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

机译:来自海洋蓝磷酸杆菌梭菌SP的生物聚磷酸纳米粒子。 PCC 7002:体外生产,表征和抗炎性能

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摘要

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 Synechococcus sp. PCC 7002 as nano-sized granules. The maximum accumulation of polyphosphates in Synechococcus 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 Synechococcus sp. PCC 7002 to produce BPNPs, an anti-inflammatory postbiotic.
机译:益生菌衍生的多磷酸盐吸引了潜在治疗剂以改善肠道健康的兴趣。目前的研究发现了海洋青杆菌梭菌SP中多磷酸盐的细胞内积累。 PCC 7002作为纳米尺寸颗粒。同系Cococcus sp中多磷酸盐的最大积累。当培养基含有0.74mm的KH2PO4,11.76mm纳米3和30.42mna4的Na 2 SO 4时,PCC 7002发现在晚期对数生长阶段。通过热水萃取完好地从藻类细胞完善生物磷酸纳米颗粒(BPNP),并通过Sephadex G-100凝胶过滤纯化以除去有机杂质。通过使用100kDa超滤,将BPNP分离成较大且小的群体,直径分别在30-70nm和10-30nm之间。 4',6-二氨基-2-苯基吲哚荧光和正磷酸盐的产生表明,在模拟的胃肠生物消化期间,BPNPS(约14-18%)的次要部分降解。使用脂多糖激活的Raw264.7细胞的体外研究表明,BPNPS抑制环氧氧酶-2,诱导型一氧化氮(NO)合成酶表达,以及促炎介质的产生,包括NO,肿瘤坏死因子-α,白细胞介素-6和白细胞介素-1β通过抑制Toll样受体4 / NF-κB信号通路。总体而言,在使用海洋角蓝的肌肉杆菌SP时存在承诺。 PCC 7002生产BPNPS,一种抗炎后生物植酸酶。

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