Cited by 350Plant nutrient uptake and metabolismPhotosynthetic Processes and MechanismsPlant Molecular Biology Research

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Regulation of Starch Biosynthesis in Response to a Fluctuating Environment

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Geigenberger, Peter·2011·Plant Physiology

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Abstract

Starch is the major storage carbohydrate in higher plants, with many important functions. In photosynthesizing leaves, starch accumulates during the day and is remobilized at night to support continued respiration, Suc export, and growth in the dark ([Geiger and Servaites, 1994][1]). In this context

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Gonzalez, E. B., Rolland, F., Thevelein, J. M., & Sheen, J. (2007) · Nature · doi:10.1038/nature06069 · Cited by 1,526
The control of flux.
KACSER, H., & Ja, B. (1973) · PubMed · Cited by 1,455
Starch: its metabolism, evolution, and biotechnological modification in plants
Zeeman, S. C., Kossmann, J., & Smith, A. M. (2010) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042809-112301 · Cited by 1,095
From Bacterial Glycogen to Starch: Understanding the Biogenesis of the Plant Starch Granule
Ball, S. G., & Morell, M. K. (2003) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.54.031902.134927 · Cited by 748
Trehalose Metabolism and Signaling
Paul, M. J., Primavesi, L. F., Jhurreea, D., & Zhang, Y. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092945 · Cited by 727
Sugars and Circadian Regulation Make Major Contributions to the Global Regulation of Diurnal Gene Expression in Arabidopsis
Bläsing, O. E., Gibon, Y., Guenther, M., Höhne, M., Morcuende, R., Osuna, D., Thimm, O., Usadel, B., Scheible, W., & Stitt, M. (2005) · The Plant Cell · doi:10.1105/tpc.105.035261 · Cited by 708
Circadian control of carbohydrate availability for growth in Arabidopsis plants at night
Graf, A., Schlereth, A., Stitt, M., & Smith, A. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914299107 · Cited by 654
Regulation of the Amount of Starch in Plant Tissues by ADP Glucose Pyrophosphorylase
Stark, D. M., Timmerman, K. P., Barry, G. F., Preiss, J., & Kishore, G. M. (1992) · Science · doi:10.1126/science.258.5080.287 · Cited by 652
Sugar-induced increases in trehalose 6-phosphate are correlated with redox activation of ADPglucose pyrophosphorylase and higher rates of starch synthesis in Arabidopsis thaliana
Lunn, J. E., Feil, R., Hendriks, J. H. M., Gibon, Y., Morcuende, R., Osuna, D., Scheible, W., Carillo, P., Hajirezaei, M., & Stitt, M. (2006) · Biochemical Journal · doi:10.1042/bj20060083 · Cited by 620
Inhibition of SNF1-Related Protein Kinase1 Activity and Regulation of Metabolic Pathways by Trehalose-6-Phosphate
Zhang, Y., Primavesi, L. F., Jhurreea, D., Andralojc, P. J., Mitchell, R. A. C., Powers, S. J., Schluepmann, H., Delatte, T., Wingler, A., & Paul, M. J. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.133934 · Cited by 604
Nitrate Acts as a Signal to Induce Organic Acid Metabolism and Repress Starch Metabolism in Tobacco.
