Oxidative stress and its effects during dehydration

França, M.B.; Panek, A.D.; Eleutherio, E.C.A.

doi:10.1016/j.cbpa.2006.02.030

Cited by 422Tardigrade Biology and EcologyRedox biology and oxidative stressPlant Stress Responses and Tolerance

Oxidative stress and its effects during dehydration

França, M.B., Panek, A.D., Eleutherio, E.C.A.·2007·Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology

DOI 10.1016/j.cbpa.2006.02.030

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Abstract

Water is usually thought to be required for the living state, but several organisms are capable of surviving complete dehydration (anhydrobiotes). Elucidation of the mechanisms of tolerance against dehydration may lead to development of new methods for preserving biological materials that do not normally support drying, which is of enormous practical importance in industry, in clinical medicine as well as in agriculture. One of the molecular mechanisms of damage leading to death in desiccation-sensitive cells upon drying is free-radical attack to phospholipids, DNA and proteins. This review aims to summarize the strategies used by anhydrobiotes to cope with the danger of oxygen toxicity and to present our recent results about the importance of some antioxidant defense systems in the dehydration tolerance of Saccharomyces cerevisiae, a usual model in the study of stress response.

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As desiccation induces oxidative stress, expanded SODs could contribute to better tolerance against desiccation.
“As desiccation induces oxidative stress, expanded SODs could contribute to better tolerance against desiccation18.”
From Extremotolerant tardigrade genome and improved radiotolerance of human cultured cells by tardigrade-unique protein (2016) · cites this paper as [18]
Desiccation causes severe oxidative stress.
“As desiccation causes severe oxidative stress18, desiccation-tolerant animals should have the ability to mitigate this type of stress.”
From Extremotolerant tardigrade genome and improved radiotolerance of human cultured cells by tardigrade-unique protein (2016) · cites this paper as [18]

