Resurrection plants: Imperative resources in developing strategies to drought and desiccation pressure
DOI:
https://doi.org/10.14719/pst.2019.6.3.542Keywords:
Drought, Resurrection, Pokilohydric, stress, toleranceAbstract
Resurrection plants are the vital assets of nature that have amazing mechanism to restrict the negative impacts of drought or desiccation stress by diminishing cell damage. These surprising plants are in minority on this planet but have the potential to serve as a powerful resource for developing new strategies for major crop plants that are unable to adapt well to the arid climate. In this review, an attempt is made to highlight the potential aspects of these resurrection plants especially the genetic engineering facet which has been done to develop drought tolerance in economically important plants.
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References
1. Shao HB, Chu LY, Jaleel CA. Understanding water deficit stress-induced changes in the basic metabolism of higher plants-biotechnologically and sustainably improving agriculture and the eco environment in arid regions of the globe. Critical Reviews in Biotechnology 2009; 29: 131-151. https://doi.org/10.1080/07388550902869792
2. Leprince O, Buitink J. Desiccation tolerance: From genomics to the field. Plant Science 2010; 179: 554-564. https://doi.org/10.1016/j.plantsci.2010.02011
3. Gaff DF. Desiccation-tolerant ?owering plants in Southern Africa. Science 1971; 174: 1033–1034. https:// doi.org/10.1126/science.174.4013.1033
4. Oliver MJ. Desiccation tolerance in vegetative plant cells. Physiologia Plantarum 1996; 97: 779–787. https://doi.org/10.1111/j.1399-3054.1996.tb00544.x
5. Farrant JM, Moore JP. Programming desiccation-tolerance: from plants to seeds to resurrection plants. Current Opinion in Plant Biology 2011; 14(3): 340-345. https://doi.org/10.1016/j.pbi.2011.03.018
6. VanBuren R, Wai, CM, Ou S, Pardo J, Bryant D, Ning Jiang N,Todd C. Mockler TC, Patrick Edger P, Todd P. Michae TP. Extreme haplotype variation in the desiccation-tolerant clubmoss Selaginella lepidophylla. Nature Communications 2018; 9:13. https://doi.org/10.1038/s41467-017-02546-5
7. Illing N, Denby KJ, Collett H, Shen A, Farrant JM. The signature of seeds in resurrection plants: a molecular and physiological comparison of desiccation tolerance in seeds and vegetative tissues. Integrative and Compartaive Biology 2005; 45: 771–787. https://doi.org/10.1093/icb/45.5.771
8. Furini A, Koncz C, Salamini F, Bartels D. High level transcription of a member of a repeated gene family confers dehydration tolerance to callus tissue of Craterostigma plantagineum. The EMBO Journal. 1997; 16: 3599-3608. https://doi.org/10.1093/emboj/16.12.3599
9. Bartels D, Salamini F. Desiccation tolerance in the resurrection plant Craterostigma plantagineum. A contribution to the study of drought tolerance at the molecular level. Plant Physiology 2001; 127: 1346–1353.
10. Mundree SG, Baker B, Mowla S, Peters S, Marais S, Vander Willigen C, et al. Physiological and molecular insights into drought tolerance. African Journal of Biotechnology 2002; 1:28–38.
11. Moore JP, Lindsey FJM, GG BWF. The South African and Namibian populations of the resurrection plant Myrothamnus ?abellifolius are genetically distinct and display variation in their galloquinic acid composition. Journal of Chemical Ecology 2005; 31: 2823–2834. https://doi.org/10.1007/s10886-005-8396-x
12. Gaff DF, Ellis RP. Southern African grasses with foliage that revives after dehydration. Bothalia 1974; 11: 305–308.
13. Gaff DF, Churchill DM. Borya nitida Labill. – an Australian species in the Liliaceae with desiccation-tolerant leaves. Australian Journal of Botany 1976; 24: 209–224.
14. Gaff DF, Latz PK. The occurrence of resurrection plants in the Australian ?ora. Australian Journal of Botany 1978; 26: 485-492.
15. Rahmanzadeh R, M€uller K, Fischer E, Bartels D, Borsch T. The Linderniaceae and Gratiolaceae are further lineages distinct from the Scrophulariaceae (Lamiales). Plant Biology 2005; 7: 1–12. https://doi.org/10.1055/s-2004-830444
16. Bartels D, Hussain SS. Resurrection Plants: Physiology and Molecular Biology. U. L€uttge et al. (eds.). Plant Desiccation Tolerance. Ecological Studies 2011; 215: 339-364. https://doi.org/10.1007/978-3-642-19106-0_16
17. Gaff DF. Responses of desiccation tolerant 'resurrection'plants to water stress. In: Kreeb KH, Richter H, Hinckley TM, eds. Structural and functional responses to environmental stresses. The Hague: SPB Academic Publishing. 1989; pp. 255-268.
18. Scott P. Resurrection plants and the secrets of eternal leaf. Annals of Botany 2000; 85: 159–166.
19. Farrant JM, Vander Willigen C, Loffell DA, Bartsch S, Whittaker A. An investigation into the role of light during desiccation of three angiosperm resurrection plants. Plant Cell and Environment 2003; 26: 1275–1286. https://doi.org/10.1046/j.0016-8025.2003.01052.x
20. Vander Willigen C, Pammenter CNW, Jaffer MA, Mundree SG, Farrant JM. An ultrastructural study using anhydrous ?xation of Eragrostis nindensis, a resurrection grass with both desiccation-tolerant and sensitice tissues. Functional Plant Biology 2003; 30: 1–10.
