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- W4385308106 abstract "Many studies aim at maximizing fungal secondary metabolite production but the influence of light during cultivation has often been neglected. Here, we combined an untargeted isotope-assisted liquid chromatography–high-resolution mass spectrometry-based metabolomics approach with standardized cultivation of Trichoderma atroviride under three defined light regimes (darkness (PD), reduced light (RL) exposure, and 12/12 h light/dark cycle (LD)) to systematically determine the effect of light on secondary metabolite production. Comparative analyses revealed a similar metabolite profile upon cultivation in PD and RL, whereas LD treatment had an inhibiting effect on both the number and abundance of metabolites. Additionally, the spatial distribution of the detected metabolites for PD and RL was analyzed. From the more than 500 detected metabolites, only 25 were exclusively produced upon fungal growth in darkness and 85 were significantly more abundant in darkness. The majority were detected under both cultivation conditions and annotation revealed a cluster of substances whose production followed the pattern observed for the well-known T. atroviride metabolite 6-pentyl-alpha-pyrone. We conclude that cultivation of T. atroviride under RL can be used to maximize secondary metabolite production." @default.
- W4385308106 created "2023-07-28" @default.
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- W4385308106 date "2023-07-26" @default.
- W4385308106 modified "2023-10-18" @default.
- W4385308106 title "Light-Induced Changes in Secondary Metabolite Production of Trichoderma atroviride" @default.
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- W4385308106 doi "https://doi.org/10.3390/jof9080785" @default.
- W4385308106 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37623556" @default.
- W4385308106 hasPublicationYear "2023" @default.
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