Oxidants, oxidative stress and the biology of ageing
Finkel, T., & Holbrook, N. J. (2000) · Nature · doi:10.1038/35041687 · Cited by 9,413 · see citing works
ASCORBATE AND GLUTATHIONE: Keeping Active Oxygen Under Control
Noctor, G., & Foyer, C. H. (1998) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.49.1.249 · Cited by 5,722 · see citing works
THE WATER-WATER CYCLE IN CHLOROPLASTS: Scavenging of Active Oxygens and Dissipation of Excess Photons
Asada, K. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.601 · Cited by 4,038 · see citing works
Living with Water Stress: Evolution of Osmolyte Systems
Yancey, P. H., Clark, M. E., Hand, S. C., Bowlus, R. D., & Somero, G. N. (1982) · Science · doi:10.1126/science.7112124 · Cited by 3,724 · see citing works
The mitochondrial generation of hydrogen peroxide. General properties and effect of hyperbaric oxygen
Boveris, A., & Chance, B. (1973) · Biochemical Journal · doi:10.1042/bj1340707 · Cited by 2,626 · see citing works
Protein carbonyl groups as biomarkers of oxidative stress
Dalle‐Donne, I., Rossi, R., Giustarini, D., Milzani, A., & Colombo, R. (2003) · Clinica Chimica Acta · doi:10.1016/s0009-8981(03)00003-2 · Cited by 2,353 · see citing works
THE MOLECULAR BASIS OF DEHYDRATION TOLERANCE IN PLANTS
Ingram, J., & Bartels, D. (1996) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.47.1.377 · Cited by 2,204 · see citing works
The role of active oxygen in the response of plants to water deficit and desiccation
Smirnoff, N. (1993) · New Phytologist · doi:10.1111/j.1469-8137.1993.tb03863.x · Cited by 2,006 · see citing works
Adaptations to Environmental Stresses.
Bohnert, H. J., Nelson, D. E., & Jensen, R. G. (1995) · The Plant Cell · doi:10.1105/tpc.7.7.1099 · Cited by 1,609 · see citing works
Mechanisms of plant desiccation tolerance
Hoekstra, F. A., Golovina, E. A., & Buitink, J. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(01)02052-0 · Cited by 1,455 · see citing works
Anhydrobiosis
Crowe, J. H., Hoekstra, F. A., & Crowe, L. M. (1992) · Annual Review of Physiology · doi:10.1146/annurev.ph.54.030192.003051 · Cited by 1,257 · see citing works
Seed Development and Germination
(2017) · Routledge eBooks · doi:10.1201/9780203740071 · Cited by 1,223 · see citing works
Antioxidants and Prevention of Chronic Disease
Willcox, J. K., Ash, S. L., & Catignani, G. L. (2004) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408690490468489 · Cited by 1,183 · see citing works
Desiccation tolerance of prokaryotes
Potts, M. (1994) · Microbiological Reviews · doi:10.1128/mr.58.4.755-805.1994 · Cited by 1,124 · see citing works
Water stress-induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up-regulates the activities of antioxidant enzymes in maize leaves
Jiang, M. (2002) · Journal of Experimental Botany · doi:10.1093/jxb/erf090 · Cited by 898 · see citing works
Dehydration-induced conformational transitions in proteins and their inhibition by stabilizers
Prestrelski, S. J., Tedeschi, N. I., Arakawa, T., & Carpenter, J. F. (1993) · Biophysical Journal · doi:10.1016/s0006-3495(93)81120-2 · Cited by 717 · see citing works
Trehalose Accumulation during Cellular Stress Protects Cells and Cellular Proteins from Damage by Oxygen Radicals
Benaroudj, N., Lee, D. H., & Goldberg, A. L. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m101487200 · Cited by 669 · see citing works
Interactions of sugars with membranes
Crowe, J. H., Crowe, L. M., Carpenter, J. F., Rudolph, A. S., Wistrom, C. A., Spargo, B. J., & Anchordoguy, T. J. (1988) · Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes · doi:10.1016/0304-4157(88)90015-9 · Cited by 624 · see citing works
Trehalose: a review of properties, history of use and human tolerance, and results of multiple safety studies
Richards, A. B., Krakowka, S. G., DEXTER, L. B., Schmid, H., Wolterbeek, A. P. M., Waalkens‐Berendsen, D. H., Shigoyuki, A., & Kurimoto, M. (2002) · Food and Chemical Toxicology · doi:10.1016/s0278-6915(02)00011-x · Cited by 596 · see citing works
Animal response to drastic changes in oxygen availability and physiological oxidative stress
Hermes‐Lima, M., & Zenteno‐Savín, T. (2002) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/s1532-0456(02)00080-7 · Cited by 591 · see citing works
Hydrogen Bonding between Sugar and Protein Is Responsible for Inhibition of Dehydration-Induced Protein Unfolding
Allison, S. D., Chang, B. S., Randolph, T. W., & Carpenter, J. F. (1999) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1999.1175 · Cited by 544 · see citing works
Membranes, metabolism, and dry organisms
Leopold, A. C. (1986) · Cited by 529 · see citing works
Intracellular trehalose improves the survival of cryopreserved mammalian cells
Eroğlu, A., Russo, M. J., Bieganski, R. M., Fowler, A., Cheley, S., Bayley, H., & Toner, M. (2000) · Nature Biotechnology · doi:10.1038/72608 · Cited by 521 · see citing works
The evolution of vegetative desiccation tolerance in land plants
Oliver, M. J., Tuba, Z., & Mishler, B. D. (2000) · Plant Ecology · doi:10.1023/a:1026550808557 · Cited by 515 · see citing works
On the role of Hsp27 in regulating apoptosis
Concannon, C. G., Gorman, A. M., & Samali, A. (2003) · Apoptosis · doi:10.1023/a:1021601103096 · Cited by 513 · see citing works
Tomato Plants Ectopically Expressing Arabidopsis CBF1 Show Enhanced Resistance to Water Deficit Stress
Hsieh, T.-H., Lee, J.-T., Charng, Y., & Chan, M. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.006783 · Cited by 442 · see citing works
Cryptobiosis — a peculiar state of biological organization
Clegg, J. S. (2001) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/s1096-4959(01)00300-1 · Cited by 438 · see citing works
Stress management – heat shock protein-70 and the regulation of apoptosis
Beere, H. M. (2001) · Trends in Cell Biology · doi:10.1016/s0962-8924(00)01874-2 · Cited by 435 · see citing works
Oxidative damage, lipid peroxidation and antioxidant protection in chloroplasts
Halliwell, B. B. (1987) · Chemistry and Physics of Lipids · doi:10.1016/0009-3084(87)90056-9 · Cited by 422 · see citing works
NUCLEAR AND MITOCHONDRIAL COMPARTMENTATION OF OXIDATIVE STRESS AND REDOX SIGNALING
Hansen, J. M., Go, Y., & Jones, D. P. (2005) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.46.120604.141122 · Cited by 401 · see citing works
Seed development and germination
Welbaum, G. (1997) · Field Crops Research · doi:10.1016/s0378-4290(97)00051-8 · Cited by 359 · see citing works
Glass formation in plant anhydrobiotes: survival in the dry state
Buitink, J., & Leprince, O. (2004) · Cryobiology · doi:10.1016/j.cryobiol.2004.02.011 · Cited by 356 · see citing works
Human Platelets Loaded with Trehalose Survive Freeze-Drying
Wolkers, W. F., Walker, N. J., Tablin, F., & Crowe, J. H. (2001) · Cryobiology · doi:10.1006/cryo.2001.2306 · Cited by 332 · see citing works
Effect of glass transition on rates of nonenzymic browning in food systems
Karmas, R., Buera, M. D. P., & Karel, M. (1992) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf00017a035 · Cited by 301 · see citing works
Desiccation Tolerance in the Resurrection PlantCraterostigma plantagineum. A Contribution to the Study of Drought Tolerance at the Molecular Level
Bartels, D., & Salamini, F. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.010765 · Cited by 301 · see citing works
Dry Biological Systems
(1978) · Elsevier eBooks · doi:10.1016/b978-0-12-198080-1.x5001-7 · Cited by 299 · see citing works
Dehydration in dormant insects
Danks, H. V. (2000) · Journal of Insect Physiology · doi:10.1016/s0022-1910(99)00204-8 · Cited by 294 · see citing works
Desiccation and Survival in Plants. Drying Without Dying
Scott, P. (2002) · South African Journal of Botany · doi:10.1016/s0254-6299(15)30385-9 · Cited by 290 · see citing works
The mechanisms of desiccation tolerance in developing seeds
Leprince, O., Hendry, G. A. F., & McKersie, B. D. (1993) · Seed Science Research · doi:10.1017/s0960258500001859 · Cited by 289 · see citing works
Revival of a resurrection plant correlates with its antioxidant status
Kranner, I., BECKETT, R. P., Wornik, S., Zorn, M., & Pfeifhofer, H. W. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01329.x · Cited by 285 · see citing works
Protection mechanisms against excess light in the resurrection plants Craterostigma wilmsii and Xerophyta viscosa
Sherwin, H. W., & Farrant, J. M. (1998) · Plant Growth Regulation · doi:10.1023/a:1005801610891 · Cited by 283 · see citing works
Antioxidants and photoprotection in a lichen as compared with its isolated symbiotic partners
Kranner, I., Cram, W. J., Zorn, M., Wornik, S., Yoshimura, I., Stabentheiner, E., & Pfeifhofer, H. W. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407716102 · Cited by 273 · see citing works
Proteome Analysis of Grain Filling and Seed Maturation in Barley
Finnie, C., Melchior, S., Roepstorff, P., & Svensson, B. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.003681 · Cited by 261 · see citing works
Preservation mechanisms of trehalose in food and biosystems
Patist, A., & Zoerb, H. F. (2004) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2004.05.003 · Cited by 245 · see citing works
Desiccation and survival in plants: drying without dying
(2002) · CABI Publishing eBooks · doi:10.1079/9780851995342.0000 · Cited by 235 · see citing works
Iron‐catalysed oxygen radical formation and its possible contribution to drought damage in nine native grasses and three cereals
Price, A. H., & Hendry, G. A. F. (1991) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1991.tb01517.x · Cited by 234 · see citing works
Winter Survival of Transgenic Alfalfa Overexpressing Superoxide Dismutase1
