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

The DOI matches its Crossref record; 124 of the 128 references it cites were found in a registry or an index.

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

Open this paper in CoChat — free account

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.

Integrity signals

Registry

Crossref · 10.1016/j.cbpa.2006.02.030

Cites

124 of 124 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Oxidants, oxidative stress and the biology of ageing
Finkel, T., & Holbrook, N. J. (2000) · Nature · doi:10.1038/35041687 · Cited by 9,413
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
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
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
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
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 2,352
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
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
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
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 1,467

Flagged first, then by citations

Show all 128 references

4 of the 128 references couldn’t be matched to a known paper.

Research works printed but not linked: 1

Kranner, 1997, Desiccation and subsequent recovery of cryptogamics that are resistant to drought, Phyton, 37, 139

Sorted by citations

Oxidative Stress Resistance in Deinococcus radiodurans
Slade, D., & Radman, M. (2011) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00015-10 · Cited by 761
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
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 435
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
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
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
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 284
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
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
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
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 231
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
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
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
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
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 173
Desiccation tolerance in Staphylococcus aureus
Chaibenjawong, P., & Foster, S. J. (2010) · Archives of Microbiology · doi:10.1007/s00203-010-0653-x · Cited by 168
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 171
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
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
Revisiting yeast trehalose metabolism
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
Self-citation
Reactive oxygen species in the world ocean and their impacts on marine ecosystems
Morris, J., Rose, A. L., & Lu, Z. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102285 · Cited by 147
Emerging Technologies and Coating Materials for Improved Probiotication in Food Products: a Review
Misra, S., Pandey, P. O., Dalbhagat, C. G., & Mishra, H. N. (2022) · Food and Bioprocess Technology · doi:10.1007/s11947-021-02753-5 · Cited by 147
Metabolic Engineering of Saccharomyces cerevisiae for Astaxanthin Production and Oxidative Stress Tolerance
Ukibe, K., Hashida, K., Yoshida, N., & Takagi, H. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01249-09 · Cited by 143
The effects of natural variation in background radioactivity on humans, animals and other organisms
Møller, A. P., & Mousseau, T. A. (2012) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/j.1469-185x.2012.00249.x · Cited by 142
Biomarkers of oxidative status: missing tools in conservation physiology
Beaulieu, M., & Costantini, D. (2014) · Conservation Physiology · doi:10.1093/conphys/cou014 · Cited by 151
Protection of Anaerobic Microbes from Processing Stressors Using Metal–Phenolic Networks
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
Anhydrobiosis in bacteria: From physiology to applications
García, A. H. (2011) · Journal of Biosciences · doi:10.1007/s12038-011-9107-0 · Cited by 131
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
The induction of anhydrobiosis in the sleeping chironomid: Current status of our knowledge
Cornette, R., & Kikawada, T. (2011) · IUBMB Life · doi:10.1002/iub.463 · Cited by 125
Seeds and the Art of Genome Maintenance
Waterworth, W. M., Bray, C. M., & West, C. E. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00706 · Cited by 124
Extreme anti-oxidant protection against ionizing radiation in bdelloid rotifers
Krisko, A., Leroy, M., Radman, M., & Meselson, M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119762109 · Cited by 121
Molecular Strategies of the Caenorhabditis elegans Dauer Larva to Survive Extreme Desiccation
Erkut, C., Vasilj, A., Boland, S., Habermann, B. H., Shevchenko, A., & Kurzchalia, T. V. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082473 · Cited by 120
Dehydration, rehydration, and overhydration alter patterns of gene expression in the Antarctic midge, Belgica antarctica
López‐Martínez, G., Benoit, J. B., Rinehart, J. P., Elnitsky, M. A., Lee, R. E., Jr., & Denlinger, D. L. (2009) · Journal of Comparative Physiology B · doi:10.1007/s00360-008-0334-0 · Cited by 119
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
Mechanisms of Desiccation Tolerance: Themes and Variations in Brine Shrimp, Roundworms, and Tardigrades
Hibshman, J. D., Clegg, J. S., & Goldstein, B. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.592016 · Cited by 115
Meeting the challenges of on-host and off-host water balance in blood-feeding arthropods
Benoit, J. B., & Denlinger, D. L. (2010) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2010.02.014 · Cited by 111
Stress‐tolerance of baker's‐yeast ( Saccharomyces cerevisiae ) cells: stress‐protective molecules and genes involved in stress tolerance
Shima, J., & Takagi, H. (2009) · Biotechnology and Applied Biochemistry · doi:10.1042/ba20090029 · Cited by 104
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
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
Desiccation tolerance in Acinetobacter baumannii is mediated by the two-component response regulator BfmR
Farrow, J. M., Wells, G., & Pesci, E. C. (2018) · PLoS ONE · doi:10.1371/journal.pone.0205638 · Cited by 101
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
Frog Skins Keep Redox Homeostasis by Antioxidant Peptides with Rapid Radical Scavenging Ability
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
Oxidative stress responses and lipid peroxidation damage are induced during dehydration in the production of dry active wine yeasts
Garré, E., Raginel, F., Palacios, A., Julien, A., & Matallana, E. (2009) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2009.10.018 · Cited by 97
When Phased without Water: Biophysics of Cellular Desiccation, from Biomolecules to Condensates
Romero-Perez, P. S., Dorone, Y., Flores, E., Sukenik, S., & Boeynaems, S. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.2c00659 · Cited by 97
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 97
Viability of microencapsulated Akkermansia muciniphila and Lactobacillus plantarum during freeze-drying, storage and in vitro simulated upper gastrointestinal tract passage
Marcial-Coba, M. S., Cieplak, T., Cahú, T. B., Blennow, A., Knøchel, S., & Nielsen, D. S. (2018) · Food & Function · doi:10.1039/c8fo01331d · Cited by 92
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
Anhydrobiosis-Associated Nuclear DNA Damage and Repair in the Sleeping Chironomid: Linkage with Radioresistance
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
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
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
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
DNA Protection Protein, a Novel Mechanism of Radiation Tolerance: Lessons from Tardigrades
Hashimoto, T., & Kunieda, T. (2017) · Life · doi:10.3390/life7020026 · Cited by 89
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
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 84
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
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
Radiation Tolerance in Tardigrades: Current Knowledge and Potential Applications in Medicine
Jonsson, K. (2019) · Cancers · doi:10.3390/cancers11091333 · Cited by 79
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
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
Optimizing oral delivery of next generation probiotics
Torp, A. M., Bahl, M. I., Boisen, A., & Licht, T. R. (2021) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2021.11.034 · Cited by 76
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
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 77
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
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
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
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
Intracellular Protective Functions and Therapeutical Potential of Trehalose
Kuczyńska‐Wiśnik, D., Stojowska‐Swędrzyńska, K., & Laskowska, E. (2024) · Molecules · doi:10.3390/molecules29092088 · Cited by 72
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
Desiccation and radiation stress tolerance in cyanobacteria
Singh, H. (2018) · Journal of Basic Microbiology · doi:10.1002/jobm.201800216 · Cited by 70
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
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
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
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
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
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
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
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
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
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
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
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
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 59
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
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
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
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 58
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
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
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
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
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
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
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
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 55
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 51
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 50
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
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
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 49

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

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Oxidative stress and its effects during dehydration

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks