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HORT640 - Metabolic Plant Physiology
References, ADP-glucose pyrophosphorylase
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Bae HH, Herman E, Bailey B, Bae HJ, Sicher R. Exogenous trehalose alters Arabidopsis transcripts involved in cell wall modification, abiotic stress, nitrogen metabolism, and plant defense. Physiol. Plant. 125: 114-126 (2005).
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Baroja-Fernandez E, Munoz FJ, Akazawa T, Pozueta-Romero J. Reappraisal of the currently prevailing model of starch biosynthesis in photosynthetic tissues: a proposal involving the cytosolic production of ADP-glucose by sucrose synthase and occurrence of cyclic turnover of starch in the chloroplast. Plant Cell Physiol. 42: 1311-1320 (2001).
Baroja-Fernandez E, Munoz FJ, Akazawa T, Pozueta-Romero J. Reappraisal of the currently prevailing model of starch biosynthesis in photosynthetic tissues: a proposal involving the cytosolic production of ADP-glucose by sucrose synthase and occurrence of cyclic turnover of starch in the chloroplast. Plant Cell Physiol. 42: 1311-1320 (2001).
Beckles DM, Craig J, Smith AM. ADP-glucose pyrophosphorylase is located in the plastid in developing tomato fruit. Plant Physiol. 126: 261-266 (2001).
Beckles DM, Smith AM, ap Rees T. A cytosolic ADP-glucose pyrophosphorylase is a feature of graminaceous endosperms, but not of other starch-storing organs. Plant Physiol. 125: 818-827 (2001).
Bejar CM, Ballicora MA, Gomez-Casati DF, Iglesias AA, Preiss J. The ADP-glucose pyrophosphorylase from Escherichia coli comprises two tightly bound distinct domains. FEBS Lett. 573: 99-104 (2004).
Bejar CM, Jin X, Ballicora MA, Preiss J. Molecular architecture of the glucose 1-phosphate site in ADP-glucose pyrophosphorylases. J. Biol. Chem. 281: 40473-40484 (2006).
Boehlein SK, Shaw JR, Stewart JD, Hannah LC. Characterization of an autonomously activated plant adenosine diphosphate glucose pyrophosphorylase. Plant Physiol. 149: 318-326 (2009).
Burger BT, Cross JM, Shaw JR, Caren JR, Greene TW, Okita TW, Hannah LC. Relative turnover numbers of maize endosperm and potato tuber ADP-glucose pyrophosphorylases in the absence and presence of 3-phosphoglyceric acid. Planta 217: 449-456 (2003).
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Carlson SJ, Chourey PS, Helentjaris T, Datta R. Gene expression studies on developing kernels of maize sucrose synthase (SuSy) mutants show evidence for a third SuSy gene. Plant Mol. Biol. 49: 15-29 (2002).
Chen BY, Janes HW. Multiple forms of ADP-glucose pyrophosphorylase from tomato fruit. Plant Physiol. 113: 235-241 (1997).
Chen LS, Qi YP, Smith BR, Liu XH. Aluminum-induced decrease in CO2 assimilation in citrus seedlings is unaccompanied by decreased activities of key enzymes involved in CO2 assimilation. Tree Physiol. 25: 317-324 (2005).
Cheng L, Zhou R, Reidel EJ, Sharkey TD, Dandekar AM. Antisense inhibition of sorbitol synthesis leads to up-regulation of starch synthesis without altering CO2 assimilation in apple leaves. Planta 220: 767-776 (2005).
Cid E, Geremia RA, Guinovart JJ, Ferrer JC. Glycogen synthase: towards a minimum catalytic unit? FEBS Lett. 528: 5-11 (2002).
Ciereszko I, Johansson H, Hurry V, Kleczkowski LA. Phosphate status affects the gene expression, protein content and enzymatic activity of UDP-glucose pyrophosphorylase in wild-type and pho mutants of Arabidopsis. Planta 212: 598-605 (2001).
Colleoni C, Dauvillee D, Mouille G, Buleon A, Gallant D, Bouchet B, Morell M, Samuel M, Delrue B, d'Hulst C, Bliard C, Nuzillard JM, Ball S. Genetic and biochemical evidence for the involvement of alpha-1,4 glucanotransferases in amylopectin synthesis. Plant Physiol. 120: 993-1004 (1999).