21. Farrant JM, Brandt W, Lindsey GG. An overview of mechanisms of desiccation tolerance in selected angiosperm resurrection plants. Plant Stress 2007; 1(1): 72–84.
22. Sherwin HW, Farrant JM. Protection mechanisms against excess light in the resurrection plants Craterostigma wilmsii and Xerophyta viscosa. Plant Growth Regulations 1998; 24: 203–210.
23. Farrant JM. A comparation of mechanisms of desiccation tolerance among three angiosperm resurrection plant species. Plant Ecology 2000; 151: 29–39.
24. Hallam ND, Luff SE. Fine structural changes in the mesophyll tissue of the leaves of Xerophyta villosa during desiccation. Botanical Gazette 1980; 141: 173–179.
25. Cosgrove DJ. Expansive growth of plant cell walls. Plant Physiology and Biochemistry 2000; 38: 109–124.
26. Farrant JM, Sherwin HW. Mechanisms of desiccation tolerance in seeds and resurrection plants. In: Taylor AG, Huang XL (eds) Progress in seed research. Proceedings of the second international conference on seed science and technology. Communication Services of the New York State Agricultural Experimental Station, Geneva, 1997; NY. pp. 109–120.
27. Thomson WW, Platt KA. Conservation of cell order in desiccated mesophyll of Selaginella lepidophylla [Hook and Grev.] Spring. Annals of Botany 1997; 79: 439–447.
28. Vicr? M, Sherwin HW, Driouich A, Jaffer MA, Farrant JM. Cell wall characteristics and structure of hydrated and dry leaves of the resurrection plant Craterostigma wilmsii, a microscopical study. Journal of Plant Physiology 1999; 155: 719–726.
29. Vicr? M, Lerouxel O, Farrant J, Lerouge P, Driouich A. Composition and desiccationinduced alterations of the cell wall in the resurrection plant Craterostigma wilmsii. Physiologia Plantarum 2004; 120: 229–239.
30. Vander Willigen C, Farrant JM, Pammenter NW. Anomalous pressure volume curves of resurrection plants do not suggest negative turgor. Annals of Botany 2001; 88: 537–543.
31. Wang Z, Zhu Y, Wang L, Liu X, LiuY, Phillips J, et al. A WRKY transcription factor participates in dehydration tolerance in Boea hygrometrica by binding to the W-box elements of the galactinol synthase (BhGolS1) promoter. Planta 2009; 230: 1155–1166. https://doi.org/10.1007/s00425-009-1014-3
32. Moon BY, Higashi S, Gombos Z, Murata N . Unsaturation of the membrane lipids of chloroplasts stabilizes the photosynthetic machinery against low-temperature photoinhibition in transgenic tobacco plants. Proceedings of the National Academy of Sciences of the United States of America. 1995; 92(14): 6219–6223. https://doi.org/10.1073/pnas.92.14.6219
33. Georgieva K, Szigeti Z, Sarvari E, et al. Photosynthetic activity of homoiochlorophyllous desiccation tolerant plant Haberlea rhodopensis during dehydration and rehydration. Planta 2007; 225: 955–964. https://doi.org/10.1007/s00425-006-0396-8
34. Deng X, Hu ZA, Wang HX, et al. A comparison of photosynthetic apparatus of the detached leaves of the resurrection plant Boea hygrometrica with its non tolerant relative Chirita heterotrichia in response to dehydration and rehydration. Plant Science 2003; 165: 851–861. https://doi.org/10.1016/S0168-9452(03)00284-X
35. Degl’Innocenti, Guidi EL, Stevanovic B, Navari F. CO2 ?xation and chlorophyll a ?uorescence in leaves of Ramonda serbica during a dehydration rehydration cycle. Journal of Plant Physiology 2008; 165: 723–733. https://doi.org/10.1016/j.jplph.2007.06.009
36. Schwab KB, Schreiber U, Heber U. Response of photosynthesis and respiration of resurrection plants to desiccation and rehydration. Planta 1989; 177: 217–227.
37. Alamillo JM, Bartels D. Effects of desiccation on photosynthesis pigments and the ELIP-like dsp22 protein complex in the resurrection plant Craterostigma plantagineum. Plant Science 2001; 160: 1161–1170.
38. Navari-Izzo F, Quartacci MF, Pinzino C, Rascio N, Vazzana C, Sgherri C. Protein dynamics in thylakoids of the desiccation-tolerant plant Boea hygroscopica during dehydration and rehydration. Plant Physiology 2000; 124: 1427–1436.
39. Quartacci MF, Forli M, Rascio N, DallaVecchia F, Bochicchio A, Navari-Izzo F. Desiccation-tolerant Sporobolus stap?anus: lipid composition and cellular ultrastructure during dehydration and rehydration. Journal of Experimental Botany 1997; 48: 1269–1279.
40. Tuba Z, Proctor MCF, Csintalan Z. Ecophysiological responses of homoiochlorophyllous and poikilochlorophyllous desiccation-tolerant plants: a comparison and an ecological perspective. Plant Growth Regulation 1998; 24: 211–217.
41. Gechev ST, Challabathula D,Benina M, Toneva V, Bartels D. Molecular mechanisms of desiccation tolerance in resurrection plants. Cellular and Molecular Life Sciences 2012; 69: 3175–3186. https://doi.org/10.1007/s00018-012-1088-0
42. Araùjo SS, Duque AS, Silva JM, etal. Water de?cit and recovery response of Medicago truncatula plants expressing the ELIP-like DSP22. Biologia Planarum 2013; 57: 159–163. https://doi.org/10.1007/s10535-012-0235-7
43. Adamska I. ELIPs: Light-induced stress proteins. Physiologia plantarum 1997; 100: 794–805.
44. Montan? MH, Dreyer S, Triantaphylides C, Kloppstech K. Early light-inducible proteins during long-term acclimation of barley to photooxidative stress caused by light and cold: high level of accumulation by posttranscriptional regulation. Planta 1997; 202: 293–302.