Scheible, W., González‐Fontes, A., Lauerer, M., Müller‐Röber, B., Caboche, M. M., & Stitt, M. (1997) · The Plant Cell · doi:10.1105/tpc.9.5.783 · Cited by 601
Response of plant metabolism to too little oxygen
Geigenberger, P. (2003) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(03)00038-4 · Cited by 580
Self-citation
The control of flux
KACSER, H., Burns, J., KACSER, H., & Fell, D. A. (1995) · Biochemical Society Transactions · doi:10.1042/bst0230341 · Cited by 576
Starch synthesis in the cereal endosperm
James, M. G., Denyer, K., & Myers, A. M. (2003) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(03)00042-6 · Cited by 559
Starch as a major integrator in the regulation of plant growth
Ronan Sulpice, A., Pyl, E., Ishihara, H., Trenkamp, S., Steinfath, M., Witucka‐Wall, H., Gibon, Y., Usadel, B., Porée, F., Piques, M., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903478106 · Cited by 553
A Robot-Based Platform to Measure Multiple Enzyme Activities in Arabidopsis Using a Set of Cycling Assays: Comparison of Changes of Enzyme Activities and Transcript Levels during Diurnal Cycles and in Prolonged Darkness[W]
Gibon, Y., Blaesing, O. E., Hannemann, J., Carillo, P., Höhne, M., Hendriks, J. H. M., Palacios, N., Cross, J., Selbig, J., & Stitt, M. (2004) · The Plant Cell · doi:10.1105/tpc.104.025973 · Cited by 552
Alterations in Growth, Photosynthesis, and Respiration in a Starchless Mutant of Arabidopsis thaliana (L.) Deficient in Chloroplast Phosphoglucomutase Activity
Caspar, T., Huber, S. C., & Somerville, C. R. (1985) · PLANT PHYSIOLOGY · doi:10.1104/pp.79.1.11 · Cited by 537
A Novel WRKY Transcription Factor, SUSIBA2, Participates in Sugar Signaling in Barley by Binding to the Sugar-Responsive Elements of theiso1Promoter [W]
Sun, C., Palmqvist, S., Olsson, H., Borén, M., Ahlandsberg, S., & Jansson, C. (2003) · The Plant Cell · doi:10.1105/tpc.014597 · Cited by 529
Starch biosynthesis in cereal endosperm
Jeon, J., Ryoo, N., Hahn, T., Walia, H., & Nakamura, Y. (2010) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2010.03.006 · Cited by 515
Large-Scale Arabidopsis Phosphoproteome Profiling Reveals Novel Chloroplast Kinase Substrates and Phosphorylation Networks
Reiland, S., Messerli, G., Baerenfaller, K., Gerrits, B., Endler, A., Grossmann, J., Gruissem, W., & Baginsky, S. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.138677 · Cited by 470
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Hendriks, J. H. M., Kolbe, A., Gibon, Y., Stitt, M., & Geigenberger, P. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.024513 · Cited by 460
Self-citation
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Satoh‐Nagasawa, N., Nagasawa, N., Malcomber, S. T., Sakai, H., & Jackson, D. P. (2006) · Nature · doi:10.1038/nature04725 · Cited by 459
Starch Synthesis in Potato Tubers Is Regulated by Post-Translational Redox Modification of ADP-Glucose Pyrophosphorylase
Tiessen, A., Hendriks, J. H. M., Stitt, M., Branscheid, A., Gibon, Y., Farré, E. M., & Geigenberger, P. (2002) · The Plant Cell · doi:10.1105/tpc.003640 · Cited by 444
Self-citation
Diurnal Changes in the Transcriptome Encoding Enzymes of Starch Metabolism Provide Evidence for Both Transcriptional and Posttranscriptional Regulation of Starch Metabolism in Arabidopsis Leaves
Smith, S. M., Fulton, D. C., Chia, T., Thorneycroft, D., Chapple, A., Dunstan, H., Hylton, C. M., Zeeman, S. C., & Smith, A. M. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.044347 · Cited by 433
The Glycogen-Binding Domain on the AMPK β Subunit Allows the Kinase to Act as a Glycogen Sensor
McBride, A., Ghilagaber, S., Nikolaev, A., & Hardie, D. G. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2008.11.008 · Cited by 432
Normal growth of Arabidopsis requires cytosolic invertase but not sucrose synthase
Barratt, D. H. P., Derbyshire, P., Findlay, K., Pike, M. J., Wellner, N., Lunn, J. E., Feil, R., Simpson, C. E., Maule, A. J., & Smith, A. M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900689106 · Cited by 432
