Abstract
This experiment was designed to determine the relationship between the ultrastructure of the embryo cells and the changes in antioxidant enzymatic activities and lipid peroxidation in oat (Avena sativa L.) seeds with different moisture contents (4, 10 and 16 %) that were aged for 0, 8, 16, 24, 32 and 40 days in 45 °C. The results showed that the declining in the germination percentage and integrity of cell ultrastructure in oat aged seeds were presented during the aged process, and these changes would be enhanced by the higher moisture content. There were consequent changes for biochemical reactions and lipid peroxidation exhibited. For oat seeds with 4 and 10 % moisture content, SOD and CAT were much more sensitive than APX at the early stages of imbibition after mild ageing, the activities of SOD, CAT, APX and MDHAR at 4 h of imbibition decreased significantly (P < 0.05) after being aged from 32 to 40 days. On the contrary, MDA and H2O2 contents both did not increase further. Upon imbibition the activities of DHAR and GR increased after mild ageing, declined after further ageing and maintained a stable level after ageing from 24 to 40 days at those moisture levels. Both activities were higher after ageing at 4 % moisture content than at 10 %. The decline in integrity of ultrastructural cells was related with accumulation of H2O2 during seed ageing, and favoured by the decrease of SOD, CAT, APX and MDHAR activities after imbibition. The activities of antioxidant enzymes and contents of MDA and H2O2 in oat seeds with 16 % moisture content all gradually decreased after ageing from 8 to 40 days, also the ultrastructure of embryo cells was severely damaged. Its ultrastructure was destroyed much more quickly in the seeds with higher moisture content. The level of moisture content could accelerate the seed deterioration, and mitochondrial damages were probably the main reason for oat seed ageing. However, the activities of antioxidant enzymes were the key factor to repair the damage from lipid peroxidation and to maintain the integrity of cell ultrastructure for oat aged seeds during imbibition.
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Abbreviations
- APX:
-
Ascorbate peroxidase
- AsA:
-
Ascorbate
- CAT:
-
Catalase
- CM:
-
Cytoplasmic membrane
- CW:
-
Cell wall
- DHA:
-
Dehydroascorbate
- DHAR:
-
Dehydroascorbate reductase
- GPX:
-
Glutathione peroxidase
- GR:
-
Glutathione reductase
- GSH:
-
Glutathione
- GSSG:
-
Oxidized glutathione
- M:
-
Mitochondria
- MDA:
-
Malondialdehyde
- MDHAR:
-
Monodehydroascorbate reductase
- N:
-
Nucleus
- NM:
-
Nuclear membrane
- ROS:
-
Reactive oxygen species
- SOD:
-
Superoxide dismutase
References
Anuradha G, Ajay KG, Inder SS (2003) Changes in oxidative stress enzymes during artificial ageing in cotton (Gossypium hirsutum L.) seeds. J Plant Physiol 160:1093–1100
Arrigoni O, Dipiero S, Borraccino G (1981) Ascorbate free radical reductase: a key enzyme of the ascorbic acid system. FEBS Lett 125:242–244
Bailly C, Benamar A, Corbineau F, Côme D (1996) Changes in malondialdehyde content and superoxide dismutase, catalase and glutathione reductase activities in sunflower seeds as related to deterioration during accelerated aging. Physiol Plant 97:104–110
Bazin J, Langlade N, Vincourt P, Arribat S, Balzergue S, EI-Maarouf-Bouteau H, Bailly C (2011) Targeted mRNA oxidation regulates sunflower seed dormancy alleviation during dry after-ripening. Plant Cell 23:2196–2208
Bewley JD, Bradford KJ, Hilhorst HWM, Nonogaki H (2013) Seeds: Physiology of development, germination and dormancy, 3rd edn. Springer Press, New York, pp 341–374
Chen ZH, Wang Z, Yun XJ, Li XF, Gao HW (2011) Physiological and biochemical responses of ultra-dry storage of Elymus dahuricus seeds. Afr J Biotechnol 10:14862–14867
Chen HY, Osuna D, Colville L, Lorenzo O, Graeber K, Küster H, Leubner-Metzger G, Kranner I (2013) Transcriptome-Wide mapping of pea seed ageing reveals a pivotal role for genes related to oxidative stress and programmed cell death. PLoS One 8:1–15
Cui K, Wang HY, Li K, Liao SX, Li L, Zhang CH (2014) Physiological and biochemical effects of ultra-dry storage on barbados nut seeds. Crop Sci 54:1748–1755
Dalton DA, Baird LM, Langeberg L, Taugher CY, Anyan WR, Vance CP, Sarath G (1993) Subcellular localization of oxygen defense enzymes in soybean (Glycine max (L.) Merr.) root nodules. Plant Physiol 102:481–489
Deepa GT, Chetti MB, Khetagoudar MC, Adavirao GM (2013) Influence of vacuum packaging on seed quality and mineral contents in chilli (Capsicum annuum L.). J Food Sci Technol 50:153–158
Donà M, Balestrazzi A, Mondoni A, Rossi G, Ventura L, Buttafava A, Macovei A, Sabatini ME, Valassi A, Carbonera D (2013) DNA profiling, telomere analysis and antioxidant properties as tools for monitoring ex situ seed longevity. Ann Bot 111:987–998
Fessehazion MK, Marais D, Robbertse PJ (2008) Predicting seedling emergence of cabbage and onion using vigour tests. S Afr J Plant Soil 25:1–7
Goel A, Sheoran IS (2003) Lipid peroxide-scavenging enzyme in cotton seeds under natural aging. Biol Plant 46:429–434
