Physiological and biochemical responses of Kinnow mandarin (Citrus nobilis × Citrus deliciosa) to EMS induced mutagenesis


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Authors

  • SUNIL KUMAR ICAR-Indian Agricultural Research Institute, New Delhi 110 012, India
  • O P AWASTHI ICAR-Indian Agricultural Research Institute, New Delhi 110 012, India
  • R M SHARMA ICAR-Indian Agricultural Research Institute, New Delhi 110 012, India
  • SATYABRATA PRADHAN ICAR-Indian Agricultural Research Institute, New Delhi 110 012, India

https://doi.org/10.56093/ijas.v91i7.115116

Keywords:

Antioxidant enzymes, Chlorophyll, EMS, Kinnow mutants, Leaf area, Phenol

Abstract

The present study was carried out to enhance the genetic variability in Kinnow mandarin (Citrus nobilis Loureiro Physiological and biochemical responses of Kinnow mandarin (Citrus nobilis × Citrus deliciosa) to EMS induced mutagenesis Citrus deliciosa Tenora) using ethyl methanesulfonate (EMS) during 2016-17 and 2017-18. Plants created with different doses of EMS concentration, viz. 0.05%, 0.1%, 0.2% and 0.5% were examined for the various physiological and biochemical alterations in putative mutants aged six years and compared with the wild type (WT). A dose-dependent decrease in leaf area was recorded in the mutants with increasing doses of EMS concentration and as compared to WT, maximum reduction of 135.52 and 104.92% was witnessed in the mutants E-19 and E-17 developed from 0.5% EMS, whereas the leaves were more succulent in E-16. Chlorophyll a content was higher than chlorophyll b in the mutated population. As compared to WT, maximum decrease in chlorophyll a, total chlorophyll was noticed in the mutants E-19 generated from 0.5% EMS. Contrary to the physiological alterations, the total phenol, proline and total protein content in the mutants were upregulated by nearly two fold in the mutants developed beyond 0.1% EMS. Significant increase was also noticed in the antioxidant enzymes SOD, CAT, POX and GR activity in the mutants E-16 to E-20 induced from 0.5% EMS. The variation in traits of interest observed in the present study such as better leaf succulency and upregulated antioxidant enzyme activity in the mutant E-16 (0.5% EMS) suggests that the developed mutant could be utilised in Kinnow improvement for abiotic stress tolerance.

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References

Acedo G N. 1983. Peroxidase activity in Arabidopsis mutant A-154. Phyton 23: 263–69.

Barnes J D, Balaguer L, Manrique E, Elvira S and Davison A W. 1992. A reappraisal of the use of DMSO for the extraction and determination of chlorophylls a and b in lichens and higher plants. Environmental and Experimental Botany 32(2): 85–100. DOI: https://doi.org/10.1016/0098-8472(92)90034-Y

Bates L S, Waldren R P and Teare I D. 1973. Rapid determination of free proline for water-stress studies. Plant and Soil 39(1): 205–07. DOI: https://doi.org/10.1007/BF00018060

Bidabadi S S, Mahmood M, Meon S, Wahab Z and Ghobadi C. 2011. Evaluation of in vitro water stress tolerance among EMS—Induced variants of banana (Musa spp., AAA), using “morphological, physiological and molecular” traits. Journal of Crop Science and Biotechnology 14(4): 255–63. DOI: https://doi.org/10.1007/s12892-011-0073-8

Bradford M M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein–dye binding. Analytical Biochemistry 72(1-2): 248–54. DOI: https://doi.org/10.1016/0003-2697(76)90527-3

Deepthi T and Remesh K N. 2016. Impact of EMS induction on morphological, anatomical and physiological traits of bhindi Abelmoschus esculentus (L.) Moench. International Journal of Recent Research in Life Sciences 3(2): 4-11.

Dhakshanamoorthy D, Selvaraj R and Chidambaram A. 2010. Physical and chemical mutagenesis in Jatropha curcas L. to induce variability in seed germination, growth and yield traits. Romanian Journal of Biology Plant Biology 55(2): 113–25.