The Ferredoxin/Thioredoxin System of Oxygenic Photosynthesis
Schürmann, P., & Buchanan, B. B. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.1931 · Cited by 430
Adjustment of diurnal starch turnover to short days: depletion of sugar during the night leads to a temporary inhibition of carbohydrate utilization, accumulation of sugars and post‐translational activation of ADP‐glucose pyrophosphorylase in the following light period
Gibon, Y., Bläsing, O. E., Palacios‐Rojas, N., Panković, D. M., Hendriks, J. H. M., Fisahn, J., Höhne, M., Guenther, M., & Stitt, M. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02173.x · Cited by 413
Trehalose 6-phosphate regulates starch synthesis via posttranslational redox activation of ADP-glucose pyrophosphorylase
Kolbe, A., Tiessen, A., Schluepmann, H., Paul, M. J., Ulrich, S., & Geigenberger, P. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503410102 · Cited by 411
Self-citation
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Fu, F., & Xue, H. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.159517 · Cited by 407
Protein Phosphorylation in Amyloplasts Regulates Starch Branching Enzyme Activity and Protein–Protein Interactions
Tetlow, I. J., Wait, R., Lu, Z., Akkasaeng, R., Bowsher, C., Esposito, S., Kosar‐Hashemi, B., Morell, M. K., & Emes, M. J. (2004) · The Plant Cell · doi:10.1105/tpc.017400 · Cited by 391
Recent developments in understanding the regulation of starch metabolism in higher plants
Tetlow, I. J. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh248 · Cited by 384
Arabidopsis and primary photosynthetic metabolism – more than the icing on the cake
Stitt, M., Lunn, J. E., & Usadel, B. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04142.x · Cited by 357
PhosPhAt: a database of phosphorylation sites in Arabidopsis thaliana and a plant-specific phosphorylation site predictor
Heazlewood, J. L., Durek, P., Hummel, J., Selbig, J., Weckwerth, W., Walther, D., & Schulze, W. X. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm812 · Cited by 347
Molecular Characterization of a Carbon Transporter in Plastids from Heterotrophic Tissues: The Glucose 6-Phosphate/Phosphate Antiporter
Kammerer, B., Fischer, K., Hilpert, B., Schubert, S., Gutensohn, M., Weber, A. P. M., & Flügge, U. (1998) · The Plant Cell · doi:10.1105/tpc.10.1.105 · Cited by 335
Adenosine Diphosphate Glucose Pyrophosphorylase
Ghosh, H. P., & Preiss, J. (1966) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)99747-4 · Cited by 334
Adjustment of growth, starch turnover, protein content and central metabolism to a decrease of the carbon supply when Arabidopsis is grown in very short photoperiods
Gibon, Y., Pyl, E., Ronan Sulpice, A., Lunn, J. E., Höhne, M., Guenther, M., & Stitt, M. (2009) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2009.01965.x · Cited by 331
SnRK1 (SNF1‐related kinase 1) has a central role in sugar and ABA signalling in Arabidopsis thaliana
Jossier, M., Bouly, J., Meimoun, P., Arjmand, A., Lessard, P., Hawley, S. A., Hardie, D. G., & Thomas, M. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03871.x · Cited by 330
Diurnal Regulation of Photosynthetic Carbon Metabolism in C3 Plants
Geiger, D. R., & Servaites, J. C. (1994) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.pp.45.060194.001315 · Cited by 329
Rice NTRC Is a High-Efficiency Redox System for Chloroplast Protection against Oxidative Damage
Pérez-Ruiz, J. M., Spínola, M. C., Kirchsteiger, K., Moreno, J., Sahrawy, M., & Cejudo, F. J. (2006) · The Plant Cell · doi:10.1105/tpc.106.041541 · Cited by 328
Plastidial Thioredoxin z Interacts with Two Fructokinase-Like Proteins in a Thiol-Dependent Manner: Evidence for an Essential Role in Chloroplast Development in Arabidopsis and Nicotiana benthamiana
Arsova, B., Hoja, U., Wimmelbacher, M., Greiner, E., Üstün, Ş., Melzer, M., Petersen, K., Lein, W., & Börnke, F. A. J. (2010) · The Plant Cell · doi:10.1105/tpc.109.071001 · Cited by 314
Enhanced ADP-glucose pyrophosphorylase activity in wheat endosperm increases seed yield