45. Zeng Q, Chen XB, Wood A J. Two early light-inducible protein (ELIP) cDNAs from the resurrection plant Tortula ruralis are differentially expressed in response to desiccation, rehydration, salinity, and high light. Journal of Experimental Botany 2002; 53(371): 1197–1205.
46. Provart NJ, Gil P, Chen W, Han B, Chang HS, Wang X, Zhu T. Gene expression phenotypes of Arabidopsis associated with sensitivity to low temperatures. Plant Physiology 2003; 132: 893–906. https://doi.org/10.1104/pp.103.021261
47. Sävenstrand H, Olofsson M, Samuelsson M, Strid A. Induction of early-inducible protein gene expression in Pisum sativum after exposure to low levels of UV-B radiation and other environmental stresses. Plant Cell Reports 2004; 22: 532–536. https://doi.org/10.1007/s00299-003-0743-1
48. Phillips JR, Hilbricht T, Salamini F, Bartels D. A novel abscisic acid- and dehydration responsive gene family from the resurrection plant Craterostigma plantagineum encodes a plastid-targeted protein with DNA binding activity. Planta 2002; 215:258–266. https://doi.org/10.1007/s00425-002-0755-z
49. Challabathula D, Puthur JT, Bartels D. Surviving metabolic arrest: photosynthesis during desiccation and rehydration in resurrection plants. Annals of the New York Academy of Sciences 2016; 1365: 89–99. https://doi.org/10.1111/nyas.12884
50. Kranner I, Beckett RP, Wornik S, Zorn M, Pfeinhofer W. Revival of a resurrection plant correlates with its antioxidant status. The Plant Journal 2002; 31: 13–24.
51. Kranner I, Birti? S. A modulating role for antioxidants in desiccation tolerance. Integrative and Comparative Biology 2005; 45: 734-740. https://doi.org/10.1093/icb/45.5.734
52. Ndima T, Farrant JM, Thomson J, Mundree S . Molecular characterization of XVT8, a stress-responsive gene from the resurrection plant Xerophyta viscosa Baker. Plant Growth Regulation 2001; 35: 137–145.
53. Mowla SB, Thomson JA, Farrant JM, Mundree SG. A novel stress-inducible antioxidant enzyme identi?ed from the resurrection plant Xerophyta viscosa Baker. Planta 2002; 215: 716–726. https://doi.org/10.1007/s00425-002-0819-0
54. Kozak CA. Genetic mapping of six mouse peroxiredoxin genes and fourteen peroxiredoxin related sequences. Mammalian Genome 1999; 10: 1017–1019.
55. Smirnoff N. The role of active oxygen in the response of plants to water deficit and desiccation. New Phytologist 1993; 125: 27-58. https://doi.org/10.1111/j.1469-8137.1993.tb03863.x
56. Asada K. The water-water cycle as alternative photon and electron sinks. Philosophical Transactions Royal Society of London B 2000; 355: 1419-1431. https://doi.org/10.1098/rstb.2000.0703
57. Sairam PK, Saxena DC. Oxidative stress and antioxidants in wheat genotypes: possible mechanism of water stress tolerance. Journal of Agronomy and Crop Science 2000; 184: 55-61. https://doi.org/10.1046/j.1439-037x.2000.00358.x
58. Reddy AR, Chaitanya KV, Vivekanandan M. Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. Journal of Plant Physiology. 2004; 161: 1189-1202. https://doi.org/10.1016/j.jplph.2004.01.013
59. Price AH, Taylor A, Ripley SJ, Griffiths A, Trewavas AJ , Knight M. Oxidative signals in tobacco increase cytosolic calcium. The Plant Cell 1994; 6: 1301-1310. https://doi.org/10.1105/tpc.6.9.1301
60. Köhler B and Blatt MR. Protein phosphorylation activates the guard cell Ca2+ channel and is a prerequisite for gating by abscisic acid. The Plant Journal: for Cell and Molecular Biology 2002; 32: 185-194.
61. Schroeder JI, Kwak JM, Allen GJ. Guard cell abscisic acid signalling and engineering drought hardiness in plants. Nature 2001; 410: 327–330. https://doi.org/10.1038/35066500
62. Gaff DF. Protoplasmic tolerance of extreme water stress. In: Turner NC, Kramer PJ (eds) Adaptation of plants to water and high temperature stress. Wiley, 1980; New York, 207–230.
63. Gaff DF, Loveys BR. Abscisic-acid content and effects during dehydration of detached leaves of desiccation tolerant plants. Journal of Experimental Botany 1984; 35: 1350–1358.
64. Bartels D, Schneider K, Terstappen G, Piatkowski D, Salamini F. Molecular cloning of abscisic acid-modulated genes which are induced during desiccation of the resurrection plant Craterostigma plantagineum. Planta 1990; 181: 27–34.
65. Reynolds TL, Bewley JD. Abscisic acid enhances the ability of the desiccation tolerant fern Polypodium virginianum to withstand drying. Journal of Experimental Botany 1993; 44: 1771–1779.
66. Hellwege EM, Dietz KJ, Volk OH, Hartung W. Abscisic acid and the induction of desiccation tolerance in the extremely xerophilic liverwort Exormotheca holstii. Planta 1994; 194: 525–531.
