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Starch turnover: pathways, regulation and role in growth

Stitt, Mark, Zeeman, Samuel C·2012·Current Opinion in Plant Biology
DOI 10.1016/j.pbi.2012.03.016
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Research works printed but not linked: 65

  1. Smith, 2007, Coordination of carbon supply and plant growth, Plant Cell Environ, 30, 1126, 10.1111/j.1365-3040.2007.01708.x · DOI · Paper page
  2. Graf, 2011, Starch and the clock: the dark side of plant productivity, Trends Plant Sci, 16, 169, 10.1016/j.tplants.2010.12.003 · DOI · Paper page
  3. Gibon, 2009, 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, Plant Cell Environ, 32, 859, 10.1111/j.1365-3040.2009.01965.x · DOI · Paper page
  4. Tschoep, 2009, Adjustment of growth and central metabolism to a mild but sustained nitrogen-limitation in Arabidopsis, Plant Cell Environ, 32, 300, 10.1111/j.1365-3040.2008.01921.x · DOI · Paper page
  5. Hummel, 2010, Arabidopsis plants acclimate to water deficit at low cost through changes of carbon usage: an integrated perspective using growth, metabolite, enzyme, and gene expression analysis, Plant Physiol, 154, 357, 10.1104/pp.110.157008 · DOI · Paper page
  6. Caspar, 1985, Alterations in growth, photosynthesis, and respiration in a starchless mutant of Arabidopsis thaliana (L.) deficient in chloroplast phosphoglucomutase activity, Plant Physiol, 79, 11, 10.1104/pp.79.1.11 · DOI · Paper page
  7. Lin, 1988, Isolation and characterization of a starchless mutant of Arabidopsis thaliana (L.) Heynh lacking ADPglucose pyrophosphorylase activity, Plant Physiol, 86, 1131, 10.1104/pp.86.4.1131 · DOI · Paper page
  8. Stitt, 2007, Multilevel genomics analysis of carbon signalling during low carbon availability: coordinating the supply and utilisation of carbon in a fluctuating environment, Funct Plant Biol, 34, 526, 10.1071/FP06249 · DOI
  9. Graf, 2010, Circadian control of carbohydrate availability for growth in Arabidopsis plants at night, Proc Natl Acad Sci U S A, 107, 9458, 10.1073/pnas.0914299107 · DOI · Paper page
  10. Yazdanbakhsh, 2011, Circadian control of root elongation and C partitioning in Arabidopsis thaliana, Plant Cell Environ, 34, 877, 10.1111/j.1365-3040.2011.02286.x · DOI
  11. Pantin, 2011, Control of leaf expansion: a developmental switch from metabolics to hydraulics, Plant Physiol, 156, 803, 10.1104/pp.111.176289 · DOI · Paper page
  12. Rasse, 2006, Leaf carbohydrate controls over Arabidopsis growth and response to elevated CO2: an experimentally based model, New Phytol, 172, 500, 10.1111/j.1469-8137.2006.01848.x · doi:10.1111/j.1469-8137.2006.01848.x
  13. Weise, 2012, Engineering starch accumulation by manipulation of phosphate metabolism of starch, Plant Biotech J, 7, 139
  14. Poorter, 2000, The role of biomass allocation in the growth response of plants to different levels of light, CO2, nutrients and water: a quantitative review, Aust J Plant Physiol, 27, 1191, 10.1071/PP99173_CO · DOI · Paper page
  15. Zeeman, 2010, Starch: its metabolism, evolution, and biotechnological modification in plants, Annu Rev Plant Biol, 61, 209, 10.1146/annurev-arplant-042809-112301 · DOI · Paper page
  16. Tsai, 2009, Starch synthesis in Arabidopsis is achieved by spatial cotranscription of core starch metabolism genes, Plant Physiol, 151, 1582, 10.1104/pp.109.144196 · DOI
