CoChat
Sign Up
Cited by 66Seed Germination and PhysiologyPlant nutrient uptake and metabolismPlant Stress Responses and Tolerance

Seed quality and carbon primary metabolism.

Open access
Domergue, Jean‐Baptiste, Abadie, Cyril, Limami, Anis, Way, Danielle, Tcherkez, Guillaume·2019·Plant, Cell & Environment
DOI 10.1111/pce.13618
Open this paper in CoChat — free accountOpen PDF

Abstract

Improving seed quality is amongst the most important challenges of contemporary agriculture. In fact, using plant varieties with better germination rates that are more tolerant to stress during seedling establishment may improve crop yield considerably. Therefore, intense efforts are currently being devoted to improve seed quality in many species, mostly using genomics tools. However, despite its considerable importance during seed imbibition and germination processes, primary carbon metabolism in seeds is less studied. Our knowledge of the physiology of seed respiration and energy generation and the impact of these processes on seed performance have made limited progress over the past three decades. In particular, (isotope‐assisted) metabolomics of seeds has only been assessed occasionally, and there is limited information on possible quantitative relationships between metabolic fluxes and seed quality. Here, we review the recent literature and provide an overview of potential links between metabolic efficiency, metabolic biomarkers, and seed quality and discuss implications for future research, including a climate change context.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1111/pce.13618

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

No references could be resolved yet.

Research works printed but not linked: 118

  1. Abdul-Baki, A. A., & Anderson, J. D. (1973). Relationship between decarboxylation of glutamic acid and vigor in soybean seed. Crop Science, 13, 227-232. https://doi.org/10.2135/cropsci1973. · DOI
  2. 0011183X001300020023x · DOI
  3. Ainsworth, E., & Long, S. (2004). What have we learned from 15 years of free-air CO 2 enrichment (FACE)? A meta-analytic review of the responses of photosynthesis, canopy properties and plant production to rising CO 2 . New Phytologist, 165, 351-372. https://doi.org/ 10.1111/j.1469-8137.2004.01224.x · DOI · Paper page
  4. Al-Ani, A., Bruzau, F., Raymond, P., Saint-Ges, V., Leblanc, J. M., & Pradet, A. (1985). Germination, respiration, and adenylate energy charge of seeds at various oxygen partial pressures. Plant Physiology, 79, 885-890. https://doi.org/10.1104/pp.79.3.885 · DOI
  5. Andalo, C., Godelle, B., Lefranc, M., Mousseau, M., & Till-Brottaud, I. (1996). Elevated CO 2 decreases seed germination in Arabidopsis thaliana. Global Change Biology, 2, 129-135. https://doi.org/10.1111/ j.1365-2486.1996.tb00057.x · DOI
  6. Anderson, J. D. (1977). Adenylate metabolism of embryonic axes from deteriorated soybean seeds. Plant Physiology, 59, 610-614. https:// doi.org/10.1104/pp.59.4.610 · DOI
  7. Anstine, W., Jacobsen, J. V., Scandalios, J. G., & Varner, J. E. (1970). Deu- terium oxide as a density label of peroxidases in germinating barley embryos. Plant Physiology, 45, 148-152. https://doi.org/10.1104/ pp.45.2.148 · DOI
  8. Ap Rees, T., & Hill, S. (1994). Metabolic control analysis of plant metabo- lism. Plant, Cell & Environment, 17, 587-599. https://doi.org/10.1111/ j.1365-3040.1994.tb00151.x · DOI
  9. Ashihara, H., & Matsumura, H. (1977). Changes in the activity and the function of the pentose phosphate pathway during germination of black gram (Phaseolus mungo) seeds. International Journal of Biochemis- try, 8, 461-471.
  10. Begcy, K., Mariano, E. D., Mattiello, L., Nunes, A. V., Mazzafera, P., Maia, I. G., & Menossi, M. (2011). An Arabidopsis mitochondrial uncoupling pro- tein confers tolerance to drought and salt stress in transgenic tobacco plants. PLoS ONE, 6, e23776. https://doi.org/10.1371/journal. pone.0023776 · DOI
  11. Bewley, J. D., & Black, M. (1982). Physiology and biochemistry of seeds in relation to germination. Volume 2: Viability, dormancy, and environmental control. Berlin: Springer.
