Phenol Content and Peroxidase Enzyme Activity in Soybean Infected with Xanthomonas axonopodis pv glycines with the Application of Bacillus subtilis JB12 and Bacillus velezensis ST32

Authors

  • Suhartiningsih Dwi Nurcahyanti Department of Plant Protection, Faculty of Agriculture, University of Jember. Jl. Kalimantan 37 Sumbersari, Jember, East Java, Indonesia. https://orcid.org/0000-0002-5160-1709
  • Wiwiek Sri Wahyuni Department of Plant Protection, Faculty of Agriculture, University of Jember. Jl. Kalimantan 37 Sumbersari, Jember, East Java, Indonesia https://orcid.org/0000-0002-7621-0288
  • Rachmi Masnilah Department of Plant Protection, Faculty of Agriculture, University of Jember. Jl. Kalimantan 37 Sumbersari, Jember, East Java, Indonesia.
  • Anggi Anwar Hendra Nurdika Postgraduate Program Phytopathology, Department of Plant Protection, Faculty of Agriculture, ¬Gadjah Mada University, Jl Flora, Bulaksumur, Sleman, Special Region of Yogyakarta, Indonesia. https://orcid.org/0000-0002-6895-2687

DOI:

https://doi.org/10.21123/bsj.2023.7406

Keywords:

Bacillus subtilis, Bacillus velezensis, Induce resistance, Soybean, Xanthomonas axonopodis pv glycines

Abstract

Xanthomonas axonopodis pv glycines (Xag) is a pathogen that causes pustule disease in soybeans. Many
techniques for controlling this disease have been widely developed, one of which is the use of biological agents.
Bacillus sp. from the soybean phyllosphere is a biological agent that has the potential to suppress the
development of pustule disease. One of the biological control mechanisms is through biochemical induction
of plant resistance which includes the accumulation of phenols, salicylic acid compounds, and peroxidase
enzymes. Bacillus subtilis JB12 and Bacillus velezensis ST32 are two bacteria isolated from the soybean
phyllosphere which have previously been known to suppress Xag through an antibiosis mechanism. This study
aimed to determine the potential of Bacillus subtilis JB12 and Bacillus velezensis ST32 in inducing soybean
resistance against Xag infection. This research was carried out in two stages, the induction of resistance to
soybean germination and an experiment in a greenhouse. This study consisted of 4 treatments and 5
replications, including P0 (Xag inoculation), P1 (Bacillus subtilis JB12 inoculation), P2 (Bacillus velezensis
ST32), and P3 (Bacillus subtilis JB12 + Bacillus velezensis ST32 inoculation). Observations were made on
the content of phenolic compounds, peroxidase enzyme activity, and the development of soybean pustule
disease. The results showed differences in phenol content and peroxidase activity at the two stages of the study.
Seed treatment with both isolates of Bacillus sp was able to increase the phenol content of soybean sprouts up
to 3 - 5 days after inoculation (dai). Phenol content then decreased and was followed by an increase in the
peroxidase activity up to 7 dai. The application of Xag and two isolates of Bacillus sp. in soybean plants caused
the phenol content to fluctuate and peroxidase activity to decrease. Bacillus subtilis JB12 in general played a
better role in increasing phenol content and peroxidase enzyme activity in soybean than Bacillus velezensis
ST32. The application of two isolates of Bacillus sp. was not able to prolong the incubation period and reduce
the severity of the pustule disease 14 days after inoculation.

References

Sain SK, Gour HN. Pathological and physio-biochemical characterization of Xanthomonas axonopodis pv. glycines, incitent of Glycine max leaf pustules. Indian Phytopathol. 2013; 66(April): 20–7.

Tchemadon GC, Zinsou VA, Salami M, Sanni HA, Natta AK. Spatial distribution of soybean bacterial leaf pustule in benin and identification of Xanthomonas axonopodis pv glycines host plants. Agron Afr.2021; 33(3): 253–62.

