Programa de Pós-Graduação em Bioquímica e Bioprospecção - Laboratório de Neuroquímica, Inflamação e Câncer, Campus Capão do Leão s/n, Universidade Federal de Pelotas, Pelotas, RS, Brazil.
Embrapa Agroindústria Tropical, Fortaleza, CE, Brazil.
Appl Biochem Biotechnol. 2023 Jul;195(7):4011-4035. doi: 10.1007/s12010-023-04328-w. Epub 2023 Jan 18.
Endophytic fungi are important sources of anticancer compounds. An endophytic fungus was isolated from the medicinal plant Achyrocline satureioides, and molecularly identified as Biscogniauxia sp. (family Xylariaceae) based on partial nucleotide sequences of the internal transcribed spacer genomic region (GenBank Accession No. ON257911). The chemical characterization and cytotoxic properties of secondary metabolites produced by Biscogniauxia sp. were evaluated in a human melanoma cell line (A375). The fungus was grown in potato-dextrose liquid medium for 25 days, and the extracted compounds were subjected to solid-phase fractionation to obtain the purified F fraction, for which the metabolites were elucidated via ultra-performance chromatography coupled to a mass spectrometer. In the present study, 17 secondary metabolites of Biscogniauxia sp., including nine polyketide derivatives, five terpenoids, and three isocoumarins, were putatively identified. This is the first study to report of the ability of Biscogniauxia sp. in the production of isocoumarin orthosporin; the terpenoids nigriterpene A and 10-xylariterpenoid; the polyketide derivatives daldinin C, 7'dechloro-5'-hydroxygriseofulvin, daldinone D, Sch-642305, curtachalasin A, cytochalasin E, epoxycytochalasins Z8, Z8 isomer, and Z17. Furthermore, this study has reported the biosynthesis of Sch-642305 by a Xylariaceae fungus for the first time. F significantly reduced the viability and proliferation of human melanoma cells at half-maximal inhibitory concentrations of 10.34 and 6.89 µg/mL, respectively, and induced late apoptosis/necrosis and cell cycle arrest in G2/M phase after 72 h of treatment. Given its ability to produce unique metabolites with promising cytotoxic effects, Biscogniauxia sp. of A. satureioides may be a reservoir of compounds with important therapeutic applications.
内生真菌是抗癌化合物的重要来源。从药用植物 Achyrocline satureioides 中分离出一株内生真菌,并根据内部转录间隔区基因组区域(GenBank 注册号 ON257911)的部分核苷酸序列,通过分子鉴定为 Biscogniauxia sp.(木霉科)。Biscogniauxia sp. 产生的次生代谢产物的化学特征和细胞毒性在人黑色素瘤细胞系(A375)中进行了评估。该真菌在土豆-葡萄糖液体培养基中培养 25 天,提取的化合物经过固相分级得到纯化的 F 级分,通过超高效色谱与质谱联用对代谢产物进行了阐明。在本研究中,鉴定了 17 种 Biscogniauxia sp. 的次生代谢产物,包括 9 种聚酮衍生物、5 种萜类化合物和 3 种异香豆素。这是首次报道 Biscogniauxia sp. 能够产生异香豆素 orthosporin;萜类化合物 nigriterpene A 和 10-xylariterpenoid;聚酮衍生物 daldinin C、7'-去氯-5'-羟基灰黄霉素、daldinone D、Sch-642305、curtachalasin A、细胞松弛素 E、环氧化物细胞松弛素 Z8、Z8 异构体和 Z17。此外,本研究首次报道了 Xylariaceae 真菌生物合成 Sch-642305。F 级分在半抑制浓度分别为 10.34 和 6.89 µg/mL 时显著降低人黑色素瘤细胞的活力和增殖,并在 72 h 处理后诱导晚期细胞凋亡/坏死和细胞周期停滞在 G2/M 期。鉴于其产生具有潜在细胞毒性作用的独特代谢产物的能力,A. satureioides 的 Biscogniauxia sp. 可能是具有重要治疗应用化合物的潜在来源。