67. Schiller P, Heilmeier H, Hartung W. Absisic acid (ABA) relations in the aquatic resurrection plant Chamaegigas intrepidus under naturally ?uctuating environmental conditions. New Phytologist 1997; 136: 603–611. https://doi.org/10.1046/j.1469-8137.1997.00789.x
68. Crowe JH, Carpenter JF, Crowe LM. The role of vitri?cation in anhydrobiosis. Annual Reviews Plant Physiology 1998; 60: 73–103. https://doi.org/10.1146/annurev.physiol.60.1.73
69. Ramanjulu S, Bartels D. Drought- and desiccation-induced modulation of gene expression in plants. Plant Cell and Environment 2002; 25: 141–151.
70. Peters S, Mundree SG, Thomson JA, Farrant JM, Keller F. Protection mechanisms in the resurrection plant Xerophyta viscosa Baker: both sucrose and raf?nose family oligosacharides (RFOs) accumulate in leaves in response to water de?cit. Journal of Experimental Botany 2007; 58(8): 1947–1956. https://doi.org/10.1093/jxb/erm056
71. Hoekstra FA. Differential longevities in desiccated anhydrobiotic plant systems. Integrative and Comparative Biology 2005; 45: 725–733. https://doi.org/10.1093/icb/45.5.725
72. Ghasempour HR, Gaff DF, Williams RPW, Gianello RD. Contents of sugars in leaves of drying desiccation-tolerant ?owering plants, particularly grasses. Plant Growth Regulation 1998; 24: 185–191.
73. Bianchi G, Gamba A, Murelli C, Salamini F, Bartels D. Novel carbohydrate metabolism in the resurrection plant Craterostigma plantagineum. The Plant Journal 1991; 1: 355–359.
74. Kleines M, Elster RC, Rodrigo MJ, Blervacq AS, Salamini F, Bartels D. Isolation and expression analysis of two stress-responsive sucrose-synthase genes from the resurrection plant Craterostigma plantagineum (Hochst.). Planta 1999; 209: 13–24. https://doi.org/10.1007/s004250050602
75. Feder ME, Hofmann GE. Heat shock proteins, evolutionary and ecological physiology. Annual Review of Physiology 1999; 61: 243–282. https://doi.org/10.1146/annurev.physiol.61.1.243
76. Tunnacliffe A, Wise M. The continuing conundrum of the LEA protein. Die Naturwissenschaften 2007; 94: 791-812. https://doi.org/10.1007/s00114-007-0254-y
77. Bernacchia G, Salamini F, Bartels D. Molecular characterization of the rehydration process in the resurrection plant Craterostigma plantagineum. Plant Physiology 1996; 111: 1043–1050. https://doi.org/10.1104/pp.111.4.1043
78. Cooper K, Farrant JM. Recovery of the resurrection plant Craterostigma wilmsii from desiccation: protection versus repair. Journal of Experimental Botany 2002; 53: 1805-813. https://doi.org/10.1093/jxb/erf028
79. Mariaux JB, Bockel C, Salamini F, Bartels D. Desiccation and abscisic acid-responsive genes encoding major intrinsic proteins (MIP) from the resurrection plant Craterostigma plantagineum. Plant Molecular Biology 1998; 38: 1089–1099. https://doi.org/10.1023/A:1006013130681.
80. Deng X, Phillips J, Brautigam A, Engstrom P, Johannesson H, Ouwerkerk PB, et al. A homeodomain leucine zipper gene from Craterostigma plantagineum regulates abscisic acid responsive gene expression and physiological responses. Plant Molecular Biology 2006; 61: 469–489. https://doi.org/10.1007/s11103-006-0023-x
81. Zhu Y, Wang Z, Jing Y, Wang L, Liu X, Liu Y, Deng X. Ectopic over-expression of BhHsf1, a heat shock factor from the resurrection plant Boea hygrometrica, leads to increased thermotolerance and retarded growth in transgenic Arabidopsis and tobacco. Plant Molecular Biology 2009; 71: 451–467. https://doi.org/10.1007/s11103-009-9538-2
82. Frank W, Munnik T, Kerkmann K, Salamini F, Bartels D. Water de?cit triggers phospholipase D activity in the resurrection plant Craterostigma plantagineum. The Plant Cell 2000; 12:111–124.