  12. Bloom, A., Burger, M., Asensio, J., & Cousins, A. (2010). Carbon dioxide enrichment inhibits nitrate assimilation in wheat and Arabidopsis. Sci- ence, 328, 899-903. https://doi.org/10.1126/science.1186440 · DOI
  13. Cantrell, R. P., Hodges, H. F., & Keim, W. F. (1972). Relationship between plant respiration and seedling vigor in Zea mays L. Crop Sci- ence, 12, 214-216. https://doi.org/10.2135/cropsci1972.0011183X 001200020020x · DOI
  14. Cao, D. D., Hu, J., Zhu, S. J., Hu, W. M., & Knapp, A. (2010). Relationship between changes in endogenous polyamines and seed quality during development of sh2 sweet corn (Zea mays L.) seed. Scientia Horticulturae, 123, 301-307. https://doi.org/10.1016/j.scienta. 2009.10.006 · DOI
  15. Catusse, J., Meinhard, J., Job, C., Strub, J.-M., Fischer, U., Pestsova, E., … Job, D. (2011). Proteomics reveals potential biomarkers of seed vigor in sugarbeet. Proteomics, 11, 1569-1580. https://doi.org/10.1002/ pmic.201000586 · DOI
  16. Catusse, J., Strub, J.-M., Job, C., Van Dorsselaer, A., & Job, D. (2008). Pro- teome-wide characterization of sugarbeet seed vigor and its tissue specific expression. Proceedings of the National Academy of Sciences, 105, 10262-10267. https://doi.org/10.1073/pnas.0800585105 · DOI
  17. Chen, S. S. C., & Varner, J. E. (1969). Metabolism of 14 C-maltose in Avena fatua seeds during germination. Plant Physiology, 44, 770-774. https://doi.org/10.1104/pp.44.5.770 · DOI
  18. Chibani, K., Ali-Rachedi, S., Job, C., Job, D., Jullien, M., & Grappin, P. (2006). Proteomic analysis of seed dormancy in Arabidopsis. Plant Physiology, 142, 1493-1510. https://doi.org/10.1104/pp.106.087452 · DOI
  19. Ching, T. M. (1973). Adenosine triphosphate content and seed vigor. Plant Physiology, 51, 400-402. https://doi.org/10.1104/pp.51.2.400 · DOI
  20. Ching, T. M., & Danielson, R. (1972). Seedling vigor and adenosine triphos- phate level of lettuce seeds. Proceedings of the Association of Official Seed Analysts, 62, 116-124.
  21. Ciais, P., Sabine, C., Bala, G., Bopp, L., Brovkin, V., Canadell, J., … Heimann, M. (2013). Carbon and other biogeochemical cycles. In M. Tignor, S. Allen, J. Boshung, A. Nauels, Y. Xia, V. Bex, & P. Midgley (Eds.), Climate change 2013: The physical science basis. Contribution of working group I to the fifth assessment report of the intergovernamental panel on climate change. Cambridge: Cambridge University Press.
  22. Corbineau, F., & Côme, D. (1995). Control of seed germination and dor- mancy by the gaseous environment. In J. Kigel, & G. Galili (Eds.), Seed development and germination (pp. 397-424). New York: CRC Press.
  23. Corbineau, F., Gay-Mathieu, C., Vinel, D., & Côme, D. (2002). Decrease in sunflower (Helianthus annuus) seed viability caused by high tempera- ture as related to energy metabolism, membrane damage and lipid composition. Physiologia Plantarum, 116, 489-496. https://doi.org/ 10.1034/j.1399-3054.2002.1160407.x · DOI
  24. Corbineau, F., Ozbingol, N., Vinel, D., & Côme, D. (2000). Improvement of tomato seed germination by osmopriming as related to energy metab- olism. In Seed biology: Advances and applications: Proceedings of the sixth international workshop on seeds (p. 467). Mérida (Mexico): CABI.
  25. Criddle, R. S., Breidenbach, R. W., & Hansen, L. D. (1991). Plant calorime- try: How to quantitatively compare apples and oranges. Thermochimica Acta, 193, 67-90. https://doi.org/10.1016/0040- 6031(91)80175-I · DOI · Paper page
  26. Day, D. A., Neuburger, M., & Douce, R. (1984). Activation of NAD-linked malic enzyme in intact plant mitochondria by exogenous coenzyme A. Archives of Biochemistry and Biophysics, 231, 233-242. https://doi. org/10.1016/0003-9861(84)90383-7 · DOI
  27. De Marchi, U., Checchetto, V., Zanetti, M., Teardo, E., Soccio, M., Formentin, E., … Szabò, I. (2010). ATP-sensitive cation-channel in wheat (Triticum durum Desf.): Identification and characterization of a plant mitochondrial channel by patch-clamp. Cellular Physiology and Bio- chemistry, 26, 975-982. https://doi.org/10.1159/000324010 · DOI
