The Influence of Azotobacter vinelandii IMV B-7076 on the Buckwheat Development and Exometabolite Composition in the Root Zone

Authors

  • I.K. Kurdish Zabolotny Institute of Microbiology and Virology, NAS of Ukraine, 154 Akademika Zabolotnoho Str., Kyiv, 03143, Ukraine
  • A.Yu. Chobotarov Zabolotny Institute of Microbiology and Virology, NAS of Ukraine, 154 Akademika Zabolotnoho Str., Kyiv, 03143, Ukraine
  • O.S. Brovarska Zabolotny Institute of Microbiology and Virology, NAS of Ukraine, 154 Akademika Zabolotnoho Str., Kyiv, 03143, Ukraine
  • N.Y. Parkhomenko Zabolotny Institute of Microbiology and Virology, NAS of Ukraine, 154 Akademika Zabolotnoho Str., Kyiv, 03143, Ukraine
  • V.V. Chobotarova Zabolotny Institute of Microbiology and Virology, NAS of Ukraine, 154 Akademika Zabolotnoho Str., Kyiv, 03143, Ukraine

DOI:

https://doi.org/10.15407/microbiolj86.05.039

Keywords:

Azotobacter vinelandii IMV B-7076, buckwheat plants, morphometric indicators, content of photosynthetic pigments, protein, carbohydrates, phenolic compounds

Abstract

During the growth and development of plants, a large quantity of root exudates is released into the rhizosphere, forming a microbiome capable of stimulating plant growth and productivity. The application of microbial preparations will be the cornerstone of soil improvement and obtaining high-quality plant products. The aim of this study was to determine the influence of Azotobacter vinelandii IMV B-7076, a component of the highly effective complex bacterial preparation Azogran, on the buckwheat development and exometabolite composition in the root zone. Methods. The effect of azotobacter on the growth of buckwheat plants and their exometabolite synthesis was investigated during a 14-day cultivation period in a Farreus medium under phytotron conditions. The content of photosynthetic pigments in plant leaves was determined using spectrophotometric methods. The protein content in the medium was determined by the Bradford method, carbohydrates by their interaction with phenol and sulfuric acid, and phenols by the Folin-Chokalteu reagent. Results. It was found that the cultivation of buckwheat in a medium with azotobacter significantly stimulated the growth activity of plants and the content of chlorophyll a in their leaves. Under these conditions, the content of chlorophyll b and carotenoids in buckwheat leaves increased less noticeably. During the 14-day cultivation of plants in a medium containing 107 CFU/mL of these bacteria, the protein content increased by 110.4% compared to the control, phenolic compounds by 48.8%, and carbohydrates by 266.4%. Conclusions. Azotobacter vinelandii IMV B-7076 noticeably improves the growth of buckwheat, increases the concentration of exometabolites in the medium during hydroponic cultivation.

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References

Avksentyeva, O. A., Petrenko, V. A. (2011). Biotechnology of higher plants: in vitro culture educational and methodological manual. KNU.

Badri, D. V., & Vivanco, J. M. (2009). Regulation and function of root exudates. Plant, Cell & Environment, 32(6), 666-681. https://doi.org/10.1111/j.1365-3040.2009.01926.x

Bradford, 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), 248-254. https://doi.org/10.1016/0003-2697(76)90527-3

Bulavenko, L.V., Bega, Z.T., Kurdish, I. K. (2000). Mobilization of phosphorus by some microorganisms from sparingly soluble inorganophosphates. Bull agricultural microbiology, 6, 55 - 56.

Canarini, A., Kaiser, C., Merchant, A., Richter, A., & Wanek, W. (2019). Root Exudation of Primary Metabolites: Mechanisms and Their Roles in Plant Responses to Environmental Stimuli. Frontiers in Plant Science, 10. https://doi.org/10.3389/fpls.2019.00157

Francis, C. A. (2005). Organic Farming. Encyclopedia of Soils in the Environment, 77-84. https://doi.org/10.1016/B0-12-348530-4/00285-X

Gray, E. J., & Smith, D. L. (2005). Intracellular and extracellular PGPR: commonalities and distinctions in the plant-bacterium signaling processes. Soil Biology and Biochemistry, 37(3), 395-412. https://doi.org/10.1016/j.soilbio.2004.08.030

Hryshchenko, R. E., Liubchych, A. G., Glieva, О. V., Кurdysh, І. К. (2020). Changes in buckwheat yield under the influence of biological products in the system of organic cultivation. Zemlerobstvo, 98(1), 139 - 151.

Innerebner, G., Knief, C., & Vorholt, J. A. (2011). Protection of Arabidopsis thaliana against Leaf-Pathogenic Pseudomonas syringae by Sphingomonas Strains in a Controlled Model System. Applied and Environmental Microbiology, 77(10), 3202-3210. https://doi.org/10.1128/AEM.00133-11

Korenblum, E., Dong, Y., Szymanski, J., Panda, S., Jozwiak, A., Massalha, H., Meir, S., Rogachev, I., & Aharoni, A. (2020). Rhizosphere microbiome mediates systemic root metabolite exudation by root-to-root signaling. Proceedings of the National Academy of Sciences, 117(7), 3874-3883. https://doi.org/10.1073/pnas.1912130117

Korus, A. (2012). Effect of preliminary and technological treatments on the content of chlorophylls and carotenoids in kale (Brassica Oleracea L. var. Acephala). Journal of Food Processing and Preservation, 37(4), 335-344. https://doi.org/10.1111/j.1745-4549.2011.00653.x

