Patwal Tania, Baranwal Manoj
Department of Biotechnology, Thapar Institute of Engineering & Technology, Patiala, Punjab 147004 India.
3 Biotech. 2021 Apr;11(4):171. doi: 10.1007/s13205-021-02720-z. Epub 2021 Mar 18.
Exopolysaccharides (EPS) isolated from microalgae are promising immune cell proliferation agents, that could be potentially used as immunostimulants. In the current study, () was grown under varying nutrient (sulphur and phosphorus) concentrations to enhance the EPS production, and the isolated EPS were assessed for their effect on cell proliferation using peripheral blood mononuclear cells (PBMC). Five different concentrations of MgSO (0, 0.25, 0.5, 1.0 and 1.25 g/L) and KHPO (0, 0.2, 0.6, 0.8 and 1.0 g/L) were taken as compared to the normal culture conditions (0.75 g/L MgSO and 0.4 g/L KHPO) with the intention to enrich EPS secretion. LC-MS, FTIR and NMR analysis revealed that isolated EPS have the characteristic spectrum of hetero-polysaccharides (octa-saccharides). Immunostimulatory property of EPS was demonstrated by their ability to augment PBMC proliferation as measured by MTT assay. Further, increase in the glucose content and proliferative index was observed for EPS obtained under higher concentrations of MgSO (1 and 1.25 g/L) and KHPO (0.6 and 0.8 g/L) relative to normal culture conditions. Effects of the generated EPS under varying concentration of MgSO ( = 0.84-0.99) and KHPO ( = 0.76-0.97) remained strongly correlated with cell count, chlorophyll content, total biomass, glucose, proliferative index and its scavenging activity. Collectively, our data not only showed that EPS generated by under higher concentration of KHPO and MgSO possess improved immunostimulatory properties, but also provides convincing evidence towards nutritional optimization of alga for enhanced EPS production with better bioactivities.
The online version contains supplementary material available at 10.1007/s13205-021-02720-z.
从微藻中分离出的胞外多糖(EPS)是很有前景的免疫细胞增殖剂,有可能用作免疫刺激剂。在当前研究中,()在不同营养物质(硫和磷)浓度下培养以提高EPS产量,并使用外周血单核细胞(PBMC)评估分离出的EPS对细胞增殖的影响。与正常培养条件(0.75 g/L MgSO₄和0.4 g/L KH₂PO₄)相比,采用了五种不同浓度的MgSO₄(0、0.25、0.5、1.0和1.25 g/L)和KH₂PO₄(0、0.2、0.6、0.8和1.0 g/L),目的是丰富EPS分泌。液相色谱 - 质谱联用(LC - MS)、傅里叶变换红外光谱(FTIR)和核磁共振(NMR)分析表明,分离出的EPS具有杂多糖(八糖)的特征光谱。通过MTT法测定,EPS增强PBMC增殖的能力证明了其免疫刺激特性。此外,相对于正常培养条件,在较高浓度的MgSO₄(1和1.25 g/L)和KH₂PO₄(0.6和0.8 g/L)下获得的EPS观察到葡萄糖含量和增殖指数增加。在不同浓度的MgSO₄(r = 0.84 - 0.99)和KH₂PO₄(r = 0.76 - 0.97)下产生的EPS的作用与细胞计数、叶绿素含量、总生物量、葡萄糖、增殖指数及其清除活性仍密切相关。总体而言,我们的数据不仅表明在较高浓度的KH₂PO₄和MgSO₄下由()产生的EPS具有改善的免疫刺激特性,而且还为藻类营养优化以提高EPS产量和更好的生物活性提供了令人信服的证据。
在线版本包含可在10.1007/s13205 - 021 - 02720 - z获取的补充材料。