  28. D'Hooghe, P., Dubousset, L., Gallardo, K., Kopriva, S., Avice, J.-C., & Trouverie, J. (2014). Evidence for proteomic and metabolic adaptations associated with alterations of seed yield and quality in sulfur-limited Brassica napus L. Molecular and Cellular Proteomics, 13, 1165-1183. https://doi.org/10.1074/mcp.M113.034215 · DOI
  29. Drake, B., Gonzalez-Meler, M., & Long, S. (1997). More efficient plants: A consequence of rising atmospheric CO 2 ? Annual Review of Plant Physi- ology and Plant Molecular Biology, 48, 609-639. https://doi.org/ 10.1146/annurev.arplant.48.1.609 · DOI
  30. Duke, E., & Doehlert, D. (1996). Effects of heat stress on enzyme activities and transcription levels in developing maize kernels grown in culture. Environmental and Experimental Botany, 36, 199-208. https://doi.org/ 10.1016/0098-8472(96)01004-0 · DOI
  31. Dürr, E., Brunel-Muguet, S., Girousse, C., Larmure, A., Larré, C., Rolland- Sabaté, A., & Wagner, M.-H. (2018). Changes in seed composition of wheat (Triticum aestivum) and pea (Pisum sativum) when exposed to high temperatures during grain filling and maturation. Crop & Pasture Science, 69, 374-386. https://doi.org/10.1071/CP17397 · DOI
  32. Eastmond, P. J., & Graham, I. A. (2001). Re-examining the role of the glyoxylate cycle in oilseeds. Trends in Plant Science, 6, 72-78. https:// doi.org/10.1016/S1360-1385(00)01835-5 · DOI
  33. Ellis, N., Hattori, C., Cheema, J., Donarski, J., Charlton, A., Dickinson, M., … Domoney, C. (2018). NMR metabolomics defining genetic variation in pea seed metabolites. Frontiers in Plant Science, 9, 1022-1022. https://doi.org/10.3389/fpls.2018.01022 FAO (2013). Seed and seed quality: Technical information for FAO emergency staff. Rome: Food and Agriculture Organization (FAO). · DOI
  34. Fedorova, M., Bollineni, R. C., & Hoffmann, R. (2014). Protein carbonyla- tion as a major hallmark of oxidative damage: Update of analytical strategies. Mass Spectrometry Reviews, 33, 79-97. https://doi.org/ 10.1002/mas.21381 · DOI
  35. Fell, D. A. (1992). Metabolic control analysis: A survey of its theoretical and experimental development. Biochemical Journal, 286, 313-333. https:// doi.org/10.1042/bj2860313 · DOI · Paper page
  36. Ferguson, J. M., TeKrony, D. M., & Egli, D. B. (1990). Changes during early seed and axes deterioration: I. Seed quality and mitochondrial respira- tion. Crop Science, 30, 175-179. https://doi.org/10.2135/ cropsci1990.0011183X003000010038x · DOI
  37. Galland, M., Huguet, R., Arc, E., Cueff, G., Job, D., & Rajjou, L. (2014). Dynamic proteomics emphasizes the importance of selective mRNA translation and protein turnover during Arabidopsis seed germination. Molecular and Cellular Proteomics, 13, 252-268. https://doi.org/ 10.1074/mcp.M113.032227 · DOI · Paper page
  38. Gallardo, K., Job, C., Groot, S. P. C., Puype, M., Demol, H., Vandekerckhove, J., & Job, D. (2002). Importance of methionine biosynthesis for Arabidopsis seed germination and seedling growth. Physiologia Plantarum, 116, 238-247. https://doi.org/10.1034/j.1399-3054. 2002.1160214.x · DOI
  39. Grafahrend-Belau, E., Schreiber, F., Koschützki, D., & Junker, B. H. (2009). Flux balance analysis of barley seeds: A computational approach to study systemic properties of central metabolism. Plant Physiology, 149, 585-598. https://doi.org/10.1104/pp.108.129635 · DOI
  40. Grass, L., & Burris, J. S. (1995). Effect of heat stress during seed develop- ment and maturation on wheat (Triticum durum) seed quality. II. Mitochondrial respiration and nucleotide pools during early germina- tion. Canadian Journal of Botany, 75, 831-839.
  41. Hampton, J. G., Boelt, B., Rolston, M. P., & Chastain, T. G. (2012). Effects of elevated CO 2 and temperature on seed quality. The Journal of Agricul- tural Science, 151, 154-162.