Smidansky, E. D., Clancy, M. A., Meyer, F. D., Lanning, S. P., Blake, N. K., Talbert, L. E., & Giroux, M. J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.022635299 · Cited by 311
The plant thioredoxin system
Gelhaye, É., Rouhier, N., Navrot, N., & Jacquot, J. (2004) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-004-4296-4 · Cited by 303
One of two different ADP-glucose pyrophosphorylase genes from potato responds strongly to elevated levels of sucrose
Müller‐Röber, B., Koßmann, J., Hannah, L. C., Willmitzer, L., & Sonnewald, U. (1990) · Molecular and General Genetics MGG · doi:10.1007/bf00259460 · Cited by 280
Malate Plays a Crucial Role in Starch Metabolism, Ripening, and Soluble Solid Content of Tomato Fruit and Affects Postharvest Softening
Centeno, D. C., Osorio, S., Nunes‐Nesi, A., Bertolo, A. L. F., Carneiro, R. T., Araújo, W. L., Steinhauser, M.-C., Michalska, J., Rohrmann, J., Geigenberger, P., et al. (2011) · The Plant Cell · doi:10.1105/tpc.109.072231 · Cited by 280
Self-citation
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Wuriyanghan, H., Zhang, B., Cao, W., Ma, B., Lei, G., Liu, Y.-F., Wei, W., Wu, H., Chen, L., Chen, H., et al. (2009) · The Plant Cell · doi:10.1105/tpc.108.065391 · Cited by 266
Analysis of Protein Complexes in Wheat Amyloplasts Reveals Functional Interactions among Starch Biosynthetic Enzymes
Tetlow, I. J., Beisel, K. G., Cameron, S., Makhmoudova, A., Liu, F., Bresolin, N. S., Wait, R., Morell, M. K., & Emes, M. J. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.116244 · Cited by 261
Measurement of Subcellular Metabolite Levels in Leaves by Fractionation of Freeze-Stopped Material in Nonaqueous Media
Gerhardt, R., & Heldt, H. W. (1984) · PLANT PHYSIOLOGY · doi:10.1104/pp.75.3.542 · Cited by 260
Analysis of the Compartmentation of Glycolytic Intermediates, Nucleotides, Sugars, Organic Acids, Amino Acids, and Sugar Alcohols in Potato Tubers Using a Nonaqueous Fractionation Method
Farré, E. M., Tiessen, A., Roessner, U., Geigenberger, P., Trethewey, R. N., & Willmitzer, L. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.010280 · Cited by 259
Self-citation
Starch Granule Initiation inArabidopsisRequires the Presence of Either Class IV or Class III Starch Synthases
Szydlowski, N., Ragel, P., Raynaud, S., Lucas, M. M., Roldán, I., Montero, M., Muñoz, F. J., Ovečka, M., Bahaji, A., Planchot, V., et al. (2009) · The Plant Cell · doi:10.1105/tpc.109.066522 · Cited by 255
Control of Arabidopsis meristem development by thioredoxin-dependent regulation of intercellular transport
Benitez‐Alfonso, Y., Heck, M. L., Roman, A. K. S., Thomas, C. L., Maule, A. J., Hearn, S., & Jackson, D. P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808717106 · Cited by 251
NTRC links built-in thioredoxin to light and sucrose in regulating starch synthesis in chloroplasts and amyloplasts
Michalska, J., Zauber, H., Buchanan, B. B., Cejudo, F. J., & Geigenberger, P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903559106 · Cited by 251
Self-citation
Redox regulation of carbon storage and partitioning in response to light and sugars
Geigenberger, P., Kolbe, A., & Tiessen, A. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/eri178 · Cited by 241
Self-citation
Evidence that SNF1‐related kinase and hexokinase are involved in separate sugar‐signalling pathways modulating post‐translational redox activation of ADP‐glucose pyrophosphorylase in potato tubers
Tiessen, A., Prescha, K., Branscheid, A., Palacios‐Rojas, N., McKibbin, R. S., Halford, N. G., & Geigenberger, P. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01823.x · Cited by 234
Self-citation
Altered plastidic ATP/ADP‐transporter activity influences potato (Solanum tuberosumL.) tuber morphology, yield and composition of tuber starch
Tjaden, J., Möhlmann, T., Kampfenkel, K., & Neuhaus, G. H. A. E. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00317.x · Cited by 229
Regulation of starch metabolism: the age of enlightenment?