83. Mulako I, Farrant JM, Collett H, Illing N. Expression of Xhdsi-1VOC, a novel member of the vicinal oxygen chelate (VOC) metalloenzyme superfamily, is upregulated in leaves and roots during desiccation in the resurrection plant Xerophyta humilis Baker Dur and Schinz. Journal of Experimental Botany 2008; 59: 3885–3901. https://doi.org/10.1093/jxb/ern226
84. Rodriguez M C S, Edsgärd D, Hussain SS, Alquezar D, Rasmussen M, Gilbert T, et al. Transcriptomes of the desiccation-tolerant resurrection plant Craterostigma plantagineum. The Plant Journal 2010; 63: 212–228. https://doi.org/10.1111/j.1365-313X.2010.04243.x
85. Rodrigo MJ, Bockel C, Blervacq AS, Bartels D. The novel gene CpEdi-9 from the resurrection plant C. plantagineum encodes a hydrophilic protein and is expressed in mature seeds as well as in response to dehydration in leaf phloem tissues. Planta 2004; 219: 579–589. https://doi.org/10.1007/s00425-004-1264-z
86. Moore JP, Westall KL, Ravenscroft N, Farrant J, Lindsey GG, Brandt W. The predominant polyphenol in the leaves of the resurrection plant Myrothamnus ?abellifolius, 3,4,5-tri-Ogalloylquinic acid, protects membranes against desiccation and free radical-induced oxidation. The Biochemical Journal 2005; 385: 301–308. https://doi.org/10.1042/BJ20040499
87. Adebusola A, Victor O, Emmanuel I, Alam A. Effect of nitrogen application on phytochemical production in Jatropha curcas L. (Angiosperms: Euphorbiaceae) during drought conditions. Plant Science Today 2019: 6(2): 183-189. https://doi,org/10.14719/pst.20196.2.523
2. Leprince O, Buitink J. Desiccation tolerance: From genomics to the field. Plant Science 2010; 179: 554-564. https://doi.org/10.1016/j.plantsci.2010.02011
3. Gaff DF. Desiccation-tolerant ?owering plants in Southern Africa. Science 1971; 174: 1033–1034. https:// doi.org/10.1126/science.174.4013.1033
4. Oliver MJ. Desiccation tolerance in vegetative plant cells. Physiologia Plantarum 1996; 97: 779–787. https://doi.org/10.1111/j.1399-3054.1996.tb00544.x
5. Farrant JM, Moore JP. Programming desiccation-tolerance: from plants to seeds to resurrection plants. Current Opinion in Plant Biology 2011; 14(3): 340-345. https://doi.org/10.1016/j.pbi.2011.03.018
6. VanBuren R, Wai, CM, Ou S, Pardo J, Bryant D, Ning Jiang N,Todd C. Mockler TC, Patrick Edger P, Todd P. Michae TP. Extreme haplotype variation in the desiccation-tolerant clubmoss Selaginella lepidophylla. Nature Communications 2018; 9:13. https://doi.org/10.1038/s41467-017-02546-5
7. Illing N, Denby KJ, Collett H, Shen A, Farrant JM. The signature of seeds in resurrection plants: a molecular and physiological comparison of desiccation tolerance in seeds and vegetative tissues. Integrative and Compartaive Biology 2005; 45: 771–787. https://doi.org/10.1093/icb/45.5.771
8. Furini A, Koncz C, Salamini F, Bartels D. High level transcription of a member of a repeated gene family confers dehydration tolerance to callus tissue of Craterostigma plantagineum. The EMBO Journal. 1997; 16: 3599-3608. https://doi.org/10.1093/emboj/16.12.3599
9. Bartels D, Salamini F. Desiccation tolerance in the resurrection plant Craterostigma plantagineum. A contribution to the study of drought tolerance at the molecular level. Plant Physiology 2001; 127: 1346–1353.
10. Mundree SG, Baker B, Mowla S, Peters S, Marais S, Vander Willigen C, et al. Physiological and molecular insights into drought tolerance. African Journal of Biotechnology 2002; 1:28–38.
11. Moore JP, Lindsey FJM, GG BWF. The South African and Namibian populations of the resurrection plant Myrothamnus ?abellifolius are genetically distinct and display variation in their galloquinic acid composition. Journal of Chemical Ecology 2005; 31: 2823–2834. https://doi.org/10.1007/s10886-005-8396-x
12. Gaff DF, Ellis RP. Southern African grasses with foliage that revives after dehydration. Bothalia 1974; 11: 305–308.
13. Gaff DF, Churchill DM. Borya nitida Labill. – an Australian species in the Liliaceae with desiccation-tolerant leaves. Australian Journal of Botany 1976; 24: 209–224.
14. Gaff DF, Latz PK. The occurrence of resurrection plants in the Australian ?ora. Australian Journal of Botany 1978; 26: 485-492.
15. Rahmanzadeh R, M€uller K, Fischer E, Bartels D, Borsch T. The Linderniaceae and Gratiolaceae are further lineages distinct from the Scrophulariaceae (Lamiales). Plant Biology 2005; 7: 1–12. https://doi.org/10.1055/s-2004-830444
16. Bartels D, Hussain SS. Resurrection Plants: Physiology and Molecular Biology. U. L€uttge et al. (eds.). Plant Desiccation Tolerance. Ecological Studies 2011; 215: 339-364. https://doi.org/10.1007/978-3-642-19106-0_16
17. Gaff DF. Responses of desiccation tolerant 'resurrection'plants to water stress. In: Kreeb KH, Richter H, Hinckley TM, eds. Structural and functional responses to environmental stresses. The Hague: SPB Academic Publishing. 1989; pp. 255-268.
18. Scott P. Resurrection plants and the secrets of eternal leaf. Annals of Botany 2000; 85: 159–166.
19. Farrant JM, Vander Willigen C, Loffell DA, Bartsch S, Whittaker A. An investigation into the role of light during desiccation of three angiosperm resurrection plants. Plant Cell and Environment 2003; 26: 1275–1286. https://doi.org/10.1046/j.0016-8025.2003.01052.x
20. Vander Willigen C, Pammenter CNW, Jaffer MA, Mundree SG, Farrant JM. An ultrastructural study using anhydrous ?xation of Eragrostis nindensis, a resurrection grass with both desiccation-tolerant and sensitice tissues. Functional Plant Biology 2003; 30: 1–10.
21. Farrant JM, Brandt W, Lindsey GG. An overview of mechanisms of desiccation tolerance in selected angiosperm resurrection plants. Plant Stress 2007; 1(1): 72–84.
22. Sherwin HW, Farrant JM. Protection mechanisms against excess light in the resurrection plants Craterostigma wilmsii and Xerophyta viscosa. Plant Growth Regulations 1998; 24: 203–210.
23. Farrant JM. A comparation of mechanisms of desiccation tolerance among three angiosperm resurrection plant species. Plant Ecology 2000; 151: 29–39.
24. Hallam ND, Luff SE. Fine structural changes in the mesophyll tissue of the leaves of Xerophyta villosa during desiccation. Botanical Gazette 1980; 141: 173–179.