McKersie, B. D., Bowley, S. R., & Jones, K. S. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.119.3.839 · Cited by 223 · see citing works
Plant Responses to Environmental Stresses
Lerner (2018) · Routledge eBooks · doi:10.1201/9780203743157 · Cited by 219 · see citing works
The origin of threhalose and its significance during the formation of encysted dormant embryos of Artmia salina
Clegg, J. S. (1965) · Comparative Biochemistry and Physiology · doi:10.1016/0010-406x(65)90014-9 · Cited by 219 · see citing works
Cytoplasmic Vitrification and Survival of Anhydrobiotic Organisms
Sun, W. Q., & Leopold, A. C. (1997) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/s0300-9629(96)00271-x · Cited by 207 · see citing works
Ion Binding Properties of the Dehydrin ERD14 Are Dependent upon Phosphorylation
Alsheikh, M. K., Heyen, B. J., & Randall, S. K. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m307151200 · Cited by 207 · see citing works
Changes in oligosaccharide content and antioxidant enzyme activities in developing bean seeds as related to acquisition of drying tolerance and seed quality
Bailly, C., Audigier, C., Ladonne, F., Wagner, M.-H., Coste, F., Corbineau, F., & Côme, D. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.357.701 · Cited by 207 · see citing works
Anhydrobiosis: An Unsolved Problem
Crowe, J. H. (1971) · The American Naturalist · doi:10.1086/282745 · Cited by 194 · see citing works
Redox regulation and storage processes during maturation in kernels of Triticum durum
Gara, L. D., de Pinto, M. C., Moliterni, V. M. C., & D’Egidio, M. G. (2003) · Journal of Experimental Botany · doi:10.1093/jxb/erg021 · Cited by 190 · see citing works
Oxidation of methyl linoleate encapsulated in amorphous lactose-based food model
Shimada, Y., Roos, Y. H., & Karel, M. (1991) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf00004a001 · Cited by 189 · see citing works
The essential mechanisms of aging: Irreparable damage accumulation of biochemical side-reactions
Yin, D., & Chen, K. (2005) · Experimental Gerontology · doi:10.1016/j.exger.2005.03.012 · Cited by 186 · see citing works
A Food Polymer Science Approach to Structure-Property Relationships in Aqueous Food Systems: Non-Equilibrium Behavior of Carbohydrate-Water Systems
Slade, L., & Levine, H. (1991) · Advances in experimental medicine and biology · doi:10.1007/978-1-4899-0664-9_3 · Cited by 185 · see citing works
Anhydrobiosis without trehalose in bdelloid rotifers
Lapinski, J., & Tunnacliffe, A. (2003) · FEBS Letters · doi:10.1016/s0014-5793(03)01062-7 · Cited by 174 · see citing works
The rehydration transcriptome of the desiccation-tolerant bryophyte Tortula ruralis: transcript classification and analysis
Oliver, M. J., Dowd, S. E., Zaragoza, J. G., Mauget, S. A., & Payton, P. (2004) · BMC Genomics · doi:10.1186/1471-2164-5-89 · Cited by 171 · see citing works
Trehalose protects Saccharomyces cerevisiae from lipid peroxidation during oxidative stress
Herdeiro, R. S., Pereira, M. D., Panek, A. D., & Eleuthério, E. C. A. (2006) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2006.01.010 · Cited by 168 · see citing works
Self-citation
Cryptobiosis 300 Years on from van Leuwenhoek: What Have We Learned about Tardigrades?
Wright, J. C. (2001) · Zoologischer Anzeiger · doi:10.1078/0044-5231-00068 · Cited by 165 · see citing works
Active Fe-Containing Superoxide Dismutase and Abundant sodF mRNA in Nostoc commune (Cyanobacteria) after Years of Desiccation
Shirkey, B., Kovarcik, D. P., Wright, D. J., Wilmoth, G., Prickett, T., Helm, R. F., Gregory, E. M., & Potts, M. (2000) · Journal of Bacteriology · doi:10.1128/jb.182.1.189-197.2000 · Cited by 159 · see citing works
Plants Under Drought-Stress Generate Activated Oxygen
Price, A. H., Atherton, N. M., & Hendry, G. A. F. (1989) · Free Radical Research Communications · doi:10.3109/10715768909087973 · Cited by 153 · see citing works
High Critical Temperature above Tg May Contribute to the Stability of Biological Systems
Buitink, J., van den Dries, I. J., Hoekstra, F. A., Alberda, M., & Hemminga, M. A. (2000) · Biophysical Journal · doi:10.1016/s0006-3495(00)76365-x · Cited by 151 · see citing works
The Maillard reaction and oxidative stress during aging of soybean seeds
Sun, W. Q., & Leopold, A. C. (1995) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1995.tb00789.x · Cited by 147 · see citing works
Catalase activity and expression in developing sunflower seeds as related to drying
Bailly, C., Leymarie, J., Lehner, A., Rousseau, S., Côme, D., & Corbineau, F. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh050 · Cited by 145 · see citing works
Role of the trehalose carrier in dehydration resistance of Saccharomyces cerevisiae
Eleuthério, E. C. A., Araujo, P. S. D., & Panek, A. D. (1993) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/0304-4165(93)90040-f · Cited by 143 · see citing works
Self-citation
NMR and Quantum Chemical Study on the OH···π and CH···O Interactions between Trehalose and Unsaturated Fatty Acids: Implication for the Mechanism of Antioxidant Function of Trehalose
Oku, K., Watanabe, H., Kubota, M., Fukuda, S., Kurimoto, M., Tsujisaka, Y., Komori, M., Inoue, Y., & Sakurai, M. (2003) · Journal of the American Chemical Society · doi:10.1021/ja034777e · Cited by 141 · see citing works
Stress tolerance and reactive oxygen metabolism in the intertidal red seaweeds Mastocarpus stellatus and Chondrus crispus
Collén, J., & Davison, I. R. (1999) · Plant Cell & Environment · doi:10.1046/j.1365-3040.1999.00477.x · Cited by 140 · see citing works
Dehydration-Specific Induction of Hydrophilic Protein Genes in the Anhydrobiotic Nematode Aphelenchus avenae
Browne, J. A., Dolan, K. M., Tyson, T., Goyal, K., Tunnacliffe, A., & Burnell, A. M. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.4.966-975.2004 · Cited by 140 · see citing works
Metabolic Dysfunction and Unabated Respiration Precede the Loss of Membrane Integrity during Dehydration of Germinating Radicles
Leprince, O., Harren, F. J. M., Buitink, J., Alberda, M., & Hoekstra, F. A. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.122.2.597 · Cited by 139 · see citing works
Antioxidant metabolism in the intertidal red seaweed Stictosiphonia arbuscula following desiccation
Burritt, D. J., Larkindale, J., & Hurd, C. L. (2002) · Planta · doi:10.1007/s00425-002-0805-6 · Cited by 137 · see citing works
Contents of sugars in leaves of drying desiccation tolerant flowering plants, particularly grasses
Ghasempour, H., Gaff, D. F., Williams, R. P. W., & Gianello, R. (1998) · Plant Growth Regulation · doi:10.1023/a:1005927629018 · Cited by 123 · see citing works
Comparison of free sugars in growing and desiccated plants of Selaginella lepidophylla
Adams, R. P., Kendall, E. J., & Kartha, K. K. (1990) · Biochemical Systematics and Ecology · doi:10.1016/0305-1978(90)90044-g · Cited by 122 · see citing works
Acquisition of tolerance against oxidative damage in Saccharomyces cerevisiae
Pereira, M. D., Eleuthério, E. C. A., & Panek, A. D. (2001) · BMC Microbiology · doi:10.1186/1471-2180-1-11 · Cited by 122 · see citing works
Self-citation
The predominant polyphenol in the leaves of the resurrection plantMyrothamnus flabellifolius, 3,4,5 tri-O-galloylquinic acid, protects membranes against desiccation and free radical-induced oxidation
Moore, J. P., WESTALL, K. L., Ravenscroft, N., Farrant, J. M., Lindsey, G. G., & BRANDT, W. F. (2004) · Biochemical Journal · doi:10.1042/bj20040499 · Cited by 119 · see citing works
p23, a simple protein with complex activities
Felts, S. J., & Toft, D. O. (2003) · Cell Stress and Chaperones · doi:10.1379/1466-1268(2003)008 · Cited by 116 · see citing works
Self-citation
A small stress protein acts synergistically with trehalose to confer desiccation tolerance on mammalian cells
Ma, X., Jamil, K., MacRae, T. H., Clegg, J. S., Russell, J. M., Villeneuve, T. S., Euloth, M., Sun, Y., Crowe, J. H., Tablin, F., et al. (2005) · Cryobiology · doi:10.1016/j.cryobiol.2005.04.007 · Cited by 116 · see citing works
Changes in DNA and microtubules during loss and re-establishment of desiccation tolerance in germinating Medicago truncatula seeds
Faria, J. M. R., Buitink, J., van Lammeren, A. A. M., & Hilhorst, H. W. M. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/eri210 · Cited by 115 · see citing works
Desiccation-Tolerance
Bewley, J. D., & Krochko, J. E. (1982) · Springer eBooks · doi:10.1007/978-3-642-68150-9_11 · Cited by 115 · see citing works
Genomic DNA of Nostoc commune (Cyanobacteria) becomes covalently modified during long-term (decades) desiccation but is protected from oxidative damage and degradation
Shirkey, B. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg404 · Cited by 114 · see citing works
Purification, Structure and In vitro Molecular‐Chaperone Activity of Artemia P26, a Small Heat‐Shockh/α‐Crystallin Protein
Liang, P., Amons, R., MacRae, T. H., & Clegg, J. S. (1997) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1997.0225a.x · Cited by 114 · see citing works
Protective Role of Trehalose during Heat Stress in Saccharomyces cerevisiae
Eleuthério, E. C. A., Araujo, P. S. D., & Panek, A. D. (1993) · Cryobiology · doi:10.1006/cryo.1993.1061 · Cited by 114 · see citing works
Self-citation
The Involvement of Respiration in Free Radical Processes during Loss of Desiccation Tolerance in Germinating Zea mays L. (An Electron Paramagnetic Resonance Study)
Leprince, O., Atherton, N. M., DELTOUR, R., & Hendry, G. A. F. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.4.1333 · Cited by 113 · see citing works