Cross JM, Clancy M, Shaw JR, Boehlein SK, Greene TW, Schmidt RR, Okita TW, Hannah LC. A polymorphic motif in the small subunit of ADP-glucose pyrophosphorylase modulates interactions between the small and large subunits. Plant J. 41: 501-511 (2005).
Cross JM, Clancy M, Shaw JR, Greene TW, Schmidt RR, Okita TW, Hannah LC. Both subunits of ADP-glucose pyrophosphorylase are regulatory. Plant Physiol. 135: 137-144 (2004).
Denyer K, Dunlap F, Thorbjornsen T, Keeling P, Smith AM. The major form of ADP-glucose pyrophosphorylase in maize endosperm is extra-plastidial. Plant Physiol. 112: 779-785 (1996).
Dian W, Jiang H, Wu P. Evolution and expression analysis of starch synthase III and IV in rice. J. Exp. Bot. 56: 623-632 (2005).
Doan DN, Rudi H, Olsen OA. The allosterically unregulated isoform of ADP-glucose pyrophosphorylase from barley endosperm is the most likely source of ADP-glucose incorporated into endosperm starch. Plant Physiol. 121: 965-975 (1999).
Dumez S, Wattebled F, Dauvillee D, Delvalle D, Planchot V, Ball SG, D'Hulst C. Mutants of Arabidopsis lacking starch branching enzyme II substitute plastidial starch synthesis by cytoplasmic maltose accumulation. Plant Cell 18: 2694-2709 (2006).
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Emes MJ, Neuhaus HE. Metabolism and transport in non-photosynthetic plastids. J. Exp. Bot. 48: 1995-2005 (1997).
Essmann J, Schmitz-Thom I, Schon H, Sonnewald S, Weis E, Scharte J. RNAi-mediated repression of cell wall invertase impairs defense in source leaves of tobacco. Plant Physiol. 147: 1288-1299 (2008).
Farre EM, Geigenberger P, Willmitzer L, Trethewey RN. A possible role for pyrophosphate in the coordination of cytosolic and plastidial carbon metabolism within the potato tuber. Plant Physiol. 123: 681-688 (2000).
Farre EM, Tiessen A, Roessner U, Geigenberger P, Trethewey RN, Willmitzer L. Analysis of the compartmentation of glycolytic intermediates, nucleotides, sugars, organic acids, amino acids, and sugar alcohols in potato tubers using a nonaqueous fractionation method. Plant Physiol. 127: 685-700 (2001).
Fritzius T, Aeschbacher R, Wiemken A, Wingler A. Induction of ApL3 expression by trehalose complements the starch-deficient Arabidopsis mutant adg2-1 lacking ApL1, the large subunit of ADP-glucose pyrophosphorylase. Plant Physiol. 126: 883-889 (2001).
Frueauf JB, Ballicora MA, Preiss J. ADP-glucose pyrophosphorylase from potato tuber: site-directed mutagenesis of homologous aspartic acid residues in the small and large subunits. Plant J. 33: 503-511 (2003).
Fu Y, Ballicora MA, Preiss J. Mutagenesis of the glucose-1-phosphate-binding site of potato tuber ADP-glucose pyrophosphorylase. Plant Physiol. 117: 989-996 (1998).
Geigenberger P. Regulation of sucrose to starch conversion in growing potato tubers. J. Exp. Bot. 54: 457-465 (2003).
Geigenberger P, Geiger M, Stitt M. High-temperature perturbation of starch synthesis is attributable to inhibition of ADP-glucose pyrophosphorylase by decreased levels of glycerate-3-phosphate in growing potato tubers. Plant Physiol. 117: 1307-1316 (1998).
Geigenberger P, Hajirezaei M, Geiger M, Deiting U, Sonnewald U, Stitt M. Overexpression of pyrophosphatase leads to increased sucrose degradation and starch synthesis, increased activities of enzymes for sucrose-starch interconversions, and increased levels of nucleotides in growing potato tubers. Planta 205: 428-437 (1998).
Geigenberger P, Kolbe A, Tiessen A. Redox regulation of carbon storage and partitioning in response to light and sugars. J. Exp. Bot. 56: 1469-1479 (2005).