25. Cosgrove DJ. Expansive growth of plant cell walls. Plant Physiology and Biochemistry 2000; 38: 109–124.
26. Farrant JM, Sherwin HW. Mechanisms of desiccation tolerance in seeds and resurrection plants. In: Taylor AG, Huang XL (eds) Progress in seed research. Proceedings of the second international conference on seed science and technology. Communication Services of the New York State Agricultural Experimental Station, Geneva, 1997; NY. pp. 109–120.
27. Thomson WW, Platt KA. Conservation of cell order in desiccated mesophyll of Selaginella lepidophylla [Hook and Grev.] Spring. Annals of Botany 1997; 79: 439–447.
28. Vicr? M, Sherwin HW, Driouich A, Jaffer MA, Farrant JM. Cell wall characteristics and structure of hydrated and dry leaves of the resurrection plant Craterostigma wilmsii, a microscopical study. Journal of Plant Physiology 1999; 155: 719–726.
29. Vicr? M, Lerouxel O, Farrant J, Lerouge P, Driouich A. Composition and desiccationinduced alterations of the cell wall in the resurrection plant Craterostigma wilmsii. Physiologia Plantarum 2004; 120: 229–239.
30. Vander Willigen C, Farrant JM, Pammenter NW. Anomalous pressure volume curves of resurrection plants do not suggest negative turgor. Annals of Botany 2001; 88: 537–543.
31. Wang Z, Zhu Y, Wang L, Liu X, LiuY, Phillips J, et al. A WRKY transcription factor participates in dehydration tolerance in Boea hygrometrica by binding to the W-box elements of the galactinol synthase (BhGolS1) promoter. Planta 2009; 230: 1155–1166. https://doi.org/10.1007/s00425-009-1014-3
32. Moon BY, Higashi S, Gombos Z, Murata N . Unsaturation of the membrane lipids of chloroplasts stabilizes the photosynthetic machinery against low-temperature photoinhibition in transgenic tobacco plants. Proceedings of the National Academy of Sciences of the United States of America. 1995; 92(14): 6219–6223. https://doi.org/10.1073/pnas.92.14.6219
33. Georgieva K, Szigeti Z, Sarvari E, et al. Photosynthetic activity of homoiochlorophyllous desiccation tolerant plant Haberlea rhodopensis during dehydration and rehydration. Planta 2007; 225: 955–964. https://doi.org/10.1007/s00425-006-0396-8
34. Deng X, Hu ZA, Wang HX, et al. A comparison of photosynthetic apparatus of the detached leaves of the resurrection plant Boea hygrometrica with its non tolerant relative Chirita heterotrichia in response to dehydration and rehydration. Plant Science 2003; 165: 851–861. https://doi.org/10.1016/S0168-9452(03)00284-X
35. Degl’Innocenti, Guidi EL, Stevanovic B, Navari F. CO2 ?xation and chlorophyll a ?uorescence in leaves of Ramonda serbica during a dehydration rehydration cycle. Journal of Plant Physiology 2008; 165: 723–733. https://doi.org/10.1016/j.jplph.2007.06.009
36. Schwab KB, Schreiber U, Heber U. Response of photosynthesis and respiration of resurrection plants to desiccation and rehydration. Planta 1989; 177: 217–227.
37. Alamillo JM, Bartels D. Effects of desiccation on photosynthesis pigments and the ELIP-like dsp22 protein complex in the resurrection plant Craterostigma plantagineum. Plant Science 2001; 160: 1161–1170.
38. Navari-Izzo F, Quartacci MF, Pinzino C, Rascio N, Vazzana C, Sgherri C. Protein dynamics in thylakoids of the desiccation-tolerant plant Boea hygroscopica during dehydration and rehydration. Plant Physiology 2000; 124: 1427–1436.
39. Quartacci MF, Forli M, Rascio N, DallaVecchia F, Bochicchio A, Navari-Izzo F. Desiccation-tolerant Sporobolus stap?anus: lipid composition and cellular ultrastructure during dehydration and rehydration. Journal of Experimental Botany 1997; 48: 1269–1279.
40. Tuba Z, Proctor MCF, Csintalan Z. Ecophysiological responses of homoiochlorophyllous and poikilochlorophyllous desiccation-tolerant plants: a comparison and an ecological perspective. Plant Growth Regulation 1998; 24: 211–217.
41. Gechev ST, Challabathula D,Benina M, Toneva V, Bartels D. Molecular mechanisms of desiccation tolerance in resurrection plants. Cellular and Molecular Life Sciences 2012; 69: 3175–3186. https://doi.org/10.1007/s00018-012-1088-0
42. Araùjo SS, Duque AS, Silva JM, etal. Water de?cit and recovery response of Medicago truncatula plants expressing the ELIP-like DSP22. Biologia Planarum 2013; 57: 159–163. https://doi.org/10.1007/s10535-012-0235-7
43. Adamska I. ELIPs: Light-induced stress proteins. Physiologia plantarum 1997; 100: 794–805.
44. Montan? MH, Dreyer S, Triantaphylides C, Kloppstech K. Early light-inducible proteins during long-term acclimation of barley to photooxidative stress caused by light and cold: high level of accumulation by posttranscriptional regulation. Planta 1997; 202: 293–302.
45. Zeng Q, Chen XB, Wood A J. Two early light-inducible protein (ELIP) cDNAs from the resurrection plant Tortula ruralis are differentially expressed in response to desiccation, rehydration, salinity, and high light. Journal of Experimental Botany 2002; 53(371): 1197–1205.