  42. Han, Z., Ku, L., Zhang, Z., Zhang, J., Guo, S., Liu, H., … Chen, Y. (2014). QTLs for seed vigor-related traits identified in maize seeds germinated under artificial aging conditions. PLoS ONE, 9, e92535. https://doi.org/ 10.1371/journal.pone.0092535 · DOI
  43. He, H., Willems, L. A. J., Batushansky, A., Fait, A., Hanson, J., Nijveen, H., … Bentsink, L. (2016). Effects of parental temperature and nitrate on seed performance are reflected by partly overlapping genetic and metabolic pathways. Plant and Cell Physiology, 57, 473-487. https://doi.org/ 10.1093/pcp/pcv207 · DOI
  44. He, Y., Cheng, J., He, Y., Yang, B., Cheng, Y., Yang, C., … Wang, Z. (2019). Influence of isopropylmalate synthase OsIPMS1 on seed vigour associated with amino acid and energy metabolism in rice. Plant Bio- technology Journal, 17, 322-337. https://doi.org/10.1111/pbi.12979 · DOI
  45. Högy, P., Franzaring, J., Schwadorf, K., Breuer, F., Schütze, W., & Fangmeier, A. (2010). Effects of free-air CO 2 enrichment on energy traits and seed quality of oilseed rape. Agriculture, Ecosystems and Envi- ronment, 139, 239-244. https://doi.org/10.1016/j.agee.2010.08.009 · DOI
  46. Högy, P., Keck, M., Niehaus, K., Franzaring, J., & Fangmeier, A. (2010). Effects of atmospheric CO 2 enrichment on biomass, yield and low molecular weight metabolites in wheat grain. Journal of Cereal Science, 52, 215-220. https://doi.org/10.1016/j.jcs.2010.05.009 · DOI
  47. Högy, P., Wieser, H., Köhler, P., Schwadorf, K., Breuer, J., & Franzaring, J. (2009). Effects of elevated CO 2 on grain yield and quality of wheat: Results from a 3-year free-air CO 2 enrichment experiment. Plant Biol- ogy, 11, 60-69. https://doi.org/10.1111/j.1438-8677.2009.00230.x · DOI
  48. Iyer, V. V., Sriram, G., Fulton, D. B., Zhou, R., Westgate, M. E., & Shanks, J. V. (2008). Metabolic flux maps comparing the effect of temperature on protein and oil biosynthesis in developing soybean cotyledons. Plant, Cell & Environment, 31, 506-517. https://doi.org/10.1111/j.1365- 3040.2008.01781.x · DOI
  49. Izdorczyk, C., Nguyen, T., Jo, S., Sons, S., Tuan, P., & Ayele, B. (2018). Spa- tiotemporal modulation of abscisic acid and gibberellin metabolism and signalling mediates the effects of suboptimal and supraoptimal temper- atures on seed germination in wheat (Triticum aestivum L.). Plant, Cell and Environment, 41, 1022-1037. https://doi.org/10.1111/pce.12949 · DOI
  50. Jablonski, L., Wang, X., & Curtis, P. (2002). Plant reproduction under ele- vated CO 2 conditions: A meta-analysis of reports. New Phytologist, 156, 9-26. https://doi.org/10.1046/j.1469-8137.2002.00494.x · DOI
  51. Jabrin, S., Ravanel, S., Gambonnet, B., Douce, R., & Rébeillé, F. (2003). One- carbon metabolism in plants. Regulation of tetrahydrofolate synthesis during germination and seedling development. Plant Physiology, 131, 1431-1439. https://doi.org/10.1104/pp.016915 · DOI
  52. Joosen, R. V. L., Arends, D., Li, Y., Willems, L. A. J., Keurentjes, J. J. B., Ligterink, W., … Hilhorst, H. W. M. (2013). Identifying genotype-by- environment interactions in the metabolism of germinating Arabidopsis seeds using generalized genetical genomics. Plant Physiology, 162, 553-566. https://doi.org/10.1104/pp.113.216176 · DOI
  53. Keeling, P., Banisadr, R., Barone, L., Wasserman, B., & Singletary, G. (1994). Effect of temperature on enzymes in the pathway of starch biosynthe- sis in developing wheat and maize grain. Australian Journal of Plant Physiology, 21, 807-827.
  54. Keigley, P., & Mullen, R. (1986). Changes in soybean seed quality from high temperature during seed fill and maturation. Crop Science, 26, 1212-1216. https://doi.org/10.2135/cropsci1986.0011183X 002600060028x · DOI
  55. Kibinza, S., Vinel, D., Côme, D., Bailly, C., & Corbineau, F. (2006). Sunflower seed deterioration as related to moisture content during ageing, energy metabolism and active oxygen species scavenging. Physiologia Plantarum, 128, 496-506. https://doi.org/10.1111/j.1399-3054. 2006.00771.x · DOI
  56. Komatsu, T., Ohishi, R., Shino, A., Akashi, K., & Kikuchi, J. (2014). Multi- spectroscopic analysis of seed quality and 13 C-stable-isotopologue monitoring in initial growth metabolism of Jatropha curcas L. Metabo- lites, 4, 1018-1033. https://doi.org/10.3390/metabo4041018 · DOI