  17. Hanson, 1988, A starchless mutant of Nicotiana sylvestris containing a modified plastid phosphoglucomutase, Plant Physiol, 88, 838, 10.1104/pp.88.3.838 · DOI
  18. Harrison, 1998, Evidence that the rug3 locus of pea (Pisum sativum L.) encodes plastidial phosphoglucomutase confirms that the imported substrate for starch synthesis in pea amyloplasts is glucose-6-phosphate, Plant J, 13, 753, 10.1046/j.1365-313X.1998.00077.x · doi:10.1046/j.1365-313x.1998.00077.x
  19. Vriet, 2010, A suite of Lotus japonicus starch mutants reveals both conserved and novel features of starch metabolism, Plant Physiol, 154, 643, 10.1104/pp.110.161844 · DOI
  20. Lytovchenko, 2002, Carbon assimilation and metabolism in potato leaves deficient in plastidial phosphoglucomutase, Planta, 215, 802, 10.1007/s00425-002-0810-9 · doi:10.1007/s00425-002-0810-9
  21. Szydlowski, 2009, Starch granule initiation in Arabidopsis requires the presence of either Class IV or Class III starch synthases, Plant Cell, 21, 2443, 10.1105/tpc.109.066522 · DOI · Paper page
  22. Crumpton-Taylor, 2012, Control of starch granule numbers in Arabidopsis chloroplasts, Plant Physiol, 158, 905, 10.1104/pp.111.186957 · DOI
  23. Vitha, 2000, Interaction of root gravitropism and phototropism in Arabidopsis wild-type and starchless mutants, Plant Physiol, 122, 453, 10.1104/pp.122.2.453 · DOI
  24. Streb, 2009, The debate on the pathway of starch synthesis: a closer look at low-starch mutants lacking plastidial phosphoglucomutase supports the chloroplast-localized pathway, Plant Physiol, 151, 1769, 10.1104/pp.109.144931 · DOI
  25. Munoz, 2005, Sucrose synthase controls both intracellular ADP glucose levels and transitory starch biosynthesis in source leaves, Plant Cell Physiol, 46, 1366, 10.1093/pcp/pci148 · DOI
  26. Barratt, 2009, Normal growth of Arabidopsis requires cytosolic invertase but not sucrose synthase, Proc Natl Acad Sci U S A, 106, 13124, 10.1073/pnas.0900689106 · DOI · Paper page
  27. Fettke, 2011, Glucose-1-phosphate transport into protoplasts and chloroplasts from leaves of Arabidopsis, Plant Physiol, 155, 1723, 10.1104/pp.110.168716 · DOI
  28. Ventriglia, 2008, Two Arabidopsis ADP-glucose pyrophosphorylase large subunits (APL1 and APL2) are catalytic, Plant Physiol, 148, 65, 10.1104/pp.108.122846 · DOI
  29. Edner, 2007, Glucan, water dikinase activity stimulates breakdown of starch granules by plastidial β-amylases, Plant Physiol, 145, 17, 10.1104/pp.107.104224 · DOI · Paper page
  30. Hizukuri, 1983, Phosphorus and amylose branching in rice starch granules, Starch-Stärke, 35, 348, 10.1002/star.19830351004 · DOI
  31. Kötting, 2009, STARCH-EXCESS4 is a laforin-like phosphoglucan phosphatase required for starch degradation in Arabidopsis thaliana, Plant Cell, 21, 334, 10.1105/tpc.108.064360 · DOI
  32. Hejazi, 2010, The laforin-like dual-specificity phosphatase SEX4 from Arabidopsis hydrolyzes both C6- and C3-phosphate esters introduced by starch-related dikinases and thereby affects phase transition of α-glucans, Plant Physiol, 152, 711, 10.1104/pp.109.149914 · DOI
  33. Santelia, 2011, The phosphoglucan phosphatase Like Sex Four2 dephosphorylates starch at the C3-position in Arabidopsis, Plant Cell, 23, 4096, 10.1105/tpc.111.092155 · doi:10.1105/tpc.111.092155
  34. Comparot-Moss, 2010, A putative phosphatase, LSF1, is required for normal starch turnover in Arabidopsis leaves, Plant Physiol, 152, 685, 10.1104/pp.109.148981 · DOI
