Department of Biotechnology and Food Microbiology, Wroclaw University of Environmental and Life Sciences, Wrocław, Poland.
Environ Sci Pollut Res Int. 2024 Nov;31(51):60869-60879. doi: 10.1007/s11356-024-35251-0. Epub 2024 Oct 12.
The use of Trichoderma filamentous fungi in the wide concept of biocontrol is still a highly relevant topic. The multifaceted nature of their impact on phytopathogenic microorganisms results from the species diversity and complexity of their antagonistic action. The presented research aimed to determine optimal cultivation conditions of two T. citrinoviride strains for the biosynthesis of major enzymes especially those involved in the biocontrol process. Culture conditions were optimized using a three-factor Box-Behnken design to maximize the yield of chitinase and lichenase. The following independent variables were included in the model: incubation temperature, initial pH, and supplementation with fungal biomass. As a result of statistical optimization, unprecedented activities of extracellular lytic enzyme were achieved. For the B1 and B3 strains, the optimal pH was 3.5 or 7.5, respectively, in the determination of chitinase biosynthesis. It was similar for the biosynthesis of β-1.3 and β-1.4 glucanases, but at higher cultivation temperature. The exception was the B3 strain, for which the optimal pH in glucanase biosynthesis was 5.5. The most stimulating culture temperature in the process of chitinase biosynthesis and β-1.3 and β-1.4 glucanases was above 25 °C. In that, the levels of enzyme biosynthesis and corresponding composition culture environment were confirmed to be strain-dependent.
在广义的生物防治中使用丝状真菌 Trichoderma 仍然是一个高度相关的话题。它们对植物病原微生物的多方面影响源于其物种多样性和拮抗作用的复杂性。本研究旨在确定两种 T. citrinoviride 菌株的最佳培养条件,以生物合成主要酶,特别是参与生物防治过程的酶。使用三因素 Box-Behnken 设计优化培养条件,以最大限度地提高几丁质酶和几丁质酶的产量。该模型包括以下独立变量:培养温度、初始 pH 值和真菌生物量的补充。通过统计优化,获得了前所未有的细胞外溶菌酶活性。对于 B1 和 B3 菌株,在确定几丁质酶生物合成时,最佳 pH 值分别为 3.5 或 7.5。β-1.3 和 β-1.4 葡聚糖酶生物合成也是如此,但培养温度更高。B3 菌株是个例外,其在葡聚糖酶生物合成中的最佳 pH 值为 5.5。在几丁质酶生物合成和 β-1.3 和 β-1.4 葡聚糖酶过程中最具刺激性的培养温度高于 25°C。在这一点上,酶生物合成和相应的培养环境的水平被证实是菌株依赖性的。