Gupta SD (2011) Reactive oxygen species and antioxidants in higher plant. CRC Press, New York, pp 1–189
Heini RL, Oksman-Caldentey KM, Lehtinen P, Lehtinen P, Poutanen K (2001) Effect of drying treatment conditions on sensory profile of germinated oat. Cereal Chem 78:707–714
Hendry GAF (1993) Oxygen, free radical processes and seed longevity. Seed Sci Res 3:141–153
ISTA (2013) International rules for seed testing: edition 2013. Bassersdorf, Zurich
Iturbe-Ormaetxe I, Matamoros MA, Rubio MC, Dalton DA, Becana M (2001) The antioxidants of legume nodule mitochondria. Mol Plant Microbe In 14:1189–1196
Jiménez A, Hernández JA, del Río LA, Sevilla F (1998) Role of the ascorbate-glutathione cycle of mitochondria and peroxisomes in the senescence of pea leaves. Plant Physiol 118:1327–1335
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. Physiol Plant 128:496–506
Kodde J, Buckley WT, de Groot CC, Retiere M, Zamora AMV, Groot SPC (2012) A fast ethanol assay to detect seed deterioration. Seed Sci Res 22:55–62
Kong LQ, Mao PS, Yu XD, Xia FS (2014) Physiological changes in oat seeds aged at different moisture contents. Seed Sci Technol 42:190–201
Kumar D, Mishra DK (2014) Variability in permeability and integrity of cell membrane and depletion of food reserves in neem (Azadirachta indica) seeds from trees of different age classes. J For Res 25:147–153
Lehner A, Mamadou N, Poels P, Côme D, Bailly C, Corbineau F (2008) Changes in soluble carbohydrates, lipid peroxidation and antioxidant enzyme activities in the embryo during ageing in wheat grains. J Cereal Sci 47:555–565
Li Y, Feng HY, Chen T, Yang XM, An LZ (2007) Physiological responses of Limonium aureum seeds to ultra-drying. J Integr Plant Biol 49:569–575
Liu X, Xing D, Li L, Zhang L (2007) Rapid deterioration of seed vigour based on the level of superoxide generation during early imbibition. Photochem Photobiol Sci 6:767–774
Madamanchi NR, Alscher RG (1991) Metabolic bases for differences in sensitivity of two pea cultivars to sulfur dioxide. Plant Physiol 97:88–93
Matamoros MA, Loscos J, Coronado MJ, Ramos J, Sato S, Testillano PS, Tabata S, Becana M (2006) Biosynthesis of ascorbic acid in legume root nodules. Plant Physiol 141:1068–1077
Matamoros MA, Fernández-García N, Wienkoop S, Loscos J, Saiz A, Becana M (2013) Mitochondria are an early target of oxidative modifications in senescing legume nodules. New Phytol 197:873–885
McDonald MB (1999) Seed deterioration: physiology, repair and assessment. Seed Sci Technol 27:177–237
Mittova V, Volokita M, Guy M, Tal M (2000) Activities of SOD and the ascorbate-glutathione cycle enzymes in subcellular compartments in leaves and roots of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii. Physiol Plant 110:42–51
Nakano Y, Asada K (1981) Hydrogen peroxide scavenged by ascorbate-specific peroxidase in spinach chloroplast. Plant Cell Physiol 22:867–880
Pasquini S, Mizzau M, Pertrussa E, Braidot E, Patui S, Gorian F, Lambardi M, Vianello A (2012) Seed storage in polyethylene bags of a recalcitrant species (Quercus ilex): analysis of some bio-energetic and oxidative parameters. Acta Physiol Plant 34:1963–1974
Patterson BD, Macrae EA, Ferguson IB (1984) Estimation of hydrogen peroxide in plants extracts using titanium (IV). Ann Biochem 139:487–492
Pukacka S, Ratajczak E (2007) Age-related biochemical changes during storage of beech (Fagus sylvatica L.) seeds. Seed Sci Res 17:45–53
Rao KVM, Sresty TVS (2000) Antioxidant parameters in the seedlings of pigeon pea (Cajanus cajan (L.) Millspaugh) in response to Zn and Ni stresses. Plant Sci 157:113–128
Rao RGS, Singh PM, Rai M (2006) Storability of onion seeds and effects of packaging and storage conditions on viability and vigour. Sci Hortic 110:1–6
Rubio MC, James EK, Clemente MR, Bucciarelli B, Fedorova M, Vance CP, Becana M (2004) Localization of superoxide dismutases and hydrogen peroxide in legume root nodules. Mol Plant Microbe In 17:1294–1305
Sarvajeet SG, Narendra T (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Bioch 48:909–930
Sung JM, Chiu CC (1995) Lipid peroxidation and peroxide-scavenging enzymes of naturally aged soybean seed. Plant Sci 110:45–52
Xin X, Tian Q, Yin GK, Chen XL, Zhang JM, Ng S, Lu XX (2014) Reduced mitochondrial and ascorbate–glutathione activity after artificial ageing in soybean seed. J Plant Physiol 171:140–147
Zhang XP, Rhodes BB (1993) RAPD molecular marker in watermelon. Hortscience 28:22–28
Acknowledgments
This research was financially supported by National Key Technologies R&D Program of the 12th Five-Year Plan (2011BAD17B01-02) and the Ph. D. Program Foundation of the Ministry of Education of China (20110008110003).
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Communicated by M. Horbowicz.
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Xia, F., Chen, L., Sun, Y. et al. Relationships between ultrastructure of embryo cells and biochemical variations during ageing of oat (Avena sativa L.) seeds with different moisture content. Acta Physiol Plant 37, 89 (2015). https://doi.org/10.1007/s11738-015-1825-8
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DOI: https://doi.org/10.1007/s11738-015-1825-8