Superoxide production by thylakoids during chilling and its implication in the susceptibility of plants to chilling-induced photoinhibition
Hodgson, R. A. J., & Raison, J. (1991) · Planta · doi:10.1007/bf00197792 · Cited by 113 · see citing works
The role of glutathione transferases in cadmium stress
Adamis, P. D. B., Gomes, D. S., Pinto, M. L. C. C., Panek, A. D., & Eleuthério, E. C. A. (2004) · Toxicology Letters · doi:10.1016/j.toxlet.2004.07.003 · Cited by 110 · see citing works
Self-citation
Non-Disaccharide-Based Mechanisms of Protection during Drying
Oliver, A. E., Leprince, O., Wolkers, W. F., Hincha, D. K., Heyer, A. G., & Crowe, J. H. (2001) · Cryobiology · doi:10.1006/cryo.2001.2359 · Cited by 108 · see citing works
Characterization of two cDNAs (ERD11 and ERD13) for dehydration‐inducible genes that encode putative glutathione S‐transferases in Arabidopsis thaliana L
Kiyosue, T., Yamaguchi‐Shinozaki, K., & Shinozaki, K. (1993) · FEBS Letters · doi:10.1016/0014-5793(93)80727-c · Cited by 107 · see citing works
Trehalose as cryoprotectant for preservation of yeast strains
Coutinho, C. C., Bernardes, E., Félix, D. B., & Panek, A. D. (1988) · Journal of Biotechnology · doi:10.1016/0168-1656(88)90032-6 · Cited by 96 · see citing works
Self-citation
Molecular Characterization of a Small Heat Shock/α-Crystallin Protein in Encysted Artemia Embryos
Liang, P., Amons, R., Clegg, J. S., & MacRae, T. H. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.30.19051 · Cited by 96 · see citing works
Desiccation and Free Radical Mediated Changes in Plant Membranes
Senaratna, T., McKersie, B. D., & Borochov, A. (1987) · Journal of Experimental Botany · doi:10.1093/jxb/38.12.2005 · Cited by 96 · see citing works
Biochemical and physiological aspects of anhydrobiosis
Womersley, C. (1981) · Comparative Biochemistry and Physiology Part B Comparative Biochemistry · doi:10.1016/0305-0491(81)90001-8 · Cited by 91 · see citing works
Modulation of oxidative mutagenesis and carcinogenesis by polymorphic forms of human DNA repair enzymes
Nohmi, T., Kim, S.-R., & Yamada, M. (2005) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.03.033 · Cited by 89 · see citing works
Loss of chlorophylls, cessation of photosynthetic CO2 assimilation and respiration in the poikilochlorophyllous plant Xerophyta scabrida during desiccation
Tuba, Z., Lichtenthaler, H. K., Csintalan, Z., Nagy, Z., & Szente, K. (1996) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1996.tb00448.x · Cited by 88 · see citing works
Do phospholipids and sucrose determine membrane phase transitions in dehydrating pollen species?
Hoekstra, F. A., Crowe, J. H., Crowe, L. M., van Roekel, T., & Vermeer, E. (1992) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1992.tb01494.x · Cited by 87 · see citing works
New insights into the anhydrobiotic phenomenon: The effects of trehalose content and differential rates of evaporative water loss on the survival of Aphelenchus avenae
Higa, L. M., & Womersley, C. (1993) · Journal of Experimental Zoology · doi:10.1002/jez.1402670205 · Cited by 77 · see citing works
Role of antioxidant defenses in the tolerance of severe dehydration by anurans. The case of the leopard frog Rana pipiens
Hermes‐Lima, M., & Storey, K. B. (1998) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006868208476 · Cited by 77 · see citing works
Significance of Thiol‐Disulfide Exchange in Resting Stages of Plant Development
Kranner, I., & Grill, D. (1996) · Botanica Acta · doi:10.1111/j.1438-8677.1996.tb00864.x · Cited by 74 · see citing works
Exploring the active site of plant glutaredoxin by site‐directed mutagenesis
Rouhier, N., Gelhaye, É., & Jacquot, J. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)03302-6 · Cited by 73 · see citing works
The role of cytoplasmic catalase in dehydration tolerance of Saccharomyces cerevisiae
França, M. B., Panek, A. D., & Eleuthério, E. C. A. (2005) · Cell Stress and Chaperones · doi:10.1379/csc-103r.1 · Cited by 71 · see citing works
Self-citation
The density profile and cholesterol concentration of serum lipoproteins in domestic and laboratory animals
Terpstra, A. H. M., Sánchez-Muniz, F. J., West, C. E., & Woodward, C. J. H. (1982) · Comparative Biochemistry and Physiology Part B Comparative Biochemistry · doi:10.1016/0305-0491(82)90479-5 · Cited by 69 · see citing works
Targets of oxidative stress in yeast sod mutants
Pereira, M. D., Herdeiro, R. S., Fernandes, P. N., Eleuthério, E. C. A., & Panek, A. D. (2003) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/s0304-4165(03)00003-5 · Cited by 68 · see citing works
Self-citation
The requirement for DNA repair in desiccation tolerance of germinating embryos
Boubriak, I., Kargiolaki, H., Lyne, L., & Osborne, D. J. (1997) · Seed Science Research · doi:10.1017/s0960258500003433 · Cited by 68 · see citing works
The role of glutathione in yeast dehydration tolerance
Santos, A. D. S. E., Gomes, D. S., Panek, A. D., & Eleuthério, E. C. A. (2003) · Cryobiology · doi:10.1016/j.cryobiol.2003.10.003 · Cited by 62 · see citing works
Self-citation
Effects of free fatty acids and transition temperature on the stability of dry liposomes
Crowe, J. H., McKersie, B. D., & Crowe, L. M. (1989) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(89)90516-6 · Cited by 59 · see citing works
Differential regulation of glutaredoxin gene expression in response to stress conditions in the yeast Saccharomyces cerevisiae
Grant, C. M., Luikenhuis, S., Beckhouse, A. G., Soderbergh, M., & Dawes, I. W. (2000) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/s0167-4781(99)00234-1 · Cited by 57 · see citing works
Improved preservation of human red blood cells by lyophilization
Han, Y., Quan, G. B., Liu, X. Z., Pu, E., Liu, A., Jin, P. F., & Cao, W. (2005) · Cryobiology · doi:10.1016/j.cryobiol.2005.06.002 · Cited by 50 · see citing works
The evolution and biological significance of seeds
Steeves, T. A. (1983) · Canadian Journal of Botany · doi:10.1139/b83-404 · Cited by 45 · see citing works
Low molecular weight solutes in desiccated and ABA-treated calli and leaves of Craterostigma plantagineum
Bianchi, G., Gamba, A., Murelli, C., Salamini, F., & Bartels, D. (1992) · Phytochemistry · doi:10.1016/0031-9422(92)80334-b · Cited by 43 · see citing works
Desiccation and protein synthesis in the moss Tortilla ruralis
Bewley, J. D. (1973) · Canadian Journal of Botany · doi:10.1139/b73-027 · Cited by 41 · see citing works
A small heat‐shock protein, p26, from the crustacean Artemia protects mammalian cells (Cos‐1) against oxidative damage
Collins, C. H., & Clegg, J. S. (2004) · Cell Biology International · doi:10.1016/j.cellbi.2004.03.014 · Cited by 40 · see citing works
Heat Shock Provides Delayed Protection against Oxidative Injury in Cultured Human Umbilical Vein Endothelial Cells
Gill, R. R., Gbur, C. J., Fisher, B. J., Hess, M. L., Fowler, A. A., Kukreja, R. C., & Sholley, M. M. (1998) · Journal of Molecular and Cellular Cardiology · doi:10.1006/jmcc.1998.0837 · Cited by 37 · see citing works
Cold-Hardiness-Specific Glutathione Reductase Isozymes in Red Spruce (Thermal Dependence of Kinetic Parameters and Possible Regulatory Mechanisms)
Hausladen, A., & Alscher, R. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.1.215 · Cited by 36 · see citing works
Rehydration of dried systems: membranes and the nuclear genome.
Osborne, D. J., Boubriak, I., & Leprince, O. (2002) · CABI Publishing eBooks · doi:10.1079/9780851995342.0343 · Cited by 30 · see citing works
Membrane malfunctions in freeze-dried Escherichia coli
Israeli, E., Giberman, E., & Kohn, A. (1974) · Cryobiology · doi:10.1016/0011-2240(74)90115-1 · Cited by 30 · see citing works
Metabolic Heat Dissipation and Internal Solute Levels of Artemia Embryos During Changes in Cell-Associated Water
Glasheen, J. S., & Hand, S. C. (1989) · Journal of Experimental Biology · doi:10.1242/jeb.145.1.263 · Cited by 29 · see citing works
EFFECTS OF OXYGEN ON DRIED ORGANISMS
Heckly, R. J. (1978) · Elsevier eBooks · doi:10.1016/b978-0-12-198080-1.50017-x · Cited by 26 · see citing works
Effects of protein perturbants on phospholipid bilayers
Anchordoquy, T. J., Carpenter, J. F., Cecchini, C. A., Crowe, J. H., & Crowe, L. M. (1990) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(90)90654-h · Cited by 21 · see citing works
Induction of desiccation tolerance by osmotic treatment in Saccharomyces uvarum var. carlsbergensis
Eleuthério, E. C. A., Maia, F. M., Pereira, M. D., Panek, A. D., Degré, R., & Cameron, D. (1997) · Canadian Journal of Microbiology · doi:10.1139/m97-070 · Cited by 20 · see citing works
Self-citation
Encyclopedia of Plant Physiology. Vol 12b. Physiological Plant Ecology II.
Grace, J., Lange, O. L., Nobel, P. S., Osmond, C. B., & Zeigler, H. (1984) · Journal of Applied Ecology · doi:10.2307/2403069 · Cited by 19 · see citing works
Exaggeration of desiccation stress by heavy metal pollution in Tortula ruralis: a pilot study
Takács, Z., Tuba, Z., & Smirnoff, N. (2001) · Plant Growth Regulation · doi:10.1023/a:1014481704892 · Cited by 14 · see citing works
Phospholipid polar heads affect the generation of oxygen active species by Fe2+ autoxidation.
Tadolini, B., Motta, P., & Sechi, A. M. (1992) · PubMed · Cited by 8 · see citing works
Studies on the role of antioxidants in the cryptobiotic cysts of the brine shrimp, Artemia parthenogenetica
Ganapathy‐Kanniappan, S., Rani, K. V., & Munuswamy, N. (1996) · Biomedical letters · Cited by 4 · see citing works
Biochemistry, cell biology and molecular biology of lipids ofSaccharomyces cerevisiae
Daum, G., Lees, N. D., Bard, M., & Dickson, R. (1998) · Yeast · doi:10.1002/(sici)1097-0061(199812)14:16

