Abstract
In order to characterize the response to drought of 19 ethyl methanesulfonate (EMS)-mutagenized lines of durum wheat (Triticum durum Desf.) derived from the variety CHAM-1 and cultivated in Morocco, growth (plant height, PLH) and yield (grain number per spike, GNS) parameters were followed for different lines and CHAM-1 variety. All were cultivated under well-watered (C) and drought conditions (T). In parallel, quantitative and qualitative aspects of leaf peroxidases (EC 1.11.1.7) were analyzed. When compared with C plant lines, the corresponding T lines showed decreases of 9–38% and 1–78%, respectively, for PLH and GNS parameters. A positive correlation was found between PLH and the yield as GNS (r2 = 0.885). When expressed as units mg−1 proteins, soluble peroxidases (SPOX) were less represented than the ionically wall-bound peroxidases (IPOX) in all mutagenized wheat lines, with 22.1% and 46.2% as respective coefficients of variation for drought-stressed lines. Drought-induced reduction in grain yields for all lines correlated positively with percentages of IPOX exhibited by stressed plants (r2 = 0.68). In addition, Averages of drought-induced decreases in GNS, calculated for five groups of mutagenized lines, were found to be positively correlated with their respective percentages of IPOX (r2 = 0.906). Drought-adapted lines showed decreases in IPOX. When subjected to electrophoresis using 6–15% polyacrylamide gradient gels, resolved IPOX of cereal line groups of limited drought-induced reduction in GNS exhibited low reactivity on native gels. These data support the hypothesis that IPOX are indicators of the sensitivity of wheat lines to drought conditions. Possible mechanisms of POX involvement in wheat resistance to drought and developing appropriate biochemical tests to screen variability and drought adaptation of EMS mutants are discussed in this study.
Similar content being viewed by others
References
Ali Dib T, Monneveux P, Acevedo E, Nachit MM (1994) Proline analysis and chlorophyll fluorescence quenching measurements as drought tolerance indicators in durum wheat (Triticum turgidum var. durum Desf.). Euphytica 79:65–73
Almagro L, Gómez Ros LV, Belchi-Navarro S, Bru R, Ros Barceló A, Pedreño MA (2009) Class III peroxidases in plant defence reactions. J Exp Bot 60:377–390
Aouad A (1997) Contribution à l’étude des peroxydases des céréales en relation avec la résistance à la salinité. Diplôme d’Etudes Supérieures, Université Cadi Ayyad, Marrakech
Aouad A, Baaziz M, Mergoum M (2000) Quantitative and qualitative aspects of peroxidases in some Moroccan cereal varieties and their relationship with the in vitro growth potential. Plant Peroxidase Newsl 15:13–21
Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plan Biol 55:373–399
Baaziz M, Aissam F, Brakez Z, Bendiab K, El Hadrami I, Cheikh R (1994) Electrophoretic patterns of acid soluble proteins and active isoforms of peroxidase and polyphenoloxidase typifying calli and somatic embryos of two reputed date palm cultivars in Morocco. Euphytica 76:159–168
Bogdanovic Pristov J, Mutavdzić D, Prodanović O, Maksimović V, Radotić K (2015) Relations of cell wall bound peroxidases, phenols and lignin in needles of Serbian spruce Picea omorika (Pančić) Purkynĕ in the natural habitat. Biochem Syst Ecol 59:271–277
Cosio C, Dunand C (2009) Specific functions of individual class III peroxidase genes. J Exp Bot 60:391–408
Csiszár J, Gallé A, Horváth E, Dancsó P, Gombos M, Váry Z, Erdei L, Györgyey J, Tari I (2012) Different peroxidase activities and expression of abiotic stress-related peroxidases in apical root segments of wheat genotypes with different drought stress tolerance under osmotic stress. Plant Physiol Biochem 52:119–129
Donini P, Law JR, Koebner RMD, Reeves JC, Cooke RJ (2000) Temporal trends in the diversity of UK wheats. Theor Appl Genet 100:912–917
Efron Y (1973) Variation in the physiological sensitivity of maize inbreds to EMS a possible correlation with alcohol dehydrogenase activity. Mutat Res Fundam Mol Mech Mutagen 19:319–324
Ellis RP, Foster BP, Robinson D, Handley LL, Gordon DC, Russell JR, Powell W, Barley W (2000) A source of genes for crop improvement in the 21st century. J Exp Bot 51:9–17
Fry SC (2004) Oxidative coupling of tyrosine and ferulic acid residues: intra- and extra-protoplasmic occurrence, predominance of trimers and larger products, and possible role in inter-polymeric cross-linking. Phytochem Rev 3:97–111
Gadjev I, Stone JM, Gechev T (2008) Programmed cell death in plants: new insights into redox regulation and the role of hydrogen peroxide. Int Rev Cell Mol Biol 270:87–144
Gechev T, Mehterov N, Denev I, Hille J (2013) A simple and powerful approach for isolation of Arabidopsis mutants with increased tolerance to H2O2-induced cell death. Methods Enzym 527:203–220
Gill S, Tuteja N (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48:909–930
