Sugars and acid invertase mediate the physiological response of Schenkia spicata root cultures to salt stress

Journal of Plant Physiology

Volumn 169, Issue 13, 2012, Pages 1281-1289

  MiŠić, Danijela ^a   Dragićević, Milan ^a   Šiler, Branislav ^a   Nestorović Živković, Jasmina ^a   Maksimović, Vuk ^b   Momčilović, Ivana ^a   Nikolic, Miroslav ^b  

^a UNIVERSITY OF BELGRADE   (Serbia)

^b UNIVERSITY OF BELGRADE   (Serbia)

Author keywords

Acid invertase; Root culture; Salt stress; Soluble sugars; Sugar uptake

Indexed keywords

BETA FRUCTOFURANOSIDASE; SODIUM CHLORIDE; SUCROSE;

ADAPTATION; ARTICLE; BIOLOGICAL MODEL; CARBOHYDRATE METABOLISM; COMPARATIVE STUDY; CULTURE TECHNIQUE; GENETIC VARIABILITY; GENETICS; GENOTYPE; GENTIANACEAE; GROWTH, DEVELOPMENT AND AGING; HALOPHYTE; METABOLISM; PHYSIOLOGICAL STRESS; PHYSIOLOGY; PLANT ROOT; SALINITY;

ADAPTATION, PHYSIOLOGICAL; BETA-FRUCTOFURANOSIDASE; CARBOHYDRATE METABOLISM; CULTURE TECHNIQUES; GENETIC VARIATION; GENOTYPE; GENTIANACEAE; MODELS, BIOLOGICAL; PLANT ROOTS; SALINITY; SALT-TOLERANT PLANTS; SODIUM CHLORIDE; STRESS, PHYSIOLOGICAL; SUCROSE;

SCHENKIA SPICATA;

EID: 84864945953     PISSN: 01761617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jplph.2012.04.018     Document Type: Article

References (44)