  57. Lawlor, D., & Mitchell, R. (1991). The effects of increasing CO 2 on crop photosynthesis and productivity: A review of field studies. Plant, Cell and Environment, 14, 807-818. https://doi.org/10.1111/j.1365- 3040.1991.tb01444.x · DOI
  58. Lemonnier, P., & Ainsworth, E. (2018). Crop responses to rising [CO 2 ] and global climate change. In S. Yada, R. Redden, J. FHatfield, A. Ebert, & D. Hunter (Eds.), Food security and climate change. Wiley-Blackwell: Hoboken. https://doi.org/10.1002/9781119180661.ch3 · DOI
  59. Leprince, O., Harren, F. J. M., Buitink, J., Alberda, M., & Hoekstra, F. A. (2000). Metabolic dysfunction and unabated respiration precede the loss of membrane integrity during dehydration of germinating radicles. Plant Physiology, 122, 597-608. https://doi.org/10.1104/pp.122.2.597 · DOI
  60. Li, T., Zhang, Y., Wang, D., Liu, Y., Dirk, L. M. A., Goodman, J., … Zhao, T. (2017). Regulation of seed vigor by manipulation of raffinose family oli- gosaccharides in maize and Arabidopsis thaliana. Molecular Plant, 10, 1540-1555. https://doi.org/10.1016/j.molp.2017.10.014 · DOI
  61. Li, Z., Peng, Y., Zhang, X.-Q., Ma, X., Huang, L.-K., & Yan, Y.-H. (2014). Exogenous spermidine improves seed germination of white clover under water stress via involvement in starch metabolism, antioxidant defenses and relevant gene expression. Molecules, 19, 18003-18024. https://doi.org/10.3390/molecules191118003 · DOI
  62. Liu, Y., Han, C., Deng, X., Liu, D., Liu, N., & Yan, Y. (2018). Integrated phys- iology and proteome analysis of embryo and endosperm highlights complex metabolic networks involved in seed germination in wheat (Triticum aestivum L.). Journal of Plant Physiology, 229, 63-76. https:// doi.org/10.1016/j.jplph.2018.06.011 · DOI
  63. Longo, C. P. (1968). Evidence for de novo synthesis of isocitratase and malate synthesis in germinating peanut cotyledons. Plant Physiology, 43, 660-664. https://doi.org/10.1104/pp.43.4.660 · DOI
  64. Lonien, J., & Schwender, J. (2009). Analysis of metabolic flux phenotypes for two Arabidopsis mutants with severe impairment in seed storage lipid synthesis. Plant Physiology, 151, 1617-1634. https://doi.org/ 10.1104/pp.109.144121 · DOI
  65. Lunn, G., & Madsen, E. (1981). ATP-levels of germinating seeds in relation to vigor. Physiologia Plantarum, 53, 164-169. https://doi.org/10.1111/ j.1399-3054.1981.tb04127.x · DOI
  66. Manickavasagan, A., Jayas, D. S., White, N. D. G., & Paliwal, J. (2010). Wheat class identification using thermal imaging. Food and Bioprocess Technology, 3, 450-460. https://doi.org/10.1007/s11947-008-0110-x · DOI
  67. Manickavasagan, A., Jayas, D. S., White, N. D. G., & Paliwal, J. (2008). Tech- nical note: Wheat class identification using thermal imaging: A potential innovative technique. Transactions of the ASABE, 51, 649-651. https://doi.org/10.13031/2013.24362 · DOI
  68. Melkus, G., Rolletschek, H., Fuchs, J., Radchuk, V., Grafahrend-Belau, E., Sreenivasulu, N., … Borisjuk, L. (2011). Dynamic 13 C/ 1 H NMR imaging uncovers sugar allocation in the living seed. Plant Biotechnology Journal, 9, 1022-1037. https://doi.org/10.1111/j.1467-7652.2011.00618.x · DOI
  69. Melkus, G., Rolletschek, H., Radchuk, R., Fuchs, J., Rutten, T., Wobus, U., … Borisjuk, L. (2009). The metabolic role of the legume endosperm: A noninvasive imaging study. Plant Physiology, 151, 1139-1154. https://doi.org/10.1104/pp.109.143974 · DOI
  70. Min, C. W., Kim, Y. J., Gupta, R., Kim, S. W., Han, W. Y., Ko, J. M., … Kim, S. T. (2016). High-throughput proteome analysis reveals changes of pri- mary metabolism and energy production under artificial aging treatment in Glycine max seeds. Applied Biological Chemistry, 59, 841-853. https://doi.org/10.1007/s13765-016-0234-z · DOI
  71. Min, C. W., Lee, S. H., Cheon, Y. E., Han, W. Y., Ko, J. M., Kang, H. W., … Kim, S. T. (2017). In-depth proteomic analysis of Glycine max seeds dur- ing controlled deterioration treatment reveals a shift in seed metabolism. Journal of Proteomics, 169, 125-135. https://doi.org/ 10.1016/j.jprot.2017.06.022 · DOI
  72. Monjardino, P., Smith, A., & Jones, R. (2005). Heat stress effects on protein accumulation of maize endosperm. Crop Science, 45, 1203-1210. https://doi.org/10.2135/cropsci2003.0122 · DOI
  73. Munz, E., Rolletschek, H., Oeltze-Jafra, S., Fuchs, J., Guendel, A., Neuberger, T., … Borisjuk, L. (2017). A functional imaging study of ger- minating oilseed rape seed. New Phytologist, 216, 1181-1190. https:// doi.org/10.1111/nph.14736 · DOI