Geigenberger P, Muller-Rober B, Stitt M. Contribution of adenosine 5'-diphosphoglucose pyrophosphorylase to the control of starch synthesis is decreased by water stress in growing potato tubers. Planta 209: 338-345 (1999).
Geigenberger P, Reimholz R, Geiger M, Merlo L, Canale V, Stitt M. Regulation of sucrose and starch metabolism in potato tubers in response to short-term water deficit. Planta 201: 502-518 (1997).
Geigenberger P, Stitt M. Diurnal changes in sucrose, nucleotides, starch synthesis and AGPS transcript in growing potato tubers that are suppressed by decreased expression of sucrose phosphate synthase. Plant J. 23: 795-806 (2000).
Geigenberger P, Stitt M, Fernie AR. Metabolic control analysis and regulation of the conversion of sucrose to starch in growing potato tubers. Plant Cell Environ. 27: 655-673 (2004).
Geiger M, Haake V, Ludewig F, Sonnewald U, Stitt M. The nitrate and ammonium nitrate supply have a major influence on the response of photosynthesis, carbon metabolism, nitrogen metabolism and growth to elevated carbon dioxide in tobacco. Plant Cell Environ. 22: 1177-1199 (1999).
Georgelis N, Braun EL, Shaw JR, Hannah LC. The two AGPase subunits evolve at different rates in angiosperms, yet they are equally sensitive to activity-altering amino acid changes when expressed in bacteria. Plant Cell 19: 1458-1472 (2007).
Gibon Y, Blasing OE, Palacios-Rojas N, Pankovic D, Hendriks JH, Fisahn J, Hohne M, Gunther M, Stitt M. Adjustment of diurnal starch turnover to short days. Plant J. 39: 847-862 (2004).
Gomez-Casati DF, Iglesias AA. ADP-glucose pyrophosphorylase from wheat endosperm. Purification and characterization of an enzyme with novel regulatory properties. Planta 214: 428-434 (2002).
Greene TW, Hannah LC. Maize endosperm ADP-glucose pyrophosphorylase SHRUNKEN2 and BRITTLE2 subunit interactions. Plant Cell 10: 1295-1306 (1998).
Greene TW, Woodbury RL, Okita TW. Aspartic acid 413 is important for the normal allosteric functioning of ADP-glucose pyrophosphorylase. Plant Physiol. 112: 1315-1320 (1996).
Halford NG, Paul MJ. Carbon metabolite sensing and signalling. Plant Biotechnol. J. 1: 381-398 (2003).
Hannah LC, Shaw JR, Giroux MJ, Reyss A, Prioul JL, Bae JM, Lee JY. Maize genes encoding the small subunit of ADP-glucose pyrophosphorylase. Plant Physiol. 127: 173-183 (2001).
Hausler RE, Schlieben NH, Schulz B, Flugge UI. Compensation of decreased triose phosphate/phosphate translocator activity by accelerated starch turnover and glucose transport in transgenic tobacco. Planta 204: 366-376 (1998).
Hendriks JH, Kolbe A, Gibon Y, Stitt M, Geigenberger P. ADP-glucose pyrophosphorylase is activated by posttranslational redox-modification in response to light and to sugars in leaves of Arabidopsis and other plant species. Plant Physiol. 133: 838-849 (2003).
Hennen-Bierwagen TA, Lin Q, Grimaud F, Planchot V, Keeling PL, James MG, Myers AM. 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. Plant Physiol. 149: 1541-1559 (2009).
Hwang SK, Salamone PR, Okita TW. Allosteric regulation of the higher plant ADP-glucose pyrophosphorylase is a product of synergy between the two subunits. FEBS Lett. 579: 983-990 (2005).
Iglesias AA, Charng YY, Ball S, Preiss J. Characterization of the kinetic, regulatory, and structural properties of ADP-glucose pyrophosphorylase from Chlamydomonas reinhardtii. Plant Physiol. 104: 1287-1294 (1994).
Johnson PE, Patron NJ, Bottrill AR, Dinges JR, Fahy BF, Parker ML, Waite DN, Denyer K. A low-starch barley mutant, Riso 16, lacking the cytosolic small subunit of ADP-glucose pyrophosphorylase, reveals the importance of the cytosolic isoform and the identity of the plastidial small subunit. Plant Physiol. 131: 684-696 (2003).
