Valencia-Revelo Daniela, Charria-Girón Esteban, Schmidt Katharina, Reinecke Silke, Vasco-Palacios Aida M, Stradal Theresia, Marin-Felix Yasmina, Caicedo-Ortega Nelson H, Ebada Sherif S
Department Microbial Drugs, Helmholtz Centre for Infection Research (HZI), Inhoffenstrasse 7, 38124, Braunschweig, Germany.
Departamento de Ciencias Biológicas, Bioprocesos y Biotecnología. Facultad de Ingeniería, Diseño y Ciencias Aplicadas, Universidad Icesi, Calle 18 No. 122-135, Cali, Colombia.
BMC Biotechnol. 2025 Jul 1;25(1):57. doi: 10.1186/s12896-025-00978-2.
Fungal species of the order Xylariales, particularly those from tropical and untapped areas like the Amazon region, denote an intriguing reservoir of biodiversity and chemically varied metabolites. Based on this potential and by implementing the One Strain Many Compounds (OSMAC) approach, herein we have cultivated a Colombian Xylaria strain in several liquid, solid or semi-solid media, under different nutrient compositions and culture conditions. Metabolomic studies of Xylaria sp. CM-UDEA-H199 across these conditions led to the isolation of diverse metabolites. Six compounds were purified from rice (BRFT) cultures, identified as griseofulvin (1), xylaropyrones B/C (2/3), akolitserin (4), hypoxylin A (5), and (-)-(R)-5-(methoxycarbonyl)mellein (6). Three compounds were isolated from liquid YM cultivation: 2-hexylidene-3-methylsuccinic acid (7), its 4-methyl ester (8), and akoenic acid (9). Notably, cultivation in the newly designed semi-solid (S-BRFT) medium significantly altered the metabolome, leading to the predominant production of cytochalasins, with five derivatives (10-14) purified and structurally characterized.Among the isolated cytochalasins, compound 12 was identified as a previously undescribed natural diepoxy derivative of cytochalasin D. Structure elucidation of all isolated compounds was achieved based on their MS and comprehensive 1D/2D NMR analyses in addition to comparisons with the reported literature. Compounds 4-6, 10 and 11 revealed mild antifungal activity, while compounds (1, 5, 6, 8, 10, 11, 13 and 14) exhibited cytotoxic activity, with hypoxylin A (5) being the most potent, displaying IC values in the nanomolar range. In cellulo studies revealed that the epimerization at C-5 of cytochalasin D (10) backbone, as in hypoxylin A (5), neither affected its activity nor reversibility on actin dynamics. However, the epoxylated variant of 10, cytochalasin R (14), enhanced actin activity accompanied by reduced cytotoxicity compared to 5 and 10. The occurrence of diverse epoxy-substituted cytochalasins suggests that specific biosynthetic enzymes were activated in response to the applied fermentation conditions. These findings provide a basis for further bioprocess optimization strategies aimed at enhancing cytochalasan production, a chemical class recognized for its promising bioactivities in recent decades.
炭角菌目真菌物种,尤其是来自热带和未开发地区(如亚马逊地区)的那些真菌,是一个具有迷人生物多样性和化学结构多样代谢产物的宝库。基于这种潜力并通过实施“一株多化合物”(OSMAC)方法,我们在此在几种液体、固体或半固体培养基中,在不同营养成分和培养条件下培养了一株哥伦比亚炭角菌菌株。对炭角菌属CM-UDEA-H199在这些条件下进行的代谢组学研究导致分离出多种代谢产物。从大米(BRFT)培养物中纯化出六种化合物,鉴定为灰黄霉素(1)、炭角菌吡喃酮B/C(2/3)、阿科利色林(4)、异阿地菌素A(5)和(-)-(R)-5-(甲氧基羰基)蜜环菌酸(6)。从液体YM培养物中分离出三种化合物:2-亚己基-3-甲基琥珀酸(7)、其4-甲酯(8)和阿科烯酸(9)。值得注意的是,在新设计的半固体(S-BRFT)培养基中培养显著改变了代谢组,导致主要产生细胞松弛素,纯化并表征了五种衍生物(10-14)。在分离出的细胞松弛素中,化合物12被鉴定为细胞松弛素D的一种先前未描述的天然双环氧衍生物。除了与已报道文献进行比较外,所有分离化合物的结构解析均基于其质谱和全面的一维/二维核磁共振分析。化合物4-6、10和11显示出轻微的抗真菌活性,而化合物(1、5、6、8、10、11、13和14)表现出细胞毒性活性,其中异阿地菌素A(5)最有效,其IC值在纳摩尔范围内。细胞内研究表明,细胞松弛素D(10)主链C-5处的差向异构化,如在异阿地菌素A(5)中,既不影响其活性,也不影响其对肌动蛋白动力学的可逆性。然而,10的环氧化变体细胞松弛素R(14)与5和10相比,增强了肌动蛋白活性并降低了细胞毒性。多种环氧取代的细胞松弛素的出现表明,特定的生物合成酶响应所应用的发酵条件而被激活。这些发现为进一步优化生物工艺策略提供了基础,旨在提高细胞松弛素的产量,细胞松弛素是近几十年来因其具有前景的生物活性而被认可的一类化学物质。