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Oxidative Stress Resistance in<i>Deinococcus radiodurans</i>
Slade, D., & Radman, M. (2011) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00015-10 · Cited by 761 · see citing works
Yeast responses to stresses associated with industrial brewery handling: Figure 1
Gibson, B. R., Lawrence, S. J., Leclaire, J. P. R., Powell, C. D., & Smart, K. A. (2007) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2007.00076.x · Cited by 490 · see citing works
Water loss in insects: An environmental change perspective
Chown, S. L., Sørensen, J. G., & Terblanche, J. S. (2011) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2011.05.004 · Cited by 418 · see citing works
Extremotolerant tardigrade genome and improved radiotolerance of human cultured cells by tardigrade-unique protein
Hashimoto, T., Horikawa, D. D., Saito, Y., Kuwahara, H., Kozuka-Hata, H., Shin-I, T., Minakuchi, Y., Ohishi, K., Motoyama, A., Aizu, T., et al. (2016) · Nature Communications · doi:10.1038/ncomms12808 · Cited by 394 · see citing works
Xerotolerant bacteria: surviving through a dry spell
Lebre, P. H., Maayer, P. D., & Cowan, D. A. (2017) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.16 · Cited by 292 · see citing works
Physiological and proteomic responses of cotton (Gossypium herbaceum L.) to drought stress
Deeba, F., Pandey, A. K., Ranjan, S., Mishra, A., Singh, R., Sharma, Y. K., Shirke, P. A., & Pandey, V. (2012) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2012.01.002 · Cited by 282 · see citing works
Resistance and survival strategies of Salmonella enterica to environmental stresses
Spector, M. P., & Kenyon, W. J. (2011) · Food Research International · doi:10.1016/j.foodres.2011.06.056 · Cited by 268 · see citing works
Dynamic cyanobacterial response to hydration and dehydration in a desert biological soil crust
Rajeev, L., da Rocha, U. N., Klitgord, N., Luning, E. G., Fortney, J. L., Axen, S. D., Shih, P. M., Bouskill, N., Bowen, B. P., Kerfeld, C. A., et al. (2013) · The ISME Journal · doi:10.1038/ismej.2013.83 · Cited by 267 · see citing works
Extreme resistance of bdelloid rotifers to ionizing radiation
Gladyshev, E. A., & Meselson, M. S. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800966105 · Cited by 258 · see citing works
A Sister Group Contrast Using Untargeted Global Metabolomic Analysis Delineates the Biochemical Regulation Underlying Desiccation Tolerance in Sporobolus stapfianus
Oliver, M. J., Guo, L., Alexander, D. C., Ryals, J. A., Wone, B. W. M., & Cushman, J. C. (2011) · The Plant Cell · doi:10.1105/tpc.110.082800 · Cited by 244 · see citing works
The role of declining adaptive homeostasis in ageing
Pomatto, L. C. D., & Davies, K. J. A. (2017) · The Journal of Physiology · doi:10.1113/jp275072 · Cited by 223 · see citing works
Biopreservation of red blood cells – the struggle with hemoglobin oxidation
Kanias, T., & Acker, J. P. (2009) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07472.x · Cited by 197 · see citing works
Transcriptional and Physiological Responses of Bradyrhizobium japonicum to Desiccation-Induced Stress
Cytryn, E. J., Sangurdekar, D. P., Streeter, J. G., Franck, W. L., Chang, W., Stacey, G. S., Emerich, D. W., Joshi, T., Xu, D. H., & Sadowsky, M. J. (2007) · Journal of Bacteriology · doi:10.1128/jb.00533-07 · Cited by 186 · see citing works
Desiccation: An environmental and food industry stress that bacteria commonly face
Esbelin, J., Santos, T., & Hébraud, M. (2017) · Food Microbiology · doi:10.1016/j.fm.2017.07.017 · Cited by 173 · see citing works
Evidence for extensive horizontal gene transfer from the draft genome of a tardigrade
Boothby, T. C., Tenlen, J. R., Smith, F. W., Wang, J. R., Patanella, K. A., Osborne Nishimura, E., Tintori, S. C., Li, Q., Jones, C. D., Yandell, M., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510461112 · Cited by 172 · see citing works
Late Embryogenesis Abundant Proteins
Shih, M., Hoekstra, F. A., & Hsing, Y.-I. C. (2008) · Advances in botanical research · doi:10.1016/s0065-2296(08)00404-7 · Cited by 172 · see citing works
Desiccation tolerance in Staphylococcus aureus
Chaibenjawong, P., & Foster, S. J. (2010) · Archives of Microbiology · doi:10.1007/s00203-010-0653-x · Cited by 168 · see citing works
Anhydrobiosis in tardigrades—The last decade
Wełnicz, W., Grohme, M. A., Kaczmarek, Ł., Schill, R. O., & Frohme, M. (2011) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2011.03.019 · Cited by 167 · see citing works
Heat shock proteins contribute to mosquito dehydration tolerance
Benoit, J. B., López‐Martínez, G., Phillips, Z. P., Patrick, K. R., & Denlinger, D. L. (2009) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2009.09.012 · Cited by 162 · see citing works
Dehydration-induced cross tolerance of Belgica antarctica larvae to cold and heat is facilitated by trehalose accumulation
Benoit, J. B., López‐Martínez, G., Elnitsky, M. A., Lee, R. E., Jr., & Denlinger, D. L. (2008) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2008.12.009 · Cited by 156 · see citing works
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Eleuthério, E. C. A., Panek, A. D., Mesquita, J. F. D., Trevisol, E. T. V., & Magalhães, R. S. S. (2014) · Current Genetics · doi:10.1007/s00294-014-0450-1 · Cited by 155 · see citing works
Self-citation
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Morris, J., Rose, A. L., & Lu, Z. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102285 · Cited by 147 · see citing works
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Ukibe, K., Hashida, K., Yoshida, N., & Takagi, H. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01249-09 · Cited by 143 · see citing works
The effects of natural variation in background radioactivity on humans, animals and other organisms
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Biomarkers of oxidative status: missing tools in conservation physiology
Beaulieu, M., & Costantini, D. (2014) · Conservation Physiology · doi:10.1093/conphys/cou014 · Cited by 142 · see citing works
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Fan, G., Wasuwanich, P., Rodriguez-Otero, M. R., & Furst, A. L. (2021) · Journal of the American Chemical Society · doi:10.1021/jacs.1c09018 · Cited by 141 · see citing works
Anhydrobiosis in bacteria: From physiology to applications
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Drying process strongly affects probiotics viability and functionalities
Iaconelli, C., Lemetais, G., Kechaou, N., Chain, F., Bermúdez‐Humarán, L. G., Langella, P., Gervais, P., & Beney, L. (2015) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2015.08.022 · Cited by 129 · see citing works
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Krisko, A., Leroy, M., Radman, M., & Meselson, M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119762109 · Cited by 121 · see citing works
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Short-term anoxic conditioning hormesis boosts antioxidant defenses, lowers oxidative damage following irradiation and enhances male sexual performance in the Caribbean fruit fly, Anastrepha suspensa
López‐Martínez, G., & Hahn, D. A. (2012) · Journal of Experimental Biology · doi:10.1242/jeb.065631 · Cited by 111 · see citing works
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Hibshman, J. D., Clegg, J. S., & Goldstein, B. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.592016 · Cited by 111 · see citing works
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Water Management by Dormant Insects: Comparisons Between Dehydration Resistance During Summer Aestivation and Winter Diapause
Benoit, J. B. (2009) · Progress in molecular and subcellular biology · doi:10.1007/978-3-642-02421-4_10 · Cited by 104 · see citing works