Jossier M, Bouly JP, Meimoun P, Arjmand A, Lessard P, Hawley S, Grahame Hardie D, Thomas M. SnRK1 (SNF1-related kinase 1) has a central role in sugar and ABA signalling in Arabidopsis thaliana. Plant J. 59: 316-328 (2009).
Kavakli IH, Kato C, Choi SB, Kim KH, Salamone PR, Ito H, Okita TW. Generation, characterization, and heterologous expression of wild-type and up-regulated forms of Arabidopsis thaliana leaf ADP-glucose pyrophosphorylase. Planta 215: 430-439 (2002).
Kawagoe Y, Kubo A, Satoh H, Takaiwa F, Nakamura Y. Roles of isoamylase and ADP-glucose pyrophosphorylase in starch granule synthesis in rice endosperm. Plant J. 42: 164-174 (2005).
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Kolbe A, Oliver SN, Fernie AR, Stitt M, van Dongen JT, Geigenberger P. Combined transcript and metabolite profiling of Arabidopsis leaves reveals fundamental effects of the thiol-disulfide status on plant metabolism. Plant Physiol. 141: 412-422 (2006).
Kram AM, Oostergetel GT, Van Bruggen E. Localization of branching enzyme in potato tuber cells with the use of immunoelectron microscopy. Plant Physiol. 101: 237-243 (1993).
Kwak MS, Oh MJ, Paek KH, Shin JS, Bae JM. Dissected effect of a transit peptide of the ADP-glucose pyrophosphorylase gene from sweetpotato (ibAGP2) in increasing foreign protein accumulation. Plant Cell Rep. 27: 1359-1367 (2008).
Laisk A, Eichelmann H, Oja V. C3 photosynthesis in silico. Photosynth. Res. 90: 45-66 (2006).
Lalonde S, Morse D, Saini HS. Expression of a wheat ADP-glucose pyrophosphorylase gene during development of normal and water-stress-affected anthers. Plant Mol. Biol. 34: 445-453 (1997).
Lee SK, Hwang SK, Han M, Eom JS, Kang HG, Han Y, Choi SB, Cho MH, Bhoo SH, An G, Hahn TR, Okita TW, Jeon JS. Identification of the ADP-glucose pyrophosphorylase isoforms essential for starch synthesis in the leaf and seed endosperm of rice (Oryza sativa L.). Plant Mol. Biol. 65: 531-546 (2007).
Li CR, Gan LJ, Xia K, Zhou X, Hew CS. Responses of carboxylating enzymes, sucrose metabolizing enzymes and plant hormones in a tropical epiphytic CAM orchid to CO2 enrichment. Plant Cell Environ. 25: 369-377 (2002).
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Li CY, Weiss D, Goldschmidt EE. Effects of carbohydrate starvation on gene expression in citrus root. Planta 217: 11-20 (2003).
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Li WD, Duan W, Fan PG, Yan ST, Li SH. Photosynthesis in response to sink-source activity and in relation to end products and activities of metabolic enzymes in peach trees. Tree Physiol. 27: 1307-1318 (2007).
Lin Y, Ulanov AV, Lozovaya V, Widholm J, Zhang G, Guo J, Goodman HM. Genetic and transgenic perturbations of carbon reserve production in Arabidopsis seeds reveal metabolic interactions of biochemical pathways. Planta 225: 153-164 (2006).
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Linebarger CR, Boehlein SK, Sewell AK, Shaw J, Hannah LC. Heat stability of maize endosperm ADP-glucose pyrophosphorylase is enhanced by insertion of a cysteine in the N terminus of the small subunit. Plant Physiol. 139: 1625-1634 (2005).
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Nagai YS, Sakulsingharoj C, Edwards GE, Satoh H, Greene TW, Blakeslee B, Okita TW. Control of starch synthesis in cereals: metabolite analysis of transgenic rice expressing an up-regulated cytoplasmic ADP-glucose pyrophosphorylase in developing seeds. Plant Cell Physiol. 50: 635-643 (2009).
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Rolletschek H, Hajirezaei MR, Wobus U, Weber H. Antisense-inhibition of ADP-glucose pyrophosphorylase in Vicia narbonensis seeds increases soluble sugars and leads to higher water and nitrogen uptake. Planta 214: 954-964 (2002).
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Number of references = 111
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