1. Balibrea M.E., Dell'Amico J., Bolarin M.C., Perez-Alfocea F. Carbon partitioning and sucrose metabolism in tomato plants growing under salinity. Physiol Plant 2000, 110:503-511.
2. Berger S., Sinha A.K., Roitch T. Plant physiology meets phytopathology: plant primary metabolism and plant-pathogen interactions. J Exp Bot 2007, 58:4019-4026.
3. Bonfig K.B., Gabler A., Simon U.K., Luschin-Ebengreuth N., Hatz M., Berger S., et al. Post-translational depression of invertase activity in source leaves via down-regulation of invertase inhibitor expression is part of the plant defense response. Mol Plant 2010, 3:1037-1048.
4. Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem 1976, 72:248-254.
5. 2] to estimate diffusional and non-diffusional limitations of photosynthetic capacity of salt-stressed olive saplings. Plant Cell Environ 2003, 26:585-594.
6. Dubey R.S. Photosynthesis in plants under stressful conditions. Handbook of Photosynthesis 2005, 717-737. CRC Press/Taylor and Francis Group, New York. 2nd ed. M. Pessarakli (Ed.).
7. Figueiredo S.F.L., Simões C., Albarello N., Viana V.R.C. Rollinia mucosa cell suspension cultures: establishment and growth conditions. Plant Cell Tissue Org Cult 2000, 63:85-92.
8. Godt D.E., Roitsch T. The developmental and organ specific expression of sucrose cleaving enzymes in sugar beet suggests a transition between apoplasmic and symplasmic phloem unloading in the tap roots. Plant Physiol Biochem 2006, 44:656-665.
9. Greiner S., Rausch T., Sonnewald U., Herbers K. Ectopic expression of a tobacco invertase inhibitor homolog prevents cold-induced sweetening of a potato tubers. Nat Biotechnol 1999, 17:708-711.
10. Hayes M.A., Feechan A., Dry I.B. Involvement of abscisic acid in the coordinated regulation of a stress-inducible hexose transporter (VvHT5) and a cell wall invertase in grapevine in response to biotrophic fungal infection. Plant Physiol 2010, 153:211-221.
11. Hill J.P., Germino M.J., Alongi D.A. Carbon-use efficiency in green sinks is increased when a blend of apoplastic fructose and glucose is available for uptake. J Exp Bot 2011, 62:2013-2022.
12. Hothorn M., Van der Ende W., Lammens W., Rybin V., Scheffzek K. Structural insights into the pH-controlled targeting of plant cell-wall invertase by a specific inhibitor protein. Proc Natl Acad Sci U S A 2010, 107:17427-17432.
13. Huang W.X., Cao Y., Huang L.J., Ren C., Xiong Z.T. Differential expression of acid invertase genes in roots of metallicolous and non-metallicolous populations of Rumex japonicas under copper stress. Chemosphere 2011, 10.1016/j.chemosphere.2011.04.053.
14. Husain S.E., Thomas B.J., Kingston-Smith A.H., Foyer C.H. Invertase protein, but not activity, is present throughout development of Lycopersicon esculentum and L. pimpinellifolium fruit. New Phytol 2000, 150:73-81.
15. Iraqi D., Le V.Q., Lamhamedi M.S., Tremblay F.M. Sucrose utilization during somatic embryo development in black spruce: involvement of apoplastic invertase in the tissue and of extracellular invertase in the medium. J Plant Physiol 2005, 162:115-124.
16. Jain M., Chourey P.S., Li Q.B., Pring D.R. Expression of cell wall invertase and several other genes of sugar metabolism in relation to seed development in sorghum (Sorghum bicolor). J Plant Physiol 2008, 165:331-344.
17. Kim J.Y., Mahe A., Brangeon J., Prioul J.L. A maize vacuolar invertase, IVR2, is induced by water stress. Organ/tissue specificity and diurnal modulation of expression. Plant Physiol 2000, 124:71-84.
18. Kingston-Smith A.H., Pollock C.J. Tissue level localization of acid invertase in leaves: an hypothesis for the regulation of carbon export. New Phytol 1996, 134:423-432.
19. Kingston-Smith A.H., Gattier N., Pollock C.J., Foyer C.H. Soluble acid invertase activity in leaves is independent of species differences in leaf carbohydrates, diurnal sugar profiles and paths of phloem loading. New Phytol 1998, 139:283-292.
20. Kretzschmar F.S., Oliveira C.J.F., Braga M.R. Differential sugar uptake by cell suspension cultures of Rudgea jasminoides, a tropical woody Rubiaceae. In Vitro Cell Dev Biol 2007, 43:71-78.
21. López M., Herrera-Carvera J.A., Iribarne C., Tejera N.A., Lluch C. Growth and nitrogen fixation in Lotus japonicas and Medicago truncatula under NaCl stress: nodule carbon metabolism. J Plant Physiol 2008, 165:641-650.
22. 2 reactions as a source of glycolate and their stimulation by hydroxyl radicals. Carbohydr Res 2006, 341:2360-2369.
23. Matthews D., Jones H., Gans P., Coates S., Smith L.M.J. Toxic secondary metabolite production in genetically modified potatoes in response to stress. J Agric Food Chem 2005, 53:7766-7776.
24. MiŠić D., Šiler B., Nestorović Živković J., Simonović A., Maksimović V., Budimir S., et al. Contribution of inorganic cations and organic compounds to osmotic adjustment in root cultures of two Centaurium species differing in tolerance to salt stress. Plant Cell Tissue Org Cult 2012, 108:389-400.
25. Momčilović I., Ristić Z. Expression of chloroplast protein synthesis elongation factor, Ef-Tu, in two lines of maize with contrasting tolerance to heat stress during early stages of plant development. J Plant Physiol 2007, 164:90-99.
26. Munns R. Genes and salt tolerance: bringing them together. New Phytol 2005, 167:645-663.
27. Munns R., Tester M. Mechanisms of salinity tolerance. Ann Rev Plant Biol 2008, 59:651-681.
28. Murashige T., Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol Plant 1962, 15:473-497.
29. Roitch T. Source-sink regulation by sugar and stress. Curr Opin Plant Biol 1999, 2:198-206.
30. Roitsch T., González M.C. Function and regulation of plant invertases: sweet sensations. Trends Plant Sci 2004, 9:606-613.
31. Rosenkranz H., Vogel R., Greiner S., Rausch T. In wounded sugar beet (Beta vulgaris L.) tap-root, hexose accumulation correlates with the induction of a vacuolar invertase isoform. J Exp Bot 2001, 52:2381-2385.
32. Saeedipour S., Moradi F. Comparison of the drought stress responses of tolerant and sensitive wheat cultivars during grain filling: impact of invertase activity on carbon metabolism during kernel development. J Agricult Sci 2011, 3:32-44.
33. Salo D.C., Pacifici R.E., Lin S.W., Giulivi C., Davies K.J.A. Superoxide dismutase undergoes proteolysis and fragmentation following oxidative modification and inactivation. J Biol Chem 1990, 265:11919-11925.
34. Schaarschmidt S., Kopka J., Ludwig-Müller J., Hause B. Regulation of arbuscular mycorrhization by apoplastic invertases: enhanced invertase activity in the leaf apoplast affects the symbiotic interaction. Plant J 2007, 51:390-405.
35. Schwachtje J., Baldwin I.T. Why does herbivore attack reconfigure primary metabolism?. Plant Physiol 2008, 146:845-851.
36. Schwimmer S., Makower R.U., Rorem E.S. Invertase and invertase inhibitor in potato. Plant Physiol 1961, 36:313-316.
37. Sherson S.M., Alford H.L., Forbes S.M., Wallace G., Smith S.M. Roles of cell-wall invertases and monosaccharide transporters in the growth and development of Arabidopsis. J Exp Bot 2003, 54:525-531.
38. Shin K.S., Chakrabarty D., Ko J.Y., Han S.S., Peak K.Y. Sucrose utilization and mineral nutrient uptake during hairy root growth of red beet (Beta vulgaris) in liquid culture. Plant Growth Regul 2003, 39:187-193.
39. Sturm A., Sebkova V., Lorenz K., Hardegger M., Lienhard S., Unger C. Development- and organ-specific expression of the genes for sucrose synthase and three isoenzymes of acid β-fructofuranosidase in carrot. Planta 1995, 195:601-610.
40. Tymowska-Lalanne Z., Kreis M. Expression of the Arabidopsis thaliana invertase gene family. Planta 1998, 207:259-265.
41. van der Sluis W.G. Chemotaxonomical Investigations of the Genera Blackstonia and Centaurium (Gentianaceae). Plant Syst Evol 1985, 149:253-286.
42. Xiang L., Le Roy K., Bolouri-Moghaddam M.R., Vanhaecke M., Lammens W., Rolland F., et al. Exploring the neutral invertase-oxidative stress defense connection in Arabidopsis thaliana. J Exp Bot 2011, 10.1093/jxb/err069.
43. Yativ M., Harary I., Wolf S. Sucrose accumulation in watermelon fruits: genetic variation and biochemical analysis. J Plant Physiol 2010, 167:589-596.
44. Zeng Y., Wu Y., Avigne W.T., Koch K.E. Rapid regression of maize invertases by low oxygen. Invertase/sucrose synthase balance, sugar signaling potential, and seedling survival. Plant Physiol 1999, 121:599-608.