Cryopreservation affects ROS-induced oxidative stress and antioxidant response in Arabidopsis seedlings
Chen, G., Ren, L., Zhang, J., Reed, B. M., Zhang, D., & Shen, X. (2014) · Cryobiology · doi:10.1016/j.cryobiol.2014.11.004 · Cited by 103 · see citing works
Desiccation tolerance in Acinetobacter baumannii is mediated by the two-component response regulator BfmR
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Tardigrade Resistance to Space Effects: First Results of Experiments on the LIFE-TARSE Mission on FOTON-M3 (September 2007)
Rebecchi, L., Altiero, T., Guidetti, R., Cesari, M., Bertolani, R., Negroni, M., & Rizzo, A. M. (2009) · Astrobiology · doi:10.1089/ast.2008.0305 · Cited by 100 · see citing works
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Liu, C., Hong, J., Yang, H., Wu, J., Ma, D., Li, D., Lin, D., & Lai, R. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.01.036 · Cited by 97 · see citing works
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Antioxidant defences in hydrated and desiccated states of the tardigrade Paramacrobiotus richtersi
Rizzo, A. M., Negroni, M., Altiero, T., Montorfano, G., Corsetto, P. A., Berselli, P., Berra, B., Guidetti, R., & Rebecchi, L. (2010) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2010.02.009 · Cited by 93 · see citing works
Viability of microencapsulated Akkermansia muciniphila and Lactobacillus plantarum during freeze-drying, storage and in vitro simulated upper gastrointestinal tract passage
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Subcellular integrities in Chroococcidiopsis sp. CCMEE 029 survivors after prolonged desiccation revealed by molecular probes and genome stability assays
Billi, D. (2008) · Extremophiles · doi:10.1007/s00792-008-0196-0 · Cited by 91 · see citing works
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Gusev, O., Nakahara, Y., Vanyagina, V., Malutina, L., Cornette, R., Sakashita, T., Hamada, N., Kikawada, T., Kobayashi, Y., & Okuda, T. (2010) · PLoS ONE · doi:10.1371/journal.pone.0014008 · Cited by 87 · see citing works
Biomarkers and energy reserves in the isopod Porcellionides pruinosus: The effects of long-term exposure to dimethoate
Ferreira, N. G. C., Morgado, R. G., Santos, M. J. G., Soares, A. M. V. M., & Loureiro, S. (2014) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2014.08.062 · Cited by 87 · see citing works
Survival kit of Saccharomyces cerevisiae for anhydrobiosis
Dupont, S., Rapoport, A. I., Gervais, P., & Beney, L. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-6028-5 · Cited by 87 · see citing works
DNA damage in storage cells of anhydrobiotic tardigrades
Neumann, S., Reuner, A., Brümmer, F., & Schill, R. O. (2009) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2009.04.611 · Cited by 85 · see citing works
DNA Protection Protein, a Novel Mechanism of Radiation Tolerance: Lessons from Tardigrades
Hashimoto, T., & Kunieda, T. (2017) · Life · doi:10.3390/life7020026 · Cited by 84 · see citing works
Metabolic regulatory mechanisms and physiological roles of functional amino acids and their applications in yeast
Takagi, H. (2019) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2019.1576500 · Cited by 83 · see citing works
Biochar coupling with phosphorus fertilization modifies antioxidant activity, osmolyte accumulation and reactive oxygen species synthesis in the leaves and xylem sap of rice cultivars under high-temperature stress
Bamagoos, A. A., Alharby, H. F., & Fahad, S. (2021) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-021-01062-7 · Cited by 83 · see citing works
Identification of Anhydrobiosis-related Genes from an Expressed Sequence Tag Database in the Cryptobiotic Midge Polypedilum vanderplanki (Diptera; Chironomidae)
Cornette, R., Kanamori, Y., Watanabe, M., Nakahara, Y., Gusev, O., Mitsumasu, K., Kadono‐Okuda, K., Shimomura, M., Mita, K., Kikawada, T., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.150623 · Cited by 81 · see citing works
Antioxidant gene–enzyme responses in Medicago truncatula genotypes with different degree of sensitivity to salinity
Mhadhbi, H., Fotopoulos, V., Mylona, P. V., Jebara, M., Aouani, M. E., & Polidoros, A. N. (2010) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2010.01433.x · Cited by 78 · see citing works
Radiation Tolerance in Tardigrades: Current Knowledge and Potential Applications in Medicine
Jonsson, K. (2019) · Cancers · doi:10.3390/cancers11091333 · Cited by 77 · see citing works
Spray-drying microencapsulation of Trichoderma harzianum conidias in carbohydrate polymers matrices
Muñoz-Celaya, A. L., Ortiz-García, M., Vernon‐Carter, E. J., Jáuregui-Rincón, J., Galindo, E., & Serrano‐Carreón, L. (2011) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2011.12.030 · Cited by 77 · see citing works
Improving ambient temperature stability of probiotics with stress adaptation and fluidized bed drying
Nag, A., & Das, S. (2012) · Journal of Functional Foods · doi:10.1016/j.jff.2012.10.001 · Cited by 76 · see citing works
Optimizing oral delivery of next generation probiotics
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Between a Rock and a Dry Place: The Water-Stressed Moss
Charron, A. J., & Quatrano, R. S. (2009) · Molecular Plant · doi:10.1093/mp/ssp018 · Cited by 75 · see citing works
Survival and DNA degradation in anhydrobiotic tardigrades
Rebecchi, L., Cesari, M., Altiero, T., Frigieri, A., & Guidetti, R. (2009) · Journal of Experimental Biology · doi:10.1242/jeb.033266 · Cited by 75 · see citing works
How widespread is preparation for oxidative stress in the animal kingdom?
Moreira, D. C., Venâncio, L. P. R., Sabino, M. A. D. C. T., & Hermes‐Lima, M. (2016) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2016.01.023 · Cited by 74 · see citing works
Principles Underlying Cryopreservation and Freeze-Drying of Cells and Tissues
Wolkers, W. F., & Oldenhof, H. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0783-1_1 · Cited by 73 · see citing works
What can we learn from the toughest animals of the Earth? Water bears (tardigrades) as multicellular model organisms in order to perform scientific preparations for lunar exploration
Guidetti, R., Rizzo, A. M., Altiero, T., & Rebecchi, L. (2012) · Planetary and Space Science · doi:10.1016/j.pss.2012.05.021 · Cited by 73 · see citing works
Proteome analysis of leaves of the desiccation-tolerant grass, Sporobolus stapfianus, in response to dehydration
Oliver, M. J., Jain, R. S. K., Balbuena, T. S., Agrawal, G., Gasulla, F., & Thelen, J. J. (2010) · Phytochemistry · doi:10.1016/j.phytochem.2010.10.020 · Cited by 72 · see citing works
Intracellular Protective Functions and Therapeutical Potential of Trehalose
Kuczyńska‐Wiśnik, D., Stojowska‐Swędrzyńska, K., & Laskowska, E. (2024) · Molecules · doi:10.3390/molecules29092088 · Cited by 70 · see citing works
Ultraviolet radiation tolerance in hydrated and desiccated eutardigrades
Altiero, T., Guidetti, R., Caselli, V., Cesari, M., & Rebecchi, L. (2011) · Journal of Zoological Systematics & Evolutionary Research · doi:10.1111/j.1439-0469.2010.00607.x · Cited by 70 · see citing works
Desiccation and radiation stress tolerance in cyanobacteria
Singh, H. (2018) · Journal of Basic Microbiology · doi:10.1002/jobm.201800216 · Cited by 70 · see citing works
Genetic and Phenotypic Characteristics of Baker's Yeast: Relevance to Baking
Rández‐Gil, F., Córcoles-Sáez, I., & Prieto, J. A. (2013) · Annual Review of Food Science and Technology · doi:10.1146/annurev-food-030212-182609 · Cited by 69 · see citing works
The S-layer Protein DR_2577 Binds Deinoxanthin and under Desiccation Conditions Protects against UV-Radiation in Deinococcus radiodurans