Ennajeh M, Vadel A M, Cochard H and Khemira H. 2010. Comparative impacts of water stress on the leaf anatomy of a drought-resistant and a drought-sensitive olive cultivar. Journal of Horticultural Science and Biotechnology 85(4): 289–94. DOI: https://doi.org/10.1080/14620316.2010.11512670

Ghani M, Kumar S and Thakur M. 2014. Physiological and biochemical responses of gerbera (Gerbera jamesonii Hook.) to physical and chemical mutagenesis. Journal of Horticultural Science and Biotechnology 89(3): 301–06. DOI: https://doi.org/10.1080/14620316.2014.11513083

Gnanamurthy S and Dhanavel D. 2014. Effect of EMS on induced morphological mutants and chromosomal variation in cowpea (Vigna unguiculata (L.) Walp). International Letters of Natural Sciences 22: 33–43. DOI: https://doi.org/10.18052/www.scipress.com/ILNS.22.33

Kaur S and Rattanpal H S. 2010. Effect of mutagens on in vitro seed germination and growth of rough lemon (Citrus jambhiri) seedlings. Indian Journal of Agricultural Sciences 80(9): 773–76.

Kumar A H and Munirajappa V. 2013. Evaluation of ethyl methane sulfonate (EMS) induced mutants of Morus species (GENOTYPE BC2-59) for nutritive and biomass productivity. International Journal of Applied and Natural Sciences 2(3): 13–24.

Kumar G and Pandey A. 2019. Ethyl methane sulphonate induced changes in cyto-morphological and biochemical aspects of Coriandrum sativum L. Journal of the Saudi Society of Agricultural Sciences 18(4): 469–75. DOI: https://doi.org/10.1016/j.jssas.2018.03.003

Kumar S, Awasthi O P, Dubey A K, Dahuja A and Singh A. 2019. Influence of rootstocks on growth, yield, quality and physiological activity of 'Kinnow' mandarin grown in a semi-arid region. Fruits 74(5): 205–13. DOI: https://doi.org/10.17660/th2019/74.5.1

Kumar S, Awasthi O P, Singh A, Sharma R R and Singh K. 2020. Physiological alteration in Kinnow developed through physical and chemical mutagen. Indian Journal of Horticulture 77(2): 267-272. DOI: https://doi.org/10.5958/0974-0112.2020.00036.5

Kumari R, Singh S and Agrawal S B. 2010. Response of ultraviolet-B induced antioxidant defense system in a medicinal plant, Acorus calamus. Journal of Environmental Biology 31(6): 907–11.

Malik C P and Singh M B. 1980. Plant Enzymology and Histoenzymology, pp 59–60. A Text Manual. New Delhi: Kalyani Publ.

Mallick M, Awasthi O P, Singh S K and Dubey A K. 2016. Physiological and biochemical changes in pre-bearing mutants of Kinnow mandarin (C. nobilis Lour× C. deliciosa Tenora). Scientia Horticulturae 199: 178–85. DOI: https://doi.org/10.1016/j.scienta.2015.12.050

Predieri S. 2001. Mutation induction and tissue culture in improving fruits. Plant Cell, Tissue and Organ Culture 64(2-3): 185–10. DOI: https://doi.org/10.1023/A:1010623203554

Rime J, Dinesh M R, Sankaran M, Shivashankara K S, Rekha A and Ravishankar K V. 2019. Evaluation and characterization of EMS derived mutant populations in mango. Scientia Horticulturae 254: 55–60. DOI: https://doi.org/10.1016/j.scienta.2019.04.015

Wani M R, Khan S and Kozgar M I. 2011. Induced chlorophyll mutations. I. Mutagenic effectiveness and efficiency of EMS, HZ and SA in mungbean. Frontiers of Agriculture in China 5(4): 514–18. DOI: https://doi.org/10.1007/s11703-011-1126-y

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Submitted

2021-09-10

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2021-09-10

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How to Cite

KUMAR, S., AWASTHI, O. P., SHARMA, R. M., & PRADHAN, S. (2021). Physiological and biochemical responses of Kinnow mandarin (Citrus nobilis × Citrus deliciosa) to EMS induced mutagenesis. The Indian Journal of Agricultural Sciences, 91(7), 1015–1019. https://doi.org/10.56093/ijas.v91i7.115116
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