Seed longevity of bread wheat forms with purple and waxy grain

Authors

  • M. Yu. Skorokhodov Plant Production Institute named after V.Ya. Yuriev of NAAS, Ukraine
  • R. L. Bohuslavskyi Plant Production Institute named after V.Ya. Yuriev of NAAS, Ukraine

DOI:

https://doi.org/10.30835/2413-7510.2020.207013

Keywords:

bread wheat, seed, longevity, accelerated aging, freezing, antioxidant activity.

Abstract

Introduction: Bread wheat forms with purple grain and waxy endosperm are promising as healthy foods. In this regard, it becomes important to evaluate the longevity of their seeds to be stored in seed production industry and in genebanks. However, this issue is very little studied.

Objective: to evaluate the longevity of bread wheat seed samples with purple and waxy grain at long-term storage.

Material and methods: Seeds harvested in 2014–2017 were studied. The seed longevity was evaluated in a experiment modeling “accelerated aging” and after storage at -20ºС. The control seeds were stored at 4 °C. The antioxidant activity (AA) was determined using the DPPH• radical (Arabshahi, Urooj, 2007).

Results and discussion: There was a positive correlation between the antioxidant activity in control on the one hand and the germination energy and germinability after accelerated aging and their change indexes on the other hand (r = 0.67 - 0.76) and strong positive correlations between the ntioxidant activity (r = 0.82) and its change indexes (r = 0.78) after accelerated ageing and freezing. The correlation coefficients between the germination energy and degrees of their changes in the both regimens were significant: from 0.63 to 0.79. Based on the response to accelerated aging, seeds of waxy wheat accession PI619376 were found to be the most longevous; purple-seed variety Chornobrova, red-grain variety Bunchuk and waxy lines PI619377 and PI619381 were the least longevous.

Conclusions. There was no clear relationship between the bread wheat seed longevity with the purple pigmentation of grain or with high amylopectin content in starch. It is highlighted a possibility to predict the longevity of bread wheat seeds from antioxidant activity levels. The bread wheat seeds are similarly responsive to such diverse stressors as accelerated aging and freezing.

 

References

Martinek P, Jirsa O, Vaculová K, Chrpová J, Watanabe N, Burešová V, Kopecký D, Štiasna K, Vyhnánek T, Trojan V. Use of wheat gene resources with different grain colour in breeding. 64. Tagung der Vereinigung der Pflanzenzüchter und Saatgutkaufleute Österreichs. 2013. P. 75–78.

Wang S, Wang J, Zhang W, Li C, Yu J, Wang S. Molecular order and functional properties of starches from three waxy wheat varieties grown in China. Food Chemistry. 2015;181: 43–50. DOI: 10.1016/j.foodchem.2015.02.065.

Eng H, Khoo HE, Azlan A, Tang ST, Lim SM. Anthocyanidins and anthocyanins: colored pigments as food, pharmaceutical ingredients, and the potential health benefits. Food Nutr. Res. 2017; 61(1): 1–21. DOI:10.1080/16546628.2017.1361779.

Sytar O, Bośko P, Živčák M, Brestic M, Smetanska I. Bioactive phytochemicals and antioxidant properties of the grains and sprouts of colored wheat genotypes. Molecules. 2018; 23(9):1–14. DOI: 10.3390/molecules23092282.

Paznocht L, Kotíková Z, Orsák M, Lachman J, Martinek P. Carotenoid changes of colored-grain wheat flours during bun-making. Food Chemistry. 2018; 277(30): 725–734. DOI: 10.1016/j.foodchem.2018.11.019.

Havrlentová M, Pšenáková I, Žofajová A, Rückschloss L, Kraic J. Anthocyanins in wheat seed—a mini review. Nova Biotechnol. Chim. 2014; 13: 1–12. DOI 10.2478/nbec-2014-0001.

Graybosch RA. Waxy wheats: Origin, properties, and prospects. Trends in Food Science and Technology. 1998; 9: 135–142.

Hung PV, Maeda T, Yamamoto S, Morita N. Effects of germination on nutritional composition of waxy wheat. Journal of the Science of Food and Agriculture. 2012; 92(3): 667–672. DOI: 10.1002/jsfa.4628.

