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海洋蓝细菌 sp. PCC 7002 来源的生物合成多聚磷酸盐纳米颗粒:生产、表征和体外抗炎特性。

Biogenic Polyphosphate Nanoparticles from a Marine Cyanobacterium sp. PCC 7002: Production, Characterization, and Anti-Inflammatory Properties In Vitro.

机构信息

College of Food Science and Engineering, Ocean University of China, 5 Yushan Road, Qingdao 266003, Shandong Province, China.

出版信息

Mar Drugs. 2018 Sep 10;16(9):322. doi: 10.3390/md16090322.

DOI:10.3390/md16090322
PMID:30201855
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6163655/
Abstract

Probiotic-derived polyphosphates have attracted interest as potential therapeutic agents to improve intestinal health. The current study discovered the intracellular accumulation of polyphosphates in a marine cyanobacterium sp. PCC 7002 as nano-sized granules. The maximum accumulation of polyphosphates in sp. PCC 7002 was found at the late logarithmic growth phase when the medium contained 0.74 mM of KH₂PO₄, 11.76 mM of NaNO₃, and 30.42 mM of Na₂SO₄. Biogenic polyphosphate nanoparticles (BPNPs) were obtained intact from the algae cells by hot water extraction, and were purified to remove the organic impurities by Sephadex G-100 gel filtration. By using 100 kDa ultrafiltration, BPNPs were fractionated into the larger and smaller populations with diameters ranging between 30⁻70 nm and 10⁻30 nm, respectively. 4',6-diamidino-2-phenylindole fluorescence and orthophosphate production revealed that a minor portion of BPNPs (about 14⁻18%) were degraded during simulated gastrointestinal digestion. In vitro studies using lipopolysaccharide-activated RAW264.7 cells showed that BPNPs inhibited cyclooxygenase-2, inducible nitric oxide (NO) synthase expression, and the production of proinflammatory mediators, including NO, tumor necrosis factor-α, interleukin-6, and interleukin-1β through suppressing the Toll-like receptor 4/NF-κB signaling pathway. Overall, there is promise in the use of the marine cyanobacterium sp. PCC 7002 to produce BPNPs, an anti-inflammatory postbiotic.

摘要

聚磷酸盐衍生自益生菌,因其作为改善肠道健康的潜在治疗剂而受到关注。本研究发现海洋蓝藻 sp. PCC 7002 中的聚磷酸盐以纳米级颗粒的形式在细胞内积累。在含有 0.74 mM KH₂PO₄、11.76 mM NaNO₃和 30.42 mM Na₂SO₄的培养基中,sp. PCC 7002 在对数生长后期达到聚磷酸盐的最大积累量。通过热水提取从藻类细胞中完整获得生物源聚磷酸盐纳米颗粒(BPNPs),并通过 Sephadex G-100 凝胶过滤纯化以去除有机杂质。通过使用 100 kDa 超滤,BPNPs 被分为直径分别在 30⁻70nm 和 10⁻30nm 之间的较大和较小群体。4',6-二脒基-2-苯基吲哚荧光和正磷酸盐生成表明,BPNPs 在模拟胃肠道消化过程中仅有一小部分(约 14⁻18%)被降解。用脂多糖激活的 RAW264.7 细胞进行的体外研究表明,BPNPs 通过抑制 Toll 样受体 4/NF-κB 信号通路,抑制环氧合酶-2、诱导型一氧化氮(NO)合酶的表达以及促炎介质(包括 NO、肿瘤坏死因子-α、白细胞介素-6 和白细胞介素-1β)的产生,发挥抗炎作用。总的来说,利用海洋蓝藻 sp. PCC 7002 生产抗炎后生元 BPNPs 具有一定的前景。

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