Mechanisms of plant desiccation tolerance.

By F. Hoekstra, E. Golovina, J. Buitink. Trends in Plant Science, 2001

1,434 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Physiology

View Paper: https://www.semanticscholar.org/paper/8edfd4841f75dc0f32715604d1c3516dbff6b750

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Citations in the corpus

Viability of the lichen Xanthoria elegans and its symbionts after 18 months of space exposure and simulated Mars conditions on the ISS (2014, background): “Anhydrobiosis provides enormous desiccation tolerance (Hoekstra et al. 2001; Schlensog et al. 2003; Rebecchi et al. 2007) and supports the importance of the poikilohydry as a fundamental life strategy of the lichen symbiosis in response to hostile conditions (Kranner et al. 2008).”
Search for nucleotide diversity patterns of local adaptation in dehydrins and other cold-related candidate genes in Scots pine (Pinus sylvestris L.) (2008, background): “…play any role in adaptive variation, as we may lack the power to detect small effects of selection at the individual possibly interacting loci, such as dehydrins, abscisic acid-induced genes, and other protective molecules such as other lea proteins or compatible solutes (see Hoekstra et al. 2001).”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “The most important mechanism used to achieve such an effect is decreasing the plant osmotic potential by active accumulation of organic ions or solutes, known as osmotic adjustment or osmoregulation (Morgan, 1984; Hoekstra et al., 2001).”
Resurrection Plants: The Puzzle of Surviving Extreme Vegetative Desiccation (2005, background): “Moderate tissue dehydration to a moisture content of about 23 percent water on a fresh weight basis (Hoekstra et al., 2001) creates a drought condition requiring the activation of drought-tolerance strategies.”
Age-related biochemical changes during storage of beech (Fagus sylvatica L.) seeds (2007, background): “Based upon electron spin resonance (ESR) data, a role of amphiphilic substances, such as phenolic compounds, in membrane protection has been proposed by Hoekstra et al. (2001).”
Salt stress affects water relations, photosynthesis, and oxidative defense mechanisms in Solanum melongena L. (2013, background): “2010), buffer immediately salt-induced toxic levels of Na and Cl (Misra and Gupta 2005), and protect and stabilize cellular structures and macromolecules in salt-stressed plants (Hoekstra et al. 2001).”
Desiccation sensitivity and tolerance in the moss Physcomitrella patens: assessing limits and damage (2010, background): “3 g g dm (dry matter) (Alpert 2005; Hoekstra et al. 2001), although the precise value depends upon the composition of the cells (Walters and Koster 2007).”
Drought and Salt Tolerance in Plants (2005, background): “Resurrection plants and seeds of many higher plants are good examples for a link of carbohydrate (in particular sucrose) accumulation and the acquisition of stress tolerance ( Hoekstra et al. , 2001 ; Phillips et al.”
Arbuscular mycorrhizal symbiosis and alleviation of osmotic stress. New perspectives for molecular studies (2003, background): “The most important mechanism which achieves such an effect, known as osmotic adjustment or osmoregulation, is a decrease in the plant osmotic potential by active accumulation of organic ions or solutes (Morgan 1984; S�nchez-D�az and Aguirreolea 1993; Hoekstra et al. 2001 ).”
Changes in germination, growth and soluble sugar contents of Sorghum bicolor (L.) Moench seeds under various abiotic stresses (2003, positive): “Accumulation of sugars, a characteristic of mature seeds appears to be central to the development of desiccation tolerance (Hoekstra et al. (2001), for review).”
Bacterial-mediated drought tolerance: Current and future prospects (2016, background): “It protects enzymes, proteins, cellular organelles and membranes against oxidative damage (Hoekstra and Buitink, 2001; Farooq et al., 2009; Huang et al., 2014).”
Hydrophilins from distant organisms can protect enzymatic activities from water limitation effects in vitro (2005, background): “Alternatively, hydrophilins could use their own polar residues to interact with the surface groups of other proteins, effectively replacing water (Close 1997; Hoekstra et al. 2001 ).”
Crop Production under Drought and Heat Stress: Plant Responses and Management Options (2017, background): “Water shortage causes shrinkage of the cell due to which a decrease in the cellular volume takes place, as a consequence the cellular material become more viscous which leads to denaturation of the proteins (Hoekstra et al., 2001).”
When Defense Pathways Collide. The Response of Arabidopsis to a Combination of Drought and Heat Stress1[w] (2004, background): “It was suggested that a moderate level of water stress is accompanied by the accumulation of compounds such as Pro and Gly-betaine, whereas a severe level of water stress is accompanied by the accumulation of sugars such as sucrose (Hoekstra et al., 2001).”