Shoeva OY, Khlestkina EK. The specific features of anthocyanin biosynthesis regulation in wheat. In: Ogihara Y, Takumi S, Handa H, eds. Advances in wheat genetics: from genome to field. Tokyo: Springer, 2015. P. 147–157. DOI: 10.1007/978-4-431-55675-6_16.

Pincino C, Capocchi A, Galleschi L, Saviozzi F, Nanni B, Zandomeneghi M. Aging, free radicals and antioxidants in wheat Seeds. J. Agric. Food Chem. 1999; 47(4): 1333–1339. DOI: 10.1021/jf980876d.

Arif MA, Nagel M, Lohwasser U, Börner A. Genetic architecture of seed longevity in bread wheat (Triticum aestivum L.). J. Biosci. 2017; 42: 81–89.

Agacka M, Rehman Arif MA, Lohwasser U, Doroszewska T, Qualset CO, Börner A. The inheritance of wheat grain longevity: a comparison between induced and natural ageing. J Appl Genet. 2016; 57: 477–481.

Dong Zh, Feng B, Liang H, Rong Ch, Zhang K, Cao Xu, Qin Hu, Liu X, Wang T, Wang D. Grain-specific reduction in lipoxygenase activity improves flour color quality and seed longevity in common wheat. Mol Breeding. 2015; 35(150): 1–18.

Lv Y, Tian P, Zhang S, Wang J, Hu Y. Dynamic proteomic changes in soft wheat seeds during accelerated ageing. Peer J. 2018; 6: 1–16. DOI: 10.7717/peerj.5874.

Chen X, Yin G, Börner A, Xin X, He J, Nagel M, Liu X, Lu X. Comparative physiology and proteomics of two wheat genotypes differing in seed storage tolerance. Plant Physiology and Biochemistry. 2018; 130: 455–463. DOI: 10.1016/j.plaphy.2018.07.022.

TeKrony DM. Accelerated aging test: principles and procedures. Seed Technology. 2005; 27(1): 135–146.

Smolikova GN. Application of the accelerated aging method to assess resistance of seeds to stresses. Vestnik SPbGU. Ser. 3. Biologiya. 2014; 2: 82–93.

Safina GF, Filipenko GI. Longevity of seeds during storage and its prediction by the accelerated aging method. Trudy po poprikladnoy botanike, genetike i selektsii. 2013; 174: 123–130.

Hampton JG, TeKrony DM. Handbook of vigour test methods. International Seed Testing Association, Zürich, 1995. 117 p.

Likhachev BS. Some methodological issues of studying the biology of seed aging. Selskokhoziaystvennaia biologia. 1980; 15(6): 842–844.

Moori S, Eisvand HR, Ismaili A, Sasani S. Effects of drought stress during seed development and subsequent accelerated ageing on wheat seed mitochondrial ultra-structure, seedling antioxidant enzymes, and malondialdehyde. Journal of Plant Process and Function. 2019; 7(28): 1–8.

Qin P, Kong Z, Liao Xi, Liu Y. Effects of accelerated aging on physiological and biochemical characteristics of waxy and non-waxy wheat seeds. Journal of Northeast Agricultural University (English edition). 2011; 18(2): 7–12. DOI: 10.1016/S1006-8104(12)60002-6.

International Seed Testing Association (ISTA). International Rules for Seed Testing, Vol. 2019. No 1/ISTA. Bassersdorf, Switzerland, 2019. URL: https://www.ingentaconnect.com/content/ista/rules/2019/00002019/00000001.

Arabshahi S, Urooj A. Antioxidant propertiesof various solvent extracts of Mulberry morusindica L. Leaves. Food Chem. 2007; 102: 1233–1240.

Udovenko GV, ed. Diagnosis of plant resistance to stress: a methodological guide. Leningrad: VIR, 1988. 226 p.

Linnyk YuO. Effect of negative temperature on the seeds viability. Visnyk Poltavskoi derzhavnoi ahrarnoi akademii. 2010; 3(58): 175–179.

Published

2020-07-03

Issue

Section

METHODS AND RESULTS SELECTION