Does anoxia tolerance involve altering the energy currency towards PPi?

Trends in Plant Science

Volumn 13, Issue 5, 2008, Pages 221-227

  Huang, Shaobai ^a   Colmer, Timothy D ^a   Millar, A Harvey ^a  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; OXYGEN; PYROPHOSPHATE; PYRUVATE PHOSPHATE DIKINASE;

ADAPTATION; ANAEROBIC GROWTH; ARTICLE; ENZYMOLOGY; EUKARYOTIC CELL; GLYCOLYSIS; METABOLISM; PHYSIOLOGY; PLANT; PROKARYOTIC CELL;

ADAPTATION, PHYSIOLOGICAL; ADENOSINE TRIPHOSPHATE; ANAEROBIOSIS; DIPHOSPHATES; EUKARYOTIC CELLS; GLYCOLYSIS; OXYGEN; PLANTS; PROKARYOTIC CELLS; PYRUVATE, ORTHOPHOSPHATE DIKINASE;

ARABIDOPSIS; PROKARYOTA;

EID: 43049176655     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2008.02.007     Document Type: Article

References (53)

1. Voesenek L.A.C.J., et al. How plants cope with the complete submergence. New Phytol. 170 (2006) 213-226
2. van-Dongen J.T., et al. Phloem import and storage metabolism are highly coordinated by the low oxygen concentrations within developing wheat seeds. Plant Physiol. 135 (2004) 1809-1821
3. Gibbs J., and Greenway H. Mechanisms of anoxia tolerance in plants. I. Growth, survival and anaerobic catabolism. Funct. Plant Biol. 30 (2003) 1-47
4. Dennis E.S., et al. Molecular strategies for improving waterlogging tolerance in plants. J. Exp. Bot. 51 (2000) 89-97
5. Fukao T., and Bailey-Serres J. Plant responses to hypoxia - is survival a balancing act?. Trends Plant Sci. 9 (2004) 449-456
6. Huang S., et al. Protein synthesis by rice coleoptiles during prolonged anoxia: implications for glycolysis, growth and energy utilization. Ann. Bot. (Lond.) 96 (2005) 703-715
7. Loreti E., et al. A genome-wide analysis of the effects of sucrose on gene expression in Arabidopsis seedlings under anoxia. Plant Physiol. 137 (2005) 1130-1138
8. Lasanthi-Kudahettige R., et al. Transcript profiling of anoxic rice coleoptile. Plant Physiol. 144 (2007) 218-231
9. Mertens E. ATP versus pyrophosphate: glycolysis revisited in parasitic protists. Parasitol. Today 9 (1993) 122-126
10. Mertens E. Pyrophosphate-dependent phosphofructokinase, an anaerobic glycolytic enzyme?. FEBS Lett. 285 (1991) 1-5
11. Wood H.G. Some reactions in which inorganic pyrophosphate replaces ATP and serves as a source of energy. Fed. Proc. 36 (1977) 2197-2205
12. Wood H.G., et al. Properties of carboxytransphosphorylase; pyruvate, phosphate dikinase; pyrophosphate-phosphofructikinase and pyrophosphate-acetate kinase and their roles in the metabolism of inorganic pyrophosphate. Adv. Enzymol. Relat. Areas. Mol. Biol. 45 (1977) 85-155
13. Reeves R.E. Metabolism of entamoeba histolytica schaudinn. Adv. Parasitol. 23 (1984) 105-142
14. Muller M., et al. Presence of prokaryotic and eukaryrotic species in all subgroups of the PPi-dependent group II phosphofructokinase protein family. J. Bacteriol. 183 (2001) 6714-6716
15. Chi A., and Kemp R.G. The primordial high energy compound: ATP or inorganic pyrophosphate?. J. Biol. Chem. 275 (2000) 35677-35679
16. Bapteste E., et al. Rampant horizontal gene transfer and phosphor-donor change in the evolution of the phosphofructokinase. Gene 318 (2003) 185-191
17. Slamovits C.H., and Keeling P.J. Pyruvate-phosphate dikinase of oxymonds and parabasalia and the evolution of pyrophosphate-dependent glycolysis in anaerobic eukaryotes. Eukaryot. Cell 5 (2006) 148-154
18. Edwards G.E., et al. Pyruvate, Pi dikinase and NADP-malate dehydrogenase in C4 photosynthesis: properties and mechanism of light/dark regulation. Annu. Rev. Plant Physiol. 36 (1985) 255-286
19. Perata P., et al. Mobilization of endosperm reserves in cereal seeds under anoxia. Ann. Bot. (Lond.) 79 (1997) 49-56
20. Gibbs J., et al. Regulation of alcoholic fermentation in coleoptiles of two rice cultivars differing in tolerance to anoxia. J. Exp. Bot. 51 (2000) 785-796
21. Mertens E., et al. Induction of pyrophosphate:fructose 6-phosphate 1-phosphotransferase by anoxia in rice seedlings. Plant Physiol. 93 (1990) 584-587
22. Kato-Noguchi N. The catalytic direction of pyrophosphate:fructose 6-phosphate 1-phosphotransferase in rice coleoptiles in anoxia. Physiol. Plant. 116 (2002) 345-350
23. Mustroph A., et al. Characterisation of the ATP-dependent phosphofructokinase gene family from Arabidopsis thaliana. FEBS Lett. 581 (2007) 2401-2410
24. Moons A., et al. Low-oxygen stress and water deficit induce cytosolic pyruvate orthophosphate dikinase (PPDK) expression in roots of rice, a C-3 plant. Plant J. 15 (1998) 89-98
25. Mohanty B., et al. Effects of anoxia on growth and carbohydrate metabolism in suspension cultures of soybean and rice. Phytochemistry 34 (1993) 75-82
26. Greenway H., and Gibbs J. Mechanism of anoxia tolerance in plants. II. Energy requirements for maintenance and energy distribution to essential processes. Funct. Plant Biol. 30 (2003) 999-1036