Kravchenko, L.V., Azarova, T. S., Leonova-Erko, E. I., Shaposhnikov, A. I., Makarova, N. M., & Tikhonovich, I. A. (2003). Root Exudates of Tomato Plants and Their Effect on the Growth and Antifungal Activity of Pseudomonas Strains. Microbiology, 72(1), 37-41. https://doi.org/10.1023/A:1022269821379

Krewulak, K. D., & Vogel, H. J. (2008). Structural biology of bacterial iron uptake. Biochimica et Biophysica Acta (BBA) - Biomembranes, 1778(9), 1781-1804. https://doi.org/10.1016/j.bbamem.2007.07.026

Kuijken, R. C. P., Snel, J. F. H., Heddes, M. M., Bouwmeester, H. J., & Marcelis, L. F. M. (2015). The importance of a sterile rhizosphere when phenotyping for root exudation. Plant and Soil, 387(1-2), 131-142. https://doi.org/10.1007/s11104-014-2283-6

Kurdish, I. K. (2019). Interaction of Microorganisms with Nanomaterials as a Basis for Creation of High-Efficiency Biotechnological Preparations. Nanotechnology in the Life Sciences, 259-287. https://doi.org/10.1007/978-3-030-17061-5_11

Kurdish, I. K., Roy, A. A., & Skoroсhod, I. A. (2021). Efficiency of the Complex Bacterial Preparation Azogran Application in Protecting Potatoes from the Colorado Potato Beetle Depending on the Stage of its Development. Mikrobiolohichnyi Zhurnal, 83(1), 3-11. https://doi.org/10.15407/microbiolj83.01.003

Kurdish, I. K. (2010). Introduction of microorganisms into agroecosystems. Scientific opinion.

Kurdish, I. K., Bega, Z. T. (2006). Strain of bacteria Azotobacter vinelandii for bacterial fertilizer obtaining for plant-growing. UA Patent 72856.

Kuske, C. R., Barns, S. M., & Busch, J. D. (1997). Diverse uncultivated bacterial groups from soils of the arid southwestern United States that are present in many geographic regions. Applied and Environmental Microbiology, 63(9), 3614-3621. https://doi.org/10.1128/aem.63.9.3614-3621.1997

Lichtenthaler, H. K. & Buschmann, C. (2001). Chlorophylls and Carotenoids: Measurement and Characterization by UV-VIS Spectroscopy. Current Protocols in Food Analytical Chemistry, 1(1). https://doi.org/10.1002/0471142913.faf0403s01

Maurya, S., & Singh, D. K. (2010). Quantitative analysis of total phenolic content in Adhatoda vasica Nees extracts. International Journal of PharmTech Research, 2, 2403-2406.

Pogorelova, V. V., Bega Z. T., Kurdish, I. K. (2012). Interrelations of Infusoria with Azotobacter and their Influence on Plants. Mikrobiolohichnyi Zhurnal, 74(5), 48-54.

Roy, A. A., Pasychnyk, L. A., Khodos, S. F., Kurdish I. K. (2012). The effect of bacteria of the genus Bacillus on the causative agents of bacterial cancer of tomatoes. Mikrobiolohichnyi Zhurnal, 74(5), 74-80.

Rubenchik, L. I. (1960). Azotobacter and its application in agriculture. Academy of Science published USSR.

Sasse, J., Martinoia, E., & Northen, T. (2018). Feed Your Friends: Do Plant Exudates Shape the Root Microbiome? Trends in Plant Science, 23(1), 25-41. https://doi.org/10.1016/j.tplants.2017.09.003

Seitz, V. A., McGivern, B. B., Daly, R. A., Chaparro, J. M., Borton, M. A., Sheflin, A. M., Kresovich, S., Shields, L., Schipanski, M. E., Wrighton, K. C., & Prenni, J. E. (2022). Variation in Root Exudate Composition Influences Soil Microbiome Membership and Function. Applied and Environmental Microbiology, 88(11). https://doi.org/10.1128/aem.00226-22

Shaposhnikov, A. I., Shakhnazarova, V. Y., Vishnevskaya, N. A., Borodina, E. V., & Strunnikova, O. K. (2020). Aromatic carboxylic acids of barley root exudates and their effect on the growth of Fusarium culmorum and Pseudomonas fluorescens. Applied Biochemistry and Microbiology, 56(3), 292-300. https://doi.org/10.1134/S0003683820030138

The Rhizosphere. (2007). Elsevier.

Varbanets, L. D., Zdorovenko, G. M., Кnirel, Yu. A. (2006). Меthods of endotoxin investigations. Naukova dumka.

Volkogon, V. V., Nadkrenichna, O. V., Kovalevska, T. M. (2006). Microbial preparations in agriculture: Theory and practice. Agrarian Science.

Wiesenbauer, J., König, A., Gorka, S., Marchand, L., Nunan, N., Kitzler, B., Inselsbacher, E., & Kaiser, C. (2024). A pulse of simulated root exudation alters the composition and temporal dynamics of microbial metabolites in its immediate vicinity. Soil Biology and Biochemistry, 189, 109259. https://doi.org/10.1016/j.soilbio.2023.109259

Wilson, K. J. (1995). Molecular techniques for the study of rhizobial ecology in the field. Soil Biology and Biochemistry, 27(4-5), 501-514. https://doi.org/10.1016/0038-0717(95)98625-X

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Published

2024-10-31

How to Cite

Kurdish, I., Chobotarov, A., Brovarska, O., Parkhomenko, N., & Chobotarova, V. (2024). The Influence of Azotobacter vinelandii IMV B-7076 on the Buckwheat Development and Exometabolite Composition in the Root Zone. Mikrobiolohichnyi Zhurnal, 86(5), 39-46. https://doi.org/10.15407/microbiolj86.05.039