  35. Fulton, 2008, Beta-AMYLASE4, a noncatalytic protein required for starch breakdown, acts upstream of three active beta-amylases in Arabidopsis chloroplasts, Plant Cell, 20, 1040, 10.1105/tpc.107.056507 · DOI · Paper page
  36. Kötting, 2010, Regulation of starch metabolism: the age of enlightenment?, Curr Opin Plant Biol, 13, 321, 10.1016/j.pbi.2010.01.003 · DOI
  37. Stitt, 2010, Arabidopsis and primary photosynthetic metabolism—more than the icing on the cake, Plant J, 61, 1067, 10.1111/j.1365-313X.2010.04142.x · DOI · Paper page
  38. Hädrich, 2011, Use of TILLING and robotised enzyme assays to generate an allelic series of Arabidopsis thaliana mutants with altered ADP-glucose pyrophosphorylase activity, J Plant Physiol, 168, 1395, 10.1016/j.jplph.2011.01.013 · DOI
  39. Michalska, 2009, NTRC links built-in thioredoxin to light and sucrose in regulating starch synthesis in chloroplasts and amyloplasts, Proc Natl Acad Sci U S A, 106, 9908, 10.1073/pnas.0903559106 · DOI · Paper page
  40. Kolbe, 2005, Trehalose 6-phosphate regulates starch synthesis via posttranslational redox activation of ADP-glucose pyrophosphorylase, Proc Natl Acad Sci U S A, 102, 11118, 10.1073/pnas.0503410102 · DOI · Paper page
  41. Hädrich, 2012, Mutagenesis of cysteine81 prevents dimerization of the APS1 subunit of ADP-glucose pyrophosphorylase and alters diurnal starch turnover in Arabidopsis thaliana leaves, Plant J, 70, 231, 10.1111/j.1365-313X.2011.04860.x · DOI
  42. Harmer, 2000, Orchestrated transcription of key pathways in Arabidopsis by the circadian clock, Science, 290, 2110, 10.1126/science.290.5499.2110 · DOI · Paper page
  43. Smith, 2004, Diurnal changes in the transcriptome encoding enzymes of starch metabolism provide evidence for both transcriptional and post-transcriptional regulation of starch metabolism in Arabidopsis leaves, Plant Physiol, 136, 2687, 10.1104/pp.104.044347 · DOI · Paper page
  44. Lu, 2005, Daylength and circadian effects on starch degradation and maltose metabolism, Plant Physiol, 138, 2280, 10.1104/pp.105.061903 · DOI · Paper page
  45. Usadel, 2008, Global transcript levels respond to small changes of the carbon status during progressive exhaustion of carbohydrates in Arabidopsis rosettes, Plant Physiol, 146, 1834, 10.1104/pp.107.115592 · DOI · Paper page
  46. Gibon, 2006, Integration of metabolite with transcript and enzyme activity profiling during diurnal cycles in Arabidopsis rosettes, Genome Biol, 7, R76, 10.1186/gb-2006-7-8-r76 · DOI · Paper page
  47. Piques, 2009, Ribosome and transcript copy numbers, polysome occupancy and enzyme dynamics in Arabidopsis, Mol Systems Biol, 5, 314, 10.1038/msb.2009.68 · DOI · Paper page
  48. Reinhold, 2011, β-Amylase-like proteins function as transcription factors in Arabidopsis, controlling shoot growth and development, Plant Cell, 23, 1391, 10.1105/tpc.110.081950 · DOI
  49. Nozue, 2007, Rhythmic growth explained by coincidence between internal and external cues, Nature, 448, 358, 10.1038/nature05946 · DOI · Paper page
  50. Nozue, 2006, Diurnal regulation of plant growth, Plant Cell Environ, 29, 396, 10.1111/j.1365-3040.2005.01489.x · DOI
  51. Wiese, 2007, Spatio-temporal leaf growth patterns of Arabidopsis thaliana and evidence for sugar control of the diel leaf growth cycle, New Phytol, 174, 752, 10.1111/j.1469-8137.2007.02053.x · DOI