46. Provart NJ, Gil P, Chen W, Han B, Chang HS, Wang X, Zhu T. Gene expression phenotypes of Arabidopsis associated with sensitivity to low temperatures. Plant Physiology 2003; 132: 893–906. https://doi.org/10.1104/pp.103.021261
47. Sävenstrand H, Olofsson M, Samuelsson M, Strid A. Induction of early-inducible protein gene expression in Pisum sativum after exposure to low levels of UV-B radiation and other environmental stresses. Plant Cell Reports 2004; 22: 532–536. https://doi.org/10.1007/s00299-003-0743-1
48. Phillips JR, Hilbricht T, Salamini F, Bartels D. A novel abscisic acid- and dehydration responsive gene family from the resurrection plant Craterostigma plantagineum encodes a plastid-targeted protein with DNA binding activity. Planta 2002; 215:258–266. https://doi.org/10.1007/s00425-002-0755-z
49. Challabathula D, Puthur JT, Bartels D. Surviving metabolic arrest: photosynthesis during desiccation and rehydration in resurrection plants. Annals of the New York Academy of Sciences 2016; 1365: 89–99. https://doi.org/10.1111/nyas.12884
50. Kranner I, Beckett RP, Wornik S, Zorn M, Pfeinhofer W. Revival of a resurrection plant correlates with its antioxidant status. The Plant Journal 2002; 31: 13–24.
51. Kranner I, Birti? S. A modulating role for antioxidants in desiccation tolerance. Integrative and Comparative Biology 2005; 45: 734-740. https://doi.org/10.1093/icb/45.5.734
52. Ndima T, Farrant JM, Thomson J, Mundree S . Molecular characterization of XVT8, a stress-responsive gene from the resurrection plant Xerophyta viscosa Baker. Plant Growth Regulation 2001; 35: 137–145.
53. Mowla SB, Thomson JA, Farrant JM, Mundree SG. A novel stress-inducible antioxidant enzyme identi?ed from the resurrection plant Xerophyta viscosa Baker. Planta 2002; 215: 716–726. https://doi.org/10.1007/s00425-002-0819-0
54. Kozak CA. Genetic mapping of six mouse peroxiredoxin genes and fourteen peroxiredoxin related sequences. Mammalian Genome 1999; 10: 1017–1019.
55. Smirnoff N. The role of active oxygen in the response of plants to water deficit and desiccation. New Phytologist 1993; 125: 27-58. https://doi.org/10.1111/j.1469-8137.1993.tb03863.x
56. Asada K. The water-water cycle as alternative photon and electron sinks. Philosophical Transactions Royal Society of London B 2000; 355: 1419-1431. https://doi.org/10.1098/rstb.2000.0703
57. Sairam PK, Saxena DC. Oxidative stress and antioxidants in wheat genotypes: possible mechanism of water stress tolerance. Journal of Agronomy and Crop Science 2000; 184: 55-61. https://doi.org/10.1046/j.1439-037x.2000.00358.x
58. Reddy AR, Chaitanya KV, Vivekanandan M. Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. Journal of Plant Physiology. 2004; 161: 1189-1202. https://doi.org/10.1016/j.jplph.2004.01.013
59. Price AH, Taylor A, Ripley SJ, Griffiths A, Trewavas AJ , Knight M. Oxidative signals in tobacco increase cytosolic calcium. The Plant Cell 1994; 6: 1301-1310. https://doi.org/10.1105/tpc.6.9.1301
60. Köhler B and Blatt MR. Protein phosphorylation activates the guard cell Ca2+ channel and is a prerequisite for gating by abscisic acid. The Plant Journal: for Cell and Molecular Biology 2002; 32: 185-194.
61. Schroeder JI, Kwak JM, Allen GJ. Guard cell abscisic acid signalling and engineering drought hardiness in plants. Nature 2001; 410: 327–330. https://doi.org/10.1038/35066500
62. Gaff DF. Protoplasmic tolerance of extreme water stress. In: Turner NC, Kramer PJ (eds) Adaptation of plants to water and high temperature stress. Wiley, 1980; New York, 207–230.
63. Gaff DF, Loveys BR. Abscisic-acid content and effects during dehydration of detached leaves of desiccation tolerant plants. Journal of Experimental Botany 1984; 35: 1350–1358.
64. Bartels D, Schneider K, Terstappen G, Piatkowski D, Salamini F. Molecular cloning of abscisic acid-modulated genes which are induced during desiccation of the resurrection plant Craterostigma plantagineum. Planta 1990; 181: 27–34.
65. Reynolds TL, Bewley JD. Abscisic acid enhances the ability of the desiccation tolerant fern Polypodium virginianum to withstand drying. Journal of Experimental Botany 1993; 44: 1771–1779.
66. Hellwege EM, Dietz KJ, Volk OH, Hartung W. Abscisic acid and the induction of desiccation tolerance in the extremely xerophilic liverwort Exormotheca holstii. Planta 1994; 194: 525–531.
67. Schiller P, Heilmeier H, Hartung W. Absisic acid (ABA) relations in the aquatic resurrection plant Chamaegigas intrepidus under naturally ?uctuating environmental conditions. New Phytologist 1997; 136: 603–611. https://doi.org/10.1046/j.1469-8137.1997.00789.x
68. Crowe JH, Carpenter JF, Crowe LM. The role of vitri?cation in anhydrobiosis. Annual Reviews Plant Physiology 1998; 60: 73–103. https://doi.org/10.1146/annurev.physiol.60.1.73
69. Ramanjulu S, Bartels D. Drought- and desiccation-induced modulation of gene expression in plants. Plant Cell and Environment 2002; 25: 141–151.