Kötting, O., Koßmann, J., Zeeman, S. C., & Lloyd, J. R. (2010) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2010.01.003 · Cited by 221
Starch Biosynthetic Enzymes from Developing Maize Endosperm Associate in Multisubunit Complexes
Hennen‐Bierwagen, T. A., Liu, F., Marsh, R. S., Kim, S., Gan, Q., Tetlow, I. J., Emes, M. J., James, M. G., & Myers, A. M. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.116285 · Cited by 219
Seed yield and plant biomass increases in rice are conferred by deregulation of endosperm ADP-glucose pyrophosphorylase
Smidansky, E. D., Martin, J. M., Hannah, C. L., Fischer, A. M., & Giroux, M. J. (2003) · Planta · doi:10.1007/s00425-002-0897-z · Cited by 214
Proteins from Multiple Metabolic Pathways Associate with Starch Biosynthetic Enzymes in High Molecular Weight Complexes: A Model for Regulation of Carbon Allocation in Maize Amyloplasts
Hennen‐Bierwagen, T. A., Lin, Q., Grimaud, F., Planchot, V., Keeling, P. L., James, M. G., & Myers, A. M. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.135293 · Cited by 210
Biosynthesis of Starch and Its Regulation
Preiss, J. (1988) · Elsevier eBooks · doi:10.1016/b978-0-08-092615-5.50012-6 · Cited by 200
Dynamic Plastid Redox Signals Integrate Gene Expression and Metabolism to Induce Distinct Metabolic States in Photosynthetic Acclimation inArabidopsis
Bräutigam, K., Dietzel, L., Kleine, T., Ströher, E., Wormuth, D., Dietz, K., Radke, D., Wirtz, M., Hell, R., Dörmann, P., et al. (2009) · The Plant Cell · doi:10.1105/tpc.108.062018 · Cited by 197
Self-citation
Regulation of spinach SNF1‐related (SnRK1) kinases by protein kinases and phosphatases is associated with phosphorylation of the T loop and is regulated by 5′‐AMP
Sugden, C., Crawford, R. M., Halford, N. G., & Hardie, D. G. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00532.x · Cited by 195
Biosynthesis of Starch and Its Regulation
Preiss, J. (1982) · Springer eBooks · doi:10.1007/978-3-642-68275-9_10 · Cited by 193
Redox-Modulation of Chloroplast Enzymes
Scheibe, R. (1991) · PLANT PHYSIOLOGY · doi:10.1104/pp.96.1.1 · Cited by 193
The complexities of starch biosynthesis in cereal endosperms
Hannah, L. C., & James, M. (2008) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2008.02.013 · Cited by 191
The Subunit Structure of Potato Tuber ADPglucose Pyrophosphorylase
Okita, T. W., Nakata, P. A., Anderson, J. M., Sowokinos, J. R., Morell, M. K., & Preiss, J. (1990) · PLANT PHYSIOLOGY · doi:10.1104/pp.93.2.785 · Cited by 190
Phosphorylation and 14‐3‐3 binding of Arabidopsis trehalose‐phosphate synthase 5 in response to 2‐deoxyglucose
Harthill, J. E., Meek, S. E. M., MORRICE, N. A., Peggie, M. W., Borch, J., Wong, B. H. C., & MacKintosh, C. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02780.x · Cited by 182
Prospects for increasing starch and sucrose yields for bioethanol production
Smith, A. M. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03468.x · Cited by 182
Nitrate Acts as a Signal to Induce Organic Acid Metabolism and Repress Starch Metabolism in Tobacco
Scheible, W., González‐Fontes, A., Lauerer, M., Müller‐Röber, B., Caboche, M. M., & Stitt, M. (1997) · The Plant Cell · doi:10.2307/3870432 · Cited by 182
A complete ferredoxin/thioredoxin system regulates fundamental processes in amyloplasts
Balmer, Y., Vensel, W. H., Cai, N., Manieri, W., Schürmann, P., Hurkman, W. J., & Buchanan, B. B. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511040103 · Cited by 180
Activation of the Potato Tuber ADP-glucose Pyrophosphorylase by Thioredoxin
Ballicora, M. A., Frueauf, J. B., Fu, Y., Schürmann, P., & Preiss, J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.2.1315 · Cited by 179
Control analysis of photosynthate partitioning
Neuhaus, H. E., & Stitt, M. D. (1990) · Planta · doi:10.1007/bf02411398 · Cited by 179
Starch content and yield increase as a result of altering adenylate pools in transgenic plants
Regierer, B., Fernie, A. R., Springer, F., Perez‐Melis, A., Andrea Leisse, A., Koehl, K., Willmitzer, L., Geigenberger, P., & Koßmann, J. (2002) · Nature Biotechnology · doi:10.1038/nbt760 · Cited by 173
