Response of plant defense enzymes against tomato early blight disease


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Authors

  • POTHIRAJ G Institute of Agricultural Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh 221 005, India
  • VINEETA SINGH Institute of Agricultural Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh 221 005, India
  • NAVEEN KUMAR R Institute of Agricultural Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh 221 005, India
  • SANJAY KUMAR GOSWAMI ICAR-Indian Institute of Sugarcane Research, Lucknow, Uttar Pradesh

https://doi.org/10.56093/ijas.v91i4.112742

Keywords:

Alternaria solani, Catalase, Peroxidase, PAL, Total phenol

Abstract

An experiment was conducted to identify the biochemical defense enzymes, viz. catalase (CAT), peroxidase (POX), phenylalanine ammonia lyase (PAL) and total phenol responsible for resistance against A. solani in resistant (cv. H-88-78-1) and susceptible (Punjab Chhuhara) cultivars of tomato after the application of Amistar 25 SC (azoxystrobin 0.1%) during 2015 crop season. Azoxystrobin was applied for their efficacy in inducing defense enzymes in tomato against A. solani. Defense-related enzymes were increased in azoxystrobin pre-treated tomato plants. Early blight resistant tomato plants (cv. H-88-78-1) treated with novel QoI (Quinone oxidation inhibitor) fungicideazxoystrobin inoculated with A. solani under glasshouse conditions showed increased accumulation of defense enzymes, viz. CAT, POX, PAL and total phenol than
control plants.

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References

Adhikari P, Oh Y and Panthee D R. 2017. Current status of early blight resistance in tomato: an update. International Journal of Molecular Science 18: 1–22.

Beers R F and I W Sizer.1952. Colorimetric method for estimation of catalase. Journal of Biological Chemistry 195: 133–39.

Benhamou N, Belanger R R and Paulitz T C. 1996. Induction of differential host responses by Pseudomonas fluorescens in Ri TDNA- transformed pea roots after challenge with Fusarium oxysporum f. sp. pisi and Pythium ultimum. Phytopathology 86: 114-18.

Bradley D J, Kjeilborn P and Lamb C J.1992. Elicitor and wound induced oxidation cross linking of a plant cell wall proline rich protein: A novel, rapid defense response. Cell 70: 21-30.

Bray W and V Thorpe.1954. Analysis of phenol compounds of interest in metabolism. Methods of Biochemical Analysis 1: 27-52.

Chaudhary A. 2018. Systemic acquired resistance (SAR) and its significance in plant disease management.https:// www.researchgate.net/.../324719141_Systemic_Acquired_ Resistance_SAR.

Dickerson D P, Pascholati S F, Hagerman A E, Butler L G and Nicholson R L. 1984. Phenylalanine ammonia-lyase and hydroxycinnamate CoA ligase in maize mesocotyls inoculated with Helminthosporium maydis. Physiological Plant Pathology 25: 111-23.

Egley G H, Paul R N, Vaughn K C and Duke S O. 1983. Role of peroxidase in the development of water-impermeable seed coats in Sidaspinosa L. Planta 157: 224-32.

EL-Tanany M M, Hafez M A, Ahmed G A and El-Mageed M A. 2018. Efficiency of biotic and abiotic inducers for controlling tomato early blight. Middle East Journal 7: 650–70.

Hammond-Kosack K E and Jones J D G. 1996. Resistance gene-dependent plant defense responses. Plant Cell 8: 1773-91.

Hashemi L, Golparvar A R, Nasr Esfahani M and Golabadi M. 2019. Correlation between cucumber genotype and resistance to damping-off disease caused by Phytophthora melonis. Biotechnology and Biotechnological Equipment. 33: 1494–1504.

Klessig D F and Malamy J. 1994. The salicylic acid signal. PIant Molecular Biology 26: 1439-1458.

Meena M, Zehra A, Dubey M K, Aamir M, Gupta V K and Upadhyay R S. 2016. Comparative evaluation of biochemical changes in tomato (Lycopersicon esculentum Mill.) infected by Alternaria alternata and its toxic metabolites (TeA, AOH, and AME). Frontiers in Plant Science 7: 1–14.

Nafisa, Shoaib A Iqbal J and Khan K A.2020. Evaluation of phenotypic, physiological and biochemical attributes connected with resistance in tomato against Alternaria solani. Acta Physiologiae Plantarum 42: 88.

Nash A F and R G Gardner. 1988. Tomato early blight resistance in a breeding line derived from Lycopersicon hirsutum PI 126445. Plant Disease 72: 206–09.

Odilbekov F, Edin E, Mostafanezhad H, Coolman H, Grenville- Briggs L and Liljeroth E. 2019. Within-season changes in Alternaria solani populations in potato in response to fungicide application strategies. European Journal of Plant Pathology 155: 953–65.

Poli Y, Nallamothu E, Balakrishnan D, Ramesh P, Desiraju S, Mangrauthia S K, Voleti S R and Neelamraju S. 2018. Increased catalase activity and maintenance of photosystem II distinguishes high-yield mutants from low-yield mutants of rice var. Nagina 22 under low-phosphorus stress. Frontiers in Plant Science 9: 1543.

Wolters P J, Vos L D, Bijsterbosch G, Woudenberg J H C, Visser R G F, Linden G V D and Vleeshouwers V G A A. 2019. A rapid method to screen wild Solanum for resistance to early blight. European Journal of Plant Pathology 154: 09–114.

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Submitted

2021-07-14

Published

2022-10-19

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Short-Communication

How to Cite

G, P., SINGH, V., R, N. K., & GOSWAMI, S. K. (2022). Response of plant defense enzymes against tomato early blight disease. The Indian Journal of Agricultural Sciences, 91(4), 644–646. https://doi.org/10.56093/ijas.v91i4.112742
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