Collaborative Innovation Center of Ecological Civilization, School of Chemistry and Chemical Engineering, Hainan University, Haikou 570228, China.
Mar Drugs. 2024 Feb 23;22(3):102. doi: 10.3390/md22030102.
The co-culture strategy, which mimics natural ecology by constructing an artificial microbial community, is a useful tool for the activation of biosynthetic gene clusters (BGCs) to generate new metabolites, as well as to increase the yield of respective target metabolites. As part of our project aiming at the discovery of structurally novel and biologically active natural products from mangrove endophytic fungi, we selected the co-culture of a strain of DHS-48 with another genus fungus DHS-11, both endophyted in mangrove considering the impart of the taxonomic criteria and ecological data. The competition interaction of the two strains was investigated through morphology observation and scanning electron microscopy (SEM), and it was found that the mycelia of the DHS-48 and DHS-11 compacted and tangled with each other with an interwoven pattern in the co-culture system. A new approach that integrates HPLC chromatogram, HNMR spectroscopy, UPLC-MS-PCA, and molecular networking enabled the targeted isolation of the induced metabolites, including three new dimeric xanthones phomoxanthones L-N (-), along with six known analogs (-). Their planar structures were elucidated by an analysis of their HRMS, MS/MS, and NMR spectroscopic data and the absolute configurations based on ECD calculations. These metabolites showed broad cytotoxic activity against the cancer cells assessed, of which compounds - displayed significant cytotoxicity towards human liver cells HepG-2 with IC values ranging from 4.83 μM to 12.06 μM. Compounds - exhibited weak immunosuppressive activity against the proliferation of ConA-induced (T-cell) and LPS-induced (B-cell) murine splenic lymphocytes. Therefore, combining co-cultivation with a metabolomics-guided strategy as a discovery tool will be implemented as a systematic strategy for the quick discovery of target bioactive compounds.
共培养策略通过构建人工微生物群落来模拟自然生态,是激活生物合成基因簇(BGCs)以产生新代谢物以及提高目标代谢物产量的有用工具。在我们从红树林内生真菌中发现结构新颖和具有生物活性的天然产物的项目中,我们选择了 DHS-48 菌株与另一种内生真菌 DHS-11 的共培养,这是基于分类标准和生态数据的考虑。通过形态观察和扫描电子显微镜(SEM)研究了两株菌的竞争相互作用,发现 DHS-48 和 DHS-11 的菌丝在共培养系统中相互缠绕,交织在一起。一种整合 HPLC 色谱、HNMR 光谱、UPLC-MS-PCA 和分子网络的新方法,使诱导代谢物的靶向分离成为可能,包括三种新的二聚体蒽酮 phomoxanthones L-N (-),以及六种已知类似物 (-)。通过分析其高分辨质谱、MS/MS 和 NMR 光谱数据以及基于 ECD 计算的绝对构型,阐明了它们的平面结构。这些代谢产物对评估的癌细胞表现出广泛的细胞毒性活性,其中化合物 - 对人肝癌细胞 HepG-2 表现出显著的细胞毒性,IC 值范围为 4.83 μM 至 12.06 μM。化合物 - 对 ConA 诱导的(T 细胞)和 LPS 诱导的(B 细胞)小鼠脾淋巴细胞增殖表现出较弱的免疫抑制活性。因此,将共培养与代谢组学指导的策略相结合作为一种发现工具,将作为快速发现目标生物活性化合物的系统策略实施。