Farci, D., Slavov, C., Tramontano, E., & Piano, D. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00155 · Cited by 69 · see citing works
The kinetics of ageing in dry-stored seeds: a comparison of viability loss and RNA degradation in unique legacy seed collections
Fleming, M. B., Hill, L. M., & Walters, C. (2018) · Annals of Botany · doi:10.1093/aob/mcy217 · Cited by 68 · see citing works
Repeated bouts of dehydration deplete nutrient reserves and reduce egg production in the mosquito Culex pipiens
Benoit, J. B., Patrick, K. R., Desai, K., Hardesty, J. J., Krause, T. B., & Denlinger, D. L. (2010) · Journal of Experimental Biology · doi:10.1242/jeb.044883 · Cited by 65 · see citing works
Gateway to genetic exchange? DNA double‐strand breaks in the bdelloid rotifer A dineta vaga submitted to desiccation
Hespeels, B., Knapen, M. F. C. M., Mambres, D. H., Heuskin, A., Pineux, F., Lucas, S., Koszul, R., & Doninck, K. V. (2014) · Journal of Evolutionary Biology · doi:10.1111/jeb.12326 · Cited by 65 · see citing works
Oxidative stress and antioxidant response in Hypericum perforatum L. plants subjected to low temperature treatment
Skyba, M., Petijová, L., Košuth, J., Koleva, D., Ganeva, T. G., Kapchina-Toteva, V. M., & Čellárová, E. (2012) · Journal of Plant Physiology · doi:10.1016/j.jplph.2012.02.017 · Cited by 65 · see citing works
Survival of Deinococcus geothermalis in Biofilms under Desiccation and Simulated Space and Martian Conditions
Frösler, J., Panitz, C., Wingender, J., Flemming, H., & Rettberg, P. (2017) · Astrobiology · doi:10.1089/ast.2015.1431 · Cited by 65 · see citing works
Reduction of oxidative cellular damage by overexpression of the thioredoxin TRX2 gene improves yield and quality of wine yeast dry active biomass
Gómez‐Pastor, R., Pérez‐Torrado, R., Cabiscol, E., Ros, J., & Matallana, E. (2010) · Microbial Cell Factories · doi:10.1186/1475-2859-9-9 · Cited by 61 · see citing works
Salmonella and Enterohemorrhagic Escherichia coli Serogroups O45, O121, O145 in Wheat Flour: Effects of Long-Term Storage and Thermal Treatments
Forghani, F., den Bakker, M., Liao, J., Payton, A. S., Futral, A. N., & Diez‐Gonzalez, F. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00323 · Cited by 61 · see citing works
Insects With Survival Kits for Desiccation Tolerance Under Extreme Water Deficits
Thorat, L., & Nath, B. B. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01843 · Cited by 60 · see citing works
A way to follow the viability of encapsulated Bifidobacterium bifidum subjected to a freeze-drying process in order to target the colon: Interest of flow cytometry
Martin-Dejardin, F., Ebel, B., Lemetais, G., Minh, H. N. T., Gervais, P., Cachon, R., & Chambin, O. (2013) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2013.02.015 · Cited by 58 · see citing works
Desiccation-induced cell damage in bacteria and the relevance for inoculant production
Greffe, V. R. G., & Michiels, J. J. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10501-6 · Cited by 57 · see citing works
Transcriptome survey of the anhydrobiotic tardigrade Milnesium tardigradum in comparison with Hypsibius dujardini and Richtersius coronifer
Mali, B., Grohme, M. A., Förster, F., Dandekar, T., Schnölzer, M., Reuter, D., Wełnicz, W., Schill, R. O., & Frohme, M. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-168 · Cited by 57 · see citing works
Heat and dehydration induced oxidative damage and antioxidant defenses following incubator heat stress and a simulated heat wave in wild caught four-striped field mice Rhabdomys dilectus
Jacobs, P. J., Oosthuizen, M. K., Mitchell, C., Blount, J. D., & Bennett, N. C. (2020) · PLoS ONE · doi:10.1371/journal.pone.0242279 · Cited by 56 · see citing works
A molecular analysis of desiccation tolerance mechanisms in the anhydrobiotic nematode Panagrolaimus superbus using expressed sequenced tags
Tyson, T., Zamora, G. O., Wong, S. C. K., Skelton, M., Daly, B., Jones, J. T., Mulvihill, E., Elsworth, B., Phillips, M., Blaxter, M., et al. (2012) · BMC Research Notes · doi:10.1186/1756-0500-5-68 · Cited by 55 · see citing works
Molecular mechanisms and highly functional development for stress tolerance of the yeastSaccharomyces cerevisiae
Takagi, H. (2021) · Bioscience Biotechnology and Biochemistry · doi:10.1093/bbb/zbab022 · Cited by 55 · see citing works
The effect of hydration state and energy balance on innate immunity of a desert reptile
Moeller, K. T., Butler, M. W., & DeNardo, D. F. (2013) · Frontiers in Zoology · doi:10.1186/1742-9994-10-23 · Cited by 54 · see citing works
An integrated diagnostic approach to understand drought tolerance in mulberry (Morus indica L.)
Guha, A., Sengupta, D., Rasineni, G. K., & Reddy, A. R. (2009) · Flora · doi:10.1016/j.flora.2009.01.004 · Cited by 54 · see citing works
Anhydrobiosis: Inside yeast cells
Rapoport, A. I., Golovina, E. A., Gervais, P., Dupont, S., & Beney, L. (2018) · Biotechnology Advances · doi:10.1016/j.biotechadv.2018.11.003 · Cited by 53 · see citing works
Microbial anhydrobiosis
Bosch, J., Varliero, G., Hallsworth, J. E., Dallas, T. D., HOPKINS, D. W., Frey, B., Kong, W., Lebre, P. H., Makhalanyane, T. P., & Cowan, D. A. (2021) · Environmental Microbiology · doi:10.1111/1462-2920.15699 · Cited by 53 · see citing works
When cells lose water: Lessons from biophysics and molecular biology
Caramelo, J. J., & Iusem, N. D. (2008) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2008.10.001 · Cited by 53 · see citing works
Selection and subsequent physiological characterization of industrial Saccharomyces cerevisiae strains during continuous growth at sub- and- supra optimal temperatures
Lip, K. Y. F., García‐Ríos, E., Costa, C. E., Guillamón, J. M., Domingues, L., Teixeira, J. A., & van Gulik, W. M. (2020) · Biotechnology Reports · doi:10.1016/j.btre.2020.e00462 · Cited by 52 · see citing works
Genes Associated with Desiccation and Osmotic Stress in Listeria monocytogenes as Revealed by Insertional Mutagenesis
Hingston, P. A., Piercey, M. J., & Hansen, L. T. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.01134-15 · Cited by 51 · see citing works
Enhancement of the proline and nitric oxide synthetic pathway improves fermentation ability under multiple baking-associated stress conditions in industrial baker's yeast
Sasano, Y., Haitani, Y., Hashida, K., Ohtsu, I., Shima, J., & Takagi, H. (2012) · Microbial Cell Factories · doi:10.1186/1475-2859-11-40 · Cited by 51 · see citing works
Stimulating Plant Tolerance Against Abiotic Stress Through Seed Priming
Dawood, M. G. (2018) · Springer eBooks · doi:10.1007/978-981-13-0032-5_10 · Cited by 51 · see citing works
Extreme-tolerance mechanisms in meiofaunal organisms: a case study with tardigrades, rotifers and nematodes
Rebecchi, L., Boschetti, C., & Nelson, D. R. (2019) · Hydrobiologia · doi:10.1007/s10750-019-04144-6 · Cited by 50 · see citing works
Mechanistic underpinnings of dehydration stress in the American dog tick revealed through RNA-Seq and metabolomics
Rosendale, A. J., Romick‐Rosendale, L. E., Watanabe, M., Dunlevy, M. E., & Benoit, J. B. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.137315 · Cited by 49 · see citing works
Antioxidants and oxidative stress in Helix pomatia snails during estivation
Nowakowska, A., Świderska-Kołacz, G., Rogalska, J., & Caputa, M. (2009) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2009.07.005 · Cited by 48 · see citing works
Integrated Proteomic and Cytological Study of Rice Endosperms at the Storage Phase
Xu, S. B., Yu, H. T., Yan, L. F., & Wang, T. (2010) · Journal of Proteome Research · doi:10.1021/pr900954p · Cited by 48 · see citing works
Role of Intrinsic Disorder in Animal Desiccation Tolerance
Janis, B. R., Belott, C. J., & Menze, M. A. (2018) · PROTEOMICS · doi:10.1002/pmic.201800067 · Cited by 48 · see citing works