  74. Ogé, L., Bourdais, G., Bove, J., Collet, B., Godin, B., Granier, F., … Grappin, P. (2008). Protein repair L-isoaspartyl methyltransferase 1 is involved in both seed longevity and germination vigor in Arabidopsis. The Plant Cell, 20, 3022-3037. https://doi.org/10.1105/tpc.108.058479 · DOI
  75. Pagamas, P., & Nawata, E. (2008). Sensitive stages of fruit and seed devel- opment of chili pepper (Capsicum annuum L. var. Shishito) exposed to high-temperature stress. Scientia Horticulturae, 117, 21-25. https:// doi.org/10.1016/j.scienta.2008.03.017 · DOI
  76. Pastore, D., Fratianni, A., Di Pede, S., & Passarella, S. (2000). Effects of fatty acids, nucleotides and reactive oxygen species on durum wheat mitochondria. FEBS Letters, 470, 88-92. https://doi.org/10.1016/ S0014-5793(00)01292-8 · DOI
  77. Pastore, D., Trono, D., Laus, M. N., Di Fonzo, N., & Flagella, Z. (2007). Pos- sible plant mitochondria involvement in cell adaptation to drought stress: A case study: Durum wheat mitochondria. Journal of Experimen- tal Botany, 58, 195-210. https://doi.org/10.1093/jxb/erl273 · DOI
  78. Penfield, S., Li, Y., Gilday, A. D., Graham, S., & Graham, I. A. (2006). Arabidopsis ABA INSENSITIVE4 regulates lipid mobilization in the embryo and reveals repression of seed germination by the endosperm. The Plant Cell, 18, 1887-1899. https://doi.org/10.1105/tpc. 106.041277 · DOI
  79. Perl, M. (1986). ATP synthesis and utilization in the early stage of seed ger- mination in relation to seed dormancy and quality. Physiologia Plantarum, 66, 177-182. https://doi.org/10.1111/j.1399-3054.1986. tb01253.x · DOI
  80. Pesis, E., & Ng, T. J. (1984). The role of anaerobic respiration in germinating muskmelon seeds: I. In relation to seed lot quality. Journal of Experimen- tal Botany, 35, 356-365.
  81. Potokina, E., Sreenivasulu, N., Altschmied, L., Michalek, W., & Graner, A. (2002). Differential gene expression during seed germination in barley (Hordeum vulgare L.). Functional and Integrative Genomics, 2, 28-39. https://doi.org/10.1007/s10142-002-0050-x · DOI
  82. Puntarulo, S., Beconi, M. T., Sánchez, R. A., & Boveris, A. (1987). Oxidative activities in soybean embryonic axes during germination. Plant Science, 52, 33-39. https://doi.org/10.1016/0168-9452(87)90102-6 · DOI
  83. Puntarulo, S., Sánchez, R. A., & Boveris, A. (1988). Hydrogen peroxide metabolism in soybean embryonic axes at the onset of germination. Plant Physiology, 86, 626-630. https://doi.org/10.1104/pp.86.2.626 · DOI
  84. Qin, W., Yang, C., Iqbal, N., Deng, J., Zhang, J., Shu, K., … Liu, J. (2017). Application of targeted 1 H-NMR profiling to assess the seed vitality of soybean [Glycine max (L.) Merr.]. Analytical Methods, 9, 1792-1799. https://doi.org/10.1039/C6AY02867E · DOI
  85. Rajjou, L., & Debeaujon, I. (2008). Seed longevity: Survival and mainte- nance of high germination ability of dry seeds. Comptes Rendus Biologies, 331, 796-805. https://doi.org/10.1016/j.crvi.2008.07.021 · DOI
  86. Rajjou, L., Duval, M., Gallardo, K., Catusse, J., Bally, J., Job, C., & Job, D. (2012). Seed germination and vigor. Annual Review of Plant Biology, 63, 507-533. https://doi.org/10.1146/annurev-arplant-042811- 105550 · DOI
  87. Rajjou, L., Lovigny, Y., Groot, S. P. C., Belghazi, M., Job, C., & Job, D. (2008). Proteome-wide characterization of seed aging in Arabidopsis: A com- parison between artificial and natural aging protocols. Plant Physiology, 148, 620-641. https://doi.org/10.1104/pp.108.123141 · DOI
  88. Saisho, D., Nakazono, M., Lee, K.-H., Tsutsumi, N., Akita, S., & Hirai, A. (2001). The gene for alternative oxidase-2 (AOX2) from Arabidopsis thaliana consists of five exons unlike other AOX genes and is tran- scribed at an early stage during germination. Genes & Genetic Systems, 76, 89-97. https://doi.org/10.1266/ggs.76.89 · DOI
  89. Sattler, S. E., Gilliland, L. U., Magallanes-Lundback, M., Pollard, M., & DellaPenna, D. (2004). Vitamin E is essential for seed longevity and for preventing lipid peroxidation during germination. The Plant Cell, 16, 1419-1432. https://doi.org/10.1105/tpc.021360 · DOI
  90. Schwender, J., & Ohlrogge, J. B. (2002). Probing in vivo metabolism by sta- ble isotope labeling of storage lipids and proteins in developing Brassica napus embryos. Plant Physiology, 130, 347-361. https://doi.org/ 10.1104/pp.004275 · DOI
