UMR 152 Pharma Dev, Université de Toulouse, IRD, UPS, France; Laboratorios de Investigación y Desarrollo, Facultad de Ciencias y Filosofía, Universidad Peruana Cayetano Heredia, Lima, Peru.
UMR 152 Pharma Dev, Université de Toulouse, IRD, UPS, France.
Fungal Biol. 2022 May;126(5):385-394. doi: 10.1016/j.funbio.2022.02.005. Epub 2022 Mar 2.
Endophytic fungi are capable of producing a great diversity of bioactive metabolites. However, the presence of silent and lowly expressed genes represents a main challenge for the discovery of novel secondary metabolites with different potential uses. Epigenetic modifiers have shown to perturb the production of fungal metabolites through the induction of silent biosynthetic pathways leading to an enhanced chemical diversity. Moreover, the addition of bioprecursors to the culture medium has been described as a useful strategy to induce specific biosynthetic pathways. The aim of this study was to assess the effects of different chemical modulators on the metabolic profiles of an endophytic fungal strain of Cophinforma mamane (Botryosphaeriaceae), known to produce 3 thiodiketopiperazine (TDKP) alkaloids (botryosulfuranols A-C), previously isolated and characterized by our team. Four epigenetic modifiers, 5-azacytidine (AZA), sodium butyrate (SB), nicotinamide (NIC), homoserine lactone (HSL) as well as 2 amino acids, l-phenylalanine and l-tryptophan, as bioprecursors of TDKPs, were used. The metabolic profiles were analysed by UHPLC-HRMS/MS under an untargeted metabolomics approach. Our results show that the addition of the two amino acids in C. mamane culture and the treatment with AZA significantly reduced the production of the TDKPs botryosulfuranols A, B and C. Interestingly, the treatment with HSL significantly induced the production of different classes of diketopiperazines (DKPs). The treatment with AZA resulted as the most effective epigenetic modifier for the alteration of the secondary metabolite profile of C. mamane by promoting the expression of cryptic genes.
内生真菌能够产生多种多样的生物活性代谢物。然而,沉默和低表达基因的存在是发现具有不同潜在用途的新型次生代谢物的主要挑战。表观遗传修饰剂已被证明通过诱导沉默的生物合成途径来扰乱真菌代谢产物的产生,从而导致化学多样性增强。此外,向培养基中添加生物前体已被描述为诱导特定生物合成途径的有用策略。本研究旨在评估不同化学调节剂对内生真菌菌株 Cophinforma mamane(Botryosphaeriaceae)代谢谱的影响,该菌株已知可产生 3 种硫代二酮哌嗪(TDKP)生物碱(botryosulfuranols A-C),这些生物碱先前已被我们的团队分离和表征。使用了 4 种表观遗传修饰剂,即 5-氮杂胞苷(AZA)、丁酸钠(SB)、烟酰胺(NIC)、同型半胱氨酸内酯(HSL)以及 2 种氨基酸,L-苯丙氨酸和 L-色氨酸,作为 TDKP 的生物前体。采用 UHPLC-HRMS/MS 进行非靶向代谢组学分析。我们的结果表明,在 C. mamane 培养物中添加这两种氨基酸以及用 AZA 处理可显著降低 TDKP botryosulfuranols A、B 和 C 的产生。有趣的是,HSL 的处理显著诱导了不同类别的二酮哌嗪(DKP)的产生。AZA 的处理是改变 C. mamane 次生代谢物谱的最有效表观遗传修饰剂,它通过促进隐匿基因的表达来实现。