Dry up and survive: the role of antioxidant defences in anhydrobiotic organisms
Rebecchi, L. (2013) · Journal of Limnology · doi:10.4081/jlimnol.2013.s1.e8 · Cited by 41 · see citing works
p23, a simple protein with complex activities
Felts, S. J., & Toft, D. O. (2003) · Cell Stress and Chaperones · doi:10.1379/1466-1268(2003)008 · Cited by 116 · see citing works
Self-citation
Non-Disaccharide-Based Mechanisms of Protection during Drying
Oliver, A. E., Leprince, O., Wolkers, W. F., Hincha, D. K., Heyer, A. G., & Crowe, J. H. (2001) · Cryobiology · doi:10.1006/cryo.2001.2359 · Cited by 108 · see citing works
Biochemistry and biophysics of tolerance systems.
Buitink, J., Hoekstra, F. A., & Leprince, O. (2002) · CABI Publishing eBooks · doi:10.1079/9780851995342.0293 · Cited by 84 · see citing works
How to Survive without Water: A Short Lesson on the Desiccation Tolerance of Budding Yeast
Robison, Z. L., Ren, Q., & Zhang, Z. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147514 · Cited by 9 · see citing works

Authors: França, M. B., Panek, A. D., & Eleutherio, E. C. A.
Affiliations: Universidade Federal do Rio de Janeiro (BR)
ORCID: França, M.B.
Venue: Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology
Publisher: Elsevier BV
Published: 2007-04
Volume: 146
Issue: 4
Pages: 621-631
ISSN: 1095-6433 (ISSN-L)
DOI: 10.1016/j.cbpa.2006.02.030
OpenAlex: W2051148648
Cited by: 422
References: 128
Citations by year: 2026: 16 · 2025: 18 · 2024: 21 · 2023: 20 · 2022: 23 · 2021: 29 · 2020: 30 · 2019: 28 · 2018: 29 · 2017: 23 · 2016: 23 · 2015: 20 · 2014: 19 · 2013: 20 · 2012: 22
FWCI: 1.27
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology (publishedVersion)
PubMed (publishedVersion)
Funders: Conselho Nacional de Desenvolvimento Científico e Tecnológico
Topics: Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Tardigrade Biology and Ecology
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Stress Responses and Tolerance
Keywords: oxidative stress, dehydration tolerance, anhydrobiosis, oxygen toxicity, antioxidant defense, oxidative damage, phospholipid oxidation, DNA damage, protein damage, Saccharomyces cerevisiae, desiccation, biological preservation
MeSH terms: Animals, Antioxidants, Catalase, Dehydration, DNA Damage, Glutathione, Proteins, Saccharomyces cerevisiae, Superoxide Dismutase, Trehalose, Lipid Peroxidation, Reactive Oxygen Species, Oxidative Stress, Lipid Metabolism

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Oxidative stress and its effects during dehydration

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