, Pardo JM (2002) Differential expression and function of Arabidopsis thaliana NHX Na+/H+ antiporters in the salt stress response. The Plant Journal 30, 529–539.
Differential expression and function of Arabidopsis thaliana NHX Na+/H+ antiporters in the salt stress response.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XlsFyktL0%3D&md5=08a83482979c4b3f4ba66c201e80e8faCAS | 12047628PubMed |

Yu J, Chen S, Zhao Q, Wang T, Yang C, Diaz C, Sun G, Dai S (2011) Physiological and proteomic analysis of salinity tolerance in Puccinellia tenuiflora. Journal of Proteome Research 10, 3852–3870.
Physiological and proteomic analysis of salinity tolerance in Puccinellia tenuiflora.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXpvVyhsbc%3D&md5=db8490723a5fe7630950ef12705b77a8CAS | 21732589PubMed |

Zhang JX, Nguyen HT, Blum A (1999) Genetic analysis of osmotic adjustment in crop plants. Journal of Experimental Botany 49, 915–929.

Zhang H, Han B, Wang T, Chen S, Li H, Zhang Y, Dai S (2012) Mechanisms of plant salt response: insights from proteomics. Journal of Proteome Research 11, 49–67.
Mechanisms of plant salt response: insights from proteomics.Crossref | GoogleScholarGoogle Scholar | 22017755PubMed |

Zhigang A, Löw R, Rausch T, Lüttge U, Ratajczak R (1996) The 32 kDa tonoplast polypeptide Di associated with the V-type H+-ATPase of Mesembryanthemum crystallinum L. in the CAM state: a proteolytically processed subunit B? FEBS Letters 389, 314–318.
The 32 kDa tonoplast polypeptide Di associated with the V-type H+-ATPase of Mesembryanthemum crystallinum L. in the CAM state: a proteolytically processed subunit B?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XktVOmtbk%3D&md5=38ed001980ad676a1e5cf72bf0931ec8CAS | 8766723PubMed |

Zhou J, Wang X, Jiao Y, Qin Y, Liu X, He K, Chen C, Ma L, Wang J, Xiong L, Zang Q, Fan L, Deng XW (2007) Global genome expression analysis of rice in response to drought and high-salinity stress in shoot, flag leaf, and panicle. Plant Molecular Biology 63, 591–608.
Global genome expression analysis of rice in response to drought and high-salinity stress in shoot, flag leaf, and panicle.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXitFKmsbw%3D&md5=a41bc9706897494e553157d4f3d2cbebCAS | 17225073PubMed |

Zhu JK (2002) Salt and drought stress signal transduction in plants. Annual Review of Plant Biology 53, 247–273.
Salt and drought stress signal transduction in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XlsVWhtbc%3D&md5=f20f5493d7e57fe0984b2dba9a510739CAS | 12221975PubMed |

Zhu JK (2003) Regulation of ion homeostasis under salt stress. Current Opinion in Plant Biology 6, 441–445.
Regulation of ion homeostasis under salt stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXntVKhsbs%3D&md5=0ddcc4f1d487026b7b052f5c1d38966dCAS | 12972044PubMed |

Zhu B, Su J, Chang M, Verma DPS, Fan YL, Wu R (1998) Overexpression of a Δ1-pyrroline-5-carboxylate synthetase gene and analysis of tolerance to water-and salt-stress in transgenic rice. Plant Science 139, 41–48.
Overexpression of a Δ1-pyrroline-5-carboxylate synthetase gene and analysis of tolerance to water-and salt-stress in transgenic rice.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXmvFWltbg%3D&md5=287dd21b0d74c8e786c650c9e01fad0eCAS |

Zörb C, Herbst R, Forreiter C, Schubert S (2009) Short-term effects of salt exposure on the maize chloroplast protein pattern. Proteomics 9, 4209–4220.
Short-term effects of salt exposure on the maize chloroplast protein pattern.Crossref | GoogleScholarGoogle Scholar | 19688749PubMed |