  52. Poire, 2010, Diel time-courses of leaf growth in monocot and dicot species: endogenous rhythms and temperature effects, J Exp Bot, 61, 1751, 10.1093/jxb/erq049 · doi:10.1093/jxb/erq049
  53. Dixon, 2011, Temporal repression of core circadian genes is mediated through EARLY FLOWERING 3 in Arabidopsis, Curr Biol, 21, 120, 10.1016/j.cub.2010.12.013 · DOI
  54. Helfer, 2011, LUX ARRHYTHMO encodes a nighttime repressor of circadian gene expression in the Arabidopsis core clock, Curr Biol, 21, 126, 10.1016/j.cub.2010.12.021 · DOI · Paper page
  55. Nusinow, 2011, The ELF4-ELF3-LUX complex links the circadian clock to diurnal control of hypocotyl growth, Nature, 475, 398, 10.1038/nature10182 · DOI · Paper page
  56. Pokhilko, 2010, Data assimilation constrains new connections and components in a complex, eukaryotic circadian clock model, Mol Syst Biol, 6, 416, 10.1038/msb.2010.69 · DOI · Paper page
  57. De Veylder, 2007, The ins and outs of the plant cell cycle, Nat Rev Mol Cell Biol, 8, 655, 10.1038/nrm2227 · DOI · Paper page
  58. Henriques, 2010, Arabidopsis S6 kinase mutants display chromosome instability and altered RBR1-E2F pathway activity, EMBO J, 29, 2979, 10.1038/emboj.2010.164 · DOI
  59. Sulpice, 2010, Network analysis of enzyme activities and metabolite levels and their relationship to biomass in a large panel of arabidopsis accessions, Plant Cell, 22, 2872, 10.1105/tpc.110.076653 · DOI
  60. Sulpice, 2009, Starch as a major integrator in the regulation of plant growth, Proc Natl Acad Sci U S A, 106, 10348, 10.1073/pnas.0903478106 · DOI · Paper page
  61. Ni, 2009, Altered circadian rhythms regulate growth vigour in hybrids and allopolyploids, Nature, 457, 327, 10.1038/nature07523 · DOI · Paper page
  62. McDowell, 2011, The interdependence of mechanisms underlying climate-driven vegetation mortality, Trends Ecol Evol, 26, 523, 10.1016/j.tree.2011.06.003 · DOI · Paper page
  63. Hoffman, 2010, Changes in diurnal patterns within the Populus transcriptome and metabolome in response to photoperiod variation, Plant Cell Environ, 33, 1298, 10.1111/j.1365-3040.2010.02148.x · doi:10.1111/j.1365-3040.2010.02148.x
  64. Resman, 2010, Components acting downstream of short day perception regulate differential cessation of cambial activity and associated responses in early and late clones of hybrid poplar, Plant Physiol, 154, 1294, 10.1104/pp.110.163907 · DOI
  65. Berrocal-Lobo, 2011, Identification of a homolog of Arabidopsis DSP4 (SEX4) in chestnut: its induction and accumulation in stem amyloplasts during winter or in response to the cold, Plant Cell Environ, 34, 1693, 10.1111/j.1365-3040.2011.02365.x · doi:10.1111/j.1365-3040.2011.02365.x

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Metadata

Authors
Stitt, M., & Zeeman, S. C.
Venue
Current Opinion in Plant Biology
Publisher
Elsevier BV
Published
2012-06
Volume
15
Issue
3
Pages
282-292
ISSN
1369-5266 (ISSN-L)
DOI
10.1016/j.pbi.2012.03.016
OpenAlex
W2018233263
Cited by
758
References
3
FWCI
5.17
Type
journal article
Language
en
Open access
closed
Licence
www.elsevier.com/tdm/userlicense/1.0/ (tdm)

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Stitt, M., & Zeeman, S. C. (2012). Starch turnover: pathways, regulation and role in growth. Current Opinion in Plant Biology. https://doi.org/10.1016/j.pbi.2012.03.016

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