Le Loarer Alexandre, Marcourt Laurence, Marcellin-Gros Rémy, Dufossé Laurent, Ramesh Chatragadda, Anwesh Maile, Bignon Jérome, Frédérich Michel, Ledoux Allison, Ferreira Queiroz Emerson, Wolfender Jean-Luc, Fouillaud Mireille, Gauvin-Bialecki Anne
Laboratory of Chemistry and Biotechnology of Natural Products, Faculty of Science and Technology, University of La Réunion, 15 Avenue René Cassin, CS 92003, CEDEX 09, 97744 Saint-Denis, France.
Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, CMU-Rue Michel-Servet 1, CH-1211 Geneva, Switzerland.
Microorganisms. 2025 Sep 2;13(9):2045. doi: 10.3390/microorganisms13092045.
The study of various microorganisms isolated from an Indian Ocean sponge, ML-263, led to the selection of a promising Actinobacteria strain, sp. SH-82. Genomic analysis identified this strain as a new species, revealing the presence of 23 biosynthetic gene clusters (BGCs), some of which are associated with the synthesis of specialized metabolites such as polyketides deriving from polyketide synthases (PKSs). The strain was cultivated under favorable conditions for the production of bioactive molecules, resulting in the isolation and identification of seven microbial metabolites. Three of them are potentially novel, two erythronolides and one erythromycin, all characterized by a rare C10-C11 double bond. Some of these compounds also display atypical conformations, forming hemiacetals or spiroacetals. Their identification was achieved through detailed chemical analyses (NMR and ESI-HRMS). A molecular networking approach was employed to assess the presence of potentially novel molecules in the microbial crude extract, supported by the identification of isolated molecules. Four molecules (, , and ) were evaluated for their cytotoxic activities against cancer cell lines (HCT-116 and MDA-MB-231) and the immortalized retinal pigment epithelial RPE1 cells. No activity was observed in the latter, suggesting a lack of toxicity toward healthy cells. Moreover, megalomicin C1 (3), one of the isolated compounds, showed interesting antiplasmodial activity against 3D7, with an IC of 6.37 ± 2.99 µM.
对从印度洋海绵ML - 263中分离出的各种微生物进行的研究,促成了一种有潜力的放线菌菌株sp. SH - 82的筛选。基因组分析将该菌株鉴定为一个新物种,发现其存在23个生物合成基因簇(BGCs),其中一些与特殊代谢产物的合成相关,比如源自聚酮合酶(PKSs)的聚酮化合物。该菌株在有利于生物活性分子产生的条件下进行培养,从而分离并鉴定出7种微生物代谢产物。其中3种可能是新的,两种是红霉内酯,一种是红霉素,它们都具有罕见的C10 - C11双键。这些化合物中的一些还呈现出非典型构象,形成半缩醛或螺缩醛。通过详细的化学分析(核磁共振和电喷雾高分辨质谱)实现了对它们的鉴定。采用分子网络方法评估微生物粗提物中潜在新分子的存在情况,并得到了已分离分子鉴定结果的支持。对4种分子(、、和)针对癌细胞系(HCT - 116和MDA - MB - 231)以及永生化视网膜色素上皮RPE1细胞的细胞毒性活性进行了评估。在后者中未观察到活性,这表明对健康细胞没有毒性。此外,分离出的化合物之一巨球霉素C1(3)对3D7显示出有趣的抗疟活性,IC为6.37 ± 2.99 μM。