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Optimization of Oligosaccharide Production from Leuconostoc lactis Using a Response Surface Methodology and the Immunostimulating Effects of These Oligosaccharides on Macrophage Cells

机译:利用响应表面方法优化乳酸乳球菌生产寡糖的能力以及这些寡糖对巨噬细胞的免疫刺激作用

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摘要

Production of oligosaccharides from Leuconostoc lactis CCK940 was optimized using a response surface methodology with a central composite design. Culture temperature and the concentrations of sucrose and maltose were used as the main factors. The predicted optimum conditions for the production of oligosaccharides were a culture temperature of 30 °C, a sucrose concentration of 9.6% (w/v), and a maltose concentration of 7.4% (w/v). Using these optimal conditions, Leuconostoc lactis CCK940 was cultured using a fermenter to produce oligosaccharides, and the resulting oligosaccharides with a degree of polymerization greater than 4 were purified by Bio-gel P2 gel permeation column chromatography and then lyophilized. When macrophages were treated with the purified oligosaccharides at concentrations of 0.1–10 mg/mL, no cytotoxicity towards the macrophages was observed. However, nitric oxide production levels were similar to those following treatment with 1 μg/mL lipopolysaccharide. The mRNA expression levels of tumor necrosis factor-α, interleukin-1β, interleukin-6, and inducible nitric oxide synthase were all also increased in a dose-dependent manner following treatment with the oligosaccharides. These data suggest that oligosaccharides produced by Leuconostoc lactis CCK940 could be used as an immune enhancer of macrophages.
机译:使用响应表面方法和中央复合设计优化了乳酸乳球菌CCK940的寡糖生产。培养温度以及蔗糖和麦芽糖的浓度是主要因素。预测的生产寡糖的最佳条件是培养温度为30°C,蔗糖浓度为9.6%(w / v),麦芽糖浓度为7.4%(w / v)。在这些最佳条件下,使用发酵罐培养乳酸乳球菌CCK940以产生寡糖,并且通过Bio-gel P2凝胶渗透柱色谱法纯化得到的聚合度大于4的寡糖,然后冻干。当用0.1-10 mg / mL的纯化寡糖处理巨噬细胞时,未观察到对巨噬细胞的细胞毒性。但是,一氧化氮的生产水平与1μg/ mL脂多糖处理后的水平相似。寡糖处理后,肿瘤坏死因子-α,白介素-1β,白介素-6和诱导型一氧化氮合酶的mRNA表达水平也均呈剂量依赖性增加。这些数据表明,乳酸乳球菌CCK940产生的寡糖可以用作巨噬细胞的免疫增强剂。

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