Mannan-Containing Polymers from Hadal Bacterium Psychrobacter pulmonis: Preparation, Structural Analysis, Immunological Activity and Antitumor Effects.

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL
Marine Drugs Pub Date : 2025-08-12 DOI:10.3390/md23080326
Mingxing Qi, Shuqiang Yan, Yukun Cui, Yanan Huang, Yang Liu, Wenhui Wu, Xi Yu, Peipei Wang
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Abstract

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 Psychrobacter pulmonis 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.

肺冷杆菌含甘露聚糖聚合物的制备、结构分析、免疫活性及抗肿瘤作用。
来自极端环境的微生物外多糖越来越成为药物开发的有价值的候选者。本研究采用柱层析法从肺冷杆菌中分离纯化了XL-1、XMRS-1、XL-1- d和XMRS-1- d四个组分。通过分子量、单糖组成、傅立叶红外光谱(FTIR)、氨基酸分析和核磁共振(NMR)表征了各组分的结构特征。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。体外生物活性实验表明,四组分均能显著增强RAW264.7巨噬细胞的增殖和吞噬能力,刺激一氧化氮(NO)和活性氧(ROS)的产生,诱导白细胞介素-6 (IL-6)、肿瘤坏死因子-α (TNF-α)的分泌和诱导型一氧化氮合酶(iNOS) mRNA的表达。此外,平板克隆实验、细胞划痕实验、细胞凋亡实验以及RT-qPCR分析表明,这四种组分均能显著抑制A549细胞的增殖。具体来说,XMRS-1和XMRS-1- d上调Bax、Caspase-3、Caspase-8和Caspase-9,下调Bcl-2,提示凋亡相关通路的转录激活。这些结果为该菌的进一步开发利用提供了参考。
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来源期刊
Marine Drugs
Marine Drugs 医学-医药化学
CiteScore
9.60
自引率
14.80%
发文量
671
审稿时长
1 months
期刊介绍: Marine Drugs (ISSN 1660-3397) publishes reviews, regular research papers and short notes on the research, development and production of drugs from the sea. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible, particularly synthetic procedures and characterization information for bioactive compounds. There is no restriction on the length of the experimental section.
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