27. Xu K., et al. Sub1A is an ethylene-response-factor-like gene that confers submergence tolerance to rice. Nature 442 (2006) 705-708
28. Perata P., and Voesenek L.A.C.J. Submergence tolerance in rice requires Sub1A, an ethylene-response-factor-like gene. Trends Plant Sci. 12 (2007) 43-46
29. Huang S., et al. Manipulation of ethanol production in anoxic rice coleoptiles by exogenous glucose determines rates of ion fluxes and provides estimates of energy requirements for cell maintenance during anoxia. J. Exp. Bot. 56 (2005) 2453-2463
30. + efflux in the coleoptile of rice seedlings during prolonged anoxia. J. Exp. Bot. 52 (2001) 1507-1517
31. Stitt M. Pyrophosphate as an energy donor in the cytosol of plant cells: an enigmatic alternative to ATP. Bot. Acta 111 (1998) 167-175
32. Plaxton W.C. Plant response to stress: biochemical adaptations to phosphate deficiency. In: Goodman R.M. (Ed). Encyclopedia of Plant and Crop Sciences (2004), Marcel Dekker 976-980
33. Davies J.M., et al. The computed free energy change of hydrolysis of inorganic pyrophosphate and ATP: apparent significance for inorganic-pyrophosphate-driven reactions of intermediary metabolism. Biochim. Biophys. Acta 1141 (1993) 233-250
34. Felle H.H. pH regulation in anoxic plants. Ann. Bot. (Lond.) 96 (2005) 519-532
35. Menegus F., et al. Response to anoxia in rice and wheat seedlings: changes in the pH of intracellular compartments, glucose-6-phosphate level, and metabolic rate. Plant Physiol. 95 (1991) 760-767
36. +-translocating pyrophosphatase is induced by anoxia or chilling in seedlings of rice. Plant Physiol. 108 (1995) 641-649
37. Ricard B., et al. Anaerobic stress induces the transcription and translation of sucrose synthase in rice. Plant Physiol. 95 (1991) 669-674
38. Guglielminetti L., et al. Effect of anoxia on carbohydrate metabolism in rice seedlings. Plant Physiol. 108 (1995) 735-741
39. Liu F., et al. Global transcription profiling reveals comprehensive insight into hypoxic response in Arabidopsis. Plant Physiol. 137 (2005) 1115-1129
40. Klok E.J., et al. Expression profile analysis of the low-oxygen response in Arabidopsis root cultures. Plant Cell 14 (2002) 2481-2494
41. Peltier J.-B., et al. The oligomeric stromal proteome of Arabidopsis thaliana chloroplasts. Mol. Cell. Proteomics 5 (2006) 114-133
42. Parsley K., and Hibberd J.M. The Arabidopsis PPDK gene is transcribed from two promoters to produce differentially expressed transcripts responsible for cytosolic and plastidic proteins. Plant Mol. Biol. 62 (2006) 339-349
43. Chastain C.J., et al. The pyruvate, orthophosphate dikinase regulatory proteins of Arabidopsis possess a novel, unprecedented Ser/Thr protein kinase primary structure. Plant J. 53 (2008) 854-863
44. Hatch M.D., and Slack C.R. A new enzyme for the interconversion of pyruvate and phosphopyruvate and its role in the C4 dicarboxylic acid pathway of photosynthesis. Biochem. J. 106 (1968) 141-147
45. Merchant S.S., et al. The chlamydomonas genome reveals the evolution of key animal and plant functions. Science 318 (2007) 245-251
46. Glackin C.A., and Grula J.W. Organ-specific transcripts of different size and abundance derive from the same pyruvate, orthophosphate dikinase gene in maize. Proc. Natl. Acad. Sci. U. S. A. 87 (1990) 3004-3008
47. Sheen J. Molecular mechanisms underlying the differential expression of maize pyruvate, orthophosphate dikinase genes. Plant Cell 3 (1991) 225-245
48. Agarie S., et al. Expression of C3 and C4 photosynthetic characteristics in the amphibious plant Eleocharis vivipara: structre and analysis of the expression of isogenes for pyruvate, orthophosphate dikinase. Plant Mol. Biol. 34 (1997) 363-369
49. Rosche E., and Westhoff P. Genomic structure and expression of the pyruvate, orthophosphate dikinase gene of the dicotyledonous C4 plant Flaveria trinervia (Asteraceae). Plant Mol. Biol. 29 (1995) 663-678
50. Fisslthaler B., et al. Age-dependent induction of pyruvate, orthophosphate dikinase in Mesembryanthemum crystailinum L. Planta 196 (1995) 492-500
51. Summers J.E., et al. Anoxia tolerance in the aquatic monocot Potamogeton pectinatus: absence of oxygen stimulates elongation in association with an unusually large Pasteur effect. J. Exp. Bot. 51 (2000) 1413-1422
52. Dixon M.H., et al. Physiological and metabolic adaptations of Potamogeton pectinatus L. tubers support rapid elongation of stem tissue in the absence of oxygen. Plant Cell Physiol. 47 (2006) 128-140
53. Ueno O., et al. Photosynthetic characteristics of an amphibious plant, Eleocharis vivipara: expression of C4 and C3 modes in contrasting environments. Proc. Natl. Acad. Sci. U. S. A. 85 (1988) 6733-6737