Acknowledgement
Supported by : Korea Science and Engineering Foundation, Kyung Hee University, Rural Development Administration
References
- ap Rees, T., Green, J.H., and Wilson, P.M. (1985). Pyrophosphate:fructose 6-phosphate 1-phosphotransferase and glycolysis in non-photosynthetic tissues of higher plants. Biochem. J. 227, 299-304 https://doi.org/10.1042/bj2270299
- Baek, I.-S., Park, H.-Y., You, M.K., Lee, J.H., and Kim, J.-K. (2008). Functional conservation and divergence of csb genes that control flowering time and cold response in rice and Arabidopsis. Mol. Cells 26, 368-372
-
Carlisle, S.M., Blakeley, S.D., Hemmingsen, S.M., Trevanion, S.J., Hiyoshi, T., Kruger, N.J., and Dennis, D.T (1990). Pyrophosphate-dependent phosphofructokinase. Conservation of protein sequence between the
$\alpha$ - and$\beta$ -subunits and with the ATPdependent phosphofructokinase. J. Biol. Chem. 265, 18366-18371 - Carnal, N.W., and Black, C.C. (1989). Soluble sugars as the carbohydrate reserve for CAM in pineapple leaves. Implications for the role of pyrophosphate:6-phosphofructokinase in glycolysis. Plant Physiol. 90, 91-100 https://doi.org/10.1104/pp.90.1.91
- Clough, S.J., and Bent, A.F. (1998). Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana, Plant J. 16, 735-743 https://doi.org/10.1046/j.1365-313x.1998.00343.x
-
Cs
$\acute{e}$ ke, C., Weeden, N.F., Buchanan, B.B., and Uyeda, K. (1982). A special fructose bisphosphate functions as a cytoplasmic regulatory metabolite in green leaves. Proc. Natl. Acad. Sci. USA 79, 4322-4326 https://doi.org/10.1073/pnas.79.14.4322 - Dennis, D.T., and Greyson, M.F. (1987). Fructose-6-phosphate metabolism in plants. Physiol. Plantarum. 69, 395-404 https://doi.org/10.1111/j.1399-3054.1987.tb04306.x
- Fernie, A.R., Tauberger, E., Lytovchenko, A., Roessner, U., Willmitzer, L., and Trethewey, R.N. (2002). Antisense repression of cytosolic phosphoglucomutase in potato (Solanum tubrosun) results in severe growth retardation, reduction in tuber number and altered carbon metabolism. Planta 214, 510-520 https://doi.org/10.1007/s004250100644
- Grant, J.J., Chini, A., Basu, D., and Loake, G.J. (2003). Targeted activation tagging of the Arabidopsis NBS_LRR gene, ADR1, conveys resistance to virulent pathogens. Mol. Plant Microbe Interact. 16, 669-680 https://doi.org/10.1094/MPMI.2003.16.8.669
- Groenewald J.H., and Botha F.C. (2008). Down-regulation of pyrophosphate: fructose 6-phosphate 1-phosphotransferase (PFP) activity in sugarcane enhances sucrose accumulation in immature internodes. Transgenic Res. 17, 85-92 https://doi.org/10.1007/s11248-007-9079-x
- Hajdukiewicz, P., Svab, Z., and Maliga, P. (1994). The small, versatile pPZP family of Agrobacterium binary vectors for plant transformation. Plant Mol. Biol. 25, 989-994 https://doi.org/10.1007/BF00014672
- Hajirezaei, M., Sonnewald, U., Viola, R., Carlisle, S., Dennis, D., and Stitt, M. (1994). Transgenic potato plants with strongly decreased expression of pyrophosphate:fructose-6-phosphate phosphotransferase show no visible phenotype and only minor changes in metabolic fluxes in their tubers. Planta 192, 16-30
- Hatzfeld, W.-D., Dancer, J., and Stitt, M. (1989). Direct evidence that pyrophosphate:fructose-6-phosphate phosphotransferase can act as a glycolytic enzyme in plants. FEBS Lett. 254, 215-218 https://doi.org/10.1016/0014-5793(89)81042-7
- Hatzfeld, W.-D., Dancer, J., and Stitt, M. (1990). Fructose-2,6-bisphosphate, metabolites and 'coarse' control of pyrophosphate: fructose-6-phosphate phosphotransferase during triosephosphate cycling in heterotrophic cell-suspension cultures of Chenopodium. Planta 180, 205-211
- Hue, L., and Rider, M.H. (1987). Role of fructose 2,6-bisphosphate in the control of glycolysis in mammalian tissues. Biochem. J. 245, 313-324 https://doi.org/10.1042/bj2450313
