Qi Mingxing, Yan Shuqiang, Cui Yukun, Huang Yanan, Liu Yang, Wu Wenhui, Yu Xi, Wang Peipei
College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China.
College of Oceanography and Ecological Science, Shanghai Ocean University, Shanghai 201306, China.
Mar Drugs. 2025 Aug 12;23(8):326. doi: 10.3390/md23080326.
Microbial exopolysaccharides from extreme environments are increasingly becoming valuable candidates for drug development. In this study, four fractions named XL-1, XMRS-1, XL-1-D, and XMRS-1-D were isolated and purified from the hadal bacterium by column chromatography. The structural features of these fractions were characterized by molecular weight, monosaccharide composition, Fourier transform infrared (FTIR) spectrum, amino acid analysis and NMR. The results showed that XL-1 and XMRS-1 were mainly composed of mannose, glucose, and glucosamine, while XL-1-D and XMRS-1-D were mainly composed of mannose. In vitro bioactivity assays demonstrated that all four fractions significantly enhanced RAW264.7 macrophage proliferation and phagocytosis, stimulated nitric oxide (NO) and reactive oxygen species (ROS) production, and induced the secretion of interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), and the expression of inducible nitric oxide synthase (iNOS) mRNA. Moreover, plate cloning tests, cell scratch tests, and apoptosis assays, along with RT-qPCR analysis, demonstrated that the four fractions significantly inhibited A549 cells' proliferation. Specifically, XMRS-1 and XMRS-1-D upregulated Bax, Caspase-3, Caspase-8, and Caspase-9, while downregulating Bcl-2, suggesting transcriptional activation of apoptosis-related pathways. These results offered a reference for the further development and utilization of this hadal bacterium in the future.
来自极端环境的微生物胞外多糖正日益成为药物开发的宝贵候选物。在本研究中,通过柱色谱法从超深渊细菌中分离并纯化出四个组分,分别命名为XL-1、XMRS-1、XL-1-D和XMRS-1-D。通过分子量、单糖组成、傅里叶变换红外(FTIR)光谱、氨基酸分析和核磁共振对这些组分的结构特征进行了表征。结果表明,XL-1和XMRS-1主要由甘露糖、葡萄糖和氨基葡萄糖组成,而XL-1-D和XMRS-1-D主要由甘露糖组成。体外生物活性测定表明,所有四个组分均显著增强RAW264.7巨噬细胞的增殖和吞噬作用,刺激一氧化氮(NO)和活性氧(ROS)的产生,并诱导白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)的分泌以及诱导型一氧化氮合酶(iNOS)mRNA的表达。此外,平板克隆试验、细胞划痕试验和凋亡检测以及RT-qPCR分析表明,这四个组分显著抑制A549细胞的增殖。具体而言,XMRS-1和XMRS-1-D上调Bax、Caspase-3、Caspase-8和Caspase-9,同时下调Bcl-2,提示凋亡相关途径的转录激活。这些结果为今后进一步开发和利用这种超深渊细菌提供了参考。
Biomolecules. 2024-9-16