Shukla AK. Pilot estimation studies of soybean (Glycine max) yield losses by various levels of bacterial pustule (Xanthomonas campestris pv glycines) infection. Int J Pest Manag. 1994; 40(3): 249–51. https://dx.doi.org/10.1080/09670879409371892 .

Habazar T, Resti Z, Yanti Y, Trisno J, Diana A. Screening of indigenous bacterial endophytes from healthy soybean root to control bacterial pustule using in planta technique. J Fitopatologi. 2012; 8(4): 103–9. https://dx.doi.org/10.14692/jfi.8.4.103 .

Algar E, Gutierrez-Mañero FJ, Garcia-Villaraco A, García-Seco D, Lucas JA, Ramos-Solano B. The role of isoflavone metabolism in plant protection depends on the rhizobacterial MAMP that triggers systemic resistance against Xanthomonas axonopodis pv. glycines in Glycine max (L.) Merr. cv. Osumi. Plant Physiol Biochem. 2014; 82: 9–16. https://dx.doi.org/10.1016/j.plaphy.2014.05.001 .

Leveau JHJ. Microbial Communities in the Phyllosphere. Annu Plant Rev online. 2018; 334–67. https://dx.doi.org/10.1002/9781119312994.apr0239 .

Nurcahyanti SD, Wahyuni WS, Masnilah R, Nurdika AAH. Diversity of Bacillus spp. from soybean phyllosphere as potential antagonist agents for Xanthomonas axonopodis pv. glycines causal of pustule disease. Biodivers. 2021; 22(11): 5003–11. https://dx.doi.org/10.13057/biodiv/d221136 .

Miljaković D, Marinković J, Balešević-Tubić S. The significance of Bacillus spp. In disease suppression and growth promotion of field and vegetable crops. Microorganisms. 2020; 8(7): 1–19. https://dx.doi.org/10.3390/microorganisms8071037 .

Köhl J, Kolnaar R, Ravensberg WJ. Mode of action of microbial biological control agents against plant diseases: Relevance beyond efficacy. Front Plant Sci. 2019; 10(July): 1–19. https://dx.doi.org/10.3389/fpls.2019.00845 .

Nurcahyanti SD, Wahyuni WS, Masnilah R. The ability of phyllosphere bacteria as biological agent of pustule disease (Xanthomonas axonopodis pv. glycines) and as soybean growth promotion. Agritrop : Jurnal Ilmu-Ilmu Pertanian. J Agric Sci. 2021; 18(2): 124–36. https://dx.doi.org/10.32528/agritrop.v18i2.3804 .

Otálvaro F, Echeverri F, Quiñones W, Torres F, Schneider B. Correlation between phenylphenalenone phytoalexins and phytopathological properties in Musa and the role of a dihydrophenylphenalene triol. Molecules. 2002; 7(3): 331–40. https://dx.doi.org/10.3390/70300331.

Lama-Muñoz A, Contreras M del M, Espínola F, Moya M, Romero I, Castro E. Content of phenolic compounds and mannitol in olive leaves extracts from six Spanish cultivars: Extraction with the Soxhlet method and pressurized liquids. Food Chem. 2020; 320. https://dx.doi.org/10.1016/j.foodchem.2020.126626 .

Saravanan T, Bhaskaran R, Muthusamy M. Pseudomonas fluorescens Induced Enzymological Changes in Banana Roots (Cv. Rasthali) against Fusarium Wilt Disease. Plant Pathol J. 2004; 3: 72–80. https://dx.doi.org/10.3923/ppj.2004.72.80 .

Nicaise V, Roux M, Zipfel C. Recent advances in PAMP-Triggered immunity against bacteria: Pattern recognition receptors watch over and raise the alarm. Plant Physiol. 2009; 150(4): 1638–47. https://dx.doi.org/10.1104/pp.109.139709 .

Kumar S, Abedin M, Singh AK, Das S. Role of phenolic compounds in plant-defensive mechanisms. Book (Plant phenolics in sustainable agriculture). Springer. Singapore. 2020. P. 517-532. https://dx.doi.org/10.1007/978-981-15-4890-1 .