  91. Seifter, E. (1954). The occurrence of coenzyme A in plants. Plant Physiol- ogy, 29, 403-406. https://doi.org/10.1104/pp.29.5.403 · DOI
  92. Sew, Y. S., Ströher, E., Fenske, R., & Millar, A. H. (2016). Loss of mitochon- drial malate dehydrogenase activity alters seed metabolism impairing seed maturation and post-germination growth in Arabidopsis. Plant Physiology, 171, 849-863. https://doi.org/10.1104/pp.16.01654 · DOI
  93. Sheteiwy, M., Shen, H., Xu, J., Guan, Y., Song, W., & Hu, J. (2017). Seed polyamines metabolism induced by seed priming with spermidine and 5-aminolevulinic acid for chilling tolerance improvement in rice (Oryza sativa L.) seedlings. Environmental and Experimental Botany, 137, 58-72. https://doi.org/10.1016/j.envexpbot.2017.02.007 · DOI
  94. Shinohara, T., Hampton, G., & Hill, M. (2006a). Effects of the field environ- ment before and after seed physiological maturity on hollow heart occurrence in garden pea (Pisum sativum). New Zealand Journal of Crop and Horticultural Science, 34, 247-255. https://doi.org/10.1080/ 01140671.2006.9514414 · DOI
  95. Shinohara, T., Hampton, G., & Hill, M. (2006b). Location of deterioration within garden pea (Pisum sativum) cotyledons is associated with the timing of exposure to high temperature. New Zealand Journal of Crop and Horticultural Science, 34, 299-309. https://doi.org/10.1080/ 01140671.2006.9514420 · DOI
  96. Soba, D., Ben Mariem, S., Fuertes-Mendizabal, T., Mendez-Espinoza, A., Gilard, F., Gonzalez-Murua, C., … Aranjuelo, I. (2019). Metabolic effects of elevated CO 2 on wheat grain development and composition. Journal of Agricultural and Food Chemistry, n/a, n/a-n/a. In press
  97. Tahir, I., & Nakata, N. (2005). Remobilization of nitrogen and carbohydrate from stem of bread wheat in response to heat stress during grain filling. Journal of Agronomy and Crop Science, 191, 106-115. https://doi.org/ 10.1111/j.1439-037X.2004.00127.x · DOI
  98. Terroine, E., Bonnet, R., & Joessel, P. (1924). L'énergie de croissance: II. La germination. Bulletin de la Société de Chimie Biologique, 6, 357-393.
  99. Thomas, J., Boote, K., Allen, L., Gallo-Meagher, M., & Davis, J. (2003). Ele- vated temperature and carbon dioxide effects on soybean seed composition and transcript abundance. Crop Science, 43, 1548-1557. https://doi.org/10.2135/cropsci2003.1548 · DOI
  100. Thomas, J., Prasad, P., Boote, K., & Allen, L. (2009). Seed composition, seedling emergence and early seedling vigour of red kidney bean seed produced at elevated temperature and carbon dioxide. Journal of Agronomy and Crop Science, 195, 148-156. https://doi.org/10.1111/ j.1439-037X.2008.00348.x · DOI
  101. Tilton, G. B., Wedemeyer, W. J., Browse, J., & Ohlrogge, J. (2006). Plant coenzyme A biosynthesis: Characterization of two pantothenate kinases from Arabidopsis. Plant Molecular Biology, 61, 629-642. https://doi.org/10.1007/s11103-006-0037-4 · DOI
  102. Vadivambal, R., Chelladurai, V., Jayas, D. S., & White, N. D. G. (2010). Detection of sprout-damaged wheat using thermal imaging. Applied Engineering in Agriculture, 26, 999-1004. https://doi.org/10.13031/ 2013.35900 · DOI
  103. Vandewalle, I., & Olsson, R. (1983). The γ-aminobutyric acid shunt in ger- minating Sinapis alba seeds. Plant Science Letters, 31, 269-273. https://doi.org/10.1016/0304-4211(83)90065-2 · DOI
  104. Villanueva, V. R., Adlakha, R. C., & Cantera-Soler, A. M. (1978). Changes in polyamine concentration during seed germination. Phytochemistry, 17, 1245-1249. https://doi.org/10.1016/S0031-9422(00)94565-5 · DOI
  105. Walker-Simmons, M., & Sesing, J. (1990). Temperature effects on embry- onic abscisic acid levels during development of wheat grain dormancy. Journal of Plant Growth Regulation, 9, 51-56. https://doi. org/10.1007/BF02041941 · DOI
  106. Wang, W.-Q., Cheng, H.-Y., Møller, I. M., & Song, S.-Q. (2012). The role of recovery of mitochondrial structure and function in desiccation toler- ance of pea seeds. Physiologia Plantarum, 144, 20-34. https://doi.org/ 10.1111/j.1399-3054.2011.01518.x · DOI
  107. Wang, W.-Q., Liu, S.-J., Song, S.-Q., & Møller, I. M. (2015). Proteomics of seed development, desiccation tolerance, germination and vigor. Plant Physiology and Biochemistry, 86, 1-15. https://doi.org/10.1016/j. plaphy.2014.11.003 · DOI
  108. Way, D., LaDeau, S., McCarthy, H., Clark, J., Oren, R., Finzi, A., & Jackson, R. (2010). Greater seed production in elevated CO2 is not accompanied by reduced seed quality in Pinus taeda L. Global Change Biology, 16, 1046-1056. https://doi.org/10.1111/j.1365-2486.2009. 02007.x · DOI