- Kowalczyk, S. (1987). The characteristics of pyrophosphate: Dfructose-6-phosphate 1-phosphotransferases from Sanseviaeria trfasciata leaves and Phaseolus coccineus stems. Acta Biochim. Pol. 34, 253-268
- Kruger, N.J., and Dennis, D.T. (1987). Molecular properties of pyrophosphate: fructose-6-phosphate phosphotransferase from potato tuber. Arch. Biochem. Biophys. 256, 273-279 https://doi.org/10.1016/0003-9861(87)90446-2
- Kubota, K., and Ashihara, H. (1990). Identification of nonequilibrium glycolytic reactions in suspension-cultured plant cells. Biochim. Biophys. Acta 1036, 138-142 https://doi.org/10.1016/0304-4165(90)90025-R
- Lu, Y., and Sharkey, T.D. (2004). The role of amylomaltase in maltose metabolism in the cytosol of photosynthetic cells. Planta 218, 466-473 https://doi.org/10.1007/s00425-003-1127-z
- Lee, Y.H., Lee, D.S., Lim, J.M., Yoon, J.M., Bhoo, S.H., Jeon, J.-S., and Hahn, T.-R. (2006). Carbon-partitioning in Arabidopsis is regulated by the fructose 6- phosphate, 2-kinase/fructose 2,6-bisphosphatase enzyme. J. Plant Biol. 49, 70-79 https://doi.org/10.1007/BF03030790
- Mertens, E., Larondelle, Y., and Hers, H.-G. (1990). Induction of pyrophosphate:fructose 6-phosphate 1-phosphotransferase by anoxia in rice seedlings. Plant Physiol. 93, 584-587 https://doi.org/10.1104/pp.93.2.584
- Mustroph, A., Albrecht, G., Hajirezaei, M., Grimm, B., and Biemelt, S. (2005). Low levels of pyrophosphate in transgenic potato plants expressing E. coli pyrophosphatase lead to decreased vitality under oxygen deficiency. Ann. Bot. 96, 717-726 https://doi.org/10.1093/aob/mci223
- Nakamura, N., Suzuki, Y., and Suzuki, H. (1992). Pyrophosphatedependent phosphofructokinase from pollen: properties and possible roles in sugar metabolism. Physiol. Plantarum 86, 616-622 https://doi.org/10.1111/j.1399-3054.1992.tb02178.x
- Nielsen, T.H. (1994). Pyrophosphate:fructose-6-phosphate 1-phosphotransferase from barley seedlings. Isolation, subunit composition and kinetic characterization. Physiol. Plantarum 92, 311-321 https://doi.org/10.1111/j.1399-3054.1994.tb05342.x
- Nielsen, T.H., and Stitt, M. (2001). Tobacco transformants with strongly decreased expression of pyrophosphate:fructose-6-phosphate expression in the base of their young growing leaves contain much higher levels of fructose-2,6-bisphosphate but no major changes in fluxes. Planta 214, 106-116 https://doi.org/10.1007/s004250100591
- Nielsen, T.H., Rung, J.H., and Villadsen, D. (2004). Fructose-2,6-bisphosphate: a traffic signal in plant metabolism. Trends Plant Sci. 9, 556-563 https://doi.org/10.1016/j.tplants.2004.09.004
- Park, S., Cho, M.-H., Bhoo, S.H., Jeon, J.-S., Kwon, Y.-K., and Hahn, T.-R. (2007). Altered sucrose synthesis in rice plants with reduced activity of fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase. J. Plant Biol. 50, 38-43 https://doi.org/10.1007/BF03030598
- Paul, M., Sonnewald, U., Hajirezaei, M., Dennis, D., and Sitt, M. (1995). Transgenic tobacco plants with strongly decreased expression of pyrophosphate:fructose-6-phosphate 1-phosphotransferase do not differ significantly from wild type in photosynthate partitioning, plant growth or their ability to cope with limiting phosphate, limiting nitrogen and suboptimal temperatures. Planta 196, 277-283
- Plaxton, W.C. (1996). The organization and regulation of plant glycolysis. Annu. Rev. Plant Physiol. Plant Mol. Biol. 47, 185-214 https://doi.org/10.1146/annurev.arplant.47.1.185
- Ratcliffe, O.J., Kumimoto, R.W., Wong, B.J., and Riechmann, J.L. (2003). Analysis of the Arabidopsis MADS AFFECTING FLOWERING gene family: MAF2 prevents vernalization by short periods of cold. Plant Cell 15, 1159-1169 https://doi.org/10.1105/tpc.009506