Jayapala N, Mallikarjunaiah NH, Puttaswamy H, Gavirangappa H, Ramachandrappa NS. Rhizobacteria Bacillus spp. induce resistance against anthracnose disease in chili (Capsicum annuum L.) through activating host defense response. Egypt J Biol Pest Control. 2019; 29(1). https://dx.doi.org/10.1186/s41938-019-0148-2 .

Djellout H, Raio A, Boutoumi H, Krimi Z. Bacillus and Pseudomonas spp. strains induce a response in phenolic profile and enhance biosynthesis of antioxidant enzymes in Agrobacterium tumefaciens infected tomato plants. Eur J Plant Pathol. 2020; 157(2): 269–80. https://dx.doi.org/10.1007/s10658-020-01975-1 .

Rais A, Jabeen Z, Shair F, Hafeez FY, Hassan MN. Bacillus spp., a bio-control agent enhances the activity of antioxidant defense enzymes in rice against Pyricularia oryzae. PLoS One. 2017; 12(11): 1–17. https://dx.doi.org/10.1371/journal.pone.0187412 .

Gerayeli N, Baghaee-Ravari S, Tarighi S. Evaluation of the antagonistic potential of Bacillus strains against Pectobacterium carotovorum subsp. carotovorum and their role in the induction of resistance to potato soft rot infection. Eur J Plant Pathol. 2018 Apr 1; 150(4): 1049–63. https://dx.doi.org/10.1007/s10658-017-1344-0 .

Ben S, Noura M, Samir O, El M, Ismail H, Hadrami E, et al. Bacillus Induces Phenolic Compounds and Enhances Resistance to Uncinula necator Infection in Grapevine Leaves. Afr J Plant Sci Biotech. 2010; 4: 46–53.

Kawano T. Roles of the reactive oxygen species-generating peroxidase reactions in plant defense and growth induction. Plant Cell Rep. 2003; 21(9): 829–37. https://dx.doi.org/10.1007/s00299-003-0591-z .

Rajput VD, Harish, Singh RK, Verma KK, Sharma L, Quiroz-Figueroa FR, et al. Recent developments in enzymatic antioxidant defence mechanism in plants with special reference to abiotic stress. Biology (Basel). 2021; 10(4). https://dx.doi.org/10.3390/biology10040267 .

Khaeruni A, Johan EA, Wijayanto T, Taufik M, Syafar AAR, Kade Sutariati GA. Induction of soybean resistance to bacterial pustule disease (Xanthomonas axonopodis pv. glycines) by rhizobacteria and organic material treatment. IOP Conf Ser Earth Environ Sci. 2018; 122(1). https://dx.doi.org/10.1088/1755-1315/122/1/012052 .

Prasannath K. Plant defense-related enzymes against pathogens: a review. AGRIEAST: J Agric Sci. 2017; 11(1): 38. https://dx.doi.org/10.4038/agrieast.v11i1.33 .

Minaeva OM, Akimova EE, Tereshchenko NN, Zyubanova TI, Apenysheva M V, Kravets A V. Effect of Pseudomonas Bacteria on Peroxidase Activity in Wheat Plants when Infected with Bipolaris sorokiniana. Russ J Plant Physiol. 2018; 65(5): 717–25. https://dx.doi.org/10.1134/S1021443718040052 .

Bashan Y, Okon Y, Henis Y. Peroxidase, polyphenoloxidase, and phenols in relation to resistance against Pseudomonas syringae pv. tomato in tomato plants. Can J Plant Sci.1987;65(2):366–72. https://dx.doi.org/10.1139/b87-047 .

Downloads

Published

2023-10-28

How to Cite

1.
Phenol Content and Peroxidase Enzyme Activity in Soybean Infected with Xanthomonas axonopodis pv glycines with the Application of Bacillus subtilis JB12 and Bacillus velezensis ST32. Baghdad Sci.J [Internet]. 2023 Oct. 28 [cited 2024 Apr. 27];20(5(Suppl.). Available from: https://bsj.uobaghdad.edu.iq/index.php/BSJ/article/view/7406

Similar Articles

You may also start an advanced similarity search for this article.