  109. Wei, Y., Xu, H., Diao, L., Zhu, Y., Xie, H., Cai, Q., … Xie, H. (2015). Protein repairl-isoaspartyl methyltransferase 1 (PIMT1) in rice improves seed longevity by preserving embryo vigor and viability. Plant Molecular Biology, 89, 475-492. https://doi.org/10.1007/ s11103-015-0383-1 · DOI
  110. Wilhelm, E., Mullen, R., Keeling, P., & Singletary, G. (1999). Heat stress during grain filling in maize: Effects on kernel growth and metabolism. Crop Science, 39, 1733-1741. https://doi.org/10.2135/ cropsci1999.3961733x · DOI
  111. Wimalasekera, R. (2015). Role of seed quality in improving crop yields. In K. Hakeem (Ed.), Crop production and global environmental issues (pp. 153-168). Cham: Springer. https://doi.org/10.1007/978-3-319- 23162-4_6 · DOI
  112. Woodstock, L. W., Furman, K., & Leffler, H. R. (1985). Relationship between weathering deterioration and germination, respiratory metabolism, and mineral leaching from cottonseeds. Crop Science, 25, 459-466. https:// doi.org/10.2135/cropsci1985.0011183X002500030008x · DOI
  113. Xia, Q., Ponnaiah, M., Cueff, G., Rajjou, L., Prodhomme, D., Gibon, Y., … El-Maarouf-Bouteau, H. (2018). Integrating proteomics and enzymatic profiling to decipher seed metabolism affected by temperature in seed dormancy and germination. Plant Science, 269, 118-125. https://doi.org/10.1016/j.plantsci.2018.01.014 · DOI
  114. Yacoubi, R., Job, C., Belghazi, M., CHaibi, W., & Job, D. (2011). Toward characterizing seed vigor in alfalfa through proteomic analysis of germination and priming. Journal of Proteome Research, 10, 3891-3903. https://doi.org/10.1021/pr101274f · DOI
  115. Yan, S., Huang, W., Gao, J., Fu, H., & Liu, J. (2018). Comparative metabolomic analysis of seed metabolites associated with seed storability in rice (Oryza sativa L.) during natural aging. Plant Physiology and Biochemistry, 127, 590-598. https://doi.org/10.1016/j. plaphy.2018.04.020 · DOI
  116. Yin, X., Xin, W., & Komatsu, S. (2018). Phosphoproteomics: Protein phos- phorylation in regulation of seed germination and plant growth. Current Protein and Peptide Science, 19, 401-412. https://doi.org/ 10.2174/1389203718666170209151048 · DOI
  117. Zhang, H., Wang, W.-Q., Liu, S.-J., Møller, I. M., & Song, S.-Q. (2015). Pro- teome analysis of poplar seed vigor. PLoS ONE, 10, e0132509. https:// doi.org/10.1371/journal.pone.0132509 · DOI
  118. Zhou, Y., Cui, M., Yin, Q., Deng, M., Hao, Y., Huang, X., & Luo, L. (2018). Analysis of coffee seed vigor by extractive electrospray ionization mass spectrometry. Analytical Methods, 10, 867-873. https://doi.org/ 10.1039/C7AY02403G How to cite this article: Domergue J-B, Abadie C, Limami A, Way D, Tcherkez G. Seed quality and carbon primary metabo- lism. Plant Cell Environ. 2019;42:2776-2778. https://doi.org/ 10.1111/pce.13618 · DOI

Cited by

Sorted by citations

Authors
Domergue, J., Abadie, C., Limami, A., Way, D., & Tcherkez, G.
Affiliations
  • Institut Agro Rennes-Angers (FR)
  • Australian National University (AU)
Corresponding author
Tcherkez, Guillaume
ORCID
Venue
Plant, Cell & Environment
Publisher
Wiley
Published
2019-08-12
Volume
42
Issue
10
Pages
2776-2788
ISSN
  • 0140-7791 (ISSN-L)
  • 1365-3040
DOI
10.1111/pce.13618
OpenAlex
W2963558199
Cited by
66
References
0
Citations by year
2026: 10 · 2025: 13 · 2024: 12 · 2023: 7 · 2022: 9 · 2021: 8 · 2020: 6 · 2019: 1
FWCI
0.54
Type
journal article
Language
en
Open access
Licence
onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations
  • Plant Cell & Environment (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
Funders
  • Research School of Biology, Australian National University
  • Universite Angers
Topics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Seed Germination and Physiology
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant nutrient uptake and metabolism
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Stress Responses and Tolerance
Keywords
seed quality, primary carbon metabolism, seed respiration, seed germination, seedling establishment, metabolic flux, metabolic biomarkers, seed imbibition, climate change
MeSH terms
Carbon, Plants, Seeds, Biomarkers, Germination, Seedlings, Metabolic Networks and Pathways, Climate Change

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review