70. Peters S, Mundree SG, Thomson JA, Farrant JM, Keller F. Protection mechanisms in the resurrection plant Xerophyta viscosa Baker: both sucrose and raf?nose family oligosacharides (RFOs) accumulate in leaves in response to water de?cit. Journal of Experimental Botany 2007; 58(8): 1947–1956. https://doi.org/10.1093/jxb/erm056
71. Hoekstra FA. Differential longevities in desiccated anhydrobiotic plant systems. Integrative and Comparative Biology 2005; 45: 725–733. https://doi.org/10.1093/icb/45.5.725
72. Ghasempour HR, Gaff DF, Williams RPW, Gianello RD. Contents of sugars in leaves of drying desiccation-tolerant ?owering plants, particularly grasses. Plant Growth Regulation 1998; 24: 185–191.
73. Bianchi G, Gamba A, Murelli C, Salamini F, Bartels D. Novel carbohydrate metabolism in the resurrection plant Craterostigma plantagineum. The Plant Journal 1991; 1: 355–359.
74. Kleines M, Elster RC, Rodrigo MJ, Blervacq AS, Salamini F, Bartels D. Isolation and expression analysis of two stress-responsive sucrose-synthase genes from the resurrection plant Craterostigma plantagineum (Hochst.). Planta 1999; 209: 13–24. https://doi.org/10.1007/s004250050602
75. Feder ME, Hofmann GE. Heat shock proteins, evolutionary and ecological physiology. Annual Review of Physiology 1999; 61: 243–282. https://doi.org/10.1146/annurev.physiol.61.1.243
76. Tunnacliffe A, Wise M. The continuing conundrum of the LEA protein. Die Naturwissenschaften 2007; 94: 791-812. https://doi.org/10.1007/s00114-007-0254-y
77. Bernacchia G, Salamini F, Bartels D. Molecular characterization of the rehydration process in the resurrection plant Craterostigma plantagineum. Plant Physiology 1996; 111: 1043–1050. https://doi.org/10.1104/pp.111.4.1043
78. Cooper K, Farrant JM. Recovery of the resurrection plant Craterostigma wilmsii from desiccation: protection versus repair. Journal of Experimental Botany 2002; 53: 1805-813. https://doi.org/10.1093/jxb/erf028
79. Mariaux JB, Bockel C, Salamini F, Bartels D. Desiccation and abscisic acid-responsive genes encoding major intrinsic proteins (MIP) from the resurrection plant Craterostigma plantagineum. Plant Molecular Biology 1998; 38: 1089–1099. https://doi.org/10.1023/A:1006013130681.
80. Deng X, Phillips J, Brautigam A, Engstrom P, Johannesson H, Ouwerkerk PB, et al. A homeodomain leucine zipper gene from Craterostigma plantagineum regulates abscisic acid responsive gene expression and physiological responses. Plant Molecular Biology 2006; 61: 469–489. https://doi.org/10.1007/s11103-006-0023-x
81. Zhu Y, Wang Z, Jing Y, Wang L, Liu X, Liu Y, Deng X. Ectopic over-expression of BhHsf1, a heat shock factor from the resurrection plant Boea hygrometrica, leads to increased thermotolerance and retarded growth in transgenic Arabidopsis and tobacco. Plant Molecular Biology 2009; 71: 451–467. https://doi.org/10.1007/s11103-009-9538-2
82. Frank W, Munnik T, Kerkmann K, Salamini F, Bartels D. Water de?cit triggers phospholipase D activity in the resurrection plant Craterostigma plantagineum. The Plant Cell 2000; 12:111–124.
83. Mulako I, Farrant JM, Collett H, Illing N. Expression of Xhdsi-1VOC, a novel member of the vicinal oxygen chelate (VOC) metalloenzyme superfamily, is upregulated in leaves and roots during desiccation in the resurrection plant Xerophyta humilis Baker Dur and Schinz. Journal of Experimental Botany 2008; 59: 3885–3901. https://doi.org/10.1093/jxb/ern226
84. Rodriguez M C S, Edsgärd D, Hussain SS, Alquezar D, Rasmussen M, Gilbert T, et al. Transcriptomes of the desiccation-tolerant resurrection plant Craterostigma plantagineum. The Plant Journal 2010; 63: 212–228. https://doi.org/10.1111/j.1365-313X.2010.04243.x
85. Rodrigo MJ, Bockel C, Blervacq AS, Bartels D. The novel gene CpEdi-9 from the resurrection plant C. plantagineum encodes a hydrophilic protein and is expressed in mature seeds as well as in response to dehydration in leaf phloem tissues. Planta 2004; 219: 579–589. https://doi.org/10.1007/s00425-004-1264-z
86. Moore JP, Westall KL, Ravenscroft N, Farrant J, Lindsey GG, Brandt W. The predominant polyphenol in the leaves of the resurrection plant Myrothamnus ?abellifolius, 3,4,5-tri-Ogalloylquinic acid, protects membranes against desiccation and free radical-induced oxidation. The Biochemical Journal 2005; 385: 301–308. https://doi.org/10.1042/BJ20040499
87. Adebusola A, Victor O, Emmanuel I, Alam A. Effect of nitrogen application on phytochemical production in Jatropha curcas L. (Angiosperms: Euphorbiaceae) during drought conditions. Plant Science Today 2019: 6(2): 183-189. https://doi,org/10.14719/pst.20196.2.523
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Alam A, Dwivedi A, Emmanuel I. Resurrection plants: Imperative resources in developing strategies to drought and desiccation pressure. Plant Sci. Today [Internet]. 2019 Jul. 23 [cited 2024 Nov. 21];6(3):333-41. Available from: https://horizonepublishing.com/journals/index.php/PST/article/view/542
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