Self-citation
The amylose extender mutant of maize conditions novel protein-protein interactions between starch biosynthetic enzymes in amyloplasts
Liu, F., Makhmoudova, A., Lee, E. A., Wait, R., Emes, M. J., & Tetlow, I. J. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp297 · Cited by 170
Production of high‐starch, low‐glucose potatoes through over‐expression of the metabolic regulator SnRK1
McKibbin, R. S., Muttucumaru, N., Paul, M. J., Powers, S. J., Burrell, M. M., Coates, S. A., Purcell, P. C., Tiessen, A., Geigenberger, P., & Halford, N. G. (2006) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2006.00190.x · Cited by 169
Self-citation
Regulation of sucrose to starch conversion in growing potato tubers
Geigenberger, P. (2002) · Journal of Experimental Botany · doi:10.1093/jxb/erg074 · Cited by 167
Self-citation
Trehalose-6-Phosphate Synthase/Phosphatase Regulates Cell Shape and Plant Architecture in Arabidopsis
Chary, S. N., Hicks, G. R., Choi, Y. G., Carter, D., & Raikhel, N. V. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.107441 · Cited by 162
Proteome and phosphoproteome analysis of starch granule-associated proteins from normal maize and mutants affected in starch biosynthesis
Grimaud, F., Rogniaux, H., James, M. G., Myers, A. M., & Planchot, V. (2008) · Journal of Experimental Botany · doi:10.1093/jxb/ern198 · Cited by 159
Mechanism of Reductive Activation of Potato Tuber ADP-glucose Pyrophosphorylase
Fu, Y., Ballicora, M. A., Leykam, J. F., & Preiss, J. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.39.25045 · Cited by 153
Metabolic control analysis and regulation of the conversion of sucrose to starch in growing potato tubers
Geigenberger, P., Stitt, M. D., & Fernie, A. R. (2004) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2004.01183.x · Cited by 146
Self-citation
Expression of the potato tuber ADP-glucose pyrophosphorylase in Escherichia coli.
Iglesias, A. Á., Barry, G. F., Meyer, C. R., Bloksberg, L. N., Nakata, P. A., Greene, T. W., Laughlin, M. J., Okita, T. W., Kishore, G. M., & Preiss, J. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)54044-8 · Cited by 144
THE EXPRESSION OF MENDELIAN FACTORS IN THE GAMETOPHYTE OF MAIZE
Mangelsdorf, P. C., & Jones, D. F. (1926) · Genetics · doi:10.1093/genetics/11.5.423 · Cited by 141
Genes driving potato tuber initiation and growth: identification based on transcriptional changes using the POCI array
Kloosterman, B., Koeyer, D. L. D., Griffiths, R., Flinn, B. S., Steuernagel, B., Scholz, U., Sonnewald, S., Sonnewald, U., Bryan, G. J., Prat, S., et al. (2008) · Functional & Integrative Genomics · doi:10.1007/s10142-008-0083-x · Cited by 136
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Authors: Geigenberger, P.
Affiliations: Ludwig-Maximilians-Universität München (DE)
Corresponding author: Geigenberger, Peter
ORCID: Geigenberger, Peter
Venue: Plant Physiology
Publisher: Oxford University Press (OUP)
Published: 2011-03-01
Volume: 155
Issue: 4
Pages: 1566-1577
ISSN: 0032-0889 (ISSN-L)
1532-2548
DOI: 10.1104/pp.110.170399
PMC: PMC3091114
OpenAlex: W1990319852
Cited by: 348
References: 123
Citations by year: 2026: 18 · 2025: 15 · 2024: 20 · 2023: 12 · 2022: 21 · 2021: 22 · 2020: 19 · 2019: 27 · 2018: 24 · 2017: 25 · 2016: 32 · 2015: 30 · 2014: 21 · 2013: 28 · 2012: 23
FWCI: 2.68
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
Locations: PLANT PHYSIOLOGY (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant nutrient uptake and metabolism
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
Keywords: starch biosynthesis, environmental variability, sucrose export, dark respiration, storage carbohydrates
MeSH terms: Light, Mitochondria, Plants, Protein Processing, Post-Translational, Starch, Transcription, Genetic, Gene Expression Regulation, Plant, Carbohydrate Metabolism, Metabolic Networks and Pathways

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Regulation of Starch Biosynthesis in Response to a Fluctuating Environment

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