Habash DZ, Baudo M, Hindle M, Powers SJ, Defoin-Platel M, Mitchell R, Saqi M, Rawlings C, Latiri K, Araus JL, Abdulkader A, Tuberosa R, Lawlor DW, Nachit MM (2014) Systems responses to progressive water stress in durum wheat. PLoS ONE 9:e108431. https://doi.org/10.1371/journal.pone.0108431
Hoisington D, Khairallah M, Reeves T, Ribaut JM, Skovmand B, Taba S, Warburton M (1999) Plant genetic resources: what can they contribute toward increased crop productivity? Proc Nat Acad Sci USA 96:5937–5943
Khales A, Baaziz M (2005) Quantitative and qualitative aspects of peroxidises extracted from cladodes of Opuntia ficus indica L. Sci Hortic 103:209–218
Kohaich K, Baaziz M (2015) New investigations on the guaiacol peroxidase of Opuntia ficus indica L. and its modulation by ascorbic acid and copper. Towards an optimization of quantitative and qualitative tests. J Mol Catal B Enzym 119:26–32
Lipiec J, Doussan C, Nosalewicz A, Kondracka K (2013) Effect of drought and heat stresses on plant growth and yield. A review. Int Agrophysics 27:463–477
Liszkay A, Van der Zalm E, Schopfer P (2004) Production of reactive oxygen intermediates (O2−, H2O2, and OH) by maize roots and their role in wall loosening and elongation growth. Plant Physiol 136:3114–3123
Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the folin-phenol reagent. J Biol Chem 193:265–275
Lüthje S, Meisrimler C-N, Hopff D, Möller B (2011) Phylogeny, topology, structure and functions of membrane-bound class III peroxidases in vascular plants. Phytochemistry 72:1124–1135
Marjamaa K, Kukkola EM, Fagerstedt KV (2009) The role of xylem class III peroxidases in lignifications. J Exp Bot 60:367–376
Miller G, Shulaevb V, Mittler R (2008) Reactive oxygen signalling and abiotic stress. Physiol Plant 133:481–489
Nsarellah N, Amri A, Nachit M (2005) Amélioration génétique du blé dur. In la création variétale à l’INRA. Méthodologie, acquis et perspectives; Abbad Andaloussi & Chahbar, Edition INRA, p 7
Parry MAJ, Madgwick PJ, Bayon C, Tearall K, Hernandez-Lopez A, Baudo M, Rakszegi M, Hamada W, Al-Yassin A, Ouabbou H, Labhilili M, Phillips AL (2009) Mutation discovery for crop improvement. J Exp Bot 60:2817–2825
Pearse IS, Heath KD, Cheeseman JM (2005) Biochemical and ecological characterization of two peroxidase isoenzymes from the mangrove, Rhizophora mangle. Plant Cell Environ 28:612–622
Porceddu E, Damania AB, Qualset CO (2014) Proceedings of the international symposium on genetics and breeding of durum Wheat—IAM Bari: CIHEAM (Centre International de Hautes Etudes Agronomiques Méditerranéennes). Sér A Mediterr Semin Options Méditerr 110:636
Qureshi MK, Radeva V, Genkov T, Minkov I, Hille J, Gechev TS (2011) Isolation and characterization of Arabidopsis mutants with enhanced tolerance to oxidative stress. Acta Physiol Plant 33:375–382
Radotić K, Dučić T, Mutavdžiæ D (2000) Changes in peroxidase activity and isoenzymes in spruce needles after exposure to different concentrations of cadmium. Environ Exp Bot 44:105–113
Rascio A, Russo M, Platani C, Ronga G, Di Fonzo N (1999) Mutants of durum wheat with alterations in tissue affinity for strongly bound water. Plant Sci 144:29–34
Singh RP, Trethowan RM (2007) Breeding spring bread wheat for irrigated and rainfed production systems of the developing world. In: Kang MS, Priyadarshan PM (eds) Breeding major food staples. Blackwell Publishing, Oxford, pp 109–139
Subira J, Alvaroa F, Garcia del Moral LF, Royo C (2015) Breeding effects on the cultivar × environment interaction of durum wheat yield. Eur J Agron 68:78–88
Xiao X, Yang F, Zhang S, Korpelainen H, Li C (2009) Physiological and proteomic responses of two contrasting Populus cathayana populations to drought stress. Physiol Plant 136:150–168
Ying YQ, Song LL, Jacobs DF, Mei L, Liu P, Jin SH, Wu JS (2015) Physiological response to drought stress in Camptotheca acuminata seedlings from two provenances. Front Plant Sci 6:361
Zhang N, Wang S, Zhang X, Dong Z, Chen F, Cui D (2016) Transcriptome analysis of the Chinese bread wheat cultivar Yunong 201 and its ethyl methanesulfonate mutant line. Gene 575:285–293
Zlatev ZS, Lidon FC, Ramalho JC, Yordanov IT (2006) Comparison of resistance to drought of three bean cultivars. Biol Plant 50:389–394
Acknowledgements
We acknowledge staff of the National Institute of Agronomic Research (INRA) at Rabat, Morocco, for help in plant culture.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Funding
This work is supported by Cadi Ayyad University, Marrakech, Morocco, accreditation 2016 and the National Institute of Agronomic Research (INRA), Morocco.
Rights and permissions
About this article
Cite this article
Kahama, I., Kohaich, K., Baaziz, M. et al. Quantitative and Qualitative Aspects of Soluble and Ionically Wall-Bound Peroxidases of EMS-Mutagenized Durum Wheat Lines (Triticum durum), as Tested for Yield at Drought Conditions. Agric Res 8, 148–157 (2019). https://doi.org/10.1007/s40003-018-0361-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s40003-018-0361-3