Drehval O. A., Lesychna A. V., Drehval I. V., Sklyar T. V.
INFLUENCE OF CARBON AND NITROGEN SOURCES ON BIOMASS YIELD AND FUNGISTATIC ACTIVITY OF TRICHODERMA VIRIDE KMB-F-15
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About the author:
Drehval O. A., Lesychna A. V., Drehval I. V., Sklyar T. V.
Heading:
MICROBIOLOGY
Type of article:
Scientific article
Annotation:
Micromycetes of the Trichoderma genus are the most common biological agents used in agriculture today to control plant mycoses. Using biological products allows us to produce environmentally friendly agricultural products and reduce the chemical burden on the environment. When choosing carbon and nitrogen sources as a basic base for developing the optimal composition of the nutrient medium for deep cultivation of microorganisms, it is necessary to consider their genus and strain characteristics. In this study, we investigated the effect of carbon and nitrogen sources on the biomass accumulation and fungistatic activity of Trichoderma viride strain KMB-F-15, an antagonist of a wide range of phytopathogenic fungi. The fungistatic activity was determined by inhibition of growth of the phytopathogenic fungus Fusarium culmorum IMBF-50716 when the filtrate of T. viride KMB-F-1 culture fluid was added to the dense medium. It was found that glycerol and green molasses at a concentration of 20 g/l resulted in the highest yield of dry biomass of T. viride KMB-F-15 (5.0 g/l and 4.9 g/l, respectively). The most favourable nitrogen sources for the fungus growth at a concentration of 5 g/l were yeast autolysate (dry biomass yield – 4.4 g/l) and ammonium chloride (3.3 g/l). The fungistatic activity of T. viride KMB-F-15, regardless of the carbon source, was high (94.7-100%). The manifestation of fungistatic activity was influenced by the source of nitrogen nutrition. The highest percentage of growth inhibition of the phytopathogen was observed when corn extract, yeast autolysate, L-glutamic acid, ammonium chloride or ammonium sulfate were used (88.5-100%).
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Bibliography:
- Rozhkova TO, Bilyavsʹka LO. Antahonistychna aktyvnistʹ hrybiv Gliocladium sp. v umovakh in vitro. Silʹsʹkohospodarsʹka mikrobiolohiya. 2022;36:55-63. [in Ukrainian].
- Singh A, Shukla N, Kabadwal BC, Tewari AK, Kumar J. Review on plant-Trichoderma-pathogen interaction. Int. J. Curr. Microbiol. App. Sci. 2018;7(2):2382-2397.
- Savchuk YI, Yurieva OM, Syrchin SO, Naconechna LT, Tuhai TI, Tuhai AV, et al. Trichoderma strains – antagonists of plant pathogenic micromycetes. Microbiol. journ. 2022;84(1):24-38.
- Asad SA, Ali N, Hameed A, Khan SA, Ahmad R, Bilal M, et al. Biocontrol efficacy of different isolates of Trichoderma against soil borne pathogen Rhizoctonia solani. Polish Journal of Microbiology. 2014;63(1):95-103.
- Hao D, Lang B, Wang Y, Wang X, Liu T, Chen J. Designing synthetic consortia of Trichoderma strains that improve antagonistic activities against pathogens and cucumber seedling growth. Microbial Cell Factories. 2022;21:234.
- Oszust K, Pylak M, Frac M. Trichoderma-based biopreparation with prebiotics supplementation for the naturalization of raspberry plant rhizosphere. Int J Mol Sci. 2021;22:6356.
- Ruocco M, Lanzuise S, Lombardi N, Woo SL, Vinale F, Marra R, et al. Multiple roles and effects of a novel Trichoderma hydrophobin. Mol Plant Microbe Interact. 2015;28(2):167-79.
- Galindo M, Rueda D, Romero P, Medina M, Bangeppagari M, Gangireddygari VSR, et al. Evaluation of the interaction of arbuscular mycorrhizal fungi and Trichoderma harzianum in the development and nutrition of potato plants (Solanum phureja). Asian J Agri &Biol. 2018;6(3):403-416.
- Pavlenko AA, Kopylov YP, Tsekhmister HV. Efektyvnistʹ zastosuvannya shtamu Trichoderma viride z vysokoyu antahonistychnoyu ta tselyulozolitychnoyu aktyvnistyu. Silʹsʹkohospodarsʹka mikrobiolohiya. 2021;33:88-95. [in Ukrainian].
- Rayhane H, Josiane M, Gregoria M, Yiannis K, Nathalie D, Ahmed M. From flasks to single used bioreactor: Scale-up of solid state fermentation process for metabolites and conidia production by Trichoderma asperellum. Journal of environmental management. 2019;252:109496.
- Locatelli OL, Pimentel MF, Bueno LA, Lobo Junior, Mascarin GM, Finkler CL. Production of microsclerotia by Trichoderma asperellum through submerged liquid fermentation using low-cost nitrogen and carbon sources. Biocatalysis and Agricultural Biotechnology. 2022;44:102455.
- Senkovs M, Dzierkale MT, Rimkus A, Grigs O, Nikolajeva V. Application of a posttreatment to improve the viability and antifungal activity of Trichoderma asperellum biomass obtained in a bioreactor during submerged cultivation. Biology. 2022;11(11):1610.
- Rimkus A, Namina A, Dzierkale MT, Grigs O, Senkovs M, Larsson S. Impact of growth conditions on the viability of Trichoderma asperellum during storage. Microorganisms. 2023;11(4):1084.
- Li Y, Song K, Li Y, Chen J. Statistical culture-based strategies to enhance chlamydospore production by Trichoderma harzianum SH2303 in liquid fermentation. J Zhejiang Univ-Sci B (Biomed & Biotechnol). 2016;17(8):619-627.
- Yeremenko AO, Drehval OA, Cherevach NV, Vinnikov AI. Antahonistychna aktivnistˊ gruntovykh. Microbiolohiya I biotekhnolohiya. 2017;1:73-84. [in Ukrainian].
- Onilude AA, Adebayo-Tayo BC, Odeniyi AO, Banjo D, Garuba EO. Comparative mycelial and spore yield by Trichoderma viride in batch and fed-batch cultures. Ann Microbiol. 2013;63:547-553.
- Rossi-Rodrigues BC, Brochetto-Braga MR, Tauk-Tornisielo SM, Carmona EC, Arruda VM, Netto JC. Comparative growth of Trichoderma strain in different nutrional sources, using bioscreen automated system. Brazilian Journal of Microbiology. 2009;40:404-410.
- Sriram S, Roopa KP, Savitha MJ. Extended shelf-life of liquid fermentation derived talc formulations of Trichoderma harzianum with the addition of glycerol in the production medium. Crop Protection. 2011;30(10):1334-1339.
Publication of the article:
«Bulletin of problems biology and medicine», 2024 Issue 1, 172, 363-371 pages, index UDC 579.264 +579.64