- Rowland, O., Zheng, H., Hepworth, S.R., Lam, P., Jetter, R., and Kunst, L. (2006). `boQ encodes an alcohol-forming fatty acylcoenzyme A reductase involved in cuticular wax production in Arabidopsis. Plant Physiol. 142, 866-877 https://doi.org/10.1104/pp.106.086785
- Smyth, D.A., and Black, C.C. (1984). Measurement of the pyrophosphate content of plant tissues. Plant Physiol. 75, 862-864 https://doi.org/10.1104/pp.75.3.862
-
Snustad, D.P., Haas, N.A., Kopczak, S.D., and Silflow C.D. (1992). The small genome of Arabidopsis contains at least nine expressed
$\beta$ -tubulin genes. Plant Cell 4, 549-556 https://doi.org/10.2307/3869554 - Stitt, M. (1990). Fructose-2,6-bisphosphate as a regulatory molecule in plants. Annu. Rev. Plant Physiol. Plant Biol.41, 153-185 https://doi.org/10.1146/annurev.pp.41.060190.001101
- Stitt, M., Lilley, R.M.C., Gerhardt, R., and Heldt, H.W. (1989). Determination of metabolite levels in specific cells and subcellular compartments of plant leaves. Method Enzymol. 174, 518-522 https://doi.org/10.1016/0076-6879(89)74035-0
- Taji, T., Ohsumi, C., Iuchi, S., Seki, M., Kasuga, M., Kobayashi, M., Yamaguchi-Shinozaki, K., and Shinozaki, K. (2002). Important roles of drought- and cold-inducible genes for galactinol synthase in stress tolerance in Arabidopsis thaliana. Plant J. 29, 417-426 https://doi.org/10.1046/j.0960-7412.2001.01227.x
- Theodorou, M.E., and Plaxton, W.C. (1996). Purification and characterization of pyrophosphate-dependent phosphofructokinase from phosphate-starved Brassica nigra suspension cells. Plant Physiol. 112, 343-351 https://doi.org/10.1104/pp.112.1.343
-
Theodorou, M.E., Cornel, F.A., Duff, S.M., and Plaxton, W.C. (1992). Phosphate starvation-inducible synthesis of the
$\alpha$ -subunit of the pyrophosphate-dependent phosphofructokinase in black mustard suspension cells. J. Biol. Chem. 267, 21901-21905 -
Todd, J.F., Blakeley, S.D., and Dennis, D.T. (1995). Structure of the genes encoding the
$\alpha$ - and$\beta$ -subunits of castor pyrophosphatedependent phosphofructokinase. Gene 152, 181-186 https://doi.org/10.1016/0378-1119(94)00646-A - Turner, W.L., and Plaxton, W.C. (2003). Purification and characterization of pyrophosphate- and ATP-dependent phosphofructokinases from banana fruit. Planta 217, 113-121
- Van Schaftingen, E. (1987). Fructose 2,6-bisphosphate. Adv. Enzymol. Relat. Areas Mol. Biol.59, 315-395
- Van Schaftingen, E., Lederer, B., Bartrons, R., and Hers H.-G. (1982) A kinetic study of pyrophosphate:fructose-6-phosphate phosphotransferase from potato tubers; Application to a microassay of fructose-2,6-bisphosphate. Eur. J. Biochem. 129, 191-195 https://doi.org/10.1111/j.1432-1033.1982.tb07039.x
- von Caemmerer, S., and Farquhar, G.D. (1981). Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves. Planta 153, 376-387 https://doi.org/10.1007/BF00384257
- Walters, R.G., Ibrahim, D.G., Horton, P., and Kruger, N.J. (2004). A mutant of Arabidopsis lacking the triose-phosphate/phosphate translocator reveals the light. Plant Physiol. 135, 891-906 https://doi.org/10.1104/pp.104.040469
- Weiner, H., Stitt, M., and Heldt, H.W. (1987). Subcellular compartmentation of pyrophosphate and alkaline pyrophosphatase in leaves. Biochim. Biophys. Acta 893, 13-21 https://doi.org/10.1016/0005-2728(87)90143-5
- Wong, J.H., Kiss, F., Wu, M.-X., and Buchanan, B.B. (1990). Pyrophosphate fructose-6-P 1-phosphotransferase from tomato fruit. Evidence for change during ripening. Plant Physiol. 94, 499-506 https://doi.org/10.1104/pp.94.2.499
- Wood, H.G. (1985). Inorganic pyrophosphate and polyphosphates as sources of energy. Curr. Top. Cell Regul. 26, 355-369
- Yan, T.-F.J., and Tao, M. (1984). Multiple forms of pyrophosphate:Dfructose-6-phosphate 1-phosphotransferase from wheat seedlings. Regulation by fructose 2,6-bisphosphate. J